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379. Foreyt, W.J., L.G. Rickard, and W. Boyce, Psoroptes sp. in two
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381. Grubb, T.L., T.W. Riebold, and M.J. Huber, Evaluation of lidocaine,
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384. Houten, D.v., et al., Reference hematologic values and morphologic
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385. Hutchinson, J.M., Immunodeficiency in juvenile llamas. Large Animal
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386. Hutchison, J.M., et al., Immunodeficiency syndrome associated with
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387. Leichty, M.D. and I.A. Davis, Llama failure to thrive syndrome.
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392. Morin, D.E., et al., Hematological features of iron deficiency
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400. Ruck, R.J., Along came a llama. 1992: Weavers Press.
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402. Smith, B.B., K.I. Timm, and P.J. Reed, Morphometric evaluation of
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406. Weiser, M.G., et al., Characterization of erythrocytic indices and
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407. Wheeler, J.C., A.Y.F. Russel, and H.F. Stanley, A measure of loss:
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408. Barreto de Bonnemaison, L., Jose\0301 Rafael Pocaterra y "La Llama
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410. Black-Schultz, L.L., et al., Diaphragmatic hernia in a llama.
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411. Braga L, W., Corynebacterium pseudotuberculosis in abscesses of
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412. Bravo, P.W., et al., Ovarian and endocrine patterns associated with
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413. Burkhardt, J.E., et al., Septicemic Enterococcus infection in an
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414. Card, C.S., Report of the committee on infectious disease of
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416. David, M., et al., Further studies on foot-and-mouth disease in the
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418. Garnica, J., L. Chavez, and P.W. Bravo, Immunoglobulin G in mammary
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419. Giussani, D.A., et al., Rapid, intense peripheral vasoconstriction
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421. Grubb, T.L., T.W. Riebold, and M.J. Huber, Evaluation of lidocaine,
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422. Hildebrand, S.V. and T. Hill, Neuromuscular blockade by use of
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423. Hutchison, J.M., E.B. Belknap, and R.J. Williams, Acute renal
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424. John of the Cross, S., C.b. Cuevas GarcÃa, and S.L.d.a.v. John of
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427. Johnson, L.W., Infertility evaluation in llamas and alpacas. 1993,
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428. Kayouli, C., C. Dardillat, and J.P. Jouany, Comparative study of
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429. Kimberling, C.V., An overview of the drug needs and present lack of
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433. Morin, D.E., F.B. Garry, and M.G. Weiser, Hematologic responses in
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434. Nasta, J.D., Sin tocayos : historias reales de co\0301mo se llama
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438. Picton, R.A., Serologic survey of llamas in Oregon for antibodies
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439. Pugh, D.G., Polioencephalomalacia in a llama herd. Equine Practice,
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446. Sijtsma, L. and B. Tan, Degradation and utilization of grass cell
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600. Lackey, M.N., et al., Single intravenous and multiple dose
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601. Lang, K.D.M., Y. Wang, and Y. Plante, Fifteen polymorphic
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602. Lemosquet, S., et al., Voluntary intake and gastric digestion of
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604. Lichtenwalner, A.B., G.L. Woods, and J.A. Weber, Seminal
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605. Malone, E., K. Roertgen, and C. Kobluk, Anaplastic sarcoma of the
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606. Moraga, F., et al., Fetal and maternal blood oxygen affinity: a
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608. Oplinger, H., Kinesthesia : University of Pennsylvania graduate
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609. Patterson, W.A., Influence of llama, horse, and foot traffic on
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610. Perkins, N.R., G.S. Frazer, and B.L. Hull, Endocrine diagnosis of
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611. Raggi, S.L., et al., Use of different methods of pregnancy
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612. Reed, P.J., Studies on luteinizing hormone and gonadal steroids in
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613. Rowan, L.L., et al., Evaluation of udder health and mastitis in
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614. Sapienza, J.S., et al., Atresia of the nasolacrimal duct in a
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615. Saun, R.J.v., B.B. Smith, and B.J. Watrous, Evaluation of vitamin D
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624. Waldridge, B.M., The effect of subcutaneous selenium administration
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625. Waller, M.M.a. and R. Waller, The leaping llama carpet. A little
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626. Aller, J.F., et al., Semen collection in llamas (Lama glama) from
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628. Anderson, D.E., et al., Multifocal polyostotic aneurysmal bone
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629. Andrews, A.H. and A. Cox, Suspected nutritional deficiency causing
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632. Bezek, D. and R.D. Walker, Additional cause of mastitis in a llama
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660. Puntel, M., Seroprevalence of viral infections in llamas (Lama
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661. Ratto, M.H., R. Gatica, and J.E. Correa, Timing of mating and
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670. Welles, E.G., et al., Liver biopsy in llamas. Equine Practice,
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680. Bennett, J., A. Kennel, and C.R. Stanhope, Surgical correction of
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681. Cavalcanti, S.M.C. and F.F. Knowlton, Evaluation of physical and
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682. Cebra, M.L., et al., Atrioventricular Septal Defects in Three
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683. Cebra, M.L., et al., Atrioventricular septal defects in three
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685. Deluca, T.H., et al., Influence of llamas, horses, and hikers on
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686. Dulphy, J.P., et al., Intake and digestibility of different forages
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687. Engelhardt, W.v., Forestomach motility in llamas and camels.
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688. Fowler, M.E., Medicine and surgery of South American camelids :
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689. Fowler, M.E., Medicine and surgery of South American camelids:
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690. Frank, N., L.L. Coutëtil, and K.A. Clarke, Listeria monocytogenes
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691. Frost, B., Research update on diagnostic tests for tuberculosis in
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692. Gerken, M., et al., Social behaviour and social distance in female
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694. Gustafson, L.L., et al., Predicting Early Mortality of Newborn
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696. Hamir, A.N. and G. Moser, Immunohistopathological findings in an
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698. Hoogmoed, L.v., et al., Role of nitric oxide in in vitro
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699. Hoogmoed, L.v., et al., Use of computed tomography to evaluate the
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700. Hoogmoed, L.v., J.R. Snyder, and P. Vasseur, Surgical repair of
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701. Hutchison, J.M., et al., Characterization of plasma immunoglobulin
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702. Iñiguez, L.C., et al., Fleece types, fiber characteristics and
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703. Karesh, W.B., et al., Health Evaluation of Free-Ranging Guanaco
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704. King, M.R., et al., Laparoscopic ovariectomy in two standing
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705. Lichtenwalner, A.B., G.L. Woods, and J.A. Weber, Male llama choice
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706. Lopez, M.J., M.D. Markel, and R. Dubielzig, Urinary obstruction in
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708. Potts, L.K., Of lentils and llamas, and other stories from the
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709. Quist, C.F., et al., Gastrointestinal ulceration and pulmonary
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710. Rodgerson, D.H., et al., Ventral abdominal approach for
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711. Smith, B.B., et al., Blood mineral and vitamin E concentrations in
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712. Stevens, J.B., et al., The immunological response of llamas (Lama
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713. Sutmoller, P. and P. Taylor, An assessment of the risk of disease
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714. Tyler, J.W., et al., Conservative management of a ruptured
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715. Waldridge, B.M., et al., Rabies in a llama. Veterinary Medicine,
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716. Waldridge, B.M., et al., Measurement of passive transfer in
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720. Aguilar Cabrera, J.C., Suplementación de heno y ensillaje de
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721. Alyakine, H., et al., Surgical treatment of a congenital flexural
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722. Anderson, D.E., Liver disease, metabolism and digestion in llamas
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728. Beier, E., Oral pharmacokinetic and clinical efficacy profiles of
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730. Carmen Aguilar, J., Supplementation of alfalfa hay and ensilage to
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731. Costarella, C.E. and D.E. Anderson, Ileocecocolic intussusception
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732. DeHart, M., Bilateral cataracts in a three month old llama. 1999.
733. Drew, M.L., et al., Presumptive Sry-negative XX sex reversal in a
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735. Feder, F.H., H. González, and P. Arias, Comparative histological
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737. Fowler, M.E. and B. Frost, Prevalence of selected diseases of
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740. Gorman, T., et al., Seroprevalence of Toxoplasma gondii infection
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741. Hinrichs, K., L.C. Buoen, and G.R. Ruth, XX/XY chimerism and
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743. Isaac, P., Understanding some of the needs and requirements of the
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744. Isaza, R., Degenerative myelopathy as a cause of spinal ataxia in
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1024. Ratto, M., et al., In vitro and in vivo maturation of llama
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1025. Sanhueza, E.M., et al., Vasodilator tone in the llama fetus: the
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1027. Smith, A.M., Do you hear what Rulfo hears? : the function of sound
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1028. Uhrig, S., Pharmacokinetics and pharmacodynamics of morphine in
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1029. Whitehead, C.E., The effect of maternal supplementation of vitamin
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1030. Wolf, D., et al., Detection of specific antibodies to Neospora
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1032. Zachary, V.A., Winter Grazing at 13,000 Feet: Improving Forages for
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1033. Ajata Avircata, Perfil metabólico y balance de nitrógeno en
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1034. Alvarez, R., S. Villca, and G. Lidén, Biogas production from llama
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1035. Anderson, D.E., Periapical tooth root infections in llamas and
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1037. Bradley, D.G., et al., Genetic Analysis of the Origins of Domestic
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1038. Bromage, G., Llamas and alpacas: a guide to management. 2006,
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1039. Cebra, C.K., R.J. Bildfell, and K.A. Fischer, Microanatomic
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1040. D Alterio, G., et al., Postal survey of the population of South
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1041. Evermann, J.F., Pestiviral infection of llamas and alpacas. Small
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1046. Harmsen, M.M., et al., Selection and optimization of
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1047. Harrison, R.A., et al., Neutralisation of venom-induced haemorrhage
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1048. Hashimoto, K., Commodification of farm products in Andes highlands,
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1050. Lakritz, J., et al., Pharmacokinetics of intravenously administered
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1055. Newman, K.D. and D.E. Anderson, Fracture management in llamas and
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1057. Pant, N., et al., Lactobacilli expressing variable domain of llama
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1058. Panuska, C., L.G. Rickard, and D.D. Rudolph, Isotype-specific serum
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1060. Ratto, M., et al., Comparison of the effect of natural mating, LH,
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1061. Ratto, M.H., Ovarian follicular synchronization, ovulation and
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1062. Ratto, M.H., et al., Comparison of the effect of ovulation-inducing
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1063. Riek, A., Investigations on milk composition, milk intake and body
weight development in the Llama (Lama glama). 2006, Cuvillier: Gottingen.
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1065. Robinson, T.F., et al., Digestibility and nitrogen retention in
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1066. Schoeniger, S., L.R. Donner, and W.G.v. Alstine, Malignant
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1067. Sheedy, C., et al., Selection, characterization, and CDR shuffling
of naive llama single-domain antibodies selected against auxin and their
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1069. Ugarte Huanca, E.G., Valor energético en llamas (Lama glama)
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1070. Valentine, B.A., et al., Compressive myelopathy due to
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1073. Wheeler, J.C., et al., Genetic Analysis of the Origins of Domestic
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1074. Whitehead, C.E. and D.E. Anderson, Neonatal diarrhea in llamas and
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1076. Fewer fires. Chile Forestal, 2007(No.331): p. 25-28.
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1079. Altenbrunner-Martinek, B., et al., Congenital malformation of the
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1080. Alvarez-Rueda, N., et al., Generation of llama single-domain
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1081. Azwai, S.M., et al., Morphological characteristics of blood cells
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1082. Bangari, D.S. and G.W. Stevenson, Carcinoma in a mixed mammary
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1083. Bianchi, C.P., et al., Uterine estrogen receptor alpha and
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1084. Bolton, M., Counting llamas and accounting for people: livestock,
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1085. Borkowski, R., P.A. Moore, and S. Mumford, Adaptations of
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1086. Borkowski, R., et al., Adaptations of subpalpebral lavage systems
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1087. Byers, S.R., et al., A fungal granuloma of the frontal sinus in a
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1089. Cebra, C., Diarrhea in llama and alpaca crias. 2007, American
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1090. Cebra, C., Uterine torsion in llamas and alpacas. 2007, American
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1091. Cebra, C., Internal parasites in llamas and alpacas: importance and
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1092. Cebra, C.K., et al., Eimeria macusaniensis infection in 15 llamas
and 34 alpacas. Journal of the American Veterinary Medical Association,
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1093. Cecchi, T., et al., Quantitative variation of melanins in llama
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1098. Foster, A., et al., Bovine viral diarrhoea virus infection of
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1099. Frank, E.N., M.V.H. Hick, and M.R. Ahumada, Argentine Llamas
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1100. Graziotti, G.H., et al., Distribution of the internal pudendal
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1101. Harmsen, M.M., et al., Passive immunization of guinea pigs with
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1102. Hultberg, A., et al., Lactobacilli expressing llama VHH fragments
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1103. Iturrizaga, D.M., et al., The materno-fetal interface in llama
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1104. Jones, M.L., M.A. Gilmour, and R.N. Streeter, Use of grid
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1105. Klein, D., et al., Esophageal dilatation in a llama - a case
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1107. Lewis, W.J.K., Novel llama antibody fusion proteins as deposition
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1108. Linden, D.R., et al., Apparent digestibility of organic zinc forms
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1109. Lyashchenko, K., et al., Antibody responses in New World camelids
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1110. Mantero, M.M.a., Poesi̕a : como llama en el diamante (1954-2004)
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1112. Nes, E.v. and M.C. Pieterse, Reproduction in the llama and alpaca.
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1114. Nichols, S., D.E. Anderson, and K. Schober, Subtotal
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1115. Niehaus, A.J. and D.E. Anderson, Tooth root abscesses in llamas and
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1116. Plant, J.D., M.A. Kutzler, and C.K. Cebra, Efficacy of topical
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1117. Polidori, P., et al., Tenderness evaluation and mineral levels of
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1120. Powell, S.A., et al., Expression of estrogen receptors α and β in
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1122. Reed, S.K., et al., Morphologic and biochemical characterization of
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1123. Riek, A. and M. Gerken, Measurements of the bodyweight and other
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1124. Riek, A., M. Gerken, and E. Moors, Measurement of milk intake in
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1125. Roth, C. and M. Ganter, Urolithiasis in a gelded llama.
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1127. Sansinena, M.J., et al., In vitro production of llama (Lama glama)
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1128. Saun, R.J.v., Rickets and vitamin D metabolism in llamas and
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1129. Schwalm, A., et al., Changes in testicular histology and sperm
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1131. Serrano-Martínez, E., et al., Evaluation of Neospora caninum and
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1132. Sherwood, L.J., et al., Rapid Assembly of Sensitive Antigen-Capture
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1133. Sherwood, L.J., et al., Rapid assembly of sensitive antigen-capture
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1136. Uhrig, S.R., et al., Pharmacokinetics and pharmacodynamics of
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1138. Woodford, N., G.L. D'Alterio, and M. Owen, Bilateral
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1139. Zielińska, P. and P. Jurka, Characteristics of llamas and alpacas
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1141. Ali Quisbert, E., Efecto de la privación de alimentos en el perfil
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1145. Cebra, C.K. and B.V. Stang, Comparison of methods to detect
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1149. Forsman, A., et al., Llama antibody fragments with cross-subtype
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1157. Moré, G., et al., Seroprevalence of Neospora caninum, Toxoplasma
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de Investigaciones Veterinarias del Perú (RIVEP), 2011. 22(1): p. 1-8.
1291. Loayza M, E., et al., Evaluation of Toxoplasma gondii in female
llamas from two peasant communities in Puno. Revista de Investigaciones
Veterinarias del Perú (RIVEP), 2011. 22(3): p. 239-243.
1292. Lusat, J., Importance and management of mange mites and
gastrointestinal parasites in alpaca and llama populations in the UK.
2011.
1293. Maw, J., Llamascape based on an interpretive cast : the inhabitanta
llama the spatial analysta geographer the common humana phantom within
the social imagination. 2011: Ottawa.
1294. Osmundson, S.D., Abdominal serosal cysts in an adult male llama
(Lama glama). 2011.
1295. Pasquel H, S., et al., Determination of the presence of
Campylobacter fetus subsp. venerealis in alpacas and llamas in the Puno
region. Revista de Investigaciones Veterinarias del Perú (RIVEP), 2011.
22(3): p. 278-282.
1296. Vásquez E, M., et al., Evaluation of two embryo cryopreservation
methods in llama on the in vivo e in vitro embryonic survival rates.
Revista de Investigaciones Veterinarias del Perú (RIVEP), 2011. 22(3): p.
190-198.
1297. Wani, N.A., et al., Biophysical and biochemical characteristics of
ejaculated semen of dromedary camel (Camelus dromedarius) and llama
(Llama glama). Journal of Camel Practice and Research, 2011. 18(1): p.
97-102.
1298. Llama Llama Zippity-Zoom. Kirkus Reviews, 2012. 80(24): p. 195-195.
1299. The Llama of Death: A Gunn Zoo Mystery. Library Journal, 2012.
137(20): p. 67-67.
1300. Llama Llama, Time to Share. School Library Journal, 2012. 58(8): p.
70-70.
1301. El sector llama a "visibilizar la utilidad" de las bibliotecas y a
"luchar para minimizar" la caida de sus presupuestos. Boletin de la
Asociacion Andaluza de Bibliotecarios, 2012. 27(104): p. 293-295.
1302. Barreta, J., Analysis of mitochondrial DNA in Bolivian llama,
alpaca and vicuna populations: a contribution to the phylogeny of the
South American camelids. 2012, Oxford: Blackwell Science. 1 online
resource LA - English NT - In: Animal genetics, Vol. 44, no. 2 (Apr.
2013), p.158-168. NT - SummaryThe objectives of this work were to assess
the mtDNA diversity of Bolivian South American camelid (SAC) populations
and to shed light on the evolutionary relationships between the Bolivian
camelids and other populations of SACs. We have analysed two different
mtDNA regions: the complete coding region of the MT―CYB gene and
513 bp of the D―loop region. The populations sampled included Bolivian
llamas, alpacas and vicunas, and Chilean guanacos. High levels of genetic
diversity were observed in the studied populations. In general, MT―CYB
was more variable than D―loop. On a species level, the vicunas showed
the lowest genetic variability, followed by the guanacos, alpacas and
llamas. Phylogenetic analyses performed by including additional available
mtDNA sequences from the studied species confirmed the existence of the
two monophyletic clades previously described by other authors for
guanacos (G) and vicunas (V). Significant levels of mtDNA hybridization
were found in the domestic species. Our sequence analyses revealed
significant sequence divergence within clade G, and some of the Bolivian
llamas grouped with the majority of the southern guanacos. This finding
supports the existence of more than the one llama domestication centre in
South America previously suggested on the basis of archaeozoological
evidence. Additionally, analysis of D―loop sequences revealed two new
matrilineal lineages that are distinct from the previously reported G and
V clades. The results presented here represent the first report on the
population structure and genetic variability of Bolivian camelids and may
help to elucidate the complex and dynamic domestication process of SAC
populations.
1303. Cano Z, L., et al., Phenotypic characterization and mitocondrial
DNA analysis of Marcapomacocha llamas, Peru. Revista de Investigaciones
Veterinarias del Perú (RIVEP), 2012. 23(3): p. 388-398.
1304. Conroy, C., Mama Wants a Llama. 2012: AuthorHouse.
1305. Dewdney, A.M.a., Llama llama red pyjama. 2012, London: Hodder
Children's. 1 volume (unpaged) : illustrations ; 27 cm.
1306. Duncanson, G.R., Veterinary treatment of llamas and alpacas. 2012,
Wallingford, Oxfordshire, UK: CAB International. xix, 248.
1307. McCarthy, M.C.e.o.c., Unexplored territory : poetry and fiction
from Cultured Llama. 2012, Teynham, Sittingbourne: Cultured Llama
Publishing. xi, 94 pages ; 21 cm LA - English.
1308. Mendoza T, G., et al., Macroscopic and microscopic characterization
of the reproductive glands of the male llama (Lama glama). Revista de
Investigaciones Veterinarias del Perú (RIVEP), 2012. 23(1): p. 27-42.
1309. Perez, A.R. and P. Walker. La sangre llama. 2012 2012///; Available
from: http://digitalcommons.georgiasouthern.edu/etd/8/.
1310. Qian, J.D.-. Affinity chromatography of camelid antibodies. 2012,
Department of Chemical Engineering and Biotechnology.
1311. Rahn-Chique, K., N. Carrion, and M. Murillo, Determination of
copper, magnesium and zinc in mononuclear leukocytes by flame atomic
absorption spectrometry. Investigación Clínica, 2012. 53(4): p. 342-352.
1312. Maria Had a Little Llama/Maria Tenia una Llamita. Library Media
Connection, 2013. 32(3): p. 54-54.
1313. Llama Llama and the Bully Goat. Publishers Weekly, 2013. 260(28):
p. 168-168.
1314. Alpers, S.A., Miss Lilly The Cute Little Llama: The Cute Little
Llama. 2013: Xlibris US.
1315. Anderson, D.E., M.L. Jones, and M.D. Miesner, Veterinary Techniques
for Llamas and Alpacas. 2013: Wiley.
1316. Apichela, S.A., et al., Llama oviductal sperm reservoirs:
involvement of bulbourethral glands. 2013, Berlin, Germany: Blackwell
Science. 1 online resource LA - English NT - In: Andrologia, Vol. 46,
no. 3 (June 2014), p.290-295. NT - Summary: Summary The aim of this
study was to elucidate the role of llama seminal plasma in the formation
of oviductal sperm reservoirs. Female llamas with follicles in the mature
phase were mated with a bulbourethral glands―removed male. Females
mated with nonbulbourethral glands―removed males were used as control.
Oviducts were obtained by surgery 24Â h after mating. The uterotubal
junction and isthmus were examined by scanning electron microscopy, and
mucopolysaccharides were identified by Alcian blue staining. To know the
proteins probably involved in sperm reservoir formation, SDS―PAGE of
seminal plasma (8% and 18% resolving gel) was made. Spermatozoa only
adhered to the oviductal mucosa surface of uterotubal junction of females
mated with nonbulbourethral glands―removed males confirming that
seminal plasma and, in particular, bulbourethral secretions are related
with the oviductal sperm reservoir formation. Histological sections
showed sperm in the lumen, immersed in substance, positive for acid
mucopolysaccharides. Alcian blue staining of seminal plasma proteins
SDS―PAGE showed a band of high molecular weight containing
mucopolysaccharides, only present in nonbulbourethral glands―removed
males. Bulbourethral glands would secrete at least eight different
proteins that most likely participate in the process of sperm storage in
the oviduct.
1317. Conraths, F., M. Peters, and M. Beer, Schmallenberg virus, a novel
orthobunyavirus infection in ruminants in Europe: potential global impact
and preventive measures. New Zealand Veterinary Journal, 2013. 61(2): p.
63-67.
1318. Cucchi, M.E.C.n., et al., Detection of fiber-digesting bacteria in
the forestomach contents of llamas (Lama glama) by PCR. Revista Argentina
de microbiologia, 2013. 45(3): p. 147-149.
1319. Dadak, A.M., et al., Establishing an efficacious dose rate of
monepantel for treating gastrointestinal nematodes in llamas under field
conditions. Veterinary Record, 2013. 172(6): p. 155.
1320. Dadak, A.M., et al., Efficacy and safety of oral praziquantel
against Dicrocoelium dendriticum in llamas. Veterinary Parasitology,
2013. 197(1/2): p. 122-125.
1321. Danquah, W. and F. Koch-Nolte, Selection and characterization of
llama-derived anti-P2X7 single domain antibodies. 2013, Staats- und
Universitätsbibliothek Hamburg: Hamburg.
1322. Dewdney, A., Llama Llama and the Bully Goat. 2013: Penguin Young
Readers Group.
1323. Dewdney, A.M.a., Llama llama shopping drama. 2013, London: Hodder
Children's Books. 32 unnumbered pages : chiefly illustrations (colour) ;
27 cm. LA - English.
1324. Gomez-Puerta, L.A., et al., A case of nasal myiasis due to Oestrus
ovis (Diptera: Oestridae) in a llama (Lama glama). Revista Brasileira de
Parasitologia Veterinária, 2013. 22(4): p. 608-610.
1325. Impey, R.a. and A.i. Pye, Llama drama : it's showtime! 2013,
London: Harper Collins Children's. 186 pages ; 20 cm.
1326. Impey, R.a. and A.i. Pye, Llama drama : in it to win it! 2013,
London: Harper Collins Children's Books. 200 pages : illustrations ; 20
cm.
1327. Mamani C, R., et al., Ovulation rate using gonadotropin releasing
hormone and seminal plasma in alpacas and llamas. Revista de
Investigaciones Veterinarias del Perú (RIVEP), 2013. 24(2): p. 194-198.
1328. Mamani-Linares, L.W., F. Cayo, and C. Gallo, Technological quality
of twelve muscles from young llamas (Lama Glama) reared under an
extensive production system. Revista de Investigaciones Veterinarias del
Perú (RIVEP), 2013. 24(2): p. 168-175.
1329. Mamani-Linares, L.W., F. Cayo, and C. Gallo, Effect of season on
proximate composition and fatty acids profile of llama meat in extensive
rearing. Revista de Investigaciones Veterinarias del Perú (RIVEP), 2013.
24(4): p. 417-424.
1330. Marcoppido, G., et al., Haemonchus-induced anemia in llamas (Lama
glama) from Argentina. International Journal of Veterinary Science, 2013.
2(3): p. 111-114.
1331. Marcoppido, G. and B. Vila, Management of extra-Andean llamas.
Comments that contribute to their welfare in non-originating context.
Revista Argentina de Producción Animal, 2013. 33(2): p. 139-154.
1332. Norambuena, M.C., et al., Relationship between systemic leptin
concentration and reproductive state in llamas (Lama glama) from southern
Chile. Small Ruminant Research, 2013. 113(2/3): p. 402-404.
1333. Parisien, A., Large-Scale Production in 'Escherichia coli' TG1 and
Purification of Llama Single Domain Antibody ToxA5.1 Against 'Clostridium
difficile' Toxin A. 2013, University of, Ottawa.
1334. Pembro, C.a., Ollie : the diary of a llama farmer. 2013, Bath:
Llama-rama Publishing. vii, 97 pages.
1335. Preciado RodrÃguez, N.A., Water dispossession at the Llano en
Llamas : a research study by a daughter of Mexican farmworkers in the
land of her consciousness. 2013.
1336. Rooney, A.L., et al., A cross-sectional study of Sarcocystis spp.
in llamas (Lama glama) in Southern Bolivia including an economic costing
of loss in income caused by the disease. 2013, Society for Veterinary
Epidemiology and Preventive Medicine: Roslin. p. 175-183.
1337. Stieger-Vanegas, S.M. and C.K. Cebra, Contrast-enhanced computed
tomography of the gastrointestinal tract in clinically normal alpacas and
llamas. Journal of the American Veterinary Medical Association, 2013.
242(2): p. 254-260.
1338. Webb, B., The Llama of Death: A Gunn Zoo Mystery. 2013: Poisoned
Pen Press, Incorporated.
1339. Llama Llama Trick or Treat. Kirkus Reviews, 2014. 82(13): p. 401-
401.
1340. A Llama Trek in New Mexico. Wall Street Journal (Online), 2014: p.
1-1.
1341. Abe, M., et al., A rice-based soluble form of a murine TNF-specific
llama variable domain of heavy-chain antibody suppresses collagen-induced
arthritis in mice. Journal of Biotechnology, 2014. 175: p. 45-52.
1342. Aguirre, I.M., M.P. Quezada, and M.O. Celedón, Antigenic
variability in bovine viral diarrhea virus (BVDV) isolates from alpaca
(Vicugna pacos), llama (Lama glama) and bovines in Chile. Veterinary
Microbiology, 2014. 168(2/4): p. 324-330.
1343. Apichela, S.A., et al., Llama oviductal sperm reservoirs:
involvement of bulbourethral glands. Andrologia, 2014. 46(3): p. 290-295.
1344. Barbieri, E.S., et al., Serological survey of antibodies against
viral diseases of public health interest in llamas (Lama glama) from
Jujuy province, Argentina. Revista Argentina de Microbiología, 2014.
46(1): p. 53-57.
1345. Barone, D. and F. Guarda, Immunology of camel, alpaca and llama.
Summa, Animali da Reddito, 2014. 9(2): p. 42-46.
1346. Beck, W., Treatment of Sarcoptes mange in Llamas and Alpacas.
Tierärztliche Umschau, 2014. 69(5): p. 185-190.
1347. Cebra, C., et al., Llama and Alpaca Care: Medicine, Surgery,
Reproduction, Nutrition, and Herd Health. 2014: Elsevier Health Sciences.
1348. Chalkley, M.D., M. Kiupel, and A.C.E. Draper, Pituitary null cell
Adenoma in a domestic llama (Lama glama). Journal of Comparative
Pathology, 2014. 151(1): p. 51-56.
1349. Daverio, M.S., et al., Genetic diversity of GH1 and LEP genes in
Argentine llama (Lama glama) populations. Small Ruminant Research, 2014.
120(1): p. 20-26.
1350. Dewdney, A., Llama Llama Jingle Bells. 2014: Penguin Young Readers
Group.
1351. Dubey, J.P., et al., Toxoplasma gondii infection in Llama (Llama
glama): acute visceral disseminated lesions, diagnosis, and development
of tissue cysts. Journal of Parasitology, 2014. 100(3): p. 288-294.
1352. Fernández, A., et al., The effect of repeated administrations of
llama ovulation-inducing factor (OIF/NGF) during the peri-ovulatory
period on corpus luteum development and function in llamas. Animal
Reproduction Science, 2014. 149(3/4): p. 345-352.
1353. Flores C, B., et al., Prevalency of fascioliasis in llamas and
alpacas in two rural communities of Jauja, Peru. Revista de
Investigaciones Veterinarias del Perú (RIVEP), 2014. 25(2): p. 284-292.
1354. Hick, M.V.H., et al., Ethno-zootechnical characterization of the
population of fiber bearing lamas from the province of Jujuy, Argentina.
Archivos Latinoamericanos de Producción Animal, 2014. 22(1/2): p. 1-8.
1355. Hunter, B., et al., Carpal valgus in llamas and alpacas:
retrospective evaluation of patient characteristics, radiographic
features and outcomes following surgical treatment. Canadian Veterinary
Journal, 2014. 55(12): p. 1153-1159.
1356. Jarvinen, J.A.C., et al., Identification of Lamanema chavezi
Becklund 1963 infection in a llama (Lama glama) in the United States.
Journal of Veterinary Diagnostic Investigation, 2014. 26(1): p. 178-183.
1357. Kreil, V., et al., Comparative pharmacokinetics of a single dose of
ampicillin following intravenous, intramuscular and subcutaneous
administration to llamas. Archivos de Medicina Veterinaria, 2014. 46(2):
p. 271-276.
1358. Mamani-Linares, L.W., F. Cayo, and C. Gallo, Carcass
characteristics, quality of meat and chemical composition of meat llama:
a review. Revista de Investigaciones Veterinarias del Perú (RIVEP), 2014.
25(2): p. 123-150.
1359. Mamani-Linares, L.W. and C.B. Gallo, Meat quality, proximate
composition and muscle fatty acid profile of young llamas (Lama glama)
supplemented with hay or concentrate during the dry season. Meat Science,
2014. 96(1): p. 394-399.
1360. McCoy, L.E., et al., Neutralisation of HIV-1 cell-cell spread by
human and llama antibodies. Retrovirology, 2014. 11: p. 83.
1361. Nevoltris, D., D. Baty, and . Développement des ligands pour l'
étude des récepteurs GPCR, Tyrosine Kinase, basée sur l'
utilisation de simple domaine d' anticorps de lamas. 2014, Marseille: .
1362. Nielsen, M.O., et al., Energy metabolism and methane production in
llamas, sheep and goats fed high- and low-quality grass-based diets.
Archives of Animal Nutrition, 2014. 68(3): p. 171-185.
1363. Pawlinski, S., Neonatal septicemia in a llama cria. 2014.
1364. Ramos G, M., et al., Adaptation of the lymphocyte culture technique
of alpacas and lamas for the analysis of sister chromatid exchange (SCE).
Revista de Investigaciones Veterinarias del Perú (RIVEP), 2014. 25(4): p.
461-467.
1365. Robinson, T.F. and B.L. Roeder, Serum and urine analyte comparison
between llamas and alpacas fed three forages. Scientific Journal of
Animal Science, 2014. 3(11): p. 275-283.
1366. Saadaoui, B., et al., Combining proteomic tools to characterize the
protein fraction of llama (Lama glama) milk. Electrophoresis, 2014.
35(10): p. 1406-1418.
1367. Seddighi, R., et al., Antinociceptive and selected physiological
effects of morphine and xylazine on tiletamine-zolazepam anesthesia in
llamas. Veterinary Anaesthesia and Analgesia, 2014. 41(4): p. 365-371.
1368. Silva, M., et al., Ovulation-inducing factor (OIF/NGF) from seminal
plasma origin enhances Corpus Luteum function in llamas regardless the
preovulatory follicle diameter. Animal Reproduction Science, 2014.
148(3/4): p. 221-227.
1369. Soler, C., et al., Ejaculate Fractioning Effect on Llama Sperm Head
Morphometry as Assessed by the ISAS® CASA system. Reproduction in
domestic animals, , no. 1 ( 2014),, 2014. Vol. 49: p. p.71-78.
1370. Soler, C., et al., Ejaculate fractioning effect on llama sperm head
morphometry as assessed by the ISAS® CASA system. Reproduction in
Domestic Animals, 2014. 49(1): p. 71-78.
1371. Soler, C., et al., Llama and alpaca comparative sperm head
morphometric analysis. Journal of Camelid Science, 2014. 7: p. 48-58.
1372. Szczepanik, M., et al., Mange mites species affecting llamas and
alpacas. Życie Weterynaryjne, 2014. 89(11): p. 953-956.
1373. Tillib, S.V., A.S. Vyatchanin, and S. Muyldermans, Molecular
analysis of heavy chain-only antibodies of Camelus bactrianus.
Biochemistry (Mosc), 2014. 79(12): p. 1382-90.
1374. Trasorras, V., et al., First llama (Lama glama) pregnancy obtained
after in vitro fertilization and in vitro culture of gametes from live
animals. Animal Reproduction Science, 2014. 148(1/2): p. 83-89.
1375. Ulloa-Leal, C., et al., Luteotrophic effect of ovulation-inducing
factor/nerve growth factor present in the seminal plasma of llamas.
Theriogenology, 2014. 81(8): p. 1101-1107.
1376. Wernery, U., J.r. Kinne, and R.K. Schuster, Camelid infectious
disorders. 2014: OIE (World Organisation for Animal Health).
1377. Zampini, R., et al., Detection of the matrix metalloproteinases
MMP-2 and MMP-9 and tissue inhibitors of metalloproteinases TIMP-1 and
TIMP-2 in llama (Lama glama) oviduct. Reproduction in Domestic Animals,
2014. 49(3): p. 492-498.
1378. Llama Llama Gram and Grandpa. School Library Journal, 2015. 61(9):
p. 110-110.
1379. Last Chance Llama Ranch. Kirkus Reviews, 2015. 83(10): p. 221-221.
1380. Lloyd Llama. Publishers Weekly, 2015. 262(16): p. 75-75.
1381. Llama Llama Sand and Sun. Publishers Weekly, 2015. 262(15): p. 79-
79.
1382. Õlvarez, B., et al., An Exopolysaccharide-Deficient Mutant of
Lactobacillus rhamnosus GG Efficiently Displays a Protective Llama
Antibody Fragment against Rotavirus on Its Surface. Appl Environ
Microbiol, 2015. 81(17): p. 5784-93.
1383. Abutarbush, S.M., Tetraplegia due to fracture of the articular
facet of the fourth cervical vertebra in a llama (Lama glama). Global
Veterinaria, 2015. 14(3): p. 366-368.
1384. Agbedanu, P.N., et al., Doxycycline as an inhibitor of p-
glycoprotein in the alpaca for the purpose of maintaining avermectins in
the CNS during treatment for parelaphostrongylosis. Vet Parasitol, 2015.
212(3-4): p. 303-7.
1385. Allen, A.J., et al., Bluetongue disease and seroprevalence in South
American camelids from the northwestern region of the United States. J
Vet Diagn Invest, 2015. 27(2): p. 226-30.
1386. Aller, J.F., et al., Birth of live llama (Lama glama) derived from
embryo transfer storage at 5°C for 24 h. Small Ruminant Research, 2015.
132: p. 99-102.
1387. Aller, J.F., et al., Embryo yield in llamas synchronized with two
different intravaginal progesterone-releasing devices and superovulated
with eCG. Spanish Journal of Agricultural Research, 2015. 13(3): p.
e04SC01.
1388. Alturki, N.A., et al., Isolation of Camelid Single-Domain
Antibodies Against Native Proteins Using Recombinant Multivalent Peptide
Ligands. Methods Mol Biol, 2015. 1348: p. 167-89.
1389. Álvarez, B., et al., An exopolysaccharide-deficient mutant of
Lactobacillus rhamnosus GG efficiently displays a protective llama
antibody fragment against rotavirus on its surface. Applied and
Environmental Microbiology, 2015. 81(17): p. 5784-5793.
1390. Andersen, K.K., et al., Neutralization of Clostridium difficile
Toxin B Mediated by Engineered Lactobacilli That Produce Single-Domain
Antibodies. Infect Immun, 2015. 84(2): p. 395-406.
1391. Arias, N. and B. Velapatiño, Cortisol as a reliable indicator of
stress in alpacas and llamas. Revista de Investigaciones Veterinarias del
Perú (RIVEP), 2015. 26(1): p. 1-8.
1392. Barker, W.H., et al., Dorsal laminectomy for treatment of cervical
vertebral stenotic myelopathy in an alpaca. J Am Vet Med Assoc, 2015.
246(10): p. 1122-8.
1393. Bennett, M.M. and N.L. Richards, Camelid wellness. Vet Clin North
Am Exot Anim Pract, 2015. 18(2): p. 255-80.
1394. Bianchi, C.P., et al., Oestrogen and Progesterone Receptors and
COX-2 Expression in Endometrial Biopsy Samples During Maternal
Recognition of Pregnancy in Llamas (Lama glama). Reprod Domest Anim,
2015. 50(6): p. 980-8.
1395. Bianchi, C.P., et al., Oestrogen and progesterone receptors and
COX-2 expression in endometrial biopsy samples during maternal
recognition of pregnancy in llamas (Lama glama). Reproduction in Domestic
Animals, 2015. 50(6): p. 980-988.
1396. Blykers, A., et al., PET Imaging of Macrophage Mannose Receptor-
Expressing Macrophages in Tumor Stroma Using 18F-Radiolabeled Camelid
Single-Domain Antibody Fragments. J Nucl Med, 2015. 56(8): p. 1265-71.
1397. Brooks, K., G. Burns, and T.E. Spencer, Biological Roles of
Hydroxysteroid (11-Beta) Dehydrogenase 1 (HSD11B1), HSD11B2, and
Glucocorticoid Receptor (NR3C1) in Sheep Conceptus Elongation. Biol
Reprod, 2015. 93(2): p. 38.
1398. Calpe, S., et al., Effective Inhibition of Bone Morphogenetic
Protein Function by Highly Specific Llama-Derived Antibodies. Mol Cancer
Ther, 2015. 14(11): p. 2527-40.
1399. Campbell, A.J., et al., Double ovulation and occurrence of twinning
in alpacas (Vicugna pacos). Theriogenology, 2015. 84(3): p. 421-4.
1400. Canaza-Cayo, A.W., et al., Modelling of growth curves and
estimation of genetic parameters for growth curve parameters in Peruvian
young llamas (Lama glama). Small Ruminant Research, 2015. 130: p. 81-89.
1401. Carretero, M.I., et al., Evaluation of the acrosomal status in Lama
glama sperm incubated with acrosome reaction inducers. Anim Reprod Sci,
2015. 160: p. 1-11.
1402. Chandramohan, B., et al., The alpaca melanocortin 1 receptor: gene
mutations, transcripts, and relative levels of expression in ventral skin
biopsies. ScientificWorldJournal, 2015. 2015: p. 265751 ST - The alpaca
melanocortin 1 receptor: gene mutations, transcripts, and relative levels
of expression in ventral skin biopsies.
1403. Chatalic, K.L., et al., A Novel ¹¹¹In-Labeled Anti-Prostate-
Specific Membrane Antigen Nanobody for Targeted SPECT/CT Imaging of
Prostate Cancer. J Nucl Med, 2015. 56(7): p. 1094-9.
1404. Chen, X., et al., Enteractinococcus lamae sp. nov. and
Enteractinococcus viverrae sp. nov., isolated from animal faeces. Antonie
Van Leeuwenhoek, 2015. 108(6): p. 1477-83.
1405. Cockcroft, P.D., et al., Serological survey for antibodies against
bovine viral diarrhoea virus and Neospora caninum in a population of
South Australian alpacas (Vicugna pacos). Aust Vet J, 2015. 93(12): p.
476-8.
1406. Corapi, W.V., et al., Heterobilharzia americana infection and
congestive heart failure in a llama (Lama glama). Veterinary Pathology,
2015. 52(3): p. 562-565.
1407. Cruz, A., Estimation of genetic parameters for reproductive traits
in alpacas. Anim Reprod Sci, 2015. 163: p. 48-55.
1408. Cui, Y., et al., Heavy chain single-domain antibodies to detect
native human soluble epoxide hydrolase. Anal Bioanal Chem, 2015. 407(24):
p. 7275-83.
1409. De Souza, E., et al., Mapping of somatostatin-28 (1-12) in the
alpaca (Lama pacos) brainstem. Microsc Res Tech, 2015. 78(5): p. 363-74.
1410. Dittmann, M.T., et al., Digesta retention patterns of solute and
different-sized particles in camelids compared with ruminants and other
foregut fermenters. J Comp Physiol B, 2015. 185(5): p. 559-73 ST -
Digesta retention patterns of solute and different-sized particles in
camelids compared with ruminants and other foregut fermenters.
1411. Dorresteijn, B., et al., Camelid heavy chain only antibody fragment
domain against β-site of amyloid precursor protein cleaving enzyme 1
inhibits β-secretase activity in vitro and in vivo. FEBS J, 2015.
282(18): p. 3618-31 ST - Camelid heavy chain only antibody fragment
domain against β-site of amyloid precursor protein cleaving enzyme 1
inhibits β-secretase activity in vitro and in vivo.
1412. Dreja, H., et al., CD4 binding site broadly neutralizing antibody
selection of HIV-1 escape mutants. J Gen Virol, 2015. 96(Pt 7): p. 1899-
905 ST - CD4 binding site broadly neutralizing antibody selection of
HIV-1 escape mutants.
1413. Erdoğan, S., S. Villar Arias, and W. Pérez, Morphofunctional
structure of the lingual papillae in three species of South American
Camelids: Alpaca, guanaco, and llama. 2015, [Place of publication not
identified]: Wiley Periodicals Inc. 1 online resource LA - English NT -
In: Microscopy research and technique, Vol. 79, no. 2 ( 2016), p.61-71.
NT - Summary: ABSTRACTThe aim of this study was to compare the
anatomical and functional characteristics of the lingual papilla among
the Camelidae. For this purpose, tongues of alpaca, guanaco, and llama
were used. Numerous long and thin filiform papillae were located in the
median groove and none were detected on the rest of the dorsal surface of
the lingual apex in alpaca. Secondary papillae originated from the base
of some filiform papillae on the ventral surface of alpaca tongue. The
bases of some filiform papillae of the lateral surface of the lingual
apex were inserted into conspicuous grooves in guanaco and tips of
filiform papillae on the dorsal surface of the lingual body were ended by
bifurcated apex. On the dorsal surface of the lingual apex of llama,
there were no filiform papillae but there were numerous filiform papillae
on both the lateral margins of the ventral surface of the lingual apex.
Fungiform papillae were distributed randomly on dorsal lingual surface
and ventral margins of the tongues of all camelid species. Lenticular
papillae were located on the lingual torus and varied in size and
topographical distribution for each species. Circumvallate papillae had
irregular surfaces in llama and alpaca, and smooth surface in guanaco. In
conclusion, llama and alpaca tongues were more similar to each other, and
tongues of all camelid species displayed more similarities to those of
Bactrian and dromedary camels in comparison with other herbivores and
ruminants.Microsc. Res. Tech. 79:61–71, 2016. © 2015 Wiley
Periodicals, Inc.
1414. Espinosa, M.I., et al., Comparison of DNA extraction methods for
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1415. Ferré, L.B., et al., Llama (Lama glama) semen collection via
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1422. Guedon, J.T., et al., Monoclonal and Single Domain Antibodies
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In Vivo Model Systems.
1423. Henry, K.A., J. Tanha, and G.D.-O.D.-p.g. Hussack, Identification
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against serum albumin using next-generation DNA sequencing.
1424. Herrera, C., et al., Mechanisms of Ricin Toxin Neutralization
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Treatment of a maxillary fibrosarcoma in an adult alpaca.
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Irvingtonian and Rancholabrean North American Land Mammal Ages) that have
been referred toCamelops, only 6 are currently recognised as valid. This
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latest Wisconsinan of the Nueces River valley of South Texas. During this
interval, there are two valid previously named species: the smaller
mainly IrvingtonianCamelops minidokaeand the larger, mainly
RancholabreanCamelopshesternus.Camelops hesternus,Camelops
sulcatus,Camelops huerfanensisandCamelopstraviswhiteiare junior synonyms
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