Refrigerating systems for the big CERN bubble chamber

por Giger, U, Pagani, P, Trepp, C
Publicado 1974

Feline Cystinuria Caused by a Missense Mutation in the SLC3A1 Gene

por Mizukami, K., Raj, K., Giger, U.
Publicado 2014

DEA 1 Expression on Dog Erythrocytes Analyzed by Immunochromatographic and Flow Cytometric Techniques

por Acierno, M.M., Raj, K., Giger, U.
Publicado 2014

Comparison of 4 Direct Coombs' Test Methods with Polyclonal Antiglobulins in Anemic and Nonanemic Dogs for In‐Clinic or Laboratory Use

por Caviezel, L.L., Raj, K., Giger, U.
Publicado 2014

Mucopolysaccharidosis VII in a Cat Caused by 2 Adjacent Missense Mutations in the GUSB Gene

por Wang, P., Sorenson, J., Strickland, S., Mingus, C., Haskins, M.E., Giger, U.
Publicado 2015

Comparison of Tube, Gel, and Immunochromatographic Strip Methods for Evaluation of Blood Transfusion Compatibility in Horses

por Luethy, D., Owens, S.D., Stefanovski, D., Nolen‐Walston, R., Giger, U.
Publicado 2016

Selective Intestinal Cobalamin Malabsorption with Proteinuria (Imerslund‐Gräsbeck Syndrome) in Juvenile Beagles

por Fyfe, J.C., Hemker, S.L., Venta, P.J., Stebbing, B., Giger, U.
Publicado 2014

Prevalence and Mode of Inheritance of the Dal Blood Group in Dogs in North America

por Goulet, S., Giger, U., Arsenault, J., Abrams‐Ogg, A., Euler, C.C., Blais, M.‐C.
Publicado 2017

Survey of Two New (Kai 1 and Kai 2) and Other Blood Groups in Dogs of North America

por Euler, C.C., Lee, J.H., Kim, H.Y., Raj, K., Mizukami, K., Giger, U.
Publicado 2016

Long‐term Treatment with Methylene Blue in a Dog with Hereditary Methemoglobinemia Caused by Cytochrome b5 Reductase Deficiency

por Jaffey, J.A., Harmon, M.R., Villani, N.A., Creighton, E.K., Johnson, G.S., Giger, U., Dodam, J.R.
Publicado 2017

Pre‐ and Post‐Transfusion Alloimmunization in Dogs Characterized by 2 Antiglobulin‐Enhanced Cross‐match Tests

por Goy‐Thollot, I., Giger, U., Boisvineau, C., Perrin, R., Guidetti, M., Chaprier, B., Barthélemy, A., Pouzot‐Nevoret, C., Canard, B.
Publicado 2017

Clinical, metabolic, and molecular genetic characterization of hereditary methemoglobinemia caused by cytochrome b(5) reductase deficiency in 30 dogs

por Jaffey, J. A., Reading, N. S., Abdulmalik, O., Kreisler, R., Bullock, G., Wiest, A., Villani, N. A., Mhlanga-Mutangadura, T., Johnson, G. S., Cohn, L. A., Isaza, N., Harvey, J. W., Giger, U.
Publicado 2020