Investigation of side effects to treatment and cause of death in 63 Scandinavian dogs suffering from meningoencephalitis of unknown origin: a retrospective study

Autor: Pernille Lindholm Heidemann, Bolette Erhald, Bodil Cathrine Koch, Hanne Gredal

Publikováno v: Acta Veterinaria Scandinavica, Vol 65, Iss 1, Pp 1-15 (2023)

Abstract Background Meningoencephalitis of unknown origin is a common cause of severe neurological disease in dogs. The term covers a heterogeneous group of noninfectious inflammatory diseases, with immune dysregulation widely accepted as the underly

Externí odkaz: https://doaj.org/article/b323db9b5c7f4da2bad9354bd80849ab

Investigation of side effects to treatment and cause of death in 63 Scandinavian dogs suffering from meningoencephalitis of unknown origin: a retrospective study.

Autor: Heidemann, Pernille Lindholm¹ (AUTHOR) pernille.heidemann@sund.ku.dk, Erhald, Bolette² (AUTHOR), Koch, Bodil Cathrine³ (AUTHOR), Gredal, Hanne¹ (AUTHOR)

Publikováno v: Acta Veterinaria Scandinavica. 10/19/2023, Vol. 65 Issue 1, p1-15. 15p.

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Kjartan Hasse Stenbuk Arctander

Autor: Truls Ryder, Michael Reginald Schneider, Kristin Eidal, Pernille Lindholm, Astrid Schjelderup Berntsen, Elisabeth Saetnan, Kim Alexander Tønseth

Publikováno v: Tidsskrift for Den norske legeforening.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e293f47e3920bfaabc4c53252171eb78
https://doi.org/10.4045/tidsskr.21.0200

Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome

Autor: Myriam Oufadem, Erica H. Gerkes, Lina Basel-Vanagaite, Adila Al-Kindy, Philippe Pellerin, Jean-Paul Bonnefont, Arnold Munnich, Peter M. Kroisel, Véronique Abadie, Angela E. Lin, Vincent Couloigner, Leonard B. Kaban, Brigitte A. Meijer, Paul Aurora, Stanislas Lyonnet, Maria Bitner-Glindzicz, S. Pierrot, Muriel Holder-Espinasse, David Kilner, Christopher T. Gordon, Ruth McGowan, Michael R. Speicher, Louise C. Wilson, Jeanne Amiel, Eya Ben Bdira, Françoise Denoyelle, Yves Manach, Florence Petit, Alex Henderson, Bruno Delobel, Mateo Sanchis-Borja, Alice Vuillot, Birgit Sikkema-Raddatz, Linda P. Jakobsen, Edward S. Tobias, Sarah S. Park, Sandrine Marlin, Marie Simon, M.-P. Vazquez, Asma Omarjee, C. Rotky-Fast, Alison Stewart, Yvonne M C Hendriks, Rodger Palmer, Sylvain Breton, Sixto García-Miñaur, Michael L. Cunningham, Pernille Lindholm

Publikováno v: Journal of Medical Genetics, 50(3), 174-186. BMJ Publishing Group
Gordon, C T, Vuillot, A, Marlin, S, Gerkes, E, Henderson, A, AlKindy, A, Holder-Espinasse, M, Park, S S, Omarjee, A, Sanchis-Borja, M, Ben Bdira, E, Oufadem, M, Sikkema-Raddatz, B, Stewart, A, Palmer, R, McGowan, R, Petit, F, Delobel, B, Speicher, M R, Aurora, P, Kilner, D, Pellerin, P, Simon, M, Bonnefont, J P, Tobias, E S, Garcia-Minaur, S, Bitner-Glindzicz, M, Lindholm, P, Meijer, B A, Abadie, V, Denoyelle, F, Vazquez, M P, Rotky-Fast, C, Couloigner, V, Pierrot, S, Manach, Y, Breton, S, Hendriks, Y M C, Munnich, A, Jakobsen, L, Kroisel, P, Lin, A, Kaban, L B, Basel-Vanagaite, L, Wilson, L, Cunningham, M L, Lyonnet, S & Amiel, J 2013, ' Heterogeneity of mutational mechanisms and modes of inheritance in auriculocondylar syndrome ', Journal of Medical Genetics, vol. 50, no. 3, pp. 174-186 . https://doi.org/10.1136/jmedgenet-2012-101331
JOURNAL OF MEDICAL GENETICS, 50(3), 174-186. BMJ PUBLISHING GROUP

Background Auriculocondylar syndrome (ACS) is a rare craniofacial disorder consisting of micrognathia, mandibular condyle hypoplasia and a specific malformation of the ear at the junction between the lobe and helix. Missense heterozygous mutations in

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af707ccd203f73f963834d0807db89a6
https://research.vumc.nl/en/publications/d0c8f8ee-8a2a-4099-9c2a-3db0c2a9dd06