Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Victoria Schiffer"'
Autor:
Victoria Schiffer, Estibaliz Santiago-Mujika, Stefanie Flunkert, Staffan Schmidt, Martina Farcher, Tina Loeffler, Irene Schilcher, Maria Posch, Joerg Neddens, Ying Sun, Jan Kehr, Birgit Hutter-Paier
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0227077 (2020)
Gaucher disease is caused by a deficiency in glucocerebrosidase that can result in non-neuronal as well as neuronal symptoms. Common visceral symptoms are an increased organ size, specifically of the spleen, and glucosylceramide as well as glucosylsp
Externí odkaz:
https://doaj.org/article/934465be4e504e42abf8e2944f2bd11d
Autor:
Ying Sun, Birgit Hutter-Paier, Victoria Schiffer, Tina Loeffler, Martina Farcher, Stefanie Flunkert, Estibaliz Santiago-Mujika, Irene Schilcher, Staffan Schmidt, Joerg Neddens, Maria Posch, Jan Kehr
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 1, p e0227077 (2020)
PLoS ONE, Vol 15, Iss 1, p e0227077 (2020)
Gaucher disease is caused by a deficiency in glucocerebrosidase that can result in non-neuronal as well as neuronal symptoms. Common visceral symptoms are an increased organ size, specifically of the spleen, and glucosylceramide as well as glucosylsp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4cbfee898875fc0c39b6c98ff61b7671
http://europepmc.org/articles/PMC6957154
http://europepmc.org/articles/PMC6957154
Autor:
Joerg Neddens, Vera Niederkofler, Magdalena Temmel, Victoria Schiffer, Birgit Hutter-Paier, Ewald Auer
Publikováno v:
Molecular Genetics and Metabolism. 129:S116-S117
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3355f18140cd609029d3ca27527c399
https://doi.org/10.1016/j.ymgme.2019.11.301
https://doi.org/10.1016/j.ymgme.2019.11.301
Autor:
Staffan Schmidt, Tina Loeffler, Ewald Auer, Jan Kehr, Victoria Schiffer, Birgit Hutter-Paier, Joerg Neddens, Vera Niederkofler
Publikováno v:
Molecular Genetics and Metabolism. 126:S109
Gaucher disease is the most common lysosomal storage disease. The neuronal disease variant is characterized by aggregated protein accumulations in the brain and associated neurological manifestations. It is autosomal recessively inherited and modeled
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::11364bf7717e82de9e6e1c3ebd9fa17e
https://doi.org/10.1016/j.ymgme.2018.12.275
https://doi.org/10.1016/j.ymgme.2018.12.275
Autor:
Stefanie Flunkert, Joerg Neddens, Maria Posch, Estibaliz Santiago Mugica, Vera Niederkofler, Martina Farcher, Victoria Schiffer, Roland Rabl, Ewald Auer, Birgit Hutter-Paier
Publikováno v:
Molecular Genetics and Metabolism. 123:S46
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0497b11da6f4afbf91445496b626bda4
https://doi.org/10.1016/j.ymgme.2017.12.104
https://doi.org/10.1016/j.ymgme.2017.12.104
Publikováno v:
Journal of Veterinary Behavior. 6:71
The biotonus test developed by Trumler (1987) in order to evaluate the vitality of pups is still very common among breeders and cynologists. Trumler assumes that pups are more viable if they are more active in their drive to reach their mother’s te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43cc28af6d3141a17f39bfd437ebfc0d
https://doi.org/10.1016/j.jveb.2010.09.031
https://doi.org/10.1016/j.jveb.2010.09.031