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Human Mutation|October 17, 2006
Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patientsCindy Krause, Hendrik Rosewich, Melissa Thanos, et al.
Neurology|March 9, 2005
Treatment of early onset multiple sclerosis with subcutaneous interferon beta-1aDaniela Pohl, Kevin Rostasy, Jutta Gärtner, et al.
JIMD Reports|February 23, 2013
Lymphoblastoid cell lines for diagnosis of peroxisome biogenesis disordersSabine Grønborg, Ralph Krätzner, Hendrik Rosewich, et al.
Therapeutic Advances in Neurological Disorders|August 28, 2019
B cell depletion can be effective in multiple sclerosis but failed in a patient with advanced childhood cerebral X-linked adrenoleukodystrophyHendrik Rosewich, Stefan Nessler, Wolfgang Brück, et al.
Journal of Inherited Metabolic Disease|November 21, 2019
Inborn errors of metabolism leading to neuronal migration defectsStina Schiller, Hendrik Rosewich, Stephanie Grünewald, et al.
Pediatric Research|February 5, 2009
Suppression of nonsense mutations in Rett syndrome by aminoglycoside antibioticsCornelia Brendel, Edith Klahold, Jutta Gärtner, et al.
European Journal of Human Genetics : EJHG|May 6, 2010
Pelizaeus-Merzbacher-like disease is caused not only by a loss of connexin47 function but also by a hemichannel dysfunctionSimone Diekmann, Marco Henneke, Birgitta C Burckhardt, et al.
European Journal of Cell Biology|May 20, 2003
The peroxisomal membrane targeting elements of human peroxin 2 (PEX2)Martina Biermanns, Jutta von Laar, Ute Brosius, et al.
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