Showing results (11-20 of 165) with videos related to
Sort By:
Pageof 17
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 International|March 6, 2021
Follow-Up of a Case of Dopamine-Mediated Yawning-Fatigue-Syndrome Responsive to Opioids, Successful Desensitization via Graded Activity TreatmentPayam Dibaj, Dagmar Seeger, Jutta Gärtner, 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.Human Molecular Genetics|May 30, 2013
Functional analysis of PEX13 mutation in a Zellweger syndrome spectrum patient reveals novel homooligomerization of PEX13 and its role in human peroxisome biogenesisCindy Krause, Hendrik Rosewich, Andrew Woehler, 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.Pageof 17