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J Gärtner

Showing results (81-90 of 106) with videos related to

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Neuropediatrics|June 15, 2006
Pitfall in metabolic screening in a patient with fatal peroxisomal beta-oxidation defectH Rosewich, H R Waterham, R J A Wanders, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 3, 2010
Intrathecal IgM synthesis in pediatric MS is not a negative prognostic marker of disease progression: quantitative versus qualitative IgM analysisC Stauch, H Reiber, M Rauchenzauner, et al.
Neuropediatrics|August 26, 1998
Paraneoplastic limbic encephalitis in two teenage girlsT Rosenbaum, J Gärtner, D Körholz, et al.
Neuropediatrics|September 3, 2005
Acute motor and sensory axonal neuropathy (AMSAN) in a 15-year-old boy presenting with severe pain and distal muscle weaknessK M Rostásy, P Huppke, B Beckers, et al.
Brain : a Journal of Neurology|May 16, 2012
Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiencyM Grapp, I A Just, T Linnankivi, et al.
Genomics|February 1, 1993
Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3J Gärtner, W Kearns, C Rosenberg, et al.
American Journal of Human Genetics|April 1, 1995
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypesA Braun, H Ambach, S Kammerer, et al.
Neuropediatrics|January 20, 2007
High dose pulsatile dexamethasone therapy in children with opsoclonus-myoclonus syndromeK Rostásy, B Wilken, M Baumann, et al.
Neurology|December 13, 2006
High seroprevalence of Epstein-Barr virus in children with multiple sclerosisD Pohl, B Krone, K Rostasy, et al.
Clinical Genetics|June 19, 2015
Obtaining a genetic diagnosis in a child with disability: impact on parental quality of lifeM Lingen, L Albers, M Borchers, et al.
Pageof 11

Showing results (81-90 of 106) with videos related to

Sort By:
Pageof 11
Neuropediatrics|June 15, 2006
Pitfall in metabolic screening in a patient with fatal peroxisomal beta-oxidation defectH Rosewich, H R Waterham, R J A Wanders, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 3, 2010
Intrathecal IgM synthesis in pediatric MS is not a negative prognostic marker of disease progression: quantitative versus qualitative IgM analysisC Stauch, H Reiber, M Rauchenzauner, et al.
Neuropediatrics|August 26, 1998
Paraneoplastic limbic encephalitis in two teenage girlsT Rosenbaum, J Gärtner, D Körholz, et al.
Neuropediatrics|September 3, 2005
Acute motor and sensory axonal neuropathy (AMSAN) in a 15-year-old boy presenting with severe pain and distal muscle weaknessK M Rostásy, P Huppke, B Beckers, et al.
Brain : a Journal of Neurology|May 16, 2012
Molecular characterization of folate receptor 1 mutations delineates cerebral folate transport deficiencyM Grapp, I A Just, T Linnankivi, et al.
Genomics|February 1, 1993
Localization of the 70-kDa peroxisomal membrane protein to human 1p21-p22 and mouse 3J Gärtner, W Kearns, C Rosenberg, et al.
American Journal of Human Genetics|April 1, 1995
Mutations in the gene for X-linked adrenoleukodystrophy in patients with different clinical phenotypesA Braun, H Ambach, S Kammerer, et al.
Neuropediatrics|January 20, 2007
High dose pulsatile dexamethasone therapy in children with opsoclonus-myoclonus syndromeK Rostásy, B Wilken, M Baumann, et al.
Neurology|December 13, 2006
High seroprevalence of Epstein-Barr virus in children with multiple sclerosisD Pohl, B Krone, K Rostasy, et al.
Clinical Genetics|June 19, 2015
Obtaining a genetic diagnosis in a child with disability: impact on parental quality of lifeM Lingen, L Albers, M Borchers, et al.
Pageof 11