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M Gencik

Showing results (21-30 of 32) with videos related to

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Clinical and Experimental Immunology|August 12, 1999
Immunogenetic risk factors for anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitisM Gencik, S Borgmann, R Zahn, et al.
Muscle & Nerve|May 16, 2001
Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophiesM Vorgerd, M Gencik, J Mortier, et al.
Clinical Genetics|January 11, 2016
The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNAH Cetin, A Wöhrer, I Rittelmeyer, et al.
European Journal of Pediatrics|July 31, 2001
Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient careU Schara, M Gencik, J Mortier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 19, 2004
Apolipoprotein E genotypes do not influence the age of onset in Huntington's diseaseC Saft, J E Andrich, N Brune, et al.
Journal of Neural Transmission. Supplementum|September 10, 2004
Methyltetrahydrofolate reductase polymorphism influences onset of Huntington's diseaseN Brune, J Andrich, M Gencik, et al.
Human Mutation|May 20, 2003
A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneityP Jagiello, C Hammans, S Wieczorek, et al.
Clinical Immunology (Orlando, Fla.)|December 23, 1999
The association of CD18 alleles with anti-myeloperoxidase subtypes of ANCA-associated systemic vasculitidesM Gencik, S Meller, S Borgmann, et al.
Neurology|January 10, 2001
A prepro-orexin gene polymorphism is associated with narcolepsyM Gencik, N Dahmen, S Wieczorek, et al.
Klinische Padiatrie|October 25, 2011
Hereditary hyperferritinemia cataract syndrome: clinical, genetic, and laboratory findings in 5 familiesL Nonnenmacher, T Langer, H Blessing, et al.
Pageof 4

Showing results (21-30 of 32) with videos related to

Sort By:
Pageof 4
Clinical and Experimental Immunology|August 12, 1999
Immunogenetic risk factors for anti-neutrophil cytoplasmic antibody (ANCA)-associated systemic vasculitisM Gencik, S Borgmann, R Zahn, et al.
Muscle & Nerve|May 16, 2001
Isolated loss of gamma-sarcoglycan: diagnostic implications in autosomal recessive limb-girdle muscular dystrophiesM Vorgerd, M Gencik, J Mortier, et al.
Clinical Genetics|January 11, 2016
The c.65-2A>G splice site mutation is associated with a mild phenotype in Danon disease due to the transcription of normal LAMP2 mRNAH Cetin, A Wöhrer, I Rittelmeyer, et al.
European Journal of Pediatrics|July 31, 2001
Alpha-sarcoglycanopathy previously misdiagnosed as Duchenne muscular dystrophy: implications for current diagnostics and patient careU Schara, M Gencik, J Mortier, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 19, 2004
Apolipoprotein E genotypes do not influence the age of onset in Huntington's diseaseC Saft, J E Andrich, N Brune, et al.
Journal of Neural Transmission. Supplementum|September 10, 2004
Methyltetrahydrofolate reductase polymorphism influences onset of Huntington's diseaseN Brune, J Andrich, M Gencik, et al.
Human Mutation|May 20, 2003
A novel splice site mutation in the TRIM37 gene causes mulibrey nanism in a Turkish family with phenotypic heterogeneityP Jagiello, C Hammans, S Wieczorek, et al.
Clinical Immunology (Orlando, Fla.)|December 23, 1999
The association of CD18 alleles with anti-myeloperoxidase subtypes of ANCA-associated systemic vasculitidesM Gencik, S Meller, S Borgmann, et al.
Neurology|January 10, 2001
A prepro-orexin gene polymorphism is associated with narcolepsyM Gencik, N Dahmen, S Wieczorek, et al.
Klinische Padiatrie|October 25, 2011
Hereditary hyperferritinemia cataract syndrome: clinical, genetic, and laboratory findings in 5 familiesL Nonnenmacher, T Langer, H Blessing, et al.
Pageof 4