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A von Moers

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Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 1, 1996
Comparison of three immunoassays for diagnosing sensitization to latex in children with spina bifidaB Niggemann, T Michael, A von Moers, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Dystrophinopathy in a boy with Chediak-Higashi syndromeA von Moers, F K van Landeghem, R D Cohn, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 24, 2001
Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per seS Endesfelder, A Krahn, K A Kreuzer, et al.
Neuropediatrics|September 16, 2003
Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)R Blattner, A Von Moers, P A J Leegwater, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophyB Kerst, D Mennerich, M Schuelke, et al.
Annals of Neurology|October 18, 2001
Autosomal dominant glut-1 deficiency syndrome and familial epilepsyK Brockmann, D Wang, C G Korenke, et al.
Neuromuscular Disorders : NMD|December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosisM von der Hagen, J Schallner, A M Kaindl, et al.
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Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Pediatric Allergy and Immunology : Official Publication of the European Society of Pediatric Allergy and Immunology|November 1, 1996
Comparison of three immunoassays for diagnosing sensitization to latex in children with spina bifidaB Niggemann, T Michael, A von Moers, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Dystrophinopathy in a boy with Chediak-Higashi syndromeA von Moers, F K van Landeghem, R D Cohn, et al.
Journal of Molecular Medicine (Berlin, Germany)|February 24, 2001
Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per seS Endesfelder, A Krahn, K A Kreuzer, et al.
Neuropediatrics|September 16, 2003
Clinical and genetic heterogeneity in megalencephalic leukoencephalopathy with subcortical cysts (MLC)R Blattner, A Von Moers, P A J Leegwater, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Heterozygous myogenic factor 6 mutation associated with myopathy and severe course of Becker muscular dystrophyB Kerst, D Mennerich, M Schuelke, et al.
Annals of Neurology|October 18, 2001
Autosomal dominant glut-1 deficiency syndrome and familial epilepsyK Brockmann, D Wang, C G Korenke, et al.
Neuromuscular Disorders : NMD|December 28, 2005
Facing the genetic heterogeneity in neuromuscular disorders: linkage analysis as an economic diagnostic approach towards the molecular diagnosisM von der Hagen, J Schallner, A M Kaindl, et al.
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