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M Vorgerd

Showing results (21-30 of 65) with videos related to

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International Journal of Colorectal Disease|February 9, 2000
Polymyositis of the skeletal muscles as an extraintestinal complication in quiescent ulcerative colitisE Voigt, T Griga, A Tromm, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Impaired aerobic glycolysis in muscle phosphofructokinase deficiency results in biphasic post-exercise phosphocreatine recovery in 31P magnetic resonance spectroscopyT Grehl, K Müller, M Vorgerd, et al.
Neurology|May 5, 1999
Phenotypic variability in rippling muscle diseaseM Vorgerd, H Bolz, T Patzold, 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.
Neuropediatrics|June 1, 2000
Fetal-onset severe skeletal muscle glycogenosis associated with phosphorylase-b kinase deficiencyC Bührer, F van Landeghem, W Brück, et al.
Electroencephalography and Clinical Neurophysiology|August 1, 1996
Enhancement of inhibitory mechanisms in the motor cortex of patients with cerebellar degeneration: a study with transcranial magnetic brain stimulationK Wessel, M Tegenthoff, M Vorgerd, et al.
Der Pathologe|July 2, 2002
[Fatal cardiomyopathy in adult in polyglucosan body disease]E Postler, E Sindern, M Vorgerd, et al.
Diabetes|September 2, 2000
Heterozygous expansion of the GAA tract of the X25/frataxin gene is associated with insulin resistance in humansJ Hebinck, C Hardt, L Schöls, et al.
Neurology|January 26, 2006
Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiencyA Schroers, R A Kley, A Stachon, et al.
Klinische Padiatrie|December 22, 2007
[Muscular magnetic resonance imaging for evaluation of myopathies in children]S A Peters, C Köhler, U Schara, et al.
Pageof 7

Showing results (21-30 of 65) with videos related to

Sort By:
Pageof 7
International Journal of Colorectal Disease|February 9, 2000
Polymyositis of the skeletal muscles as an extraintestinal complication in quiescent ulcerative colitisE Voigt, T Griga, A Tromm, et al.
Neuromuscular Disorders : NMD|November 26, 1998
Impaired aerobic glycolysis in muscle phosphofructokinase deficiency results in biphasic post-exercise phosphocreatine recovery in 31P magnetic resonance spectroscopyT Grehl, K Müller, M Vorgerd, et al.
Neurology|May 5, 1999
Phenotypic variability in rippling muscle diseaseM Vorgerd, H Bolz, T Patzold, 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.
Neuropediatrics|June 1, 2000
Fetal-onset severe skeletal muscle glycogenosis associated with phosphorylase-b kinase deficiencyC Bührer, F van Landeghem, W Brück, et al.
Electroencephalography and Clinical Neurophysiology|August 1, 1996
Enhancement of inhibitory mechanisms in the motor cortex of patients with cerebellar degeneration: a study with transcranial magnetic brain stimulationK Wessel, M Tegenthoff, M Vorgerd, et al.
Der Pathologe|July 2, 2002
[Fatal cardiomyopathy in adult in polyglucosan body disease]E Postler, E Sindern, M Vorgerd, et al.
Diabetes|September 2, 2000
Heterozygous expansion of the GAA tract of the X25/frataxin gene is associated with insulin resistance in humansJ Hebinck, C Hardt, L Schöls, et al.
Neurology|January 26, 2006
Gentamicin treatment in McArdle disease: failure to correct myophosphorylase deficiencyA Schroers, R A Kley, A Stachon, et al.
Klinische Padiatrie|December 22, 2007
[Muscular magnetic resonance imaging for evaluation of myopathies in children]S A Peters, C Köhler, U Schara, et al.
Pageof 7