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M Vorgerd

Showing results (31-40 of 65) with videos related to

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Journal of the Neurological Sciences|September 15, 1996
Muscle phosphofructokinase deficiency in two generationsM Vorgerd, J Karitzky, M Ristow, et al.
Biochemical and Biophysical Research Communications|July 30, 1999
Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormalityB Burwinkel, J Kreuder, S Schweitzer, et al.
Annals of Neurology|July 12, 2002
Creatine supplementation results in elevated phosphocreatine/adenosine triphosphate (ATP) ratios in the calf muscle of athletes but not in patients with myopathiesJ Zange, C Kornblum, K Müller, et al.
Acta Neurologica Scandinavica|December 19, 1998
Reduced intracortical facilitation in patients with cerebellar degenerationJ Liepert, K Wessel, P Schwenkreis, et al.
Human Genetics|April 1, 1988
Phenylketonuria: distribution of DNA diagnostic patterns in German familiesC Aulehla-Scholz, M Vorgerd, E Sautter, et al.
Der Nervenarzt|September 14, 1999
[Adult polyglucosan antibody disease. Case report with predominant involvement of the central and peripheral nervous system and branching enzyme defect in leukocytes]E Sindern, T Patzold, M Vorgerd, et al.
Journal of Inherited Metabolic Disease|July 9, 2008
Molecular diagnosis of German patients with late-onset glycogen storage disease type IIP R Joshi, D Gläser, S Schmidt, et al.
Journal of Neuromuscular Diseases|June 28, 2021
Diffusion Tensor Imaging Shows Differences Between Myotonic Dystrophy Type 1 and Type 2R Rehmann, C Schneider-Gold, M Froeling, et al.
Diabetes|July 30, 1999
Deficiency of phosphofructo-1-kinase/muscle subtype in humans is associated with impairment of insulin secretory oscillationsM Ristow, H Carlqvist, J Hebinck, et al.
European Journal of Neurology|April 5, 2005
Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions: a placebo-controlled, double-blind 31P-MRS crossover studyC Kornblum, R Schröder, K Müller, et al.
Pageof 7

Showing results (31-40 of 65) with videos related to

Sort By:
Pageof 7
Journal of the Neurological Sciences|September 15, 1996
Muscle phosphofructokinase deficiency in two generationsM Vorgerd, J Karitzky, M Ristow, et al.
Biochemical and Biophysical Research Communications|July 30, 1999
Carnitine transporter OCTN2 mutations in systemic primary carnitine deficiency: a novel Arg169Gln mutation and a recurrent Arg282ter mutation associated with an unconventional splicing abnormalityB Burwinkel, J Kreuder, S Schweitzer, et al.
Annals of Neurology|July 12, 2002
Creatine supplementation results in elevated phosphocreatine/adenosine triphosphate (ATP) ratios in the calf muscle of athletes but not in patients with myopathiesJ Zange, C Kornblum, K Müller, et al.
Acta Neurologica Scandinavica|December 19, 1998
Reduced intracortical facilitation in patients with cerebellar degenerationJ Liepert, K Wessel, P Schwenkreis, et al.
Human Genetics|April 1, 1988
Phenylketonuria: distribution of DNA diagnostic patterns in German familiesC Aulehla-Scholz, M Vorgerd, E Sautter, et al.
Der Nervenarzt|September 14, 1999
[Adult polyglucosan antibody disease. Case report with predominant involvement of the central and peripheral nervous system and branching enzyme defect in leukocytes]E Sindern, T Patzold, M Vorgerd, et al.
Journal of Inherited Metabolic Disease|July 9, 2008
Molecular diagnosis of German patients with late-onset glycogen storage disease type IIP R Joshi, D Gläser, S Schmidt, et al.
Journal of Neuromuscular Diseases|June 28, 2021
Diffusion Tensor Imaging Shows Differences Between Myotonic Dystrophy Type 1 and Type 2R Rehmann, C Schneider-Gold, M Froeling, et al.
Diabetes|July 30, 1999
Deficiency of phosphofructo-1-kinase/muscle subtype in humans is associated with impairment of insulin secretory oscillationsM Ristow, H Carlqvist, J Hebinck, et al.
European Journal of Neurology|April 5, 2005
Creatine has no beneficial effect on skeletal muscle energy metabolism in patients with single mitochondrial DNA deletions: a placebo-controlled, double-blind 31P-MRS crossover studyC Kornblum, R Schröder, K Müller, et al.
Pageof 7