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American Journal of Medical Genetics
|
April 24, 1996
VACTERL with the mitochondrial np 3243 point mutation
M S Damian, P Seibel, W Schachenmayr, et al.
Annals of Neurology
|
January 1, 1992
Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy
H Reichmann, H Scheel, B Bier, et al.
Journal of Neurology
|
December 1, 1990
Duchenne muscular dystrophy: evidence for somatic reversion of the mutation in man
R Gold, B Meurers, H Reichmann, et al.
Clinical Neuropathology
|
January 1, 1996
Mitochondrial changes in muscle phosphoglycerate kinase deficiency
J M Schröder, R Dodel, J Weis, et al.
Journal of Neurology
|
April 1, 1996
Investigation on the mitochondrial transfer RNA(Leu)(UUR) in blood cells from patients with cluster headache
P Seibel, T Grünewald, A Gundolla, et al.
Journal of Neurology
|
October 31, 2003
Schnitzler's syndrome with neurological findings
G Gossrau, C Pfeiffer, M Meurer, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency
H Porschke, W Kress, H Reichmann, et al.
Pflugers Archiv : European Journal of Physiology
|
May 1, 1985
Biochemical and ultrastructural changes of skeletal muscle mitochondria after chronic electrical stimulation in rabbits
H Reichmann, H Hoppeler, O Mathieu-Costello, et al.
Archives of Neurology
|
September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration
H Reichmann, R Rohkamm, M Zeviani, et al.
Der Nervenarzt
|
September 24, 2002
[Entacapone for treatment of motor fluctuations in idiopathic Parkinson syndrome]
U Sommer, A Müller, B Herting, et al.
Page
of 28
Search research articles
Search
Showing results (151-160 of 273) with videos related to
Sort By:
Page
of 28
American Journal of Medical Genetics
|
April 24, 1996
VACTERL with the mitochondrial np 3243 point mutation
M S Damian, P Seibel, W Schachenmayr, et al.
Annals of Neurology
|
January 1, 1992
Cytochrome c oxidase deficiency and long-chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy
H Reichmann, H Scheel, B Bier, et al.
Journal of Neurology
|
December 1, 1990
Duchenne muscular dystrophy: evidence for somatic reversion of the mutation in man
R Gold, B Meurers, H Reichmann, et al.
Clinical Neuropathology
|
January 1, 1996
Mitochondrial changes in muscle phosphoglycerate kinase deficiency
J M Schröder, R Dodel, J Weis, et al.
Journal of Neurology
|
April 1, 1996
Investigation on the mitochondrial transfer RNA(Leu)(UUR) in blood cells from patients with cluster headache
P Seibel, T Grünewald, A Gundolla, et al.
Journal of Neurology
|
October 31, 2003
Schnitzler's syndrome with neurological findings
G Gossrau, C Pfeiffer, M Meurer, et al.
Neuromuscular Disorders : NMD
|
December 10, 1997
Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency
H Porschke, W Kress, H Reichmann, et al.
Pflugers Archiv : European Journal of Physiology
|
May 1, 1985
Biochemical and ultrastructural changes of skeletal muscle mitochondria after chronic electrical stimulation in rabbits
H Reichmann, H Hoppeler, O Mathieu-Costello, et al.
Archives of Neurology
|
September 1, 1986
Mitochondrial myopathy due to complex III deficiency with normal reducible cytochrome b concentration
H Reichmann, R Rohkamm, M Zeviani, et al.
Der Nervenarzt
|
September 24, 2002
[Entacapone for treatment of motor fluctuations in idiopathic Parkinson syndrome]
U Sommer, A Müller, B Herting, et al.
Page
of 28