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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
March 18, 2003
[Pigmented retinopathy as a presenting sign of mitochondrial encephalomyopathy without external ophthalmoplegia]
S Staudt, A M Joussen, D Rating, et al.
Molecular Biology of the Cell
|
April 6, 2000
Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression
Y Tang, E A Schon, E Wilichowski, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 15, 2009
Distinct inflammatory properties of late-activated macrophages in inflammatory myopathies
K M Rostasy, J Schmidt, E Bahn, et al.
Journal of Child Neurology
|
August 21, 2001
Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndrome
M Cacić, E Wilichowski, V Mejaski-Bosnjak, et al.
Annals of Neurology
|
August 1, 1996
Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype
G C Korenke, S Fuchs, E Krasemann, et al.
Developmental Medicine and Child Neurology
|
September 1, 1994
Proton spectroscopy in patients with Leigh's disease and mitochondrial enzyme deficiency
B Kruse, F Hanefeld, U Holzbach, et al.
Journal of the Neurological Sciences
|
June 10, 1998
Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns-Sayre/MELAS overlap syndrome and A3243G mtDNA mutation
E Wilichowski, G C Korenke, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Progressive fatal pancytopenia, psychomotor retardation and muscle carnitine deficiency in a child with ethylmalonic aciduria and ethylmalonic acidaemia
G F Hoffmann, D H Hunneman, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 28, 2009
Aromatic L-amino acid decarboxylase deficiency: clinical features, drug therapy and follow-up
C Manegold, G F Hoffmann, I Degen, et al.
Pediatric Research
|
February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome
E Wilichowski, A Grüters, K Kruse, et al.
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Search research articles
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Showing results (21-30 of 34) with videos related to
Sort By:
Page
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Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
March 18, 2003
[Pigmented retinopathy as a presenting sign of mitochondrial encephalomyopathy without external ophthalmoplegia]
S Staudt, A M Joussen, D Rating, et al.
Molecular Biology of the Cell
|
April 6, 2000
Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression
Y Tang, E A Schon, E Wilichowski, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
April 15, 2009
Distinct inflammatory properties of late-activated macrophages in inflammatory myopathies
K M Rostasy, J Schmidt, E Bahn, et al.
Journal of Child Neurology
|
August 21, 2001
Cytochrome c oxidase partial deficiency-associated Leigh disease presenting as an extrapyramidal syndrome
M Cacić, E Wilichowski, V Mejaski-Bosnjak, et al.
Annals of Neurology
|
August 1, 1996
Cerebral adrenoleukodystrophy (ALD) in only one of monozygotic twins with an identical ALD genotype
G C Korenke, S Fuchs, E Krasemann, et al.
Developmental Medicine and Child Neurology
|
September 1, 1994
Proton spectroscopy in patients with Leigh's disease and mitochondrial enzyme deficiency
B Kruse, F Hanefeld, U Holzbach, et al.
Journal of the Neurological Sciences
|
June 10, 1998
Pyruvate dehydrogenase complex deficiency and altered respiratory chain function in a patient with Kearns-Sayre/MELAS overlap syndrome and A3243G mtDNA mutation
E Wilichowski, G C Korenke, W Ruitenbeek, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1990
Progressive fatal pancytopenia, psychomotor retardation and muscle carnitine deficiency in a child with ethylmalonic aciduria and ethylmalonic acidaemia
G F Hoffmann, D H Hunneman, C Jakobs, et al.
Journal of Inherited Metabolic Disease
|
January 28, 2009
Aromatic L-amino acid decarboxylase deficiency: clinical features, drug therapy and follow-up
C Manegold, G F Hoffmann, I Degen, et al.
Pediatric Research
|
February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndrome
E Wilichowski, A Grüters, K Kruse, et al.
Page
of 4