Search research articles
Contact Us
Filters
Showing results (81-90 of 184) with videos related to
Page
of 19
Sort By:
American Journal of Medical Genetics
|
December 1, 1986
Metabolic myopathies
S DiMauro, A F Miranda, S Sakoda, et al.
Annals of Neurology
|
February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation
V Tiranti, L D'Agruma, D Pareyson, et al.
Journal of Neurology
|
October 13, 2007
Mitochondrial complex III deficiency in a case of HCV related noninflammatory myopathy
P Cortelli, J Mandrioli, M Zeviani, et al.
Journal of Bioenergetics and Biomembranes
|
June 1, 1988
Molecular defects in cytochrome oxidase in mitochondrial diseases
S DiMauro, M Zeviani, R Rizzuto, et al.
Biochemical and Biophysical Research Communications
|
May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient
F M Santorelli, E Bertini, V Petruzzella, et al.
Journal of Neurology
|
September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study
C Mariotti, G Uziel, F Carrara, et al.
Journal of Medical Genetics
|
November 25, 2003
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son
G Puoti, F Carrara, S Sampaolo, et al.
American Journal of Medical Genetics
|
December 1, 1991
Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?
C T Moraes, M Zeviani, E A Schon, et al.
Annals of the New York Academy of Sciences
|
January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneity
S DiMauro, M Zeviani, S Servidei, et al.
Advances in Neurology
|
January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiency
S DiMauro, M Zeviani, S Servidei, et al.
Page
of 19
Search research articles
Search
Showing results (81-90 of 184) with videos related to
Sort By:
Page
of 19
American Journal of Medical Genetics
|
December 1, 1986
Metabolic myopathies
S DiMauro, A F Miranda, S Sakoda, et al.
Annals of Neurology
|
February 5, 1998
A novel mutation in the mitochondrial tRNA(Val) gene associated with a complex neurological presentation
V Tiranti, L D'Agruma, D Pareyson, et al.
Journal of Neurology
|
October 13, 2007
Mitochondrial complex III deficiency in a case of HCV related noninflammatory myopathy
P Cortelli, J Mandrioli, M Zeviani, et al.
Journal of Bioenergetics and Biomembranes
|
June 1, 1988
Molecular defects in cytochrome oxidase in mitochondrial diseases
S DiMauro, M Zeviani, R Rizzuto, et al.
Biochemical and Biophysical Research Communications
|
May 8, 1998
A novel insertion mutation (A169i) in the CLN1 gene is associated with infantile neuronal ceroid lipofuscinosis in an Italian patient
F M Santorelli, E Bertini, V Petruzzella, et al.
Journal of Neurology
|
September 1, 1995
Early-onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: a morphological, biochemical and molecular-genetic study
C Mariotti, G Uziel, F Carrara, et al.
Journal of Medical Genetics
|
November 25, 2003
Identical large scale rearrangement of mitochondrial DNA causes Kearns-Sayre syndrome in a mother and her son
G Puoti, F Carrara, S Sampaolo, et al.
American Journal of Medical Genetics
|
December 1, 1991
Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?
C T Moraes, M Zeviani, E A Schon, et al.
Annals of the New York Academy of Sciences
|
January 1, 1986
Cytochrome oxidase deficiency: clinical and biochemical heterogeneity
S DiMauro, M Zeviani, S Servidei, et al.
Advances in Neurology
|
January 1, 1988
Biochemical and molecular aspects of cytochrome C oxidase deficiency
S DiMauro, M Zeviani, S Servidei, et al.
Page
of 19