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Archives of Neurology
|
November 1, 1986
Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency
M Zeviani, D H Van Dyke, S Servidei, et al.
Journal of Neurology
|
May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA
C Mariotti, N Savarese, A Suomalainen, et al.
The American Journal of Medicine
|
August 15, 2001
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication
V Cicconi, E Carloni, F Franceschi, et al.
Annals of Neurology
|
October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndrome
S DiMauro, S Servidei, M Zeviani, et al.
The New England Journal of Medicine
|
May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
C T Moraes, S DiMauro, M Zeviani, et al.
Neurology
|
February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach
H J Tritschler, E Bonilla, A Lombes, et al.
The Journal of Pediatrics
|
December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletion
M R Mazziotta, E Ricci, E Bertini, et al.
American Journal of Medical Genetics
|
February 25, 1998
Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity
M Sabatelli, T Mignogna, G Lippi, et al.
The Journal of Pediatrics
|
January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts
A B Burlina, C Dionisi-Vici, M J Bennett, et al.
The American Journal of Pathology
|
December 1, 1988
Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy
E Bonilla, B Schmidt, C E Samitt, et al.
Page
of 15
Search research articles
Search
Showing results (121-130 of 146) with videos related to
Sort By:
Page
of 15
Archives of Neurology
|
November 1, 1986
Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency
M Zeviani, D H Van Dyke, S Servidei, et al.
Journal of Neurology
|
May 1, 1995
Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA
C Mariotti, N Savarese, A Suomalainen, et al.
The American Journal of Medicine
|
August 15, 2001
Disappearance of antiphospholipid antibodies syndrome after Helicobacter pylori eradication
V Cicconi, E Carloni, F Franceschi, et al.
Annals of Neurology
|
October 1, 1987
Cytochrome c oxidase deficiency in Leigh syndrome
S DiMauro, S Servidei, M Zeviani, et al.
The New England Journal of Medicine
|
May 18, 1989
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
C T Moraes, S DiMauro, M Zeviani, et al.
Neurology
|
February 1, 1991
Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach
H J Tritschler, E Bonilla, A Lombes, et al.
The Journal of Pediatrics
|
December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletion
M R Mazziotta, E Ricci, E Bertini, et al.
American Journal of Medical Genetics
|
February 25, 1998
Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity
M Sabatelli, T Mignogna, G Lippi, et al.
The Journal of Pediatrics
|
January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblasts
A B Burlina, C Dionisi-Vici, M J Bennett, et al.
The American Journal of Pathology
|
December 1, 1988
Normal and dystrophin-deficient muscle fibers in carriers of the gene for Duchenne muscular dystrophy
E Bonilla, B Schmidt, C E Samitt, et al.
Page
of 15