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European Journal of Pediatrics
|
November 1, 1996
Diagnostic problems in congenital myotonic dystrophy
M DiRocco, M Gennarelli, E Veneselli, et al.
Clinical Genetics
|
July 18, 2002
Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletion
C Bruno, P Gandullia, F M Santorelli, et al.
Neuromuscular Disorders : NMD
|
May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria
C Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletion
C Bruno, C Minetti, Y Tang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 21, 2004
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect
E Di Maria, R Gulli, P Balestra, et al.
Annals of Neurology
|
May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutation
P Mandich, G L Mancardi, A Varese, et al.
Biochemical and Biophysical Research Communications
|
August 12, 1999
Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy
S Repetto, M Bado, P Broda, et al.
Neuromuscular Disorders : NMD
|
November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy
C Bruno, M DiRocco, L D Lamba, et al.
Neurology
|
April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia
I Carbone, C Bruno, F Sotgia, et al.
Nature Genetics
|
April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
C Minetti, F Sotgia, C Bruno, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 31) with videos related to
Sort By:
Page
of 4
European Journal of Pediatrics
|
November 1, 1996
Diagnostic problems in congenital myotonic dystrophy
M DiRocco, M Gennarelli, E Veneselli, et al.
Clinical Genetics
|
July 18, 2002
Tubulopathy, endocrinopathies and encephalomyopathy in a child with a novel large-scale mitochondrial DNA deletion
C Bruno, P Gandullia, F M Santorelli, et al.
Neuromuscular Disorders : NMD
|
May 5, 1998
Very-long-chain acyl-coenzyme A dehydrogenase deficiency in a child with recurrent myoglobinuria
C Minetti, B Garavaglia, M Bado, et al.
Journal of Inherited Metabolic Disease
|
May 19, 1998
Primary adrenal insufficiency in a child with a mitochondrial DNA deletion
C Bruno, C Minetti, Y Tang, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 21, 2004
A novel mutation of GDAP1 associated with Charcot-Marie-Tooth disease in three Italian families: evidence for a founder effect
E Di Maria, R Gulli, P Balestra, et al.
Annals of Neurology
|
May 13, 1999
Congenital hypomyelination due to myelin protein zero Q215X mutation
P Mandich, G L Mancardi, A Varese, et al.
Biochemical and Biophysical Research Communications
|
August 12, 1999
Increased number of caveolae and caveolin-3 overexpression in Duchenne muscular dystrophy
S Repetto, M Bado, P Broda, et al.
Neuromuscular Disorders : NMD
|
November 2, 1999
A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy
C Bruno, M DiRocco, L D Lamba, et al.
Neurology
|
April 4, 2000
Mutation in the CAV3 gene causes partial caveolin-3 deficiency and hyperCKemia
I Carbone, C Bruno, F Sotgia, et al.
Nature Genetics
|
April 16, 1998
Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy
C Minetti, F Sotgia, C Bruno, et al.
Page
of 4