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Italian Journal of Neurological Sciences
|
August 11, 2000
Nuclear gene defects in mitochondrial disorders
M Zeviani, P Corona, L Nijtmans, et al.
Human Molecular Genetics
|
November 5, 1999
Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybrids
M Toompuu, V Tiranti, M Zeviani, et al.
Neurologic Clinics
|
February 1, 1989
Mitochondrial diseases
M Zeviani, E Bonilla, D C DeVivo, et al.
The Biochemical Journal
|
November 15, 1984
Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibres
G Salviati, R Betto, D Danieli Betto, et al.
Neurology
|
January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second case
M Zeviani, P Peterson, S Servidei, et al.
Human Molecular Genetics
|
September 25, 1997
Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous system
G Battaglia, A Princivalle, F Forti, et al.
International Journal of Clinical Pharmacology Research
|
December 4, 2004
Accelerated cardiomyopathy in maternally inherited diabetes and deafness
R A Mangiafico, M Zeviani, G Bartoloni, et al.
Journal of Medical Genetics
|
May 3, 2005
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
M Bugiani, V Tiranti, L Farina, et al.
Muscle & Nerve
|
June 1, 1985
Effects of thyroid hormones on the biochemical specialization of human muscle fibers
G Salviati, M Zeviani, R Betto, et al.
Clinical and Experimental Immunology
|
November 1, 1985
Demonstration and characterization of anti-human mitochondria autoantibodies in idiopathic hypoparathyroidism and in other conditions
C Betterle, A Caretto, M Zeviani, et al.
Page
of 19
Search research articles
Search
Showing results (21-30 of 184) with videos related to
Sort By:
Page
of 19
Italian Journal of Neurological Sciences
|
August 11, 2000
Nuclear gene defects in mitochondrial disorders
M Zeviani, P Corona, L Nijtmans, et al.
Human Molecular Genetics
|
November 5, 1999
Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybrids
M Toompuu, V Tiranti, M Zeviani, et al.
Neurologic Clinics
|
February 1, 1989
Mitochondrial diseases
M Zeviani, E Bonilla, D C DeVivo, et al.
The Biochemical Journal
|
November 15, 1984
Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibres
G Salviati, R Betto, D Danieli Betto, et al.
Neurology
|
January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second case
M Zeviani, P Peterson, S Servidei, et al.
Human Molecular Genetics
|
September 25, 1997
Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous system
G Battaglia, A Princivalle, F Forti, et al.
International Journal of Clinical Pharmacology Research
|
December 4, 2004
Accelerated cardiomyopathy in maternally inherited diabetes and deafness
R A Mangiafico, M Zeviani, G Bartoloni, et al.
Journal of Medical Genetics
|
May 3, 2005
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiency
M Bugiani, V Tiranti, L Farina, et al.
Muscle & Nerve
|
June 1, 1985
Effects of thyroid hormones on the biochemical specialization of human muscle fibers
G Salviati, M Zeviani, R Betto, et al.
Clinical and Experimental Immunology
|
November 1, 1985
Demonstration and characterization of anti-human mitochondria autoantibodies in idiopathic hypoparathyroidism and in other conditions
C Betterle, A Caretto, M Zeviani, et al.
Page
of 19