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Advances in Neurology
|
January 1, 1988
Immunological and biochemical studies and pilot therapeutic trial with ubidecarenone in Kearns-Sayre patients
N Bresolin, L Bet, C Ferrante, et al.
Human Mutation
|
September 5, 2003
Mutational analysis of the AGL gene: five novel mutations in GSD III patients
S Lucchiari, M A Donati, D Melis, et al.
Revue Neurologique
|
January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies
G Scarlato, N Bresolin, I Moroni, et al.
Journal of the Neurological Sciences
|
May 1, 1990
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues
C Ponzetto, N Bresolin, A Bordoni, et al.
European Neurology
|
January 1, 1993
Muscle mitochondria investigation in myotonic dystrophy
G Vita, A Toscano, A Prelle, et al.
Clinical Neuropathology
|
September 1, 1994
Neural regulation of acid maltase in an unusual adult onset deficiency
G Meola, V Sansone, G Rotondo, et al.
Neurotoxicology
|
October 26, 2005
Parkinson's disease, chronic hydrocarbon exposure and striatal neuronal damage: a 1-H MRS study
M Rango, M Canesi, I Ghione, et al.
Journal of the Neurological Sciences
|
July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis
A Prelle, M Moggio, N Checcarelli, et al.
Cytotechnology
|
February 24, 2012
CK-MM PGAM-MM G6PD and am biochemical markers of functional innervated cultured human muscle fibers
G Meola, M Velicogna, C Brigato, et al.
Minerva Chirurgica
|
April 15, 1989
[Evaluation of plasma carnitine levels after orthotopic transplantation of the liver]
G Iapichino, G Ronzoni, N Bresolin, et al.
Page
of 21
Search research articles
Search
Showing results (71-80 of 206) with videos related to
Sort By:
Page
of 21
Advances in Neurology
|
January 1, 1988
Immunological and biochemical studies and pilot therapeutic trial with ubidecarenone in Kearns-Sayre patients
N Bresolin, L Bet, C Ferrante, et al.
Human Mutation
|
September 5, 2003
Mutational analysis of the AGL gene: five novel mutations in GSD III patients
S Lucchiari, M A Donati, D Melis, et al.
Revue Neurologique
|
January 1, 1991
Multicenter trial with ubidecarenone: treatment of 44 patients with mitochondrial myopathies
G Scarlato, N Bresolin, I Moroni, et al.
Journal of the Neurological Sciences
|
May 1, 1990
Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues
C Ponzetto, N Bresolin, A Bordoni, et al.
European Neurology
|
January 1, 1993
Muscle mitochondria investigation in myotonic dystrophy
G Vita, A Toscano, A Prelle, et al.
Clinical Neuropathology
|
September 1, 1994
Neural regulation of acid maltase in an unusual adult onset deficiency
G Meola, V Sansone, G Rotondo, et al.
Neurotoxicology
|
October 26, 2005
Parkinson's disease, chronic hydrocarbon exposure and striatal neuronal damage: a 1-H MRS study
M Rango, M Canesi, I Ghione, et al.
Journal of the Neurological Sciences
|
July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis
A Prelle, M Moggio, N Checcarelli, et al.
Cytotechnology
|
February 24, 2012
CK-MM PGAM-MM G6PD and am biochemical markers of functional innervated cultured human muscle fibers
G Meola, M Velicogna, C Brigato, et al.
Minerva Chirurgica
|
April 15, 1989
[Evaluation of plasma carnitine levels after orthotopic transplantation of the liver]
G Iapichino, G Ronzoni, N Bresolin, et al.
Page
of 21