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Neuromuscular Disorders : NMD
|
January 1, 1993
Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency
N B Romero, C Marsac, M Paturneau-Jouas, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1990
[Presence of dystrophine-like protein at the neuromuscular junction in Duchenne muscular dystrophy and in "mdx" mutant mice]
M Fardeau, F M Tomé, H Collin, et al.
Revue Neurologique
|
October 1, 1977
[Eaton-Lambert myasthenic syndrome: clinical, electrophysiologic, histological and ultrastructural study]
P Castaigne, P Rondot, M Fardeau, et al.
Revue Neurologique
|
January 1, 1991
[Clinical and electrophysiologic study of the peripheral nerve in 28 cases of mitochondrial disease]
B Eymard, A Penicaud, J M Leger, et al.
Neurology
|
January 1, 1992
Decreased cerebral glucose utilization in myotonic dystrophy
M Fiorelli, D Duboc, B M Mazoyer, et al.
Human Molecular Genetics
|
November 16, 2001
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor
N Monnier, N B Romero, J Lerale, et al.
FEBS Letters
|
April 25, 1988
Storage of phosphorylated desmin in a familial myopathy
L Rappaport, F Contard, J L Samuel, et al.
Muscle & Nerve
|
September 1, 1996
Elevated levels of complement components C5 and C9 and decreased antitrypsin activity in the serum of patients with X-linked vacuolated myopathy
J P Louboutin, M Villanova, G Ulrich, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales
|
January 1, 1994
[Muscular reconstruction by myogenic cell graft]
H Alameddine, M Dehaupas, J P Louboutin, et al.
Cahiers De Sociologie Et De Demographie Medicales
|
January 1, 1982
[Multidiscipline aspects and approach to the evaluation of care for diabetics]
A Triomphe, J L Lanoe, D Costagliola, et al.
Page
of 29
Search research articles
Search
Showing results (141-150 of 289) with videos related to
Sort By:
Page
of 29
Neuromuscular Disorders : NMD
|
January 1, 1993
Infantile familial cardiomyopathy due to mitochondrial complex I and IV associated deficiency
N B Romero, C Marsac, M Paturneau-Jouas, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie
|
January 1, 1990
[Presence of dystrophine-like protein at the neuromuscular junction in Duchenne muscular dystrophy and in "mdx" mutant mice]
M Fardeau, F M Tomé, H Collin, et al.
Revue Neurologique
|
October 1, 1977
[Eaton-Lambert myasthenic syndrome: clinical, electrophysiologic, histological and ultrastructural study]
P Castaigne, P Rondot, M Fardeau, et al.
Revue Neurologique
|
January 1, 1991
[Clinical and electrophysiologic study of the peripheral nerve in 28 cases of mitochondrial disease]
B Eymard, A Penicaud, J M Leger, et al.
Neurology
|
January 1, 1992
Decreased cerebral glucose utilization in myotonic dystrophy
M Fiorelli, D Duboc, B M Mazoyer, et al.
Human Molecular Genetics
|
November 16, 2001
Familial and sporadic forms of central core disease are associated with mutations in the C-terminal domain of the skeletal muscle ryanodine receptor
N Monnier, N B Romero, J Lerale, et al.
FEBS Letters
|
April 25, 1988
Storage of phosphorylated desmin in a familial myopathy
L Rappaport, F Contard, J L Samuel, et al.
Muscle & Nerve
|
September 1, 1996
Elevated levels of complement components C5 and C9 and decreased antitrypsin activity in the serum of patients with X-linked vacuolated myopathy
J P Louboutin, M Villanova, G Ulrich, et al.
Comptes Rendus Des Seances De La Societe De Biologie Et De Ses Filiales
|
January 1, 1994
[Muscular reconstruction by myogenic cell graft]
H Alameddine, M Dehaupas, J P Louboutin, et al.
Cahiers De Sociologie Et De Demographie Medicales
|
January 1, 1982
[Multidiscipline aspects and approach to the evaluation of care for diabetics]
A Triomphe, J L Lanoe, D Costagliola, et al.
Page
of 29