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Molecular and Cellular Biochemistry
|
October 8, 1990
Liver fatty acid-binding protein in two cases of human lipid storage
L Vergani, M Fanin, A Martinuzzi, et al.
American Journal of Medical Genetics
|
March 1, 1994
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy
M L Mostacciuolo, M Miorin, L Vitiello, et al.
Muscle & Nerve
|
September 1, 1997
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitine
G Brevetti, M Fanin, V De Amicis, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 4, 2006
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
C Pizzanelli, M Mancuso, R Galli, et al.
The Journal of Clinical Investigation
|
October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency
A Martinuzzi, L Vergani, R Carrozzo, et al.
Clinical Genetics
|
April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps
M Fanin, F Benedicenti, C Fritegotto, et al.
Developmental Medicine and Child Neurology
|
March 18, 2006
Early onset calpainopathy with normal non-functional calpain 3 level
R Lanzillo, S Aurino, M Fanin, et al.
Neuromuscular Disorders : NMD
|
July 1, 1994
Prevalent cardiac involvement in dystrophin Becker type mutation
G Siciliano, M Fanin, C Angelini, et al.
European Journal of Neurology
|
June 11, 2011
Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele
M Meznaric, L Gonzalez-Quereda, E Gallardo, et al.
Neurology
|
September 29, 2004
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy
P Prandini, A Berardinelli, M Fanin, et al.
Page
of 7
Search research articles
Search
Showing results (41-50 of 68) with videos related to
Sort By:
Page
of 7
Molecular and Cellular Biochemistry
|
October 8, 1990
Liver fatty acid-binding protein in two cases of human lipid storage
L Vergani, M Fanin, A Martinuzzi, et al.
American Journal of Medical Genetics
|
March 1, 1994
Occurrence of two different intragenic deletions in two male relatives affected with Duchenne muscular dystrophy
M L Mostacciuolo, M Miorin, L Vitiello, et al.
Muscle & Nerve
|
September 1, 1997
Changes in skeletal muscle histology and metabolism in patients undergoing exercise deconditioning: effect of propionyl-L-carnitine
G Brevetti, M Fanin, V De Amicis, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 4, 2006
Epilepsy and limb girdle muscular dystrophy type 2A: double trouble, serendipitous finding or new phenotype?
C Pizzanelli, M Mancuso, R Galli, et al.
The Journal of Clinical Investigation
|
October 1, 1993
Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency
A Martinuzzi, L Vergani, R Carrozzo, et al.
Clinical Genetics
|
April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the Alps
M Fanin, F Benedicenti, C Fritegotto, et al.
Developmental Medicine and Child Neurology
|
March 18, 2006
Early onset calpainopathy with normal non-functional calpain 3 level
R Lanzillo, S Aurino, M Fanin, et al.
Neuromuscular Disorders : NMD
|
July 1, 1994
Prevalent cardiac involvement in dystrophin Becker type mutation
G Siciliano, M Fanin, C Angelini, et al.
European Journal of Neurology
|
June 11, 2011
Abnormal expression of dysferlin in skeletal muscle and monocytes supports primary dysferlinopathy in patients with one mutated allele
M Meznaric, L Gonzalez-Quereda, E Gallardo, et al.
Neurology
|
September 29, 2004
LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy
P Prandini, A Berardinelli, M Fanin, et al.
Page
of 7