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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 1, 1996
Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle
C P Trevisan, F Martinello, E Ferruzza, et al.
Muscle & Nerve
|
May 19, 1998
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient
C Angelini, M Fanin, E Menegazzo, et al.
Neuromuscular Disorders : NMD
|
March 1, 1993
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients
M Fanin, E P Hoffman, F A Saad, et al.
Neurology
|
April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
M Fanin, A C Nascimbeni, S Aurino, et al.
Neurological Research
|
January 23, 2010
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)
C Angelini, L Nardetto, C Borsato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2008
Sphingomonas paucimobilis associated with localised calf myositis
E Pegoraro, C Borsato, F Dal Bello, et al.
Neuromuscular Disorders : NMD
|
October 1, 1996
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy
P Melacini, A Vianello, C Villanova, et al.
Neurology
|
January 28, 1999
The clinical spectrum of sarcoglycanopathies
C Angelini, M Fanin, M P Freda, et al.
Journal of Medical Genetics
|
May 29, 2007
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A
M Fanin, L Nardetto, A C Nascimbeni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
September 30, 2005
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1
S Salvatori, M Fanin, C P Trevisan, et al.
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of 7
Search research articles
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Showing results (31-40 of 68) with videos related to
Sort By:
Page
of 7
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
October 1, 1996
Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle
C P Trevisan, F Martinello, E Ferruzza, et al.
Muscle & Nerve
|
May 19, 1998
Homozygous alpha-sarcoglycan mutation in two siblings: one asymptomatic and one steroid-responsive mild limb-girdle muscular dystrophy patient
C Angelini, M Fanin, E Menegazzo, et al.
Neuromuscular Disorders : NMD
|
March 1, 1993
Dystrophin-positive myotubes in innervated muscle cultures from Duchenne and Becker muscular dystrophy patients
M Fanin, E P Hoffman, F A Saad, et al.
Neurology
|
April 22, 2009
Frequency of LGMD gene mutations in Italian patients with distinct clinical phenotypes
M Fanin, A C Nascimbeni, S Aurino, et al.
Neurological Research
|
January 23, 2010
The clinical course of calpainopathy (LGMD2A) and dysferlinopathy (LGMD2B)
C Angelini, L Nardetto, C Borsato, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
September 18, 2008
Sphingomonas paucimobilis associated with localised calf myositis
E Pegoraro, C Borsato, F Dal Bello, et al.
Neuromuscular Disorders : NMD
|
October 1, 1996
Cardiac and respiratory involvement in advanced stage Duchenne muscular dystrophy
P Melacini, A Vianello, C Villanova, et al.
Neurology
|
January 28, 1999
The clinical spectrum of sarcoglycanopathies
C Angelini, M Fanin, M P Freda, et al.
Journal of Medical Genetics
|
May 29, 2007
Correlations between clinical severity, genotype and muscle pathology in limb girdle muscular dystrophy type 2A
M Fanin, L Nardetto, A C Nascimbeni, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
September 30, 2005
Decreased expression of DMPK: correlation with CTG repeat expansion and fibre type composition in myotonic dystrophy type 1
S Salvatori, M Fanin, C P Trevisan, et al.
Page
of 7