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Journal of Neurology, Neurosurgery, and Psychiatry
|
August 19, 2008
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patients
R Del Bo, S Ghezzi, S Corti, et al.
Journal of Neurology
|
June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophy
A Prelle, G P Comi, C Rigoletto, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patient
R Cagliani, A Bardoni, M Sironi, et al.
Neurology
|
April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathies
M Sciacco, G Fagiolari, C Lamperti, et al.
Clinical Neuropathology
|
February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsy
P Bazzi, M Moggio, A Prelle, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population
R Cagliani, F Fortunato, R Giorda, et al.
Annals of Neurology
|
August 17, 2001
Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis
G P Comi, F Fortunato, S Lucchiari, et al.
Acta Neuropathologica
|
November 26, 1998
Sarcoglycan deficiency in a large Italian population of myopathic patients
A Prelle, G P Comi, L Tancredi, et al.
Clinical Neuropathology
|
August 5, 2000
A sporadic, atypical case of desminopathy: morphological and immunological characterization
A Prelle, M Sciacco, G P Comi, et al.
Minerva Anestesiologica
|
March 1, 1996
[Respiratory failure caused by myopathy in severe sepsis]
G Veschi, G Zanforlin, G Breda, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 84) with videos related to
Sort By:
Page
of 9
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 19, 2008
DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patients
R Del Bo, S Ghezzi, S Corti, et al.
Journal of Neurology
|
June 1, 1997
An atypical case of partial merosin deficiency congenital muscular dystrophy
A Prelle, G P Comi, C Rigoletto, et al.
Neuromuscular Disorders : NMD
|
December 7, 2002
Two dystrophin proteins and transcripts in a mild dystrophinopathic patient
R Cagliani, A Bardoni, M Sironi, et al.
Neurology
|
April 26, 2001
Lack of apoptosis in mitochondrial encephalomyopathies
M Sciacco, G Fagiolari, C Lamperti, et al.
Clinical Neuropathology
|
February 13, 1999
Critically ill patients: immunological evidence of inflammation in muscle biopsy
P Bazzi, M Moggio, A Prelle, et al.
Neuromuscular Disorders : NMD
|
December 18, 2003
Molecular analysis of LGMD-2B and MM patients: identification of novel DYSF mutations and possible founder effect in the Italian population
R Cagliani, F Fortunato, R Giorda, et al.
Annals of Neurology
|
August 17, 2001
Beta-enolase deficiency, a new metabolic myopathy of distal glycolysis
G P Comi, F Fortunato, S Lucchiari, et al.
Acta Neuropathologica
|
November 26, 1998
Sarcoglycan deficiency in a large Italian population of myopathic patients
A Prelle, G P Comi, L Tancredi, et al.
Clinical Neuropathology
|
August 5, 2000
A sporadic, atypical case of desminopathy: morphological and immunological characterization
A Prelle, M Sciacco, G P Comi, et al.
Minerva Anestesiologica
|
March 1, 1996
[Respiratory failure caused by myopathy in severe sepsis]
G Veschi, G Zanforlin, G Breda, et al.
Page
of 9