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Neuromuscular Disorders : NMD
|
March 1, 1994
Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy
G Piccolo, G Azan, P Tonin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 5, 2013
A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation
S Saredi, S Gibertini, A Ardissone, et al.
The American Journal of Gastroenterology
|
July 1, 1996
An unusual association: celiac disease and Becker muscular dystrophy
A Meini, L Morandi, M Mora, et al.
The Journal of Clinical Investigation
|
August 1, 1995
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine
P Bernasconi, E Torchiana, P Confalonieri, et al.
Neuromuscular Disorders : NMD
|
May 1, 1994
Lysosomal glycogen storage with normal acid maltase: a familial study with successful heart transplant
F Dworzak, F Casazza, M Mora, et al.
Neurology
|
May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathy
G Vattemi, P Tonin, M Mora, et al.
Pulmonary Pharmacology & Therapeutics
|
January 29, 2014
Randomized Controlled Trials and real life studies. Approaches and methodologies: a clinical point of view
S Saturni, F Bellini, F Braido, et al.
Oral Oncology
|
March 30, 2017
Clonal analysis as a prognostic factor in multiple oral squamous cell carcinoma
D B Gissi, A Tarsitano, E Leonardi, et al.
Acta Neuropathologica
|
February 3, 1999
Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression
M Lanfossi, F Cozzi, D Bugini, et al.
American Journal of Human Genetics
|
March 1, 1985
Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids
L Roncuzzi, S Fadda, M Mochi, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 101) with videos related to
Sort By:
Page
of 11
Neuromuscular Disorders : NMD
|
March 1, 1994
Dilated cardiomyopathy requiring cardiac transplantation as initial manifestation of Xp21 Becker type muscular dystrophy
G Piccolo, G Azan, P Tonin, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 5, 2013
A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation
S Saredi, S Gibertini, A Ardissone, et al.
The American Journal of Gastroenterology
|
July 1, 1996
An unusual association: celiac disease and Becker muscular dystrophy
A Meini, L Morandi, M Mora, et al.
The Journal of Clinical Investigation
|
August 1, 1995
Expression of transforming growth factor-beta 1 in dystrophic patient muscles correlates with fibrosis. Pathogenetic role of a fibrogenic cytokine
P Bernasconi, E Torchiana, P Confalonieri, et al.
Neuromuscular Disorders : NMD
|
May 1, 1994
Lysosomal glycogen storage with normal acid maltase: a familial study with successful heart transplant
F Dworzak, F Casazza, M Mora, et al.
Neurology
|
May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathy
G Vattemi, P Tonin, M Mora, et al.
Pulmonary Pharmacology & Therapeutics
|
January 29, 2014
Randomized Controlled Trials and real life studies. Approaches and methodologies: a clinical point of view
S Saturni, F Bellini, F Braido, et al.
Oral Oncology
|
March 30, 2017
Clonal analysis as a prognostic factor in multiple oral squamous cell carcinoma
D B Gissi, A Tarsitano, E Leonardi, et al.
Acta Neuropathologica
|
February 3, 1999
Development of muscle pathology in canine X-linked muscular dystrophy. I. Delayed postnatal maturation of affected and normal muscle as revealed by myosin isoform analysis and utrophin expression
M Lanfossi, F Cozzi, D Bugini, et al.
American Journal of Human Genetics
|
March 1, 1985
Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids
L Roncuzzi, S Fadda, M Mochi, et al.
Page
of 11