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Journal of the Neurological Sciences
|
August 18, 1999
Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteins
M Fanin, C Angelini
Neuropathology and Applied Neurobiology
|
November 26, 2002
Muscle pathology in dysferlin deficiency
M Fanin, C Angelini
Neuropathology and Applied Neurobiology
|
June 13, 2002
Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes
M Fanin, C Angelini
Italian Journal of Neurological Sciences
|
January 1, 1993
Multifactorial study of inflammatory myopathies. Report of 29 cases
C Angelini, E Menegazzo, M Fanin
Journal of the Neurological Sciences
|
May 1, 1994
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients
M Fanin, E Pegoraro, C Angelini
Journal of Medical Genetics
|
September 15, 2006
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations
M Fanin, A C Nascimbeni, C Angelini
Neuropathology and Applied Neurobiology
|
February 19, 2013
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular study
M Fanin, A C Nascimbeni, C Angelini
The American Journal of Pathology
|
June 11, 1999
McArdle's disease. The unsolved mystery of the reappearing enzyme
A Martinuzzi, G Schievano, A Nascimbeni, et al.
Journal of Molecular and Cellular Cardiology
|
July 29, 1999
Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
M Fanin, P Melacini, C Angelini, et al.
Neuromuscular Disorders : NMD
|
July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy
E Pegoraro, M Fanin, C Angelini, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 68) with videos related to
Sort By:
Page
of 7
Journal of the Neurological Sciences
|
August 18, 1999
Regeneration in sarcoglycanopathies: expression studies of sarcoglycans and other muscle proteins
M Fanin, C Angelini
Neuropathology and Applied Neurobiology
|
November 26, 2002
Muscle pathology in dysferlin deficiency
M Fanin, C Angelini
Neuropathology and Applied Neurobiology
|
June 13, 2002
Defective assembly of sarcoglycan complex in patients with beta-sarcoglycan gene mutations. Study of aneural and innervated cultured myotubes
M Fanin, C Angelini
Italian Journal of Neurological Sciences
|
January 1, 1993
Multifactorial study of inflammatory myopathies. Report of 29 cases
C Angelini, E Menegazzo, M Fanin
Journal of the Neurological Sciences
|
May 1, 1994
Absence of dystrophin and spectrin in regenerating muscle fibers from Becker dystrophy patients
M Fanin, E Pegoraro, C Angelini
Journal of Medical Genetics
|
September 15, 2006
Screening of calpain-3 autolytic activity in LGMD muscle: a functional map of CAPN3 gene mutations
M Fanin, A C Nascimbeni, C Angelini
Neuropathology and Applied Neurobiology
|
February 19, 2013
Muscle atrophy in Limb Girdle Muscular Dystrophy 2A: a morphometric and molecular study
M Fanin, A C Nascimbeni, C Angelini
The American Journal of Pathology
|
June 11, 1999
McArdle's disease. The unsolved mystery of the reappearing enzyme
A Martinuzzi, G Schievano, A Nascimbeni, et al.
Journal of Molecular and Cellular Cardiology
|
July 29, 1999
Could utrophin rescue the myocardium of patients with dystrophin gene mutations?
M Fanin, P Melacini, C Angelini, et al.
Neuromuscular Disorders : NMD
|
July 17, 1999
Prenatal diagnosis in a family affected with beta-sarcoglycan muscular dystrophy
E Pegoraro, M Fanin, C Angelini, et al.
Page
of 7