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Journal of Medical Genetics
|
May 15, 2003
Novel sarcoglycan gene mutations in a large cohort of Italian patients
C Boito, M Fanin, G Siciliano, et al.
Minerva Medica
|
July 7, 1976
[Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract]
G Conte, C Angelini, C Locatelli, et al.
Journal of Clinical Pathology
|
January 29, 2005
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism
G Cenacchi, M Fanin, L B De Giorgi, et al.
Cell Death and Differentiation
|
May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)
A C Nascimbeni, M Fanin, E Masiero, et al.
Journal of Neurology
|
May 14, 1999
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy
F Martinello, A Piazza, E Pastorello, et al.
European Journal of Neurology
|
October 8, 2004
Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathy
K Kawabe, K Goto, I Nishino, et al.
Clinical Genetics
|
March 4, 2008
Cardioembolic stroke in Danon disease
M Spinazzi, M Fanin, P Melacini, et al.
Japanese Heart Journal
|
January 1, 1990
Evolution of cardiac involvement in progressive ophthalmoplegia with deleted mitochondrial DNA
P Melacini, C Angelini, G Buja, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri
|
April 1, 1984
[Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results]
P Fardin, G F Micaglio, C Angelini, et al.
Human Mutation
|
February 6, 1998
Mutations of the same sequence of the myelin P0 gene causing two different phenotypes
F Schiavon, A Rampazzo, L Merlini, et al.
Page
of 54
Search research articles
Search
Showing results (91-100 of 531) with videos related to
Sort By:
Page
of 54
Journal of Medical Genetics
|
May 15, 2003
Novel sarcoglycan gene mutations in a large cohort of Italian patients
C Boito, M Fanin, G Siciliano, et al.
Minerva Medica
|
July 7, 1976
[Benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract]
G Conte, C Angelini, C Locatelli, et al.
Journal of Clinical Pathology
|
January 29, 2005
Ultrastructural changes in dysferlinopathy support defective membrane repair mechanism
G Cenacchi, M Fanin, L B De Giorgi, et al.
Cell Death and Differentiation
|
May 19, 2012
The role of autophagy in the pathogenesis of glycogen storage disease type II (GSDII)
A C Nascimbeni, M Fanin, E Masiero, et al.
Journal of Neurology
|
May 14, 1999
Clinical and neuroimaging study of central nervous system in congenital myotonic dystrophy
F Martinello, A Piazza, E Pastorello, et al.
European Journal of Neurology
|
October 8, 2004
Dysferlin mutation analysis in a group of Italian patients with limb-girdle muscular dystrophy and Miyoshi myopathy
K Kawabe, K Goto, I Nishino, et al.
Clinical Genetics
|
March 4, 2008
Cardioembolic stroke in Danon disease
M Spinazzi, M Fanin, P Melacini, et al.
Japanese Heart Journal
|
January 1, 1990
Evolution of cardiac involvement in progressive ophthalmoplegia with deleted mitochondrial DNA
P Melacini, C Angelini, G Buja, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri
|
April 1, 1984
[Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results]
P Fardin, G F Micaglio, C Angelini, et al.
Human Mutation
|
February 6, 1998
Mutations of the same sequence of the myelin P0 gene causing two different phenotypes
F Schiavon, A Rampazzo, L Merlini, et al.
Page
of 54