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International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
October 1, 1995
Utrophin expression during human fetal development
C Rigoletto, A Prelle, P Ciscato, et al.
Acta Neuropathologica
|
January 1, 1995
High serum creatine kinase levels associated with cylindrical spirals at muscle biopsy
S Rapuzzi, A Prelle, M Moggio, et al.
Journal of the Neurological Sciences
|
September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle
A Prelle, C Rigoletto, M Moggio, et al.
Human Molecular Genetics
|
November 1, 1995
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient
G P Comi, E Ciafaloni, H A de Silva, 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.
Acta Neuropathologica
|
November 26, 1998
Sarcoglycan deficiency in a large Italian population of myopathic patients
A Prelle, G P Comi, L Tancredi, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|
October 1, 1995
Utrophin expression during human fetal development
C Rigoletto, A Prelle, P Ciscato, et al.
Acta Neuropathologica
|
January 1, 1995
High serum creatine kinase levels associated with cylindrical spirals at muscle biopsy
S Rapuzzi, A Prelle, M Moggio, et al.
Journal of the Neurological Sciences
|
September 1, 1996
Asymptomatic familial hyperCKemia associated with desmin accumulation in skeletal muscle
A Prelle, C Rigoletto, M Moggio, et al.
Human Molecular Genetics
|
November 1, 1995
A G+1-->A transversion at the 5' splice site of intron 69 of the dystrophin gene causing the absence of peripheral nerve Dp116 and severe clinical involvement in a DMD patient
G P Comi, E Ciafaloni, H A de Silva, 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.
Acta Neuropathologica
|
November 26, 1998
Sarcoglycan deficiency in a large Italian population of myopathic patients
A Prelle, G P Comi, L Tancredi, et al.
Page
of 1