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Lancet (London, England)
|
July 25, 1987
Muscle G6PD deficiency
N Bresolin, L Bet, M Moggio, et al.
Acta Neuropathologica
|
January 1, 1992
Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathy
M Sciacco, E Scarpini, P L Baron, et al.
Journal of Neurology
|
December 1, 1989
Rapid quantitative immunohistochemical assessment of human peripheral neuropathies using a monoclonal antibody against nerve growth factor receptor
E Scarpini, S Beretta, A H Ross, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1983
Discordant HLA haplotype segregation in a family with progressive extrinsic ophthalmoplegia and ragged red fibres
R Scorza Smeraldi, G Fabio, M Vanoli, et al.
Biochemical Society Transactions
|
August 1, 1985
Cytochrome c oxidase deficiency
S DiMauro, M Zeviani, E Bonilla, et al.
Journal of Neurology
|
February 1, 1992
Dystrophin deficiency in a case of congenital myopathy
A Prelle, R Medori, M Moggio, et al.
Neurology
|
August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype
C Minetti, H W Chang, R Medori, et al.
Journal of the Neurological Sciences
|
July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis
A Prelle, M Moggio, N Checcarelli, et al.
Muscle & Nerve
|
November 1, 1989
Ultrastructural localization of calcium binding sites on human muscle cell surface
M Moggio, S Jann, L Adobbati, 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.
Page
of 13
Search research articles
Search
Showing results (31-40 of 121) with videos related to
Sort By:
Page
of 13
Lancet (London, England)
|
July 25, 1987
Muscle G6PD deficiency
N Bresolin, L Bet, M Moggio, et al.
Acta Neuropathologica
|
January 1, 1992
Sural nerve immunoreactivity for nerve growth factor receptor in a case of localized hypertrophic neuropathy
M Sciacco, E Scarpini, P L Baron, et al.
Journal of Neurology
|
December 1, 1989
Rapid quantitative immunohistochemical assessment of human peripheral neuropathies using a monoclonal antibody against nerve growth factor receptor
E Scarpini, S Beretta, A H Ross, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 1, 1983
Discordant HLA haplotype segregation in a family with progressive extrinsic ophthalmoplegia and ragged red fibres
R Scorza Smeraldi, G Fabio, M Vanoli, et al.
Biochemical Society Transactions
|
August 1, 1985
Cytochrome c oxidase deficiency
S DiMauro, M Zeviani, E Bonilla, et al.
Journal of Neurology
|
February 1, 1992
Dystrophin deficiency in a case of congenital myopathy
A Prelle, R Medori, M Moggio, et al.
Neurology
|
August 1, 1991
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype
C Minetti, H W Chang, R Medori, et al.
Journal of the Neurological Sciences
|
July 1, 1993
Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis
A Prelle, M Moggio, N Checcarelli, et al.
Muscle & Nerve
|
November 1, 1989
Ultrastructural localization of calcium binding sites on human muscle cell surface
M Moggio, S Jann, L Adobbati, 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.
Page
of 13