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Neuropediatrics
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August 1, 1985
A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line
G Pellegrini, S Barbieri, M Moggio, et al.
Acta Neurologica
|
December 1, 1982
Morphological studies and quantitative assessment of the effect of chick embryo extract on monolayer cultures of normal human muscle
E Scarpini, G Meola, P Baron, et al.
Italian Journal of Neurological Sciences
|
February 1, 1989
Normal muscle mitochondrial function in Ramsay-Hunt syndrome
T Sacquegna, P Montagna, M Moggio, et al.
Acta Neuropathologica
|
January 1, 1983
Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblings
G Pellegrini, M Moggio, A Cheldi, et al.
European Journal of Basic and Applied Histochemistry
|
January 1, 1991
Lysosomotropic agents induce morphological and functional changes in human muscle cells in vitro
P L Baron, G Meola, E Scarpini, et al.
Journal of the Neurological Sciences
|
December 15, 1993
Decrease of nerve Na+,K(+)-ATPase activity in the pathogenesis of human diabetic neuropathy
E Scarpini, R Bianchi, M Moggio, et al.
Neuropediatrics
|
November 1, 1982
Familial nemaline myopathy
G Scarlato, G Pellegrini, M Moggio, et al.
Muscle & Nerve
|
May 1, 1994
Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy
M Moggio, A Prelle, G Fagiolari, et al.
Annals of Neurology
|
April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient
M Zeviani, I Nonaka, E Bonilla, et al.
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.
Page
of 13
Search research articles
Search
Showing results (21-30 of 121) with videos related to
Sort By:
Page
of 13
Neuropediatrics
|
August 1, 1985
A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line
G Pellegrini, S Barbieri, M Moggio, et al.
Acta Neurologica
|
December 1, 1982
Morphological studies and quantitative assessment of the effect of chick embryo extract on monolayer cultures of normal human muscle
E Scarpini, G Meola, P Baron, et al.
Italian Journal of Neurological Sciences
|
February 1, 1989
Normal muscle mitochondrial function in Ramsay-Hunt syndrome
T Sacquegna, P Montagna, M Moggio, et al.
Acta Neuropathologica
|
January 1, 1983
Familial megaconial myopathy: a real nosologic entity. Clinical and histopathologic studies in two siblings
G Pellegrini, M Moggio, A Cheldi, et al.
European Journal of Basic and Applied Histochemistry
|
January 1, 1991
Lysosomotropic agents induce morphological and functional changes in human muscle cells in vitro
P L Baron, G Meola, E Scarpini, et al.
Journal of the Neurological Sciences
|
December 15, 1993
Decrease of nerve Na+,K(+)-ATPase activity in the pathogenesis of human diabetic neuropathy
E Scarpini, R Bianchi, M Moggio, et al.
Neuropediatrics
|
November 1, 1982
Familial nemaline myopathy
G Scarlato, G Pellegrini, M Moggio, et al.
Muscle & Nerve
|
May 1, 1994
Anionic phospholipids calcium binding sites in Duchenne and murine X-linked muscular dystrophy
M Moggio, A Prelle, G Fagiolari, et al.
Annals of Neurology
|
April 1, 1985
Fatal infantile mitochondrial myopathy and renal dysfunction caused by cytochrome c oxidase deficiency: immunological studies in a new patient
M Zeviani, I Nonaka, E Bonilla, et al.
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.
Page
of 13