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L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
May 1, 1976
[Duchenne muscular dystrophy in girls (author's transl)]
E Grassi, A Marbini, C Marchini, et al.
Journal of the Neurological Sciences
|
September 1, 1983
Immunological abnormalities in a family with progressive external ophthalmoplegia
S Calzetti, F Gemignani, A Marbini, et al.
Acta Neuropathologica
|
December 9, 1998
Congenital myopathy with mosaic fibers and interlacing sarcomeres: a new structural myopathy
A Marbini, F Gemignani, L Badiali, et al.
Journal of the Neurological Sciences
|
November 1, 1996
Immunohistochemical localization of utrophin and other cytoskeletal proteins in skin smooth muscle in neuromuscular diseases
A Marbini, F Gemignani, M F Bellanova, et al.
Acta Neuropathologica
|
August 1, 1997
Immunohistochemical study of merosin-negative congenital muscular dystrophy: laminin alpha 2 deficiency in skin biopsy
A Marbini, M F Bellanova, A Ferrari, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 29, 2010
Non-length-dependent small fibre neuropathy. Confocal microscopy study of the corneal innervation
F Gemignani, G Ferrari, F Vitetta, et al.
Chirurgia E Patologia Sperimentale
|
June 1, 1980
[Ultrastructural changes of the gastrocnemius and rectus muscles of the femur in chronic arterial insufficiency]
A M Farinon, M M Bragaglia, E Govoni, et al.
Neurology
|
April 2, 1999
Charcot-Marie-Tooth disease type 2 with restless legs syndrome
F Gemignani, A Marbini, G Di Giovanni, et al.
Clinical Neurology and Neurosurgery
|
May 1, 1994
Hereditary sensory and autonomic neuropathy with ataxia and late onset
A Marbini, G Pavesi, G Cenacchi, et al.
Acta Neuropathologica
|
January 1, 1992
Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous. Report of nerve biopsy in four cases and review of the literature
F Gemignani, D Guidetti, P Bizzi, et al.
Page
of 7
Search research articles
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Showing results (21-30 of 61) with videos related to
Sort By:
Page
of 7
L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma
|
May 1, 1976
[Duchenne muscular dystrophy in girls (author's transl)]
E Grassi, A Marbini, C Marchini, et al.
Journal of the Neurological Sciences
|
September 1, 1983
Immunological abnormalities in a family with progressive external ophthalmoplegia
S Calzetti, F Gemignani, A Marbini, et al.
Acta Neuropathologica
|
December 9, 1998
Congenital myopathy with mosaic fibers and interlacing sarcomeres: a new structural myopathy
A Marbini, F Gemignani, L Badiali, et al.
Journal of the Neurological Sciences
|
November 1, 1996
Immunohistochemical localization of utrophin and other cytoskeletal proteins in skin smooth muscle in neuromuscular diseases
A Marbini, F Gemignani, M F Bellanova, et al.
Acta Neuropathologica
|
August 1, 1997
Immunohistochemical study of merosin-negative congenital muscular dystrophy: laminin alpha 2 deficiency in skin biopsy
A Marbini, M F Bellanova, A Ferrari, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
June 29, 2010
Non-length-dependent small fibre neuropathy. Confocal microscopy study of the corneal innervation
F Gemignani, G Ferrari, F Vitetta, et al.
Chirurgia E Patologia Sperimentale
|
June 1, 1980
[Ultrastructural changes of the gastrocnemius and rectus muscles of the femur in chronic arterial insufficiency]
A M Farinon, M M Bragaglia, E Govoni, et al.
Neurology
|
April 2, 1999
Charcot-Marie-Tooth disease type 2 with restless legs syndrome
F Gemignani, A Marbini, G Di Giovanni, et al.
Clinical Neurology and Neurosurgery
|
May 1, 1994
Hereditary sensory and autonomic neuropathy with ataxia and late onset
A Marbini, G Pavesi, G Cenacchi, et al.
Acta Neuropathologica
|
January 1, 1992
Peroneal muscular atrophy with hereditary spastic paraparesis (HMSN V) is pathologically heterogeneous. Report of nerve biopsy in four cases and review of the literature
F Gemignani, D Guidetti, P Bizzi, et al.
Page
of 7