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Clinical Neuropathology
|
July 1, 1997
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
G Di Trapani, B Gregori, S Servidei, et al.
Journal of the Neurological Sciences
|
May 24, 2011
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation
M Luigetti, G M Fabrizi, F Taioli, et al.
Muscle & Nerve
|
July 21, 2009
Ultrasound visualization of nerve morphological alteration at the site of conduction block
G Granata, C Pazzaglia, P Calandro, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 30, 2001
A useful electrophysiological test for diagnosis of minimal conduction block
L Padua, I Aprile, P D'Amico, et al.
Journal of the Neurological Sciences
|
May 1, 1992
Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle
M Sabatelli, E Bertini, E Ricci, et al.
Acta Neuropathologica
|
January 1, 1991
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study
E Bertini, C Bosman, E Ricci, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 1, 1995
Interferon-alpha may benefit steroid unresponsive chronic inflammatory demyelinating polyneuropathy
M Sabatelli, T Mignogna, G Lippi, et al.
Neurology
|
June 3, 2009
Teaching NeuroImages: the full-blown neuroimaging of Wernicke encephalopathy
M Luigetti, S De Paulis, P Spinelli, et al.
La Clinica Terapeutica
|
June 15, 2017
Recurrent miller fisher: a new case report and a literature review
F Barbato, A Di Paolantonio, M Distefano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2000
Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome
E Bertini, M Sabatelli, M Di Capua, et al.
Page
of 8
Search research articles
Search
Showing results (31-40 of 77) with videos related to
Sort By:
Page
of 8
Clinical Neuropathology
|
July 1, 1997
Mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS)
G Di Trapani, B Gregori, S Servidei, et al.
Journal of the Neurological Sciences
|
May 24, 2011
Clinical, electrophysiological and pathological findings of a patient with CMT2 due to the p.Ala738Val mitofusin 2 mutation
M Luigetti, G M Fabrizi, F Taioli, et al.
Muscle & Nerve
|
July 21, 2009
Ultrasound visualization of nerve morphological alteration at the site of conduction block
G Granata, C Pazzaglia, P Calandro, et al.
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology
|
May 30, 2001
A useful electrophysiological test for diagnosis of minimal conduction block
L Padua, I Aprile, P D'Amico, et al.
Journal of the Neurological Sciences
|
May 1, 1992
Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle
M Sabatelli, E Bertini, E Ricci, et al.
Acta Neuropathologica
|
January 1, 1991
Neuromyopathy and restrictive cardiomyopathy with accumulation of intermediate filaments: a clinical, morphological and biochemical study
E Bertini, C Bosman, E Ricci, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
May 1, 1995
Interferon-alpha may benefit steroid unresponsive chronic inflammatory demyelinating polyneuropathy
M Sabatelli, T Mignogna, G Lippi, et al.
Neurology
|
June 3, 2009
Teaching NeuroImages: the full-blown neuroimaging of Wernicke encephalopathy
M Luigetti, S De Paulis, P Spinelli, et al.
La Clinica Terapeutica
|
June 15, 2017
Recurrent miller fisher: a new case report and a literature review
F Barbato, A Di Paolantonio, M Distefano, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
March 22, 2000
Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome
E Bertini, M Sabatelli, M Di Capua, et al.
Page
of 8