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Lancet (London, England)
|
November 3, 1998
Simultaneous occurrence of spongiform encephalopathy in a man and his cat in Italy
G Zanusso, E Nardelli, A Rosati, et al.
Acta Neuropathologica
|
January 1, 1995
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy
N Rizzuto, T Cavallaro, S Monaco, et al.
Neurology
|
May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathy
G Vattemi, P Tonin, M Mora, et al.
European Neurology
|
October 25, 2008
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study
S Mazzucco, G P Anzola, M Ferrarini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 18, 2009
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life
Luca Padua, D Pareyson, I Aprile, et al.
Archives of Internal Medicine
|
March 11, 1996
Stereotactic brain biopsy in human immunodeficiency virus-infected patients
R Luzzati, S Ferrari, A Nicolato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 10, 2008
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study
L Padua, I Aprile, T Cavallaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 5, 1997
Multiple sclerosis associated with duplicated CMT1A: a report of two cases
E Frasson, A Polo, A Di Summa, et al.
Human Mutation
|
September 12, 2000
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations
M G Lira, M Mottes, P F Pignatti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 16, 2000
PMP22 related congenital hypomyelination neuropathy
G M Fabrizi, A Simonati, F Taioli, et al.
Page
of 19
Search research articles
Search
Showing results (161-170 of 190) with videos related to
Sort By:
Page
of 19
Lancet (London, England)
|
November 3, 1998
Simultaneous occurrence of spongiform encephalopathy in a man and his cat in Italy
G Zanusso, E Nardelli, A Rosati, et al.
Acta Neuropathologica
|
January 1, 1995
Role of HIV in the pathogenesis of distal symmetrical peripheral neuropathy
N Rizzuto, T Cavallaro, S Monaco, et al.
Neurology
|
May 26, 2004
Expression of protein kinase C isoforms and interleukin-1beta in myofibrillar myopathy
G Vattemi, P Tonin, M Mora, et al.
European Neurology
|
October 25, 2008
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy and right-to-left shunt: lack of evidence for an association in a prevalence study
S Mazzucco, G P Anzola, M Ferrarini, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
December 18, 2009
Natural history of Charcot-Marie-Tooth 2: 2-year follow-up of muscle strength, walking ability and quality of life
Luca Padua, D Pareyson, I Aprile, et al.
Archives of Internal Medicine
|
March 11, 1996
Stereotactic brain biopsy in human immunodeficiency virus-infected patients
R Luzzati, S Ferrari, A Nicolato, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
July 10, 2008
Relationship between clinical examination, quality of life, disability and depression in CMT patients: Italian multicenter study
L Padua, I Aprile, T Cavallaro, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
November 5, 1997
Multiple sclerosis associated with duplicated CMT1A: a report of two cases
E Frasson, A Polo, A Di Summa, et al.
Human Mutation
|
September 12, 2000
Detection of mutations in the ALD gene (ABCD1) in seven Italian families: description of four novel mutations
M G Lira, M Mottes, P F Pignatti, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
December 16, 2000
PMP22 related congenital hypomyelination neuropathy
G M Fabrizi, A Simonati, F Taioli, et al.
Page
of 19