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Neurology
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May 29, 2003
Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?
D Pareyson, D Testa, M Morbin, et al.
Neurology
|
April 13, 2000
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation
D Pareyson, F Taroni, S Botti, et al.
Neurology
|
April 1, 1996
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion
D Pareyson, V Scaioli, F Taroni, et al.
Italian Journal of Neurological Sciences
|
February 1, 1994
Homozygous hypertrophic hereditary motor and sensory neuropathies
A Sghirlanzoni, D Pareyson, R Marazzi, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
Affective disorders and multiple sclerosis: a controlled study on 65 Italian patients
A Salmaggi, R Palumbo, L Fontanillas, et al.
Neurology
|
November 1, 1992
HMSN III phenotype due to homozygous expression of a dominant HMSN II gene
A Sghirlanzoni, D Pareyson, M R Balestrini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 18, 2007
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy
M Muglia, G Vazza, A Patitucci, et al.
European Journal of Neurology
|
April 2, 2019
Longitudinal quantitative magnetic resonance imaging in adrenomyeloneuropathy
L S Politi, A Castellano, N Papinutto, et al.
Neuromuscular Disorders : NMD
|
February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective study
L Padua, D Pareyson, I Aprile, et al.
AJNR. American Journal of Neuroradiology
|
April 5, 2008
Can MR imaging diagnose adult-onset Alexander disease?
L Farina, D Pareyson, L Minati, et al.
Page
of 12
Search research articles
Search
Showing results (61-70 of 113) with videos related to
Sort By:
Page
of 12
Neurology
|
May 29, 2003
Does CMT1A homozygosity cause more severe disease with root hypertrophy and higher CSF proteins?
D Pareyson, D Testa, M Morbin, et al.
Neurology
|
April 13, 2000
Cranial nerve involvement in CMT disease type 1 due to early growth response 2 gene mutation
D Pareyson, F Taroni, S Botti, et al.
Neurology
|
April 1, 1996
Phenotypic heterogeneity in hereditary neuropathy with liability to pressure palsies associated with chromosome 17p11.2-12 deletion
D Pareyson, V Scaioli, F Taroni, et al.
Italian Journal of Neurological Sciences
|
February 1, 1994
Homozygous hypertrophic hereditary motor and sensory neuropathies
A Sghirlanzoni, D Pareyson, R Marazzi, et al.
Italian Journal of Neurological Sciences
|
August 10, 2000
Affective disorders and multiple sclerosis: a controlled study on 65 Italian patients
A Salmaggi, R Palumbo, L Fontanillas, et al.
Neurology
|
November 1, 1992
HMSN III phenotype due to homozygous expression of a dominant HMSN II gene
A Sghirlanzoni, D Pareyson, M R Balestrini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
October 18, 2007
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy
M Muglia, G Vazza, A Patitucci, et al.
European Journal of Neurology
|
April 2, 2019
Longitudinal quantitative magnetic resonance imaging in adrenomyeloneuropathy
L S Politi, A Castellano, N Papinutto, et al.
Neuromuscular Disorders : NMD
|
February 5, 2008
Natural history of CMT1A including QoL: a 2-year prospective study
L Padua, D Pareyson, I Aprile, et al.
AJNR. American Journal of Neuroradiology
|
April 5, 2008
Can MR imaging diagnose adult-onset Alexander disease?
L Farina, D Pareyson, L Minati, et al.
Page
of 12