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Brain & Development
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July 1, 1993
Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression
M T Dotti, A Malandrini, S Bartolini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 20, 1999
Novel mutation of the P0 extracellular domain causes a Déjérine-Sottas syndrome
G M Fabrizi, T Cavallaro, M Morbin, et al.
Journal of Neurology
|
January 11, 2001
Heteroplasmy of the A3243G transition of mitochondrial tRNA(Leu(UUR)) in a MELAS case and in a 25-week-old miscarried fetus
E Cardaioli, G M Fabrizi, G S Grieco, et al.
Neurology
|
July 11, 2001
A somatic and germline mosaic mutation in MPZ/P(0) mimics recessive inheritance of CMT1B
G M Fabrizi, M Ferrarini, T Cavallaro, 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.
Nucleic Acids Research
|
August 11, 1989
Sequence of a cDNA specifying subunit VIa of human cytochrome c oxidase
G M Fabrizi, R Rizzuto, H Nakase, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 27, 2003
Hereditary neuropathy with liability to pressure palsies: electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation
R Del Colle, G M Fabrizi, M Turazzini, et al.
Journal of the Neurological Sciences
|
October 1, 1995
Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter
A Malandrini, C Scarpini, G M Fabrizi, et al.
Journal of the Neurological Sciences
|
June 6, 2012
Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
S Testi, G Malerba, M Ferrarini, et al.
Neurology
|
July 20, 2007
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease
G M Fabrizi, M Ferrarini, T Cavallaro, et al.
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
Brain & Development
|
July 1, 1993
Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression
M T Dotti, A Malandrini, S Bartolini, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 20, 1999
Novel mutation of the P0 extracellular domain causes a Déjérine-Sottas syndrome
G M Fabrizi, T Cavallaro, M Morbin, et al.
Journal of Neurology
|
January 11, 2001
Heteroplasmy of the A3243G transition of mitochondrial tRNA(Leu(UUR)) in a MELAS case and in a 25-week-old miscarried fetus
E Cardaioli, G M Fabrizi, G S Grieco, et al.
Neurology
|
July 11, 2001
A somatic and germline mosaic mutation in MPZ/P(0) mimics recessive inheritance of CMT1B
G M Fabrizi, M Ferrarini, T Cavallaro, 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.
Nucleic Acids Research
|
August 11, 1989
Sequence of a cDNA specifying subunit VIa of human cytochrome c oxidase
G M Fabrizi, R Rizzuto, H Nakase, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 27, 2003
Hereditary neuropathy with liability to pressure palsies: electrophysiological and genetic study of a family with carpal tunnel syndrome as only clinical manifestation
R Del Colle, G M Fabrizi, M Turazzini, et al.
Journal of the Neurological Sciences
|
October 1, 1995
Early-onset benign limb-girdle myopathy with contractures and facial involvement affecting a father and daughter
A Malandrini, C Scarpini, G M Fabrizi, et al.
Journal of the Neurological Sciences
|
June 6, 2012
Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
S Testi, G Malerba, M Ferrarini, et al.
Neurology
|
July 20, 2007
Two novel mutations in dynamin-2 cause axonal Charcot-Marie-Tooth disease
G M Fabrizi, M Ferrarini, T Cavallaro, et al.
Page
of 7