Search research articles
Contact Us
Filters
Showing results (101-110 of 113) with videos related to
Page
of 12
Sort By:
Clinical Genetics
|
September 27, 2007
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease
F Caroli, R Biancheri, M Seri, et al.
European Journal of Neurology
|
May 5, 2016
No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype
C Bertolin, G Querin, E Da Re, et al.
European Journal of Neurology
|
July 15, 2016
Nerve conduction velocity in CMT1A: what else can we tell?
F Manganelli, C Pisciotta, M M Reilly, et al.
Neurology
|
July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations
J M Polke, M Laurá, D Pareyson, et al.
Journal of the Peripheral Nervous System : JPNS
|
October 11, 2024
Patient-reported disease burden in the Accelerate Clinical Trials in Charcot-Marie-Tooth Disease Study
T Rehbein, J Purks, N Dilek, et al.
European Journal of Neurology
|
October 14, 2017
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy
A Cortese, M Laurà, C Casali, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 25, 2014
Is overwork weakness relevant in Charcot-Marie-Tooth disease?
G Piscosquito, M M Reilly, A Schenone, et al.
European Journal of Neurology
|
August 1, 2015
Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease
G Piscosquito, M M Reilly, A Schenone, et al.
Journal of the Neurological Sciences
|
March 23, 2016
Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment
A Cortese, D Franciotta, E Alfonsi, et al.
Journal of Neurology
|
April 22, 2016
Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area
A Cortese, G Vita, M Luigetti, et al.
Page
of 12
Search research articles
Search
Showing results (101-110 of 113) with videos related to
Sort By:
Page
of 12
Clinical Genetics
|
September 27, 2007
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease
F Caroli, R Biancheri, M Seri, et al.
European Journal of Neurology
|
May 5, 2016
No effect of AR polyG polymorphism on spinal and bulbar muscular atrophy phenotype
C Bertolin, G Querin, E Da Re, et al.
European Journal of Neurology
|
July 15, 2016
Nerve conduction velocity in CMT1A: what else can we tell?
F Manganelli, C Pisciotta, M M Reilly, et al.
Neurology
|
July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutations
J M Polke, M Laurá, D Pareyson, et al.
Journal of the Peripheral Nervous System : JPNS
|
October 11, 2024
Patient-reported disease burden in the Accelerate Clinical Trials in Charcot-Marie-Tooth Disease Study
T Rehbein, J Purks, N Dilek, et al.
European Journal of Neurology
|
October 14, 2017
Altered TDP-43-dependent splicing in HSPB8-related distal hereditary motor neuropathy and myofibrillar myopathy
A Cortese, M Laurà, C Casali, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 25, 2014
Is overwork weakness relevant in Charcot-Marie-Tooth disease?
G Piscosquito, M M Reilly, A Schenone, et al.
European Journal of Neurology
|
August 1, 2015
Responsiveness of clinical outcome measures in Charcot-Marie-Tooth disease
G Piscosquito, M M Reilly, A Schenone, et al.
Journal of the Neurological Sciences
|
March 23, 2016
Combined central and peripheral demyelination: Clinical features, diagnostic findings, and treatment
A Cortese, D Franciotta, E Alfonsi, et al.
Journal of Neurology
|
April 22, 2016
Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area
A Cortese, G Vita, M Luigetti, et al.
Page
of 12