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Journal of Neurology
|
January 1, 1993
Evidence of a genetic marker associated with early onset in Friedreich's ataxia
S Cocozza, A Antonelli, G Campanella, et al.
Acta Neurologica Scandinavica
|
August 9, 2016
Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex<sup>®</sup>
A Carotenuto, R Iodice, M Petracca, et al.
Neurology
|
December 31, 1997
Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia
M Ragno, G De Michele, F Cavalcanti, et al.
Brain Imaging and Behavior
|
October 6, 2016
The influence of interoceptive awareness on functional connectivity in patients with irritable bowel syndrome
Mariachiara Longarzo, M Quarantelli, M Aiello, et al.
Neurology
|
February 11, 2000
Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene
G De Michele, A Filla, F Cavalcanti, et al.
Neurology
|
March 27, 2002
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy
A Filla, G De Michele, S Cocozza, et al.
Journal of Medical Genetics
|
August 14, 2008
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients
I Castaldo, M Pinelli, A Monticelli, et al.
Artery
|
January 1, 1993
XbaI polymorphism of the apolipoprotein B gene in patients with hyperlipidemia and echo-Doppler evidence of arterial lesions
F De Lorenzo, P Rubba, A Monticelli, et al.
Neurology
|
November 26, 2003
Intergenerational instability and marked anticipation in SCA-17
F Maltecca, A Filla, I Castaldo, et al.
Nutrition Research (New York, N.Y.)
|
September 7, 2014
Test meals rich in marine long-chain n-3 polyunsaturated fatty acids increase postprandial chylomicron response
E Griffo, L Di Marino, L Patti, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 81) with videos related to
Sort By:
Page
of 9
Journal of Neurology
|
January 1, 1993
Evidence of a genetic marker associated with early onset in Friedreich's ataxia
S Cocozza, A Antonelli, G Campanella, et al.
Acta Neurologica Scandinavica
|
August 9, 2016
Upper motor neuron evaluation in multiple sclerosis patients treated with Sativex<sup>®</sup>
A Carotenuto, R Iodice, M Petracca, et al.
Neurology
|
December 31, 1997
Broadened Friedreich's ataxia phenotype after gene cloning. Minimal GAA expansion causes late-onset spastic ataxia
M Ragno, G De Michele, F Cavalcanti, et al.
Brain Imaging and Behavior
|
October 6, 2016
The influence of interoceptive awareness on functional connectivity in patients with irritable bowel syndrome
Mariachiara Longarzo, M Quarantelli, M Aiello, et al.
Neurology
|
February 11, 2000
Atypical Friedreich ataxia phenotype associated with a novel missense mutation in the X25 gene
G De Michele, A Filla, F Cavalcanti, et al.
Neurology
|
March 27, 2002
Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy
A Filla, G De Michele, S Cocozza, et al.
Journal of Medical Genetics
|
August 14, 2008
DNA methylation in intron 1 of the frataxin gene is related to GAA repeat length and age of onset in Friedreich ataxia patients
I Castaldo, M Pinelli, A Monticelli, et al.
Artery
|
January 1, 1993
XbaI polymorphism of the apolipoprotein B gene in patients with hyperlipidemia and echo-Doppler evidence of arterial lesions
F De Lorenzo, P Rubba, A Monticelli, et al.
Neurology
|
November 26, 2003
Intergenerational instability and marked anticipation in SCA-17
F Maltecca, A Filla, I Castaldo, et al.
Nutrition Research (New York, N.Y.)
|
September 7, 2014
Test meals rich in marine long-chain n-3 polyunsaturated fatty acids increase postprandial chylomicron response
E Griffo, L Di Marino, L Patti, et al.
Page
of 9