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Human Genetics
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April 4, 2008
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL, exon 2 mutation
Silvia Bianchi, M T Dotti, N De Stefano, et al.
Neuromuscular Disorders : NMD
|
March 1, 1997
Abnormal oxidative metabolism in exercise intolerance of undetermined origin
Z Argov, N De Stefano, T Taivassalo, et al.
Muscle & Nerve
|
October 15, 1998
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy study
Z Argov, T Taivassalo, N De Stefano, et al.
Muscle & Nerve
|
August 24, 1999
Short-term aerobic training response in chronic myopathies
T Taivassalo, N De Stefano, J Chen, et al.
Brain & Development
|
March 1, 1993
Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study
M T Dotti, L Manneschi, A Malandrini, et al.
Annals of Neurology
|
February 9, 2000
Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree
F Dubeau, N De Stefano, B G Zifkin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 16, 2017
The Italian Neuroimaging Network Initiative (INNI): enabling the use of advanced MRI techniques in patients with MS
M Filippi, G Tedeschi, P Pantano, et al.
Acta Neurologica
|
April 1, 1990
Serum vitamin E in inherited ataxias
M P Eusebi, C Battisti, N De Stefano, et al.
Neurology
|
June 1, 1995
Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disorders
N De Stefano, P M Matthews, B Ford, et al.
Neuroimage
|
November 2, 2005
fMRI resting state networks define distinct modes of long-distance interactions in the human brain
M De Luca, C F Beckmann, N De Stefano, et al.
Page
of 13
Search research articles
Search
Showing results (31-40 of 124) with videos related to
Sort By:
Page
of 13
Human Genetics
|
April 4, 2008
Novel human pathological mutations. Gene symbol: NOTCH3. Disease: CADASIL, exon 2 mutation
Silvia Bianchi, M T Dotti, N De Stefano, et al.
Neuromuscular Disorders : NMD
|
March 1, 1997
Abnormal oxidative metabolism in exercise intolerance of undetermined origin
Z Argov, N De Stefano, T Taivassalo, et al.
Muscle & Nerve
|
October 15, 1998
Intracellular phosphates in inclusion body myositis--a 31P magnetic resonance spectroscopy study
Z Argov, T Taivassalo, N De Stefano, et al.
Muscle & Nerve
|
August 24, 1999
Short-term aerobic training response in chronic myopathies
T Taivassalo, N De Stefano, J Chen, et al.
Brain & Development
|
March 1, 1993
Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical study
M T Dotti, L Manneschi, A Malandrini, et al.
Annals of Neurology
|
February 9, 2000
Oxidative phosphorylation defect in the brains of carriers of the tRNAleu(UUR) A3243G mutation in a MELAS pedigree
F Dubeau, N De Stefano, B G Zifkin, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
March 16, 2017
The Italian Neuroimaging Network Initiative (INNI): enabling the use of advanced MRI techniques in patients with MS
M Filippi, G Tedeschi, P Pantano, et al.
Acta Neurologica
|
April 1, 1990
Serum vitamin E in inherited ataxias
M P Eusebi, C Battisti, N De Stefano, et al.
Neurology
|
June 1, 1995
Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disorders
N De Stefano, P M Matthews, B Ford, et al.
Neuroimage
|
November 2, 2005
fMRI resting state networks define distinct modes of long-distance interactions in the human brain
M De Luca, C F Beckmann, N De Stefano, et al.
Page
of 13