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Neuromuscular Disorders : NMD
|
November 28, 2012
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases
M Mancuso, C Angelini, E Bertini, et al.
Neurology
|
August 24, 2005
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition
L Salviati, S Sacconi, L Murer, et al.
Journal of Neurology
|
July 2, 2010
Right hemisphere dysfunction and emotional processing in ALS: an fMRI study
A Palmieri, M Naccarato, S Abrahams, et al.
Neurology
|
April 12, 2003
Cerebellar ataxia and coenzyme Q10 deficiency
C Lamperti, A Naini, M Hirano, et al.
Scientific Reports
|
November 29, 2019
Identification of potential molecular pathogenesis mechanisms modulated by microRNAs in patients with Intestinal Neuronal Dysplasia type B
Marcos C Angelini, Alana Maia E Silva, Tainara F Felix, et al.
ESMO Open
|
May 25, 2023
Prognostic role and interaction of TERT promoter status, telomere length and MGMT promoter methylation in newly diagnosed IDH wild-type glioblastoma patients
S Giunco, M Padovan, C Angelini, et al.
European Journal of Neurology
|
February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
R Del Bo, S Ghezzi, S Corti, et al.
Neuromuscular Disorders : NMD
|
January 1, 1997
Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis
G Fouad, M Dalakas, S Servidei, et al.
Human Molecular Genetics
|
November 1, 1996
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy
E M McNally, D Duggan, J R Gorospe, et al.
European Journal of Neurology
|
January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia
T Kyriakides, K Aleksovska, C Angelini, et al.
Page
of 54
Search research articles
Search
Showing results (301-310 of 531) with videos related to
Sort By:
Page
of 54
Neuromuscular Disorders : NMD
|
November 28, 2012
Fatigue and exercise intolerance in mitochondrial diseases. Literature revision and experience of the Italian Network of mitochondrial diseases
M Mancuso, C Angelini, E Bertini, et al.
Neurology
|
August 24, 2005
Infantile encephalomyopathy and nephropathy with CoQ10 deficiency: a CoQ10-responsive condition
L Salviati, S Sacconi, L Murer, et al.
Journal of Neurology
|
July 2, 2010
Right hemisphere dysfunction and emotional processing in ALS: an fMRI study
A Palmieri, M Naccarato, S Abrahams, et al.
Neurology
|
April 12, 2003
Cerebellar ataxia and coenzyme Q10 deficiency
C Lamperti, A Naini, M Hirano, et al.
Scientific Reports
|
November 29, 2019
Identification of potential molecular pathogenesis mechanisms modulated by microRNAs in patients with Intestinal Neuronal Dysplasia type B
Marcos C Angelini, Alana Maia E Silva, Tainara F Felix, et al.
ESMO Open
|
May 25, 2023
Prognostic role and interaction of TERT promoter status, telomere length and MGMT promoter methylation in newly diagnosed IDH wild-type glioblastoma patients
S Giunco, M Padovan, C Angelini, et al.
European Journal of Neurology
|
February 25, 2009
TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations
R Del Bo, S Ghezzi, S Corti, et al.
Neuromuscular Disorders : NMD
|
January 1, 1997
Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysis
G Fouad, M Dalakas, S Servidei, et al.
Human Molecular Genetics
|
November 1, 1996
Mutations that disrupt the carboxyl-terminus of gamma-sarcoglycan cause muscular dystrophy
E M McNally, D Duggan, J R Gorospe, et al.
European Journal of Neurology
|
January 31, 2026
EAN 2024 Guideline on the Diagnostic Approach to Oligo/Asymptomatic HyperCKemia
T Kyriakides, K Aleksovska, C Angelini, et al.
Page
of 54