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Journal of Neurology
|
November 15, 2011
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years
C Angelini, C Semplicini, S Ravaglia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 19, 2015
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population
O Musumeci, G la Marca, M Spada, et al.
Nature Genetics
|
September 10, 1998
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
J Liu, M Aoki, I Illa, et al.
Neurology
|
July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients
E Pegoraro, H Marks, C A Garcia, et al.
Neurology
|
July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy
M Aoki, J Liu, I Richard, et al.
Journal of Neurology
|
July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian Network
D Orsucci, C Angelini, E Bertini, et al.
Neuromuscular Disorders : NMD
|
June 26, 2009
Reliability of the North Star Ambulatory Assessment in a multicentric setting
E S Mazzone, S Messina, G Vasco, et al.
Persoonia
|
August 30, 2021
Fungal Planet description sheets: 1112-1181
P W Crous, D A Cowan, G Maggs-Kölling, et al.
Persoonia
|
September 11, 2023
Fungal Planet description sheets: 1284-1382
P W Crous, E R Osieck, Ž Jurjević, et al.
Physical Review Letters
|
February 13, 2016
Observation of B→D(*) π^(+)π^(-)ℓ^(-)ν Decays in e^(+)e^(-) Collisions at the Υ(4S) Resonance
J P Lees, V Poireau, V Tisserand, et al.
Page
of 54
Search research articles
Search
Showing results (321-330 of 531) with videos related to
Sort By:
Page
of 54
Journal of Neurology
|
November 15, 2011
Observational clinical study in juvenile-adult glycogenosis type 2 patients undergoing enzyme replacement therapy for up to 4 years
C Angelini, C Semplicini, S Ravaglia, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
March 19, 2015
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population
O Musumeci, G la Marca, M Spada, et al.
Nature Genetics
|
September 10, 1998
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
J Liu, M Aoki, I Illa, et al.
Neurology
|
July 23, 1998
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients
E Pegoraro, H Marks, C A Garcia, et al.
Neurology
|
July 27, 2001
Genomic organization of the dysferlin gene and novel mutations in Miyoshi myopathy
M Aoki, J Liu, I Richard, et al.
Journal of Neurology
|
July 12, 2017
Revisiting mitochondrial ocular myopathies: a study from the Italian Network
D Orsucci, C Angelini, E Bertini, et al.
Neuromuscular Disorders : NMD
|
June 26, 2009
Reliability of the North Star Ambulatory Assessment in a multicentric setting
E S Mazzone, S Messina, G Vasco, et al.
Persoonia
|
August 30, 2021
Fungal Planet description sheets: 1112-1181
P W Crous, D A Cowan, G Maggs-Kölling, et al.
Persoonia
|
September 11, 2023
Fungal Planet description sheets: 1284-1382
P W Crous, E R Osieck, Ž Jurjević, et al.
Physical Review Letters
|
February 13, 2016
Observation of B→D(*) π^(+)π^(-)ℓ^(-)ν Decays in e^(+)e^(-) Collisions at the Υ(4S) Resonance
J P Lees, V Poireau, V Tisserand, et al.
Page
of 54