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Journal of Medical Genetics
|
October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes
S Tezenas du Montcel, F Clot, M Vidailhet, et al.
Brain : a Journal of Neurology
|
January 21, 2009
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA)
F Mochel, F Sedel, A Vanderver, et al.
Neurology
|
October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
C Goizet, A Boukhris, D Maltete, et al.
NPJ Vaccines
|
October 21, 2020
Experimental and in silico evidence suggests vaccines are unlikely to be affected by D614G mutation in SARS-CoV-2 spike protein
Alexander J McAuley, Michael J Kuiper, Peter A Durr, et al.
Journal of Internal Medicine
|
October 27, 2020
Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56
A Legrand, C Pujol, C M Durand, et al.
Neurology
|
November 12, 2010
Tapping linked to function and structure in premanifest and symptomatic Huntington disease
N Bechtel, R I Scahill, H D Rosas, et al.
Scientific Reports
|
November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein
L L Mariani, S Rivaud-Péchoux, P Charles, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease
L Djoussé, B Knowlton, M Hayden, et al.
Brain : a Journal of Neurology
|
August 22, 2009
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
M Anheim, B Monga, M Fleury, et al.
European Journal of Neurology
|
June 20, 2020
Deciphering the natural history of SCA7 in children
M G Bah, D Rodriguez, C Cazeneuve, et al.
Page
of 17
Search research articles
Search
Showing results (151-160 of 163) with videos related to
Sort By:
Page
of 17
Journal of Medical Genetics
|
October 18, 2005
Epsilon sarcoglycan mutations and phenotype in French patients with myoclonic syndromes
S Tezenas du Montcel, F Clot, M Vidailhet, et al.
Brain : a Journal of Neurology
|
January 21, 2009
Cerebellar ataxia with elevated cerebrospinal free sialic acid (CAFSA)
F Mochel, F Sedel, A Vanderver, et al.
Neurology
|
October 7, 2009
SPG15 is the second most common cause of hereditary spastic paraplegia with thin corpus callosum
C Goizet, A Boukhris, D Maltete, et al.
NPJ Vaccines
|
October 21, 2020
Experimental and in silico evidence suggests vaccines are unlikely to be affected by D614G mutation in SARS-CoV-2 spike protein
Alexander J McAuley, Michael J Kuiper, Peter A Durr, et al.
Journal of Internal Medicine
|
October 27, 2020
Pseudoxanthoma elasticum overlaps hereditary spastic paraplegia type 56
A Legrand, C Pujol, C M Durand, et al.
Neurology
|
November 12, 2010
Tapping linked to function and structure in premanifest and symptomatic Huntington disease
N Bechtel, R I Scahill, H D Rosas, et al.
Scientific Reports
|
November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein
L L Mariani, S Rivaud-Péchoux, P Charles, et al.
American Journal of Medical Genetics. Part A
|
June 5, 2003
Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease
L Djoussé, B Knowlton, M Hayden, et al.
Brain : a Journal of Neurology
|
August 22, 2009
Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients
M Anheim, B Monga, M Fleury, et al.
European Journal of Neurology
|
June 20, 2020
Deciphering the natural history of SCA7 in children
M G Bah, D Rodriguez, C Cazeneuve, et al.
Page
of 17