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F Hentati

Showing results (111-120 of 120) with videos related to

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Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
Science (New York, N.Y.)|November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophyS Noguchi, E M McNally, K Ben Othmane, et al.
Neurology|December 22, 2010
An independent replication of PARK16 in Asian samplesC Vilariño-Güell, O A Ross, J O Aasly, et al.
Neurology|August 8, 2008
PINK1 mutations and parkinsonismL Ishihara-Paul, M M Hulihan, J Kachergus, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Human Molecular Genetics|May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 familiesG Cancel, A Dürr, O Didierjean, et al.
Nature Genetics|September 10, 1998
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyJ Liu, M Aoki, I Illa, et al.
Journal of Neurology|August 28, 2010
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arraysD H'mida-Ben Brahim, A M'zahem, M Assoum, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
Neurology|June 10, 2009
Characterization of DCTN1 genetic variability in neurodegenerationC Vilariño-Güell, C Wider, A I Soto-Ortolaza, et al.
Pageof 12

Showing results (111-120 of 120) with videos related to

Sort By:
Pageof 12
You have reached the last page of results.This site can display upto 120 results.
Neurology|November 23, 2000
Novel mutations in spastin gene and absence of correlation with age at onset of symptomsA Hentati, H X Deng, H Zhai, et al.
Science (New York, N.Y.)|November 3, 1995
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophyS Noguchi, E M McNally, K Ben Othmane, et al.
Neurology|December 22, 2010
An independent replication of PARK16 in Asian samplesC Vilariño-Güell, O A Ross, J O Aasly, et al.
Neurology|August 8, 2008
PINK1 mutations and parkinsonismL Ishihara-Paul, M M Hulihan, J Kachergus, et al.
Neurology|December 10, 2008
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North AfricaP Richard, K Gaudon, H Haddad, et al.
Human Molecular Genetics|May 1, 1997
Molecular and clinical correlations in spinocerebellar ataxia 2: a study of 32 familiesG Cancel, A Dürr, O Didierjean, et al.
Nature Genetics|September 10, 1998
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyJ Liu, M Aoki, I Illa, et al.
Journal of Neurology|August 28, 2010
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arraysD H'mida-Ben Brahim, A M'zahem, M Assoum, et al.
Journal of Neurology|December 17, 2009
Phenotype genotype analysis in 15 patients presenting a congenital myasthenic syndrome due to mutations in DOK7A Ben Ammar, F Petit, N Alexandri, et al.
Neurology|June 10, 2009
Characterization of DCTN1 genetic variability in neurodegenerationC Vilariño-Güell, C Wider, A I Soto-Ortolaza, et al.
Pageof 12