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R Tawil

Showing results (11-20 of 40) with videos related to

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Muscle & Nerve. Supplement|January 1, 1995
Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation. FSH-DY GroupR C Griggs, R Tawil, M McDermott, et al.
Neurology|December 8, 2006
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophyR J Osborne, S Welle, S L Venance, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 1999
Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutationS Bendahhou, T R Cummins, R Tawil, et al.
Muscle & Nerve. Supplement|April 12, 2013
Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlationR C Griggs, R Tawil, M McDermott, et al.
Neurology|March 1, 1994
Facioscapulohumeral muscular dystrophy (FSHD): design of natural history study and results of baseline testing. FSH-DY GroupR Tawil, M P McDermott, J R Mendell, et al.
Archives of Neurology|January 1, 1994
Dementia of adult polyglucosan body disease. Evidence of cortical and subcortical dysfunctionZ Rifai, M Klitzke, R Tawil, et al.
Journal of the American Veterinary Medical Association|March 19, 2025
Needle sharpness is minimally affected by vaccine vial punctureJulia R Tawil, Emma C Vitello, Gina M Agostini-Walesch, et al.
Neurology|June 17, 1999
Definitive molecular diagnosis of facioscapulohumeral dystrophyR W Orrell, R Tawil, J Forrester, et al.
Neurology|January 1, 1997
A pilot trial of prednisone in facioscapulohumeral muscular dystrophy. FSH-DY GroupR Tawil, M P McDermott, S Pandya, et al.
Neurology|November 30, 2006
Pregnancy and birth outcomes in women with facioscapulohumeral muscular dystrophyE Ciafaloni, E K Pressman, A M Loi, et al.
Pageof 4

Showing results (11-20 of 40) with videos related to

Sort By:
Pageof 4
Muscle & Nerve. Supplement|January 1, 1995
Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation. FSH-DY GroupR C Griggs, R Tawil, M McDermott, et al.
Neurology|December 8, 2006
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophyR J Osborne, S Welle, S L Venance, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|June 15, 1999
Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutationS Bendahhou, T R Cummins, R Tawil, et al.
Muscle & Nerve. Supplement|April 12, 2013
Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlationR C Griggs, R Tawil, M McDermott, et al.
Neurology|March 1, 1994
Facioscapulohumeral muscular dystrophy (FSHD): design of natural history study and results of baseline testing. FSH-DY GroupR Tawil, M P McDermott, J R Mendell, et al.
Archives of Neurology|January 1, 1994
Dementia of adult polyglucosan body disease. Evidence of cortical and subcortical dysfunctionZ Rifai, M Klitzke, R Tawil, et al.
Journal of the American Veterinary Medical Association|March 19, 2025
Needle sharpness is minimally affected by vaccine vial punctureJulia R Tawil, Emma C Vitello, Gina M Agostini-Walesch, et al.
Neurology|June 17, 1999
Definitive molecular diagnosis of facioscapulohumeral dystrophyR W Orrell, R Tawil, J Forrester, et al.
Neurology|January 1, 1997
A pilot trial of prednisone in facioscapulohumeral muscular dystrophy. FSH-DY GroupR Tawil, M P McDermott, S Pandya, et al.
Neurology|November 30, 2006
Pregnancy and birth outcomes in women with facioscapulohumeral muscular dystrophyE Ciafaloni, E K Pressman, A M Loi, et al.
Pageof 4