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R Tawil

Showing results (31-40 of 40) with videos related to

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Annals of Neurology|October 23, 1997
Andersen's syndrome: a distinct periodic paralysisV Sansone, R C Griggs, G Meola, et al.
Neurology|January 19, 2007
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4K L Deak, R J L F Lemmers, J M Stajich, et al.
Annals of Neurology|January 13, 2000
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic ParalysisR Tawil, M P McDermott, R Brown, et al.
Neuromuscular Disorders : NMD|January 1, 1997
Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysisG Fouad, M Dalakas, S Servidei, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Neurology|March 10, 2010
Six-Minute Walk Test demonstrates motor fatigue in spinal muscular atrophyJ Montes, M P McDermott, W B Martens, et al.
Neurology|June 11, 2003
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndromeM R Donaldson, J L Jensen, M Tristani-Firouzi, et al.
Neurology|November 10, 2004
Correlating phenotype and genotype in the periodic paralysesT M Miller, M R Dias da Silva, H A Miller, et al.
Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.
Cell|May 24, 2001
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeN M Plaster, R Tawil, M Tristani-Firouzi, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
Annals of Neurology|October 23, 1997
Andersen's syndrome: a distinct periodic paralysisV Sansone, R C Griggs, G Meola, et al.
Neurology|January 19, 2007
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4K L Deak, R J L F Lemmers, J M Stajich, et al.
Annals of Neurology|January 13, 2000
Randomized trials of dichlorphenamide in the periodic paralyses. Working Group on Periodic ParalysisR Tawil, M P McDermott, R Brown, et al.
Neuromuscular Disorders : NMD|January 1, 1997
Genotype-phenotype correlations of DHP receptor alpha 1-subunit gene mutations causing hypokalemic periodic paralysisG Fouad, M Dalakas, S Servidei, et al.
Journal of Clinical Neuromuscular Disease|December 17, 2008
Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular DystrophyR W Tim, J R Gilbert, J M Stajich, et al.
Neurology|March 10, 2010
Six-Minute Walk Test demonstrates motor fatigue in spinal muscular atrophyJ Montes, M P McDermott, W B Martens, et al.
Neurology|June 11, 2003
PIP2 binding residues of Kir2.1 are common targets of mutations causing Andersen syndromeM R Donaldson, J L Jensen, M Tristani-Firouzi, et al.
Neurology|November 10, 2004
Correlating phenotype and genotype in the periodic paralysesT M Miller, M R Dias da Silva, H A Miller, et al.
Neurology|October 27, 2010
Clinical features of facioscapulohumeral muscular dystrophy 2J C de Greef, R J L F Lemmers, P Camaño, et al.
Cell|May 24, 2001
Mutations in Kir2.1 cause the developmental and episodic electrical phenotypes of Andersen's syndromeN M Plaster, R Tawil, M Tristani-Firouzi, et al.
Pageof 4