au.\*:("TAWIL R")
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COMPARISON OF ORAL PROPRANOLOL AND VERAPAMIL FOR COMBINED SYSTEMIC HYPERTENSION AND ANGINA PECTORIS: A PLACEBO-CONTROLLED DOUBLE-BLIND RANDOMIZED CROSSOVER TRIALFRISHMAN WH; KLEIN NA; KLEIN P et al.1982; AM. J. CARDIOL.; ISSN 0002-9149; USA; DA. 1982; VOL. 50; NO 5; PP. 1164-1172; BIBL. 44 REF.Article
Gastrointestinal heminths of the crevice spiny lizard, Sceloporus poinsettii (Phrynosomatidae)GOLDBERG, S. R; BURSEY, C. R; TAWIL, R et al.Journal of the Helminthological Society of Washington. 1993, Vol 60, Num 2, pp 263-265, issn 1049-233XArticle
A puzzling case of periodic paralysisGRIGGS, R. C; BENDER, A. N; TAWIL, R et al.Muscle & nerve. 1996, Vol 19, Num 3, pp 362-364, issn 0148-639XArticle
Gastrointestinal helminths of Sceloporus lizards (Phrynosomatidae) from ArizonaGOLDBERG, S. R; BURSEY, C. R; TAWIL, R et al.Journal of the Helminthological Society of Washington. 1994, Vol 61, Num 1, pp 73-83, issn 1049-233XArticle
Aplectana macintoshii (Nematoda: Cosmocercidae) in Eumeces latiscutatus (Sauria: Scincidae), from JapanGOLDBERG, S. R; BURSEY, C. R; TAWIL, R et al.Journal of the Helminthological Society of Washington. 1993, Vol 60, Num 2, pp 283-284, issn 1049-233XArticle
Gastrointestinal helminths of five horned lizard species, Phrynosoma (Phrynosomatidae) from ArizonaGOLDBERG, S. R; BURSEY, C. R; TAWIL, R et al.Journal of the Helminthological Society of Washington. 1993, Vol 60, Num 2, pp 234-238, issn 1049-233XArticle
Scapuloperoneal syndromes : absence of linkage to the 4q35 FSHD locusTAWIL, R; MYERS, G. J; WEIFFENBACH, B et al.Archives of neurology (Chicago). 1995, Vol 52, Num 11, pp 1069-1072, issn 0003-9942Article
Genetics of facioscapsulohumeral muscular dystrophy : new mutations in sporadic casesGRIGGS, R. C; TAWIL, R; STORVICK, D et al.Neurology. 1993, Vol 43, Num 11, pp 2369-2372, issn 0028-3878Article
Linkage of atypical myotonia congenita to a sodium channel locusPTACEK, L. J; TAWIL, R; GRIGGS, R. C et al.Neurology. 1992, Vol 42, Num 2, pp 431-433, issn 0028-3878Article
Facioscapulohumeral dystrophy : A distinct regional myopathy with a novel molecular pathogenesisTAWIL, R; FIGLEWICZ, D. A; GRIGGS, R. C et al.Annals of neurology. 1998, Vol 43, Num 3, pp 279-282, issn 0364-5134Article
Definitive molecular diagnosis of facioscapulohumeral dystrophyORRELL, R. W; TAWIL, R; FORRESTER, J et al.Neurology. 1999, Vol 52, Num 9, pp 1822-1826, issn 0028-3878Article
Pregnancy and birth outcomes in women with facioscapulohumeral muscular dystrophyCIAFALONI, E; PRESSMAN, E. K; LOI, A. M et al.Neurology. 2006, Vol 67, Num 10, pp 1887-1889, issn 0028-3878, 3 p.Article
A pilot trial of prednisone in facioscapulohumeral muscular dystrophyTAWIL, R; MCDERMOTT, M. P; PANDYA, S et al.Neurology. 1997, Vol 48, Num 1, pp 46-49, issn 0028-3878Article
A new TL finger ring dosimetry system with automated ring identificationDUFTSCHMID, K. E; MAJEVSKI, M; MICHLER, E et al.Radiation protection dosimetry. 1996, Vol 66, Num 1-4, pp 111-112, issn 0144-8420Conference Paper
A new extremity system and performance at INELPERRY, O. R; TAWIL, R. A; VELBECK, K. J et al.Radiation protection dosimetry. 1996, Vol 66, Num 1-4, pp 113-118, issn 0144-8420Conference Paper
Monozygotic twins with facioscapulohumeral dystrophy (FSHD) : implications for genotype/phenotype correlationGRIGGS, R. C; TAWIL, R; MCDERMOTT, M et al.Muscle & nerve. 1995, pp S50-S55, issn 0148-639X, SUP2Conference Paper
Evidence for anticipation and association of deletion size with severity in facioscapulohumeral muscular dystrophyTAWIL, R; FORRESTER, J; GRIGGS, R. C et al.Annals of neurology. 1996, Vol 39, Num 6, pp 744-748, issn 0364-5134Article
Identification of a mutation in the gene causing hyerkalemic periodic paralysisPTACEK, L. J; GEORGE, A. L; GRIGGS, R. C et al.Cell (Cambridge). 1991, Vol 67, Num 5, pp 1021-1027, issn 0092-8674Article
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4DEAK, K. L; LEMMERS, R. J. L. F; STAJICH, J. M et al.Neurology. 2007, Vol 68, Num 8, pp 578-582, issn 0028-3878, 5 p.Article
Andersen's syndrome : A distinct periodic paralysisSANSONE, V; GRIGGS, R. C; RIRIE, D et al.Annals of neurology. 1997, Vol 42, Num 3, pp 305-312, issn 0364-5134Conference Paper
The primary periodic paralyses : diagnosis, pathogenesis and treatmentVENANCE, S. L; CANNON, S. C; FIALHO, D et al.Brain. 2006, Vol 129, pp 8-17, issn 0006-8950, 10 p., 1Article
Pilot trial of albuterol in facioscapulohumeral muscular dystrophyKISSEL, J. T; MCDERMOTT, M. P; NATARAJAN, R et al.Neurology. 1998, Vol 50, Num 5, pp 1402-1406, issn 0028-3878Article
Low energy X ray dosimetry studies (7 to 17.5 keV) with synchrotron radiationIPE, N. E; BELLAMY, H; FLOOD, J. R et al.Radiation protection dosimetry. 1996, Vol 66, Num 1-4, pp 69-74, issn 0144-8420Conference Paper
Randomized trials of dichlorphenamide in the periodic paralysesTAWIL, R; MCDERMOTT, M. P; GRIGGS, R. C et al.Annals of neurology. 2000, Vol 47, Num 1, pp 46-53, issn 0364-5134Article
Clinical features of facioscapulohumeral muscular dystrophy 2DE GREEF, J. C; LEMMERS, R. J. L. F; DESNUELLE, C et al.Neurology. 2010, Vol 75, Num 17, pp 1548-1554, issn 0028-3878, 7 p.Article