Tawil R - Search Results

1

Clinical and Genetic Characteristics in Young, Glucocorticoid-Naive Boys With Duchenne Muscular Dystrophy.

Schiava M, Amos R, VanRuiten H, McDermott MP, Martens WB, Gregory S, Mayhew A, McColl E, Tawil R, Willis T, Bushby K, Griggs RC, Guglieri M; FOR-DMD Investigators of the Muscle Study Group. Schiava M, et al. Among authors: tawil r. Neurology. 2022 Jan 24;98(4):e390-e401. doi: 10.1212/WNL.0000000000013122. Neurology. 2022. PMID: 34857536 Free PMC article.

2

Linkage of atypical myotonia congenita to a sodium channel locus.

Ptacek LJ, Tawil R, Griggs RC, Storvick D, Leppert M. Ptacek LJ, et al. Among authors: tawil r. Neurology. 1992 Feb;42(2):431-3. doi: 10.1212/wnl.42.2.431. Neurology. 1992. PMID: 1310531

3

Scapuloperoneal syndromes. Absence of linkage to the 4q35 FSHD locus.

Tawil R, Myers GJ, Weiffenbach B, Griggs RC. Tawil R, et al. Arch Neurol. 1995 Nov;52(11):1069-72. doi: 10.1001/archneur.1995.00540350055017. Arch Neurol. 1995. PMID: 7487558

4

Monozygotic twins with facioscapulohumeral dystrophy (FSHD): implications for genotype/phenotype correlation. FSH-DY Group.

Griggs RC, Tawil R, McDermott M, Forrester J, Figlewicz D, Weiffenbach B. Griggs RC, et al. Among authors: tawil r. Muscle Nerve Suppl. 1995;2:S50-5. Muscle Nerve Suppl. 1995. PMID: 7739626

5

Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis.

Ptáĉek LJ, Tawil R, Griggs RC, Meola G, McManis P, Barohn RJ, Mendell JR, Harris C, Spitzer R, Santiago F, et al. Ptáĉek LJ, et al. Among authors: tawil r. Neurology. 1994 Aug;44(8):1500-3. doi: 10.1212/wnl.44.8.1500. Neurology. 1994. PMID: 8058156

6

Andersen's syndrome: potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features.

Tawil R, Ptacek LJ, Pavlakis SG, DeVivo DC, Penn AS, Ozdemir C, Griggs RC. Tawil R, et al. Ann Neurol. 1994 Mar;35(3):326-30. doi: 10.1002/ana.410350313. Ann Neurol. 1994. PMID: 8080508

7

Extreme variability of expression in monozygotic twins with FSH muscular dystrophy.

Tawil R, Storvick D, Feasby TE, Weiffenbach B, Griggs RC. Tawil R, et al. Neurology. 1993 Feb;43(2):345-8. doi: 10.1212/wnl.43.2.345. Neurology. 1993. PMID: 8094896

8

Chromosome 4q DNA rearrangement in monozygotic twins discordant for facioscapulohumeral muscular dystrophy.

Tawil R, Storvick D, Weiffenbach B, Altherr MR, Feasby TE, Griggs RC. Tawil R, et al. Hum Mutat. 1993;2(6):492-4. doi: 10.1002/humu.1380020612. Hum Mutat. 1993. PMID: 8111417 No abstract available.

9

Facioscapulohumeral muscular dystrophy (FSHD): design of natural history study and results of baseline testing. FSH-DY Group.

Tawil R, McDermott MP, Mendell JR, Kissel J, Griggs RC. Tawil R, et al. Neurology. 1994 Mar;44(3 Pt 1):442-6. doi: 10.1212/wnl.44.3_part_1.442. Neurology. 1994. PMID: 8145913

10

Acetazolamide-induced nephrolithiasis: implications for treatment of neuromuscular disorders.

Tawil R, Moxley RT 3rd, Griggs RC. Tawil R, et al. Neurology. 1993 Jun;43(6):1105-6. doi: 10.1212/wnl.43.6.1105. Neurology. 1993. PMID: 8170551

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