139 related articles for article (PubMed ID: 3231989)
1. Myotonia levior: contribution to the nosography.
Siciliano G; Risaliti R; Vignocchi G; Rossi B
Riv Neurol; 1988; 58(5):204-9. PubMed ID: 3231989
[TBL] [Abstract][Full Text] [Related]
2. Genetic approaches to the nosology of muscular disease: myotonias and similar diseases.
Becker PE
Birth Defects Orig Artic Ser; 1971 Feb; 7(2):52-62. PubMed ID: 5293617
[TBL] [Abstract][Full Text] [Related]
3. Autosomal recessive generalized myotonia.
Zellweger H; Pavone L; Biondi A; Cimino V; Gullotta F; Hart M; Ionasescu V; Mollica F; Schieken R
Muscle Nerve; 1980; 3(2):176-80. PubMed ID: 7366606
[TBL] [Abstract][Full Text] [Related]
4. [Myotonia congenital (Thomsen) and recessive generalized myotonia (Becker)].
Kuhn E
Nervenarzt; 1993 Dec; 64(12):766-9. PubMed ID: 8114977
[TBL] [Abstract][Full Text] [Related]
5. The myotonias: their diagnosis and treatment.
Moxley RT
Compr Ther; 1996 Jan; 22(1):8-21. PubMed ID: 8654027
[No Abstract] [Full Text] [Related]
6. [Becker's myotonia in Peru].
Torres L; Vélez M; Cosentino C
Rev Neurol; 2000 Jun 1-15; 30(11):1033-6. PubMed ID: 10904948
[TBL] [Abstract][Full Text] [Related]
7. Autosomal recessive generalized myotonia.
Sun SF; Streib EW
Muscle Nerve; 1983 Feb; 6(2):143-8. PubMed ID: 6855798
[TBL] [Abstract][Full Text] [Related]
8. Myotonia congenita--a cause of muscle weakness and stiffness.
Chrestian N; Puymirat J; Bouchard JP; Dupré N
Nat Clin Pract Neurol; 2006 Jul; 2(7):393-9; quiz following 399. PubMed ID: 16932590
[TBL] [Abstract][Full Text] [Related]
9. Myotonia levior is a chloride channel disorder.
Lehmann-Horn F; Mailänder V; Heine R; George AL
Hum Mol Genet; 1995 Aug; 4(8):1397-402. PubMed ID: 7581380
[TBL] [Abstract][Full Text] [Related]
10. The autosomal recessive (Becker) form of myotonia congenita.
Kuhn E; Fiehn W; Seiler D; Schröder JM
Muscle Nerve; 1979; 2(2):109-17. PubMed ID: 397412
[TBL] [Abstract][Full Text] [Related]
11. [Regional clinico-genetic features of myotonias].
Khannanova FK
Zh Nevropatol Psikhiatr Im S S Korsakova; 1986; 86(3):342-6. PubMed ID: 2939672
[TBL] [Abstract][Full Text] [Related]
12. Myotonia congenita (Thomsen's disease) report of five cases in a family.
Pusponegoro HD; Zacharia J; Passat J
Paediatr Indones; 1991; 31(5-6):170-8. PubMed ID: 1896199
[TBL] [Abstract][Full Text] [Related]
13. [Steinert's myotonic dystrophy and Thomsen's congenital myotonia. Observation of a family (author's transl)].
Cognazzo A; Grasso E; Gerbino Promis PC
Riv Patol Nerv Ment; 1979; 100(4):209-19. PubMed ID: 555540
[TBL] [Abstract][Full Text] [Related]
14. Identification of five new mutations and three novel polymorphisms in the muscle chloride channel gene (CLCN1) in 20 Italian patients with dominant and recessive myotonia congenita. Mutations in brief no. 118. Online.
Sangiuolo F; Botta A; Mesoraca A; Servidei S; Merlini L; Fratta G; Novelli G; Dallapiccola B
Hum Mutat; 1998; 11(4):331. PubMed ID: 10215406
[TBL] [Abstract][Full Text] [Related]
15. A novel CLCN1 mutation (G1652A) causing a mild phenotype of thomsen disease.
Kumar KR; Ng K; Vandebona H; Davis MR; Sue CM
Muscle Nerve; 2010 Mar; 41(3):412-5. PubMed ID: 20120005
[TBL] [Abstract][Full Text] [Related]
16. Phenotypic variability of autosomal dominant myotonia congenita in a Taiwanese family with muscle chloride channel (CLCN1) mutation.
Chang TY; Kuo HC; Hsiao KM; Huang CC
Acta Neurol Taiwan; 2007 Dec; 16(4):214-20. PubMed ID: 18220014
[TBL] [Abstract][Full Text] [Related]
17. Dosage effect of a dominant CLCN1 mutation: a novel syndrome.
Bernard G; Poulin C; Puymirat J; Sternberg D; Shevell M
J Child Neurol; 2008 Feb; 23(2):163-6. PubMed ID: 18263754
[TBL] [Abstract][Full Text] [Related]
18. [A case of familial muscle weakness corrected by exercise (author's transl)].
Sabouraud O; Pinel JF; Le Bars R; Menault F; Saudeau D
Rev Neurol (Paris); 1979 Oct; 135(8-9):583-92. PubMed ID: 531413
[TBL] [Abstract][Full Text] [Related]
19. Thomsen or Becker myotonia? A novel autosomal recessive nonsense mutation in the CLCN1 gene associated with a mild phenotype.
Gurgel-Giannetti J; Senkevics AS; Zilbersztajn-Gotlieb D; Yamamoto LU; Muniz VP; Pavanello RC; Oliveira AB; Zatz M; Vainzof M
Muscle Nerve; 2012 Feb; 45(2):279-83. PubMed ID: 22246887
[TBL] [Abstract][Full Text] [Related]
20. Decrement of compound muscle action potential is related to mutation type in myotonia congenita.
Colding-Jørgensen E; DunØ M; Schwartz M; Vissing J
Muscle Nerve; 2003 Apr; 27(4):449-55. PubMed ID: 12661046
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]