153 related articles for article (PubMed ID: 84061)
1. Fenoterol precipitating myotonia in a minimally affected case of recessive myotonia congenita.
Ricker K; Haass A; Glötzner F
J Neurol; 1978 Dec; 219(4):279-82. PubMed ID: 84061
[TBL] [Abstract][Full Text] [Related]
2. Electrical myotonia in heterozygous carriers of recessive myotonia congenita.
Deymeer F; Lehmann-Horn F; Serdaroğlu P; Cakirkaya S; Benz S; Rüdel R; Ozdemir C
Muscle Nerve; 1999 Jan; 22(1):123-5. PubMed ID: 9883868
[TBL] [Abstract][Full Text] [Related]
3. Transient muscular weakness in severe recessive myotonia congenita. Improvement of isometric muscle force by drugs relieving myotomic stiffness.
Ricker K; Haass A; Hertel G; Mertens HG
J Neurol; 1978 Aug; 218(4):253-62. PubMed ID: 81274
[TBL] [Abstract][Full Text] [Related]
4. Novel CLCN1 mutation in carbamazepine-responsive myotonia congenita.
Lyons MJ; Duron R; Molinero I; Sangiuolo F; Holden KR
Pediatr Neurol; 2010 May; 42(5):365-8. PubMed ID: 20399394
[TBL] [Abstract][Full Text] [Related]
5. 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]
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. Heterozygote manifestation in recessive generalized myotonia.
Becker PE
Hum Genet; 1979 Feb; 46(3):325-9. PubMed ID: 437775
[TBL] [Abstract][Full Text] [Related]
8. [Analysis of CLCN1 gene mutations in 2 patients with myotonia congenita].
Chen ZT; He J; Chen WJ; Chen SG; Lin JL; Ye QY; Huang HP
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2012 Dec; 29(6):690-2. PubMed ID: 23225051
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. Asymptomatic myotonia congenita unmasked by severe hypothyroidism.
Passeri E; Sansone VA; Verdelli C; Mendola M; Corbetta S
Neuromuscul Disord; 2014 Apr; 24(4):365-7. PubMed ID: 24530047
[TBL] [Abstract][Full Text] [Related]
11. The needle EMG findings in myotonia congenita.
Nojszewska M; Lusakowska A; Gawel M; Sierdzinski J; Sulek A; Krysa W; Elert-Dobkowska E; Seroka A; Kaminska AM; Kostera-Pruszczyk A
J Electromyogr Kinesiol; 2019 Dec; 49():102362. PubMed ID: 31610484
[TBL] [Abstract][Full Text] [Related]
12. [A case of myotonic dystrophy diagnosed after delivery].
Yorinaga Y; Nishimura S; Ohara M
Nihon Sanka Fujinka Gakkai Zasshi; 1989 May; 41(5):613-6. PubMed ID: 2754292
[No Abstract] [Full Text] [Related]
13. Effect of mexiletine on transitory depression of compound motor action potential in recessive myotonia congenita.
Lo Monaco M; D'Amico A; Luigetti M; Desaphy JF; Modoni A
Clin Neurophysiol; 2015 Feb; 126(2):399-403. PubMed ID: 25065301
[TBL] [Abstract][Full Text] [Related]
14. A family with autosomal recessive generalised myotonia with Herculean appearance.
Sinha MK; Chaurasia RN; Verma R
J Assoc Physicians India; 2011 Feb; 59():120-2. PubMed ID: 21751653
[TBL] [Abstract][Full Text] [Related]
15. A Becker myotonia patient with compound heterozygosity for CLCN1 mutations and Prinzmetal angina pectoris.
Zielonka D; Jurkat-Rott K; Stachowiak P; Bryl A; Marcinkowski JT; Lehmann-Horn F
Neuromuscul Disord; 2012 Apr; 22(4):355-60. PubMed ID: 22197187
[TBL] [Abstract][Full Text] [Related]
16. Myotonia Congenita (Thomsen's disease).
Kim C; Yamada S
Hawaii Med J; 1974 Jan; 33(1):15-8. PubMed ID: 4811601
[No Abstract] [Full Text] [Related]
17. [Myotonia congenita with familial spastic paraparesis].
Wessel K; Kessler C; Rosengart A; Kömpf D
Nervenarzt; 1988 Nov; 59(11):675-8. PubMed ID: 3211250
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Maternal morbidity due to beta-adrenergic therapy. Pre-existing cardiomyopathy aggravated by fenoterol.
Eskes TK; Kornman JJ; Bots RS; Hein PR; Gimbrère JS; Vonk JT
Eur J Obstet Gynecol Reprod Biol; 1980 Jan; 10(1):41-6. PubMed ID: 7189159
[TBL] [Abstract][Full Text] [Related]
20. Dystrophia myotonica and myotonia congenita concurring in one family. A clinical and genetic study.
Höweler CJ; Busch HF; Bernini LF; van Loghem E; Meera Khan P; Nijenhuis LE
Brain; 1980 Sep; 103(3):497-513. PubMed ID: 7417778
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
