111 related articles for article (PubMed ID: 19768756)
1. Relief from episodic weakness with pyridostigmine in paramyotonia congenita: a family study.
Khadilkar SV; Singh RK; Mansukhani KA; Urtizberea JA; Sternberg D
Muscle Nerve; 2010 Jan; 41(1):133-7. PubMed ID: 19768756
[TBL] [Abstract][Full Text] [Related]
2. Comparative efficacy of repetitive nerve stimulation, exercise, and cold in differentiating myotonic disorders.
Michel P; Sternberg D; Jeannet PY; Dunand M; Thonney F; Kress W; Fontaine B; Fournier E; Kuntzer T
Muscle Nerve; 2007 Nov; 36(5):643-50. PubMed ID: 17654559
[TBL] [Abstract][Full Text] [Related]
3. Distinguishing paramyotonia congenita and myotonia congenita by electromyography.
Subramony SH; Malhotra CP; Mishra SK
Muscle Nerve; 1983 Jun; 6(5):374-9. PubMed ID: 6888415
[TBL] [Abstract][Full Text] [Related]
4. Paramyotonia congenita: abnormal short exercise test, and improvement after mexiletine therapy.
Jackson CE; Barohn RJ; Ptacek LJ
Muscle Nerve; 1994 Jul; 17(7):763-8. PubMed ID: 8008003
[TBL] [Abstract][Full Text] [Related]
5. Paramyotonia congenita due to a de novo mutation: a case report.
Fukudome T; Izumoto H; Goto H; Matsuo H; Yoshimura T; Sakoda S; Shibuya N
Muscle Nerve; 2003 Aug; 28(2):232-5. PubMed ID: 12872329
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. A new case of autosomal dominant myotonia associated with the V1589M missense mutation in the muscle sodium channel gene and its phenotypic classification.
Ferriby D; Stojkovic T; Sternberg D; Hurtevent JF; Hurtevent JP; Vermersch P
Neuromuscul Disord; 2006 May; 16(5):321-4. PubMed ID: 16624558
[TBL] [Abstract][Full Text] [Related]
8. Prolonged attacks of weakness with hypokalemia in SCN4A-related paramyotonia congenita.
van Osch T; Stunnenberg BC; Sternberg D; Kerklaan BJ
Muscle Nerve; 2018 Oct; 58(4):E27-E28. PubMed ID: 30028520
[No Abstract] [Full Text] [Related]
9. Muscle Na+ channelopathies: MRI detects intracellular 23Na accumulation during episodic weakness.
Weber MA; Nielles-Vallespin S; Essig M; Jurkat-Rott K; Kauczor HU; Lehmann-Horn F
Neurology; 2006 Oct; 67(7):1151-8. PubMed ID: 16931510
[TBL] [Abstract][Full Text] [Related]
10. [Eulenburg's paramyotonia congenita].
Sallansonnet-Froment M; Bounolleau P; De Greslan T; Ricard D; Taillia H; Renard JL
Rev Neurol (Paris); 2007 Nov; 163(11):1083-90. PubMed ID: 18033047
[TBL] [Abstract][Full Text] [Related]
11. Paramyotonia congenita in 22 members of an Arab (Omani) kindred.
Koul R; Alfutaisi A; Hira M
J Child Neurol; 2010 Feb; 25(2):212-5. PubMed ID: 19168830
[TBL] [Abstract][Full Text] [Related]
12. Paramyotonia Congenita with Persistent Distal and Facial Muscle Weakness: A Case Report with Literature Review.
Taminato T; Mori-Yoshimura M; Miki J; Sasaki R; Sato N; Oya Y; Nishino I; Takahashi Y
J Neuromuscul Dis; 2020; 7(2):193-201. PubMed ID: 32083589
[TBL] [Abstract][Full Text] [Related]
13. Autosomal recessive limb girdle myasthenia in two sisters.
Shankar A; Solomon T; Joseph TP; Gnanamuthu C
Neurol India; 2002 Dec; 50(4):500-3. PubMed ID: 12577107
[TBL] [Abstract][Full Text] [Related]
14. Reduced muscle-fiber conduction but normal slowing after cold exposure in paramyotonia congenita.
Blijham PJ; Drost G; Stegeman DF; Zwarts MJ
Muscle Nerve; 2008 Jan; 37(1):23-6. PubMed ID: 17823953
[TBL] [Abstract][Full Text] [Related]
15. The expanding clinical and genetic spectrum of the myotonic dystrophies.
Ricker K
Acta Neurol Belg; 2000 Sep; 100(3):151-5. PubMed ID: 11098287
[TBL] [Abstract][Full Text] [Related]
16. Exercise test on the patients with normokalaemic periodic paralysis from a Chinese family with a mutation in the SCN4A gene.
Feng Y; Zhang Y; Liu ZL; Zhang CD
Chin Med J (Engl); 2008 Oct; 121(19):1915-9. PubMed ID: 19080124
[TBL] [Abstract][Full Text] [Related]
17. Myasthenia gravis as a cause of head drop in Parkinson disease.
Uludag IF; Korucuk M; Sener U; Zorlu Y
Neurologist; 2011 May; 17(3):144-6. PubMed ID: 21532382
[TBL] [Abstract][Full Text] [Related]
18. A case of paramyotonia congenita without periodic paralysis: electrophysiological and molecular genetic studies.
Park JH; Lee YW; Park SA; Lee TK; Rho HJ; Sung KB
Neurologist; 2010 May; 16(3):203-5. PubMed ID: 20445432
[TBL] [Abstract][Full Text] [Related]
19. Pyridostigmine toxicity. Electrophysiological study.
Park KH; Kim DE; Arnold TW; Oh SJ; Bradley R
Electromyogr Clin Neurophysiol; 1993 Sep; 33(6):323-8. PubMed ID: 8223330
[TBL] [Abstract][Full Text] [Related]
20. Dropped head as an unusual presenting sign of myasthenia gravis.
D'Amelio M; Di Benedetto N; Ragonese P; Daniele O; Brighina F; Fierro B; Savettieri G
Neurol Sci; 2007 Apr; 28(2):104-6. PubMed ID: 17464475
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
