These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

252 related articles for article (PubMed ID: 17140792)

  • 41. Myokymia and neuromyotonia 2004.
    Gutmann L; Gutmann L
    J Neurol; 2004 Feb; 251(2):138-42. PubMed ID: 14991346
    [No Abstract]   [Full Text] [Related]  

  • 42. Management of voltage-gated potassium channel antibody disorders.
    Merchut MP
    Neurol Clin; 2010 Nov; 28(4):941-59. PubMed ID: 20816272
    [TBL] [Abstract][Full Text] [Related]  

  • 43. A novel KCNA1 mutation associated with global delay and persistent cerebellar dysfunction.
    Demos MK; Macri V; Farrell K; Nelson TN; Chapman K; Accili E; Armstrong L
    Mov Disord; 2009 Apr; 24(5):778-82. PubMed ID: 19205071
    [TBL] [Abstract][Full Text] [Related]  

  • 44. The origin of spontaneous discharges in acquired neuromyotonia. A Macro EMG study.
    Arimura K; Arimura Y; Ng A; Uehara A; Nakae M; Osame M; Stålberg E
    Clin Neurophysiol; 2005 Aug; 116(8):1835-9. PubMed ID: 15979405
    [TBL] [Abstract][Full Text] [Related]  

  • 45. Ion channel and striational antibodies define a continuum of autoimmune neuromuscular hyperexcitability.
    Vernino S; Lennon VA
    Muscle Nerve; 2002 Nov; 26(5):702-7. PubMed ID: 12402293
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Clinical, genetic, neurophysiological and functional study of new mutations in episodic ataxia type 1.
    Tomlinson SE; Rajakulendran S; Tan SV; Graves TD; Bamiou DE; Labrum RW; Burke D; Sue CM; Giunti P; Schorge S; Kullmann DM; Hanna MG
    J Neurol Neurosurg Psychiatry; 2013 Oct; 84(10):1107-12. PubMed ID: 23349320
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Generalized myokymia, or neuromyotonia, or both in dogs with or without spinocerebellar ataxia.
    Vanhaesebrouck A; Van Poucke M; Stee K; Granger N; Ives E; Van Soens I; Cornelis I; Bossens K; Peelman L; Van Ham L; Bhatti SFM
    J Vet Intern Med; 2023; 37(6):2310-2314. PubMed ID: 37905444
    [TBL] [Abstract][Full Text] [Related]  

  • 48. A novel mutation in KCNA1 causes episodic ataxia without myokymia.
    Lee H; Wang H; Jen JC; Sabatti C; Baloh RW; Nelson SF
    Hum Mutat; 2004 Dec; 24(6):536. PubMed ID: 15532032
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Potassium current suppression in patients with peripheral nerve hyperexcitability.
    Nagado T; Arimura K; Sonoda Y; Kurono A; Horikiri Y; Kameyama A; Kameyama M; Pongs O; Osame M
    Brain; 1999 Nov; 122 ( Pt 11)():2057-66. PubMed ID: 10545391
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Deletions involving both KCNQ2 and CHRNA4 present with benign familial neonatal seizures.
    Kurahashi H; Wang JW; Ishii A; Kojima T; Wakai S; Kizawa T; Fujimoto Y; Kikkawa K; Yoshimura K; Inoue T; Yasumoto S; Ogawa A; Kaneko S; Hirose S
    Neurology; 2009 Oct; 73(15):1214-7. PubMed ID: 19822871
    [TBL] [Abstract][Full Text] [Related]  

  • 51. [Isaacs' syndrome. Diagnosis and differential diagnosis of neuromyotonia].
    Fischer D; Schröder R
    Nervenarzt; 2004 Jun; 75(6):531-5. PubMed ID: 15257376
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Finger flexion resembling focal dystonia in Isaacs' syndrome.
    Jamora RD; Umapathi T; Tan LC
    Parkinsonism Relat Disord; 2006 Jan; 12(1):61-3. PubMed ID: 16337423
    [TBL] [Abstract][Full Text] [Related]  

  • 53. IgM-containing fraction suppressed voltage-gated potassium channels in acquired neuromyotonia.
    Kurono A; Arimura K; Watanabe O; Tomimitsu H; Nagado T; Sonoda Y; Kameyama M; Osame M
    Acta Neurol Scand; 2006 Mar; 113(3):185-8. PubMed ID: 16441249
    [TBL] [Abstract][Full Text] [Related]  

  • 54. [Case of Isaacs' syndrome associated with Hashimoto disease].
    Iguchi M; Morimatsu A; Kondo T; Shirata A; Yamane K
    Rinsho Shinkeigaku; 2007 Oct; 47(10):662-4. PubMed ID: 18095500
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.
    Volkers L; Rook MB; Das JH; Verbeek NE; Groenewegen WA; van Kempen MJ; Lindhout D; Koeleman BP
    Neurosci Lett; 2009 Oct; 462(1):24-9. PubMed ID: 19559753
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Thymoma-associated neuromyotonia with antibodies against voltage-gated potassium channels presenting as chronic intestinal pseudo-obstruction.
    Viallard JF; Vincent A; Moreau JF; Parrens M; Pellegrin JL; Ellie E
    Eur Neurol; 2005; 53(2):60-3. PubMed ID: 15753614
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Episodic ataxias].
    Herrmann A; Braathen GJ; Russell MB
    Tidsskr Nor Laegeforen; 2005 Aug; 125(15):2005-7. PubMed ID: 16100538
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea.
    Shook SJ; Mamsa H; Jen JC; Baloh RW; Zhou L
    Muscle Nerve; 2008 Mar; 37(3):399-402. PubMed ID: 17912752
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Paraneoplastic Isaacs' syndrome: a case series and review of the literature.
    Rana SS; Ramanathan RS; Small G; Adamovich B
    J Clin Neuromuscul Dis; 2012 Jun; 13(4):228-33. PubMed ID: 22622168
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Impairment of peripheral nerve excitability].
    Arimura K
    Rinsho Shinkeigaku; 1997 Dec; 37(12):1109-10. PubMed ID: 9577660
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.