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 *

84 related articles for article (PubMed ID: 12984563)

  • 21. 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]  

  • 22. [Thomsen disease (myotonia congenita].
    Colding-Jørgensen E
    Ugeskr Laeger; 2004 Sep; 166(37):3179-84. PubMed ID: 15384367
    [No Abstract]   [Full Text] [Related]  

  • 23. Aerobic training in myotonia congenita: Effect on myotonia and fitness.
    Andersen G; Løkken N; Vissing J
    Muscle Nerve; 2017 Oct; 56(4):696-699. PubMed ID: 28039888
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Thomsen disease with ptosis and abnormal MR findings.
    Mori Y; Yamashita S; Kato M; Masuda T; Takamatsu K; Kumamoto T; Sasaki R; Ando Y
    Neuromuscul Disord; 2016 Nov; 26(11):805-808. PubMed ID: 27666773
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Limbic encephalitis with anti-GAD antibodies and Thomsen myotonia: a casual or causal association?
    Licchetta L; Bisulli F; Naldi I; Mainieri G; Tinuper P
    Epileptic Disord; 2014 Sep; 16(3):362-5. PubMed ID: 25036107
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Some remarks on laboratory study of myotonia congenita and myasthenia gravis].
    MULLER J; KUCHLER J; KUBAJUROVA A
    Z Gesamte Inn Med; 1961 Apr; 16():296-8. PubMed ID: 13726709
    [No Abstract]   [Full Text] [Related]  

  • 27. 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]  

  • 28. Neuromuscular excitability changes produced by sustained voluntary contraction and response to mexiletine in myotonia congenita.
    Ginanneschi F; Mignarri A; Lucchiari S; Ulzi G; Comi GP; Rossi A; Dotti MT
    Neurophysiol Clin; 2017 Jun; 47(3):247-252. PubMed ID: 28153715
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Genotype-phenotype correlation of F484L mutation in three Italian families with Thomsen myotonia.
    Cassone M; Ferradini V; Longo G; Sarchielli P; Murasecco D; Romoli M; Pasquini E; Novelli G; Prontera P; Sangiuolo F
    Muscle Nerve; 2017 Jun; 55(6):E24-E25. PubMed ID: 27639085
    [No Abstract]   [Full Text] [Related]  

  • 30. [Dominant myotonia congenita(Thomsen disease)].
    Saito K; Yazaki E
    Ryoikibetsu Shokogun Shirizu; 2001; (35):120-2. PubMed ID: 11555886
    [No Abstract]   [Full Text] [Related]  

  • 31. Thomsen's disease. Observations on strength-duration curves in myotonia.
    PASTERNACK A; LINDQVIST C
    Ann Paediatr Fenn; 1962; 8():284-91. PubMed ID: 13941730
    [No Abstract]   [Full Text] [Related]  

  • 32. Structural modeling of altered CLCN1 conformation following a novel mutation in a patient affected by autosomal dominant myotonia congenita (Thomsen disease).
    Ferese R; Albano V; Falconi M; Iacovelli F; Campopiano R; Scala S; Griguoli AM; Gaglione A; Giardina E; Zampatti S; Storto M; Fornai F; D'Alessio C; Novelli G; Gambardella S
    Arch Ital Biol; 2017 Dec; 155(4):118-130. PubMed ID: 29405036
    [No Abstract]   [Full Text] [Related]  

  • 33. [Value of mexiletine in the treatment of Thomsen-Becker myotonia].
    Leheup B; Himon F; Morali A; Brichet F; Vidailhet M
    Arch Fr Pediatr; 1986 Jan; 43(1):49-50. PubMed ID: 3707279
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Heterozygous CLCN1 mutations can modulate phenotype in sodium channel myotonia.
    Furby A; Vicart S; Camdessanché JP; Fournier E; Chabrier S; Lagrue E; Paricio C; Blondy P; Touraine R; Sternberg D; Fontaine B
    Neuromuscul Disord; 2014 Nov; 24(11):953-9. PubMed ID: 25088311
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Anesthetic managements of a patient with myasthenia gravis and myotonia congenita].
    Miyabe M; Dohi S; Iwasaki H; Omote K; Takahashi T
    Masui; 1982 Jun; 31(6):650-4. PubMed ID: 7131741
    [No Abstract]   [Full Text] [Related]  

  • 36. Recessive CLCN1 mutation presenting as Thomsen disease.
    Thomas J; Tarleton J; Baker SK
    Muscle Nerve; 2008 Nov; 38(5):1515-1517. PubMed ID: 18816629
    [TBL] [Abstract][Full Text] [Related]  

  • 37. [Myotonia congenita (Thomsen's disease); clinical observations in two siblings].
    TOBLER R
    Helv Paediatr Acta; 1954 Oct; 9(4):351-72. PubMed ID: 13221170
    [No Abstract]   [Full Text] [Related]  

  • 38. 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]  

  • 39. Role of acetylcholine in pathophysiology and therapy of myotonia congenita.
    STERN P; BOSKOVIC B
    Rev Can Biol; 1962; 21():613-23. PubMed ID: 13983953
    [No Abstract]   [Full Text] [Related]  

  • 40. Clinical study of paramyotonia congenita with and without myotonia in a warm environment.
    Haass A; Ricker K; Rüdel R; Lehmann-Horn F; Böhlen R; Dengler R; Mertens HG
    Muscle Nerve; 1981; 4(5):388-95. PubMed ID: 6793868
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.