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 *

153 related articles for article (PubMed ID: 4629290)

  • 21. [ON THE GENETICS OF MYOTONIAS (A PRELIMINARY SURVEY)].
    BECKER PE
    Internist (Berl); 1963 Sep; 4():384-92. PubMed ID: 14092155
    [No Abstract]   [Full Text] [Related]  

  • 22. The myotonic disorders and the periodic paralyses.
    Griggs RC
    Adv Neurol; 1977; 17():143-59. PubMed ID: 888733
    [No Abstract]   [Full Text] [Related]  

  • 23. [Light and electron microscopic studies of muscle in adynamia episodica hereditaria (Gamstorp's syndrome)].
    Auböck L; Fladerer H
    Wien Z Nervenheilkd Grenzgeb; 1970 Jun; 28(2):104-28. PubMed ID: 4248684
    [No Abstract]   [Full Text] [Related]  

  • 24. Myopathology of myotonic dystrophy. A morphometric study.
    Casanova G; Jerusalem F
    Acta Neuropathol; 1979 Mar; 45(3):231-40. PubMed ID: 442988
    [No Abstract]   [Full Text] [Related]  

  • 25. The myotonias: their diagnosis and treatment.
    Moxley RT
    Compr Ther; 1996 Jan; 22(1):8-21. PubMed ID: 8654027
    [No Abstract]   [Full Text] [Related]  

  • 26. [VALUE OF MUSCLE BIOPSY IN MUSCULAR AND NERVOUS SYSTEM DISEASES].
    CHRISTENSEN E
    Nord Med; 1965 Apr; 73():340-2. PubMed ID: 14265343
    [No Abstract]   [Full Text] [Related]  

  • 27. [Hreditary myopathies].
    Kuhn E
    Ergeb Inn Med Kinderheilkd; 1969; 28():188-290. PubMed ID: 4897097
    [No Abstract]   [Full Text] [Related]  

  • 28. Type 2B muscle fibre deficiency in myotonia and paramyotonia congenita. A genetically determined histochemical fibre type pattern?
    Heene R; Gabriel RR; Manz F; Schimrigk K
    J Neurol Sci; 1986 Mar; 73(1):23-30. PubMed ID: 2939200
    [TBL] [Abstract][Full Text] [Related]  

  • 29. A summary review of the diagnosis and pathology of the primary familial periodic paralyses.
    Meyers KR
    Ann Clin Lab Sci; 1975; 5(3):216-21. PubMed ID: 1094905
    [No Abstract]   [Full Text] [Related]  

  • 30. [Paramyotonia congenita of Eulenberg].
    Kamraj-Mazurkiewicz K; Mierzejewska E; Litwińska T
    Neurol Neurochir Pol; 1973; 7(5):671-7. PubMed ID: 4763006
    [No Abstract]   [Full Text] [Related]  

  • 31. [Thomsen's myotonia congenita. (Clinical study of 4 cases)].
    Castello MA; Tucciarone L; Lendvai D
    Policlinico Prat; 1969 Oct; 76(43):1377-82. PubMed ID: 5402142
    [No Abstract]   [Full Text] [Related]  

  • 32. GENETICS AND DISEASES OF MUSCLE.
    BOYER SH; FAINER DC
    Am J Med; 1963 Nov; 35():622-31. PubMed ID: 14076016
    [No Abstract]   [Full Text] [Related]  

  • 33. Evidence of myotonic origin of type 2B muscle fibre deficiency in myotonia and paramyotonia congenita.
    Heene R
    J Neurol Sci; 1986 Dec; 76(2-3):357-9. PubMed ID: 3794755
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Myotonia congenita and myotonic dystrophy in the same family: coexistence of a CLCN1 mutation and expansion in the CNBP (ZNF9) gene.
    Sun C; Van Ghelue M; Tranebjærg L; Thyssen F; Nilssen Ø; Torbergsen T
    Clin Genet; 2011 Dec; 80(6):574-80. PubMed ID: 21204798
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Modifications in the sarcoplasmic reticulum and subcellular calcium distribution in skeletal muscle in a case of Westphal's disease (hypokalemic periodic paralysis).
    Porte A; Stoeckel ME; Ledeaut JY; Guez S; Hindelang-Gertner C; Mack G
    Virchows Arch A Pathol Anat Histol; 1979 Aug; 383(3):345-50. PubMed ID: 158876
    [TBL] [Abstract][Full Text] [Related]  

  • 37. PROGRESSIVE NEUROLOGICAL DISORDER AND MYOTONIA CONGENITA ASSOCIATED WITH PARAMYOTONIA.
    HUDSON AJ
    Brain; 1963 Dec; 86():811-26. PubMed ID: 14090531
    [No Abstract]   [Full Text] [Related]  

  • 38. Clinical observations on 8 cases of myotonia dystrophica.
    Aburaya T; Sakikawa C; Takeichi O; Hamajo T; Sakashita O
    Tokushima J Exp Med; 1967 Nov; 14(3):114-25. PubMed ID: 5610188
    [No Abstract]   [Full Text] [Related]  

  • 39. Histopathological study of the biopsied muscles from juvenile patients with congenital myotonic dystrophy.
    Wakai S; Kameda K; Okabe M; Nagaoka M; Minami R; Tachi N
    Acta Paediatr Jpn; 1988 Feb; 30(1):7-12. PubMed ID: 3148263
    [No Abstract]   [Full Text] [Related]  

  • 40. Case report. Ultrastructural changes of muscles during attacks of adynamia episodica hereditaria.
    Walter GF; Auböck L
    Neuropathol Appl Neurobiol; 1980; 6(4):313-7. PubMed ID: 7413016
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.