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 *

144 related articles for article (PubMed ID: 8272119)

  • 41. Detection of heterozygotes for myotonic dystrophy.
    Bundey S
    Clin Genet; 1974; 5(2):107-9. PubMed ID: 4829421
    [No Abstract]   [Full Text] [Related]  

  • 42. [Myotonic dystrophy in children; how can you recognise the symptoms in a child and in family members?].
    Bonouvrié K; Panis B
    Ned Tijdschr Geneeskd; 2016; 160():A9932. PubMed ID: 27378259
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Pre-symptomatic detection and genetic counselling in myotonic dystrophy.
    Harper PS
    Clin Genet; 1973; 4(2):134-40. PubMed ID: 4730942
    [No Abstract]   [Full Text] [Related]  

  • 44. [Electrocardiographic aspects of hereditary degenerative diseases of the nervous system].
    Franken RA; Sanvito WL; Tilbery CP; Chryssovergis G; Campana JO
    AMB Rev Assoc Med Bras; 1975 Jun; 21(6):181-4. PubMed ID: 1080861
    [No Abstract]   [Full Text] [Related]  

  • 45. [A pedigree with myotonic dystrophy: non-CTG, non-CCTG repeat expansion].
    Zhao XP; Xie HJ; Zheng HM; Yu ZL; Cui Y; Ding SJ; Ren DM; Tang GM
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Oct; 21(5):459-62. PubMed ID: 15476170
    [TBL] [Abstract][Full Text] [Related]  

  • 46. [Familial myopathies (D.M.). Electroclinical study].
    Pérez Maiquez F
    Rev Clin Esp; 1976 Oct; 143(2):125-33. PubMed ID: 1013449
    [No Abstract]   [Full Text] [Related]  

  • 47. [Abnormal values of immunological indicators in dystrophia myotonica (results of complex screening of members of 3 generations of a family)].
    Opavský J; Podivínský J; Trnecka J; Matousková I; Válková Z
    Vnitr Lek; 1981 Dec; 27(12):1152-9. PubMed ID: 7336621
    [No Abstract]   [Full Text] [Related]  

  • 48. Anticipation in myotonic dystrophy: a parental-sex-related phenomenon.
    López de Munain A; Blanco A; Emparanza JI; Martí Massó JF; Cobo A; Basauri B; Martorell L; Baiget M; Martínez Lage JM
    Neuroepidemiology; 1994; 13(1-2):75-8. PubMed ID: 8190210
    [TBL] [Abstract][Full Text] [Related]  

  • 49. [Myotonic dystrophy in the neonate (author's transl)].
    Messer J; Brochard A; Willard D; Jesel M
    Acta Paediatr Belg; 1973; 27(4):263-72. PubMed ID: 4589108
    [No Abstract]   [Full Text] [Related]  

  • 50. [Clinical manifestations of myotonic dystrophy: epidemiologic survey].
    López de Munain A; Emparanza JI; Blanco A; Cobo A; Poza JJ; Basauri B; Baiget M; Martí Massó JF
    Med Clin (Barc); 1993 Jun; 101(5):161-4. PubMed ID: 8332007
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Slow motor nerve conduction in myotonic dystrophy.
    Roohi F; List T; Lovelace RE
    Electromyogr Clin Neurophysiol; 1981; 21(2-3):97-105. PubMed ID: 7262015
    [No Abstract]   [Full Text] [Related]  

  • 52. Subtle cognitive dysfunction in adult onset myotonic dystrophy type 1 (DM1) and type 2 (DM2).
    Gaul C; Schmidt T; Windisch G; Wieser T; Müller T; Vielhaber S; Zierz S; Leplow B
    Neurology; 2006 Jul; 67(2):350-2. PubMed ID: 16864839
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [DNA analysis of a pedigree with myotonic dystrophy in Songjiang county, Shanghai].
    Xie H; Zheng H; Zheng S; Deng B; Xu J; Cui Y; Wang Y; Xu Z; Ren D
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Oct; 17(5):319-22. PubMed ID: 11024209
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Instability of a premutation allele in homozygous patients with myotonic dystrophy type 1.
    Abbruzzese C; Costanzi Porrini S; Mariani B; Gould FK; McAbney JP; Monckton DG; Ashizawa T; Giacanelli M
    Ann Neurol; 2002 Oct; 52(4):435-41. PubMed ID: 12325072
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Mutation analysis in the CTG-base multiplication in a family with myotonic dystrophy in three generations].
    Molnár J; Kis A; Melegh B; Nádasi E; Varjas T; Kovács E; Kosztolanyi G
    Orv Hetil; 1998 May; 139(18):1083-5. PubMed ID: 9608771
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Outcome and effect of pregnancy in myotonic dystrophy type 2.
    Rudnik-Schöneborn S; Schneider-Gold C; Raabe U; Kress W; Zerres K; Schoser BG
    Neurology; 2006 Feb; 66(4):579-80. PubMed ID: 16505316
    [TBL] [Abstract][Full Text] [Related]  

  • 57. [Abnormal values of the immunological parameters in dystrophia myotonica. The results of complex research on the members of 3 generations of a family].
    Opavský J; Podivínský J; Trnecka J; Matousková I; Válková Z
    Acta Univ Palacki Olomuc Fac Med; 1982; 102():311-21. PubMed ID: 6242585
    [No Abstract]   [Full Text] [Related]  

  • 58. Myotonic dystrophy: relative sensitivity of symptoms signs and abnormal investigations.
    Avaria M; Patterson V
    Ulster Med J; 1994 Oct; 63(2):151-4. PubMed ID: 8650827
    [TBL] [Abstract][Full Text] [Related]  

  • 59. [DNA diagnosis in myotonic dystrophy].
    Tachi N
    Hokkaido Igaku Zasshi; 1996 Jan; 71(1):3-8. PubMed ID: 8727368
    [TBL] [Abstract][Full Text] [Related]  

  • 60. [Ocular findings in patients with Steinert myotonic dystrophy].
    Markowska E; Zalewska R; Mariak Z; Wojnar M
    Przegl Lek; 2006; 63(8):662-3. PubMed ID: 17441379
    [TBL] [Abstract][Full Text] [Related]  

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