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 *

53 related articles for article (PubMed ID: 143177)

  • 1. [Demography of several hereditary diseases of the nervous system among the population of the Fergan valley].
    Dahuraev A
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977; 77(8):1163-6. PubMed ID: 143177
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Frequency of hereditary neurologic diseases. A clinical study].
    Leone M; Baldini S; Voltolin G; Norat M; Bottacchi E
    Minerva Med; 1993 Sep; 84(9):453-9. PubMed ID: 8247316
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Epidemiology and cases of early manifestations of Huntington chorea].
    Khannanova FK
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1987; 87(3):340-2. PubMed ID: 2953156
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Early onset rigid Huntington's disease.
    Bird MT; Paulson GW
    Neurology; 1970 Apr; 20(4):400. PubMed ID: 4254549
    [No Abstract]   [Full Text] [Related]  

  • 5. [Epidemiological aspects of Huntington chorea in the Genoa region from 1930 to 1977 (author's transl)].
    Roccatagliata G; De Marchi C; Maffini M; Albano C
    Riv Patol Nerv Ment; 1979; 100(5):239-44. PubMed ID: 162354
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [A clinico-electromyographic study of patients suffering Strumpel's familial spastic paraplegia].
    Billevich AS
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1969; 69(6):822-8. PubMed ID: 5364229
    [No Abstract]   [Full Text] [Related]  

  • 7. [Clinical manifestations and mode of inheritance of hereditary spastic paraplegia in 20 families].
    Gao HW
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1985 Feb; 18(1):24-6. PubMed ID: 3987454
    [No Abstract]   [Full Text] [Related]  

  • 8. [Clinico-genalogic characteristics of hereditary diseases of the nervous system in the Kuibyshev region].
    Nesterov LN; Sushcheva GP; Viatkina SIa
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(10):1506-12. PubMed ID: 152555
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Mutations in the skeletal muscle alpha-actin gene in patients with actin myopathy and nemaline myopathy.
    Nowak KJ; Wattanasirichaigoon D; Goebel HH; Wilce M; Pelin K; Donner K; Jacob RL; Hübner C; Oexle K; Anderson JR; Verity CM; North KN; Iannaccone ST; Müller CR; Nürnberg P; Muntoni F; Sewry C; Hughes I; Sutphen R; Lacson AG; Swoboda KJ; Vigneron J; Wallgren-Pettersson C; Beggs AH; Laing NG
    Nat Genet; 1999 Oct; 23(2):208-12. PubMed ID: 10508519
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [HLA antigens in certain hereditary diseases of the central nervous system].
    Fedrunova VS; Nazarova EK; Pevnitskiĭ LA; Ivanova-Smolenskaia IA; Alieva LM
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(11):1500-3. PubMed ID: 160174
    [No Abstract]   [Full Text] [Related]  

  • 11. Hereditary spastic paraplegia: a clinical and genetic study of cases in the north-east of England.
    Livingstone IR; Roberts DF
    J Genet Hum; 1983 Dec; 31(4):295-305. PubMed ID: 6582228
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Myopathy as a first symptom of Huntington's disease in a Marathon runner.
    Kosinski CM; Schlangen C; Gellerich FN; Gizatullina Z; Deschauer M; Schiefer J; Young AB; Landwehrmeyer GB; Toyka KV; Sellhaus B; Lindenberg KS
    Mov Disord; 2007 Aug; 22(11):1637-40. PubMed ID: 17534945
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Simulation of Huntington's disease onset.
    Markson LE; Chase GA; Brookmeyer R
    Genet Epidemiol; 1989; 6(3):451-9. PubMed ID: 2526776
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genetic aspects of Huntington's chorea: results of a national survey.
    Hayden MR; Beighton P
    Am J Med Genet; 1982 Feb; 11(2):135-41. PubMed ID: 6461251
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Alport syndrome. Molecular genetic aspects.
    Hertz JM
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Huntington's chorea in a South Australian comminity of aboriginal descent.
    Gale F; Bennett JH
    Med J Aust; 1969 Sep; 2(10):482-4. PubMed ID: 4241979
    [No Abstract]   [Full Text] [Related]  

  • 17. [Medico-genetical study of the Uzbekistan population. IX. Variability of hereditary pathology, territorial distribution of hereditary diseases and hereditary disease load in the population of the Urgut district of the Samarkand region].
    Ginter EK; Budagova KA; Revazov AA; Petrin AN; Bugaeva EA
    Genetika; 1986 Jul; 22(7):1199-206. PubMed ID: 2943634
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Heterogeneity and several clinico-genetic correlations in epilepsy under inbred conditions].
    Utin AV
    Genetika; 1975; 11(1):122-31. PubMed ID: 1225742
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Population-demographic and clinico-genetic characteristics of Huntington chorea in one region of Azerbaijan].
    Kozlova SI; Dadali EL; Prytkov AN; Bol'shakova LP; Sibiriakova LG
    Genetika; 1986 Oct; 22(10):2534-9. PubMed ID: 2947830
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Huntington's chorea in Queensland. A not uncommon disease.
    Wallace DC
    Med J Aust; 1972 Feb; 1(7):299-307. PubMed ID: 4260193
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 3.