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 *

135 related articles for article (PubMed ID: 8355122)

  • 1. Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant.
    Hamiel OP; Raas-Rothschild A; Upadhyaya M; Frydman M; Sarova-Pinhas I; Brand N; Passwell JH
    J Pediatr; 1993 Sep; 123(3):431-4. PubMed ID: 8355122
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafness.
    Cornell J; Sellars S; Beighton P
    Clin Genet; 1984 Feb; 25(2):163-5. PubMed ID: 6705250
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of the DNA duplication 17p11.2 in Charcot-Marie-Tooth neuropathy type 1 pedigrees: additional evidence for a third autosomal CMT1 locus.
    Chance PF; Matsunami N; Lensch W; Smith B; Bird TD
    Neurology; 1992 Oct; 42(10):2037-41. PubMed ID: 1407588
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness].
    Murakami K; Sobue G; Takahashi A; Mitsuma T
    Rinsho Shinkeigaku; 1986 Sep; 26(9):952-9. PubMed ID: 3791775
    [No Abstract]   [Full Text] [Related]  

  • 5. Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2.
    Holmberg BH; Holmgren G; Nelis E; van Broeckhoven C; Westerberg B
    J Med Genet; 1994 Jun; 31(6):435-41. PubMed ID: 8071969
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Localization of the mutation in an extended family with Charcot-Marie-Tooth neuropathy (HMSN I).
    Raeymaekers P; Timmerman V; De Jonghe P; Swerts L; Gheuens J; Martin JJ; Muylle L; De Winter G; Vandenberghe A; Van Broeckhoven C
    Am J Hum Genet; 1989 Dec; 45(6):953-8. PubMed ID: 2589322
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic linkage of hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease) to markers of chromosomes 1 and 17.
    Defesche JC; Hoogendijk JE; de Visser M; de Visser O; Bolhuis PA
    Neurology; 1990 Sep; 40(9):1450-3. PubMed ID: 2392234
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Charcot-Marie-Tooth disease and sleep apnoea syndrome: a family study.
    Dematteis M; Pépin JL; Jeanmart M; Deschaux C; Labarre-Vila A; Lévy P
    Lancet; 2001 Jan; 357(9252):267-72. PubMed ID: 11214130
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Duplication of part of chromosome 17 is commonly associated with hereditary motor and sensory neuropathy type I (Charcot-Marie-Tooth disease type 1).
    Hallam PJ; Harding AE; Berciano J; Barker DF; Malcolm S
    Ann Neurol; 1992 May; 31(5):570-2. PubMed ID: 1596093
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Correlation between the histopathologic, genotypic, and phenotypic features of hereditary peripheral neuropathies in childhood.
    Ouvrier R
    J Child Neurol; 1996 Mar; 11(2):133-46. PubMed ID: 8881991
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Allelic heterogeneity in hereditary motor and sensory neuropathy type Ia (Charcot-Marie-Tooth disease type 1a).
    Hoogendijk JE; Janssen EA; Gabreëls-Festen AA; Hensels GW; Joosten EM; Gabreëls FJ; Zorn I; Valentijn LJ; Baas F; Ongerboer de Visser BW
    Neurology; 1993 May; 43(5):1010-5. PubMed ID: 8492918
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I).
    Chance PF; Bird TD; O'Connell P; Lipe H; Lalouel JM; Leppert M
    Am J Hum Genet; 1990 Dec; 47(6):915-25. PubMed ID: 2239969
    [TBL] [Abstract][Full Text] [Related]  

  • 13. X-linked motor-sensory neuropathy type-II with deafness and mental retardation: a new disorder.
    Cowchock FS; Duckett SW; Streletz LJ; Graziani LJ; Jackson LG
    Am J Med Genet; 1985 Feb; 20(2):307-15. PubMed ID: 3856385
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Absence of linkage with the Duffy blood group in a family with Charcot-Marie-Tooth neuropathy.
    Raeymaekers P; De Jonghe P; Swerts L; Muylle L; Gheuens J; Martin JJ; Van Broeckhoven C; Vandenberghe A
    J Neurol Sci; 1988 Dec; 88(1-3):145-50. PubMed ID: 3225617
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N; Mihatov I
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Chromosome 1 Charcot-Marie-Tooth disease (CMT1B) locus in the Fc gamma receptor gene region.
    Lebo RV; Chance PF; Dyck PJ; Redila-Flores MT; Lynch ED; Golbus MS; Bird TD; King MC; Anderson LA; Hall J
    Hum Genet; 1991 Nov; 88(1):1-12. PubMed ID: 1683643
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Exclusion analysis of Charcot-Marie-Tooth neuropathy (CMT1) with chromosome 1p markers.
    Raeymaekers P; De Jonghe P; Swerts L; De Winter G; Gheuens J; Martin JJ; Vandenberghe A; Van Broeckhoven C
    Cytogenet Cell Genet; 1989; 50(2-3):178-80. PubMed ID: 2570676
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Molecular genetics of Charcot-Marie-Tooth disease and related neuropathies.
    Chance PF; Fischbeck KH
    Hum Mol Genet; 1994; 3 Spec No():1503-7. PubMed ID: 7849745
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A novel locus for X-linked recessive CMT with deafness and optic neuropathy maps to Xq21.32-q24.
    Kim HJ; Hong SH; Ki CS; Kim BJ; Shim JS; Cho SH; Park JH; Kim JW
    Neurology; 2005 Jun; 64(11):1964-7. PubMed ID: 15955956
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic linkage relationships of Charcot-Marie-Tooth disease (HMSN-Ib) to chromosome 1 markers.
    Chance PF; Murray JC; Bird TD; Kochin RS
    Neurology; 1987 Feb; 37(2):325-9. PubMed ID: 3468376
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.