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 *

174 related articles for article (PubMed ID: 3856385)

  • 1. 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]  

  • 2. X-linked Charcot-Marie-Tooth disease: molecular analysis of interfamilial variability.
    Niewiadomski LA; Kelly TE
    Am J Med Genet; 1996 Dec; 66(2):175-8. PubMed ID: 8958325
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Hereditary motor-sensory neuropathies. Charcot-Marie-Tooth syndrome.
    Bird TD
    Neurol Clin; 1989 Feb; 7(1):9-23. PubMed ID: 2646524
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease). Molecular-genetic aspects].
    Hertz MJ; Jensen AD; Brandt CA; Bisgård C
    Ugeskr Laeger; 1995 Jun; 157(25):3613-8. PubMed ID: 7652980
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A locus for axonal motor-sensory neuropathy with deafness and mental retardation maps to Xq24-q26.
    Priest JM; Fischbeck KH; Nouri N; Keats BJ
    Genomics; 1995 Sep; 29(2):409-12. PubMed ID: 8666389
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Genetic linkage evidence for heterogeneity in Charcot-Marie-Tooth neuropathy (HMSN type I).
    Bird TD; Ott J; Giblett ER; Chance PF; Sumi SM; Kraft GH
    Ann Neurol; 1983 Dec; 14(6):679-84. PubMed ID: 6651251
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Hereditary motor sensory neuropathy type II with neurofilament accumulation: new finding or new disorder?
    Vogel P; Gabriel M; Goebel HH; Dyck PJ
    Ann Neurol; 1985 May; 17(5):455-61. PubMed ID: 3859241
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Hereditary neuropathy with dominant inheritance, giant axons and cardiac involvement].
    Gabriel M; Vogel P; Goebel HH
    Klin Padiatr; 1986; 198(1):17-20. PubMed ID: 3007857
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Molecular genetics of inherited neuropathies].
    Takashima H
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hypertrophic motor and sensory neuropathy type I (Charcot-Marie-Tooth disease): ultrastructural study of sural nerve biopsy in members of a family.
    Calore EE; Alonso Neto JL; Cavaliere MJ; Perez NM; Russo DH; Wakamatsu A; Maeda MY; Kitamura C
    Pathologica; 1994 Jun; 86(3):279-83. PubMed ID: 7808799
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Charcot-Marie-Tooth type X: A novel mutation in the Cx32 gene with central conduction slowing.
    Seeman P; Mazanec R; Ctvrtecková M; Smilková D
    Int J Mol Med; 2001 Oct; 8(4):461-8. PubMed ID: 11562788
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [From gene to disease; Charcot-Marie-Tooth disease or the hereditary motor and sensory neuropathies].
    Verhamme C; Baas F
    Ned Tijdschr Geneeskd; 2005 Jul; 149(27):1505-9. PubMed ID: 16032995
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: a 20-year study.
    Bird TD; Kraft GH; Lipe HP; Kenney KL; Sumi SM
    Ann Neurol; 1997 Apr; 41(4):463-9. PubMed ID: 9124803
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.
    Sabatelli M; Mignogna T; Lippi G; Servidei S; Zollino M; Padua L; Lo Monaco M; De Armas L; Mereu ML; Tonali P
    Am J Med Genet; 1998 Jan; 75(3):309-13. PubMed ID: 9475604
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hereditary motor and sensory neuropathy. Clinical, genetic and electrodiagnostic studies.
    Vasilescu C
    Rom J Neurol Psychiatry; 1993; 31(3-4):207-19. PubMed ID: 8011484
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Electrophysiological findings in hereditary motor and sensory neuropathy type I and II--a conduction velocity study.
    Emeryk-Szajewska B; Badurska B; Kostera-Pruszczyk A
    Electromyogr Clin Neurophysiol; 1998 Mar; 38(2):95-101. PubMed ID: 9553747
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Screening of dominantly inherited Charcot-Marie-Tooth neuropathies.
    Ionasescu VV; Ionasescu R; Searby C
    Muscle Nerve; 1993 Nov; 16(11):1232-8. PubMed ID: 8413376
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Hereditary sensory radicular neuropathy: defective neurogenic inflammation.
    Westerman RA; Block A; Nunn A; Delaney CA; Hahn A; Dennett X; Carr RW
    Clin Exp Neurol; 1992; 29():189-209. PubMed ID: 1343862
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Confirmation of a hereditary motor and sensory neuropathy IIC locus at chromosome 12q23-q24.
    McEntagart ME; Reid SL; Irrthum A; Douglas JB; Eyre KE; Donaghy MJ; Anderson NE; Rahman N
    Ann Neurol; 2005 Feb; 57(2):293-7. PubMed ID: 15668982
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies.
    Verhalle D; Löfgren A; Nelis E; Dehaene I; Theys P; Lammens M; Dom R; Van Broeckhoven C; Robberecht W
    Ann Neurol; 1994 Jun; 35(6):704-8. PubMed ID: 8210227
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.