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 *

184 related articles for article (PubMed ID: 10815132)

  • 21. Linkage of autosomal dominant type I hereditary motor and sensory neuropathy to the Duffy locus on chromosome 1.
    Guiloff RJ; Thomas PK; Contreras M; Armitage S; Schwarz G; Sedgwick EM
    J Neurol Neurosurg Psychiatry; 1982 Aug; 45(8):669-74. PubMed ID: 7130990
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Hereditary motor and sensory neuropathy IIB: clinical and electrodiagnostic characteristics.
    Elliott JL; Kwon JM; Goodfellow PJ; Yee WC
    Neurology; 1997 Jan; 48(1):23-8. PubMed ID: 9008488
    [TBL] [Abstract][Full Text] [Related]  

  • 24. 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]  

  • 25. Charcot-Marie-Tooth disease and related inherited neuropathies.
    Murakami T; Garcia CA; Reiter LT; Lupski JR
    Medicine (Baltimore); 1996 Sep; 75(5):233-50. PubMed ID: 8862346
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci.
    Bellone E; Rodolico C; Toscano A; Di Maria E; Cassandrini D; Pizzuti A; Pigullo S; Mazzeo A; Macaione V; Girlanda P; Vita G; Ajmar F; Mandich P
    Neuromuscul Disord; 2002 Mar; 12(3):286-91. PubMed ID: 11801401
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hereditary motor and sensory neuropathy: HMSN type II (neuronal type) and X-linked HMSN.
    Hahn AF
    Brain Pathol; 1993 Apr; 3(2):147-55. PubMed ID: 8293176
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. 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]  

  • 30. 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]  

  • 31. Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an update.
    Tazir M; Hamadouche T; Nouioua S; Mathis S; Vallat JM
    J Neurol Sci; 2014 Dec; 347(1-2):14-22. PubMed ID: 25454638
    [TBL] [Abstract][Full Text] [Related]  

  • 32. The p.R1109X mutation in SH3TC2 gene is predominant in Spanish Gypsies with Charcot-Marie-Tooth disease type 4.
    Claramunt R; Sevilla T; Lupo V; Cuesta A; Millán JM; Vílchez JJ; Palau F; Espinós C
    Clin Genet; 2007 Apr; 71(4):343-9. PubMed ID: 17470135
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B).
    Gambardella A; Bolino A; Muglia M; Valentino P; Bono F; Oliveri RL; Sabatelli M; Brancolini V; Van Broeckhoven C; Romeo G; Devoto M; Quattrone A
    Neurology; 1998 Mar; 50(3):799-801. PubMed ID: 9521281
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Hereditary motor and sensory neuropathy with diaphragm and vocal cord paresis.
    Dyck PJ; Litchy WJ; Minnerath S; Bird TD; Chance PF; Schaid DJ; Aronson AE
    Ann Neurol; 1994 May; 35(5):608-15. PubMed ID: 8179305
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Penetrance of the hereditary motor and sensory neuropathy Ia mutation: assessment by nerve conduction studies.
    Nicholson GA
    Neurology; 1991 Apr; 41(4):547-52. PubMed ID: 2011255
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Rapid quantitative PCR diagnostic strategy for Charcot-Marie-Tooth 1A and hereditary neuropathy with liability to pressure palsies.
    Chen SS
    J Chin Med Assoc; 2006 Feb; 69(2):58-9. PubMed ID: 16570571
    [No Abstract]   [Full Text] [Related]  

  • 38. Continuum of phenotypes in hereditary motor and sensory neuropathy with proximal predominance and Charcot-Marie-Tooth patients with TFG mutation.
    Khani M; Taheri H; Shamshiri H; Houlden H; Efthymiou S; Alavi A; Nafissi S; Elahi E
    Am J Med Genet A; 2019 Aug; 179(8):1507-1515. PubMed ID: 31111683
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Heat shock protein 27 R127W mutation: evidence of a continuum between axonal Charcot-Marie-Tooth and distal hereditary motor neuropathy.
    Solla P; Vannelli A; Bolino A; Marrosu G; Coviello S; Murru MR; Tranquilli S; Corongiu D; Benedetti S; Marrosu MG
    J Neurol Neurosurg Psychiatry; 2010 Sep; 81(9):958-62. PubMed ID: 20660910
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Gene for hereditary motor and sensory neuropathy (proximal dominant form) mapped to 3q13.1.
    Takashima H; Nakagawa M; Suehara M; Saito M; Saito A; Kanzato N; Matsuzaki T; Hirata K; Terwilliger JD; Osame M
    Neuromuscul Disord; 1999 Oct; 9(6-7):368-71. PubMed ID: 10545038
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.