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 *

210 related articles for article (PubMed ID: 9126058)

  • 21. Nerve conduction studies in Charcot-Marie-Tooth polyneuropathy associated with a segmental duplication of chromosome 17.
    Kaku DA; Parry GJ; Malamut R; Lupski JR; Garcia CA
    Neurology; 1993 Sep; 43(9):1806-8. PubMed ID: 8414036
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Charcot-Marie-Tooth (CMT) disease: an update].
    Vallat JM; Funalot B
    Med Sci (Paris); 2010 Oct; 26(10):842-7. PubMed ID: 20929675
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hereditary motor and sensory neuropathy with myelin outfolding: clinical, genetic and neuropathological study of three cases.
    Schenone A; Abbruzzese M; Uccelli A; Mandich P; James R; Bellone E; Giunchedi M; Rolando S; Capello E; Mandich R [corrected to Mandich P]
    J Neurol Sci; 1994 Mar; 122(1):20-7. PubMed ID: 8195799
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Analysis of 17p11.2 chromosome region rearrangements in CMT1 patients from Ukraine.
    Hryshchenko NV; Livshits LA
    Tsitol Genet; 2009; 43(1):36-41. PubMed ID: 19663313
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [A family of X-linked motor and sensory neuropathy with a new type of connexin32 mutation].
    Ohnishi A; Yoshimura T; Takazawa A; Hashimoto T; Yamamoto T; Fukushima Y
    Rinsho Shinkeigaku; 1995 Aug; 35(8):843-9. PubMed ID: 8665724
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication.
    Uncini A; Di Guglielmo G; Di Muzio A; Gambi D; Sabatelli M; Mignogna T; Tonali P; Marzella R; Finelli P; Archidiacono N
    Muscle Nerve; 1995 Jun; 18(6):628-35. PubMed ID: 7753126
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 17p duplicated Charcot-Marie-Tooth 1A: characteristics of a new population.
    Marques W; Freitas MR; Nascimento OJ; Oliveira AB; Calia L; Melo A; Lucena R; Rocha V; Barreira AA
    J Neurol; 2005 Aug; 252(8):972-9. PubMed ID: 15765265
    [TBL] [Abstract][Full Text] [Related]  

  • 28. 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]  

  • 29. Overview of Charcot-Marie-Tooth Disease Type 1A.
    Thomas PK
    Ann N Y Acad Sci; 1999 Oct; 883(1):1-5. PubMed ID: 29086919
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Duplication within chromosome 17p11.2 in 12 families of French ancestry with Charcot-Marie-Tooth disease type 1a. The French CMT Research Group.
    Brice A; Ravisé N; Stevanin G; Gugenheim M; Bouche P; Penet C; Agid Y
    J Med Genet; 1992 Nov; 29(11):807-12. PubMed ID: 1453432
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Patients homozygous for the 17p11.2 duplication in Charcot-Marie-Tooth type 1A disease.
    LeGuern E; Gouider R; Mabin D; Tardieu S; Birouk N; Parent P; Bouche P; Brice A
    Ann Neurol; 1997 Jan; 41(1):104-8. PubMed ID: 9005872
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Linkage analysis of distal hereditary motor neuropathy type II (distal HMN II) in a single pedigree.
    Timmerman V; Raeymaekers P; Nelis E; De Jonghe P; Muylle L; Ceuterick C; Martin JJ; Van Broeckhoven C
    J Neurol Sci; 1992 May; 109(1):41-8. PubMed ID: 1517763
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. Insights into phenotypic variability caused by GARS1 pathogenic variants.
    Jiménez-Jiménez J; Navarrete I; Azorín I; Martí P; Vílchez R; Muelas N; Cabello-Murgui J; Millet E; Vázquez-Costa JF; Vílchez JJ; Sevilla T; Sivera R
    Eur J Neurol; 2024 Oct; 31(10):e16416. PubMed ID: 39051710
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. Early onset severe and late-onset mild Charcot-Marie-Tooth disease with mitofusin 2 (MFN2) mutations.
    Chung KW; Kim SB; Park KD; Choi KG; Lee JH; Eun HW; Suh JS; Hwang JH; Kim WK; Seo BC; Kim SH; Son IH; Kim SM; Sunwoo IN; Choi BO
    Brain; 2006 Aug; 129(Pt 8):2103-18. PubMed ID: 16835246
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38. 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]  

  • 39. Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths: clinical, electrophysiologic, and genetic aspects of a large family.
    Quattrone A; Gambardella A; Bono F; Aguglia U; Bolino A; Bruni AC; Montesi MP; Oliveri RL; Sabatelli M; Tamburrini O; Valentino P; Van Broeckhoven C; Zappia M
    Neurology; 1996 May; 46(5):1318-24. PubMed ID: 8628474
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [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]  

    [Previous]   [Next]    [New Search]
    of 11.