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 *

208 related articles for article (PubMed ID: 33272751)

  • 21. [Charcot-Marie-Tooth disease].
    Lee YC; Chang MH; Lin KP
    Acta Neurol Taiwan; 2008 Sep; 17(3):203-13. PubMed ID: 18975529
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Rigid spine syndrome associated with sensory-motor axonal neuropathy resembling Charcot-Marie-Tooth disease is characteristic of Bcl-2-associated athanogene-3 gene mutations even without cardiac involvement.
    Noury JB; Maisonobe T; Richard P; Delague V; Malfatti E; Stojkovic T
    Muscle Nerve; 2018 Feb; 57(2):330-334. PubMed ID: 28224639
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Bilateral sudden sensorineural hearing loss caused by Charcot-Marie-Tooth disease.
    Papadakis CE; Hajiioannou JK; Kyrmizakis DE; Bizakis JG
    J Laryngol Otol; 2003 May; 117(5):399-401. PubMed ID: 12803792
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Charcot-Marie-Tooth neuropathy score and ambulation index are both predictors of orthotic need for patients with CMT.
    Prada V; Zuccarino R; Schenone C; Mennella G; Grandis M; Shy ME; Schenone A
    Neurol Sci; 2022 Apr; 43(4):2759-2764. PubMed ID: 34613504
    [TBL] [Abstract][Full Text] [Related]  

  • 26. [Non-fortuitous dynamin II mutation-related association: neutropenia and Charcot-Marie-Tooth disease].
    Saint-Lézer A; Solé G; Ribeiro E; Latour P; Mercié P; Longy-Boursier M
    Rev Neurol (Paris); 2012 Apr; 168(4):367-70. PubMed ID: 22385972
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Characteristics of demyelinating Charcot-Marie-Tooth disease with concurrent diabetes mellitus.
    Yu Z; Wu X; Xie H; Han Y; Guan Y; Qin Y; Zheng H; Jiang J; Niu Z
    Int J Clin Exp Pathol; 2014; 7(7):4329-38. PubMed ID: 25120817
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Novel GJB1 mutation causing adult-onset Charcot-Marie-Tooth disease in a female patient.
    Martikainen MH; Majamaa K
    Neuromuscul Disord; 2013 Nov; 23(11):899-901. PubMed ID: 23838279
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [The genetics of type 1 Charcot-Marie-Tooth disease, the hereditary focal neuropathies and the hereditary distal motor neuropathies].
    Sevilla T
    Rev Neurol; 2000 Jan 1-15; 30(1):71-9. PubMed ID: 10743001
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [The application of scales and characteristics of disability in the common genotypes of Charcot-Marie-Tooth disease].
    Liu X; Zhang RX; Liu L; Xie YZ; Lin ZQ; Zhao Q; Cao WQ; Zhu XY; Li XB
    Zhonghua Yi Xue Za Zhi; 2021 Jan; 101(2):131-136. PubMed ID: 33455129
    [No Abstract]   [Full Text] [Related]  

  • 31. Heterogeneity of hereditary motor and sensory neuropathy type I (HMSN I): electroneurographical findings, visual evoked potentials and blood group markers in a family with Charcot-Marie-Tooth disease (CMT).
    Leblhuber F; Reisecker F; Mayr WR; Deisenhammer E
    Acta Neurol Scand; 1986 Aug; 74(2):145-9. PubMed ID: 3022527
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Atypical presentation of Charcot-Marie-Tooth disease 1A: A case report.
    Kulkarni SD; Sayed R; Garg M; Patil VA
    Neuromuscul Disord; 2015 Nov; 25(11):916-9. PubMed ID: 26432165
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Charcot-Marie-Tooth 2F (Hsp27 mutations): A review.
    Schwartz NU
    Neurobiol Dis; 2019 Oct; 130():104505. PubMed ID: 31212070
    [TBL] [Abstract][Full Text] [Related]  

  • 34. 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]  

  • 35. Diaphragmatic dysfunction in siblings with hereditary motor and sensory neuropathy (Charcot-Marie-Tooth disease).
    Chan CK; Mohsenin V; Loke J; Virgulto J; Sipski ML; Ferranti R
    Chest; 1987 Apr; 91(4):567-70. PubMed ID: 3829750
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Charcot-Marie-Tooth disease associated with "essential tremor": Report of 7 cases and a review of the literature.
    Salisachs P
    J Neurol Sci; 1976 May; 28(1):17-40. PubMed ID: 932772
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Neuromuscular hip dysplasia in Charcot-Marie-Tooth disease type 1A.
    Bamford NS; White KK; Robinett SA; Otto RK; Gospe SM
    Dev Med Child Neurol; 2009 May; 51(5):408-11. PubMed ID: 19388151
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A National French Consensus on Gene List for the Diagnosis of Charcot-Marie-Tooth Disease and Related Disorders Using Next-Generation Sequencing.
    Benquey T; Pion E; Cossée M; Krahn M; Stojkovic T; Perrin A; Cerino M; Molon A; Lia AS; Magdelaine C; Francou B; Guiochon-Mantel A; Malinge MC; Leguern E; Lévy N; Attarian S; Latour P; Bonello-Palot N
    Genes (Basel); 2022 Feb; 13(2):. PubMed ID: 35205364
    [TBL] [Abstract][Full Text] [Related]  

  • 39. [Clinical practice of hereditary motor neuropathy (HMN) and hereditary sensory and autonomic neuropathy (HSAN)].
    Takashima H
    Rinsho Shinkeigaku; 2014; 54(12):957-9. PubMed ID: 25672680
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Foot surgery for adults with Charcot-Marie-Tooth disease.
    Laurá M; Barnett J; Benfield J; Ramdharry GM; Welck MJ
    Pract Neurol; 2024 Jul; 24(4):275-284. PubMed ID: 38631902
    [TBL] [Abstract][Full Text] [Related]  

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