BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

154 related articles for article (PubMed ID: 2171842)

  • 1. A family with tomaculous neuropathy mimicking Charcot-Marie-Tooth disease.
    Barbieri F; Santangelo R; Crisci C; Ragno M; Perretti A; Santoro L
    Clin Neurol Neurosurg; 1990; 92(3):289-94. PubMed ID: 2171842
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Peripheral myelin protein 22 gene duplication with atypical presentations: a new example of the wide spectrum of Charcot-Marie-Tooth 1A disease.
    Mathis S; Corcia P; Tazir M; Camu W; Magdelaine C; Latour P; Biberon J; Guennoc AM; Richard L; Magy L; Funalot B; Vallat JM
    Neuromuscul Disord; 2014 Jun; 24(6):524-8. PubMed ID: 24792522
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Hereditary neuropathy with liability to pressure palsies].
    Smith TA; Rasmussen K; Hertz JM
    Ugeskr Laeger; 1999 Jun; 161(23):3463-5. PubMed ID: 10388355
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Tomaculous neuropathy in chromosome 1 Charcot-Marie-Tooth syndrome.
    Thomas FP; Lebo RV; Rosoklija G; Ding XS; Lovelace RE; Latov N; Hays AP
    Acta Neuropathol; 1994; 87(1):91-7. PubMed ID: 7511317
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Neuropathy, heredity, and monoclonal gammopathy.
    Latov N
    Arch Neurol; 2000 May; 57(5):641-2. PubMed ID: 10815127
    [No Abstract]   [Full Text] [Related]  

  • 6. [Hereditary neuropathy with liability to pressure palsies in childhood].
    de las Cuevas I; Arteaga R; García A; Herranz JL
    Rev Neurol; 2000 Jul 1-15; 31(1):38-41. PubMed ID: 10948581
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 17p11.2 duplication is a common finding in sporadic cases of Charcot-Marie-Tooth type 1.
    Mancardi GL; Uccelli A; Bellone E; Sghirlanzoni A; Mandich P; Pareyson D; Schenone A; Abbruzzese M; Ajmar F
    Eur Neurol; 1994; 34(3):135-9. PubMed ID: 8033938
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Late-onset HMSN 2: further evidence of genetic heterogeneity.
    Dyck PJ
    Neurology; 2008 Jul; 71(1):9-10. PubMed ID: 18591500
    [No Abstract]   [Full Text] [Related]  

  • 10. Are electrophysiological criteria useful in distinguishing childhood demyelinating neuropathies?
    Potulska-Chromik A; Ryniewicz B; Aragon-Gawinska K; Kabzinska D; Seroka A; Lipowska M; Kaminska AM; Kostera-Pruszczyk A
    J Peripher Nerv Syst; 2016 Mar; 21(1):22-6. PubMed ID: 26663344
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Variability of presentation in hereditary neuropathy with liability to pressure palsy results in underrecognition.
    Kumar N; Cole J; Parry GJ
    Ann N Y Acad Sci; 1999 Sep; 883():344-50. PubMed ID: 10586259
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Guidelines for the diagnosis of Charcot-Marie-Tooth disease and related neuropathies. Ad hoc Working Group of the Peripheral Nervous System Study Group, Italian Neurological Society.
    Pareyson D
    Ital J Neurol Sci; 1999 Aug; 20(4):207-16. PubMed ID: 10551906
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. Friedreich's ataxia mimicking hereditary motor and sensory neuropathy.
    Panas M; Kalfakis N; Karadima G; Davaki P; Vassilopoulos D
    J Neurol; 2002 Nov; 249(11):1583-6. PubMed ID: 12420100
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Assessment of Targeted Next-Generation Sequencing as a Tool for the Diagnosis of Charcot-Marie-Tooth Disease and Hereditary Motor Neuropathy.
    Lupo V; García-García F; Sancho P; Tello C; García-Romero M; Villarreal L; Alberti A; Sivera R; Dopazo J; Pascual-Pascual SI; Márquez-Infante C; Casasnovas C; Sevilla T; Espinós C
    J Mol Diagn; 2016 Mar; 18(2):225-34. PubMed ID: 26752306
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical and electrophysiologic features of HNPP patients with 17p11.2 deletion.
    Hong YH; Kim M; Kim HJ; Sung JJ; Kim SH; Lee KW
    Acta Neurol Scand; 2003 Nov; 108(5):352-8. PubMed ID: 14616306
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Differential diagnosis of Charcot-Marie-Tooth disease and related neuropathies.
    Pareyson D
    Neurol Sci; 2004 Jun; 25(2):72-82. PubMed ID: 15221625
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. Unilateral oculomotor palsy in Charcot-Marie-Tooth disease 1A (CMT 1A).
    Posa A; Emmer A; Kornhuber ME
    Clin Neurol Neurosurg; 2017 Apr; 155():20-21. PubMed ID: 28214652
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.