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1018 related items for PubMed ID: 10962051

  • 1. Neurophysiology and molecular genetics of Charcot-Marie-Tooth type 1 neuropathy in Croatian children: follow-up study.
    Barisić N, Mihatov I.
    Croat Med J; 2000 Sep; 41(3):306-13. PubMed ID: 10962051
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Neurophysiologic abnormalities in children with Charcot-Marie-Tooth disease type 1A.
    Yiu EM, Burns J, Ryan MM, Ouvrier RA.
    J Peripher Nerv Syst; 2008 Sep; 13(3):236-41. PubMed ID: 18844790
    [Abstract] [Full Text] [Related]

  • 4. Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families.
    Bouhouche A, Birouk N, Azzedine H, Benomar A, Durosier G, Ente D, Muriel MP, Ruberg M, Slassi I, Yahyaoui M, Dubourg O, Ouazzani R, LeGuern E.
    Brain; 2007 Apr; 130(Pt 4):1062-75. PubMed ID: 17347251
    [Abstract] [Full Text] [Related]

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Gene dosage is a mechanism for Charcot-Marie-Tooth disease type 1A.
    Lupski JR, Wise CA, Kuwano A, Pentao L, Parke JT, Glaze DG, Ledbetter DH, Greenberg F, Patel PI.
    Nat Genet; 1992 Apr; 1(1):29-33. PubMed ID: 1301995
    [Abstract] [Full Text] [Related]

  • 8. Duplication of the PMP22 gene in 17p partial trisomy patients with Charcot-Marie-Tooth type-1 neuropathy.
    Roa BB, Greenberg F, Gunaratne P, Sauer CM, Lubinsky MS, Kozma C, Meck JM, Magenis RE, Shaffer LG, Lupski JR.
    Hum Genet; 1996 May; 97(5):642-9. PubMed ID: 8655146
    [Abstract] [Full Text] [Related]

  • 9. Is the duplication present in all family members affected with Charcot-Marie-Tooth neuropathy type 1 A?
    Ionăşescu V, Ionăşescu G, Searby C, Barker DF.
    Rom J Neurol Psychiatry; 1993 May; 31(3-4):179-87. PubMed ID: 8011481
    [Abstract] [Full Text] [Related]

  • 10. Overview of Charcot-Marie-Tooth disease type 1A.
    Thomas PK.
    Ann N Y Acad Sci; 1999 Sep 14; 883():1-5. PubMed ID: 10586223
    [Abstract] [Full Text] [Related]

  • 11. Charcot-Marie-Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit.
    Pentao L, Wise CA, Chinault AC, Patel PI, Lupski JR.
    Nat Genet; 1992 Dec 14; 2(4):292-300. PubMed ID: 1303282
    [Abstract] [Full Text] [Related]

  • 12. Charcot-Marie-Tooth disease type 1A: a family study with microsatellites.
    Qu Y, Carpenter NJ, Whetsell L, Smith SP, Say B.
    J Okla State Med Assoc; 1996 Nov 14; 89(11):395-9. PubMed ID: 8972170
    [Abstract] [Full Text] [Related]

  • 13. 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 14; 8(4):461-8. PubMed ID: 11562788
    [Abstract] [Full Text] [Related]

  • 14. Hereditary motor and sensory neuropathy type I: clinical and neurographical features of the 17p duplication subtype.
    Hoogendijk JE, De Visser M, Bolhuis PA, Hart AA, Ongerboer de Visser BW.
    Muscle Nerve; 1994 Jan 14; 17(1):85-90. PubMed ID: 8264707
    [Abstract] [Full Text] [Related]

  • 15. Genotype/phenotype correlations in X-linked dominant Charcot-Marie-Tooth disease.
    Hahn AF, Bolton CF, White CM, Brown WF, Tuuha SE, Tan CC, Ainsworth PJ.
    Ann N Y Acad Sci; 1999 Sep 14; 883():366-82. PubMed ID: 10586261
    [Abstract] [Full Text] [Related]

  • 16. Severe vincristine neuropathy in Charcot-Marie-Tooth disease type 1A.
    Graf WD, Chance PF, Lensch MW, Eng LJ, Lipe HP, Bird TD.
    Cancer; 1996 Apr 01; 77(7):1356-62. PubMed ID: 8608515
    [Abstract] [Full Text] [Related]

  • 17. [Studies of electromyography and genetics in children with Charcot-Marie-Tooth disease type 1].
    Pan XL, Zhang NN, Ye HL, Zhao YF, Gao H.
    Zhongguo Dang Dai Er Ke Za Zhi; 2011 Aug 01; 13(8):647-50. PubMed ID: 21849115
    [Abstract] [Full Text] [Related]

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  • 19. A large family with Charcot-Marie-Tooth Type 1a and Type 2 diabetes mellitus.
    Koç F, Sarica Y, Yerdelen D, Baris I, Battaloglu E, Sert M.
    Int J Neurosci; 2006 Feb 01; 116(2):103-14. PubMed ID: 16393877
    [Abstract] [Full Text] [Related]

  • 20. [A family of early childhood-onset Charcot-Marie-Tooth disease type 2].
    Hinuma Y, Aoki M, Takahashi T, Tateyama M, Nagai M, Yoshioka M, Itoyama Y.
    Rinsho Shinkeigaku; 2001 Jan 01; 41(1):64-7. PubMed ID: 11433771
    [Abstract] [Full Text] [Related]

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