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Journal Abstract Search

318 related items for PubMed ID: 15776672

  • 1. [Charcot-Marie-Tooth disease associated with a pyramidal syndrome: clinical, electrophysiological, and neuropathological study of neuro-muscular biopsies in 14 cases].
    Thiam A, Sene FD, Ndao AK, Ndiaye M, Ndiaye IP.
    Dakar Med; 2002; 47(2):182-7. PubMed ID: 15776672
    [Abstract] [Full Text] [Related]

  • 2. Clinical, electrophysiological and morphological findings of Charcot-Marie-Tooth neuropathy with vocal cord palsy and mutations in the GDAP1 gene.
    Sevilla T, Cuesta A, Chumillas MJ, Mayordomo F, Pedrola L, Palau F, Vílchez JJ.
    Brain; 2003 Sep; 126(Pt 9):2023-33. PubMed ID: 12821518
    [Abstract] [Full Text] [Related]

  • 3. 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
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  • 4. [Charcot-Marie-Tooth disease. Study of sural nerve biopsy in 41 patients].
    Freitas MR, Nascimento OJ, Chimelli L, de Freitas GR.
    Arq Neuropsiquiatr; 1995 Sep; 53(3-B):560-9. PubMed ID: 8585811
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  • 6. Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C.
    Tazir M, Azzedine H, Assami S, Sindou P, Nouioua S, Zemmouri R, Hamadouche T, Chaouch M, Feingold J, Vallat JM, Leguern E, Grid D.
    Brain; 2004 Jan; 127(Pt 1):154-63. PubMed ID: 14607793
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  • 7. Charcot-Marie-Tooth disease type 1A: clinicopathological correlations in 24 patients.
    Carvalho AA, Vital A, Ferrer X, Latour P, Lagueny A, Brechenmacher C, Vital C.
    J Peripher Nerv Syst; 2005 Mar; 10(1):85-92. PubMed ID: 15703022
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  • 9. Charcot-Marie-Tooth disease type 1A duplication: spectrum of clinical and magnetic resonance imaging features in leg and foot muscles.
    Gallardo E, García A, Combarros O, Berciano J.
    Brain; 2006 Feb; 129(Pt 2):426-37. PubMed ID: 16317020
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  • 10. Charcot-Marie-Tooth disease in northern Finland.
    Rantala H, Tolonen U, Myllylä V.
    Ann Clin Res; 1986 Feb; 18(3):154-9. PubMed ID: 3740791
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  • 11. Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.
    Berciano J, García A, Gallardo E, Peeters K, Pelayo-Negro AL, Álvarez-Paradelo S, Gazulla J, Martínez-Tames M, Infante J, Jordanova A.
    J Neurol; 2017 Aug; 264(8):1655-1677. PubMed ID: 28364294
    [Abstract] [Full Text] [Related]

  • 12. Hypertrophic motor and sensory neuropathy type I (Charcot-Marie-Tooth disease): ultrastructural study of sural nerve biopsy in members of a family.
    Calore EE, Alonso Neto JL, Cavaliere MJ, Perez NM, Russo DH, Wakamatsu A, Maeda MY, Kitamura C.
    Pathologica; 1994 Jun; 86(3):279-83. PubMed ID: 7808799
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  • 14. [An autopsy case of neuronal type Charcot-Marie-Tooth disease (HMSN type II) with nerve deafness and psychiatric symptoms].
    Yoshimura I, Yoshimura N, Hanazono T, Usutani S, Muramoto Y, Fukushima Y.
    No To Shinkei; 1992 Jun; 44(6):571-8. PubMed ID: 1389565
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  • 15. [The clinical and pathologic features of Charcot-Marie-Tooth disease].
    Xiao B, Xie J, Yang X, Wu Z, Xiao J, Li J.
    Zhonghua Nei Ke Za Zhi; 2002 Nov; 41(11):736-8. PubMed ID: 12485517
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  • 16. Charcot-Marie-tooth disease.
    Casasnovas C, Cano LM, Albertí A, Céspedes M, Rigo G.
    Foot Ankle Spec; 2008 Dec; 1(6):350-4. PubMed ID: 19825739
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  • 18. Vocal cord paresis and diaphragmatic dysfunction are severe and frequent symptoms of GDAP1-associated neuropathy.
    Sevilla T, Jaijo T, Nauffal D, Collado D, Chumillas MJ, Vilchez JJ, Muelas N, Bataller L, Domenech R, Espinós C, Palau F.
    Brain; 2008 Nov; 131(Pt 11):3051-61. PubMed ID: 18812441
    [Abstract] [Full Text] [Related]

  • 19. [Molecular genetics of inherited neuropathies].
    Takashima H.
    Rinsho Shinkeigaku; 2006 Jan; 46(1):1-18. PubMed ID: 16541790
    [Abstract] [Full Text] [Related]

  • 20. [Clinical electrophysiological studies of peroneal muscular atrophy--report of 32 cases].
    Cui LY.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1989 Jun; 11(3):175-9. PubMed ID: 2529984
    [Abstract] [Full Text] [Related]

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