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Journal Abstract Search

247 related items for PubMed ID: 7330503

  • 21. [Peroneal muscular atrophy associated with intellectual impairment and pyramidal signs].
    Sobue G, Ibi T, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1985 Jul; 25(7):818-25. PubMed ID: 4075646
    [No Abstract] [Full Text] [Related]

  • 22.
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  • 23. [Heterogeneity of neural muscular atrophies].
    Leblhuber F, Reisecker F, Mayr WR, Deisenhammer E.
    Nervenarzt; 1986 Jul; 57(7):419-21. PubMed ID: 3462518
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  • 25. Palmoplantar keratoderma and Charcot-Marie-Tooth disease.
    Rabbiosi G, Borroni G, Pinelli P, Cosi V.
    Arch Dermatol; 1980 Jul; 116(7):789-90. PubMed ID: 6446889
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  • 26. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness].
    Murakami K, Sobue G, Takahashi A, Mitsuma T.
    Rinsho Shinkeigaku; 1986 Sep; 26(9):952-9. PubMed ID: 3791775
    [No Abstract] [Full Text] [Related]

  • 27. 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]

  • 28. [Chronic distal spinal amyotrophy or spinal forms of Charcot-Marie disease. A report on six sporadic adult cases (author's transl)].
    Serratrice G, Gastaut JL.
    Rev Neurol (Paris); 1979 Jan; 135(11):815-26. PubMed ID: 555021
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  • 31. 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
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  • 32.
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  • 33. [Usefulness Of electromyographic examination of families of patients affected with hypertrophic sensory-motor neuropathy (Charcot-Marie-Tooth disease). Preliminary results].
    Fardin P, Micaglio GF, Angelini C, Negrin P, Siciliano G.
    Riv Neurobiol; 1984 Nov; 30(2-3):222-8. PubMed ID: 6544478
    [No Abstract] [Full Text] [Related]

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  • 35. 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]

  • 36. [Familial hypertrophic neuropathies. Conceptual and critical outline. Report of a family with Dyck and Lambert's type IV disease (author's transl)].
    Sadaba Garay F, Franco Vicario R, Miguel de la Villa F, Ibarmia Lahuerta J, Bustamante Murga V.
    Med Clin (Barc); 1980 Oct 10; 75(6):240-6. PubMed ID: 7421358
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  • 37. [Latent hyperbilirubinemias elicited by nicotinic acid test among the family of a case of Gilbert's syndrome with a kind of muscle atrophy which is similar to Charcot-Marie-Tooth disease (author's transl)].
    Mizoguchi Y, Okubo A, Imawari M, Itakura H, Miyagawa Y.
    Nihon Naika Gakkai Zasshi; 1975 Mar 10; 64(3):254-60. PubMed ID: 1171919
    [No Abstract] [Full Text] [Related]

  • 38. [Three cases of Charcot-Marie-Tooth disease with neural deafness-the classification and sural nerve pathology (author's transl)].
    Kim I, Ohnishi A, Kuroiwa Y.
    Rinsho Shinkeigaku; 1980 Apr 10; 20(4):264-70. PubMed ID: 7408330
    [No Abstract] [Full Text] [Related]

  • 39. Controversy in genetic disorders.
    Sybert VP.
    Arch Dermatol; 1981 Jul 10; 117(7):380-1. PubMed ID: 6455091
    [No Abstract] [Full Text] [Related]

  • 40. Clinical, electrophysiological and molecular genetic studies in a family with X-linked dominant Charcot-Marie-Tooth neuropathy presenting a novel mutation in GJB1 Promoter and a rare polymorphism in LITAF/SIMPLE.
    Beauvais K, Furby A, Latour P.
    Neuromuscul Disord; 2006 Jan 10; 16(1):14-8. PubMed ID: 16373087
    [Abstract] [Full Text] [Related]

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