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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 3791775

  • 21.
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  • 25. X-linked motor-sensory neuropathy type-II with deafness and mental retardation: a new disorder.
    Cowchock FS, Duckett SW, Streletz LJ, Graziani LJ, Jackson LG.
    Am J Med Genet; 1985 Feb; 20(2):307-15. PubMed ID: 3856385
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  • 26. Hereditary motor-sensory neuropathy (Charcot-Marie-Tooth disease) with nerve deafness: a new variant.
    Hamiel OP, Raas-Rothschild A, Upadhyaya M, Frydman M, Sarova-Pinhas I, Brand N, Passwell JH.
    J Pediatr; 1993 Sep; 123(3):431-4. PubMed ID: 8355122
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  • 27. [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
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  • 28. [Ocular findings in Charcot-Marie-Tooth disease, HMSN type I].
    Bürki E.
    Klin Monbl Augenheilkd; 1981 Aug; 179(2):94-6. PubMed ID: 7347789
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  • 29. Malignant melanoma and Charcot-Marie-Tooth disease.
    Greene MH, Mead GD, Reimer RR, Bergfeld WF, Fraumeni JF.
    Am J Med Genet; 1980 Aug; 5(1):69-71. PubMed ID: 7395902
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  • 30. [A family with progressive neural muscular atrophy--with special reference to relation with allied diseases (author's transl)].
    Hayashi Y, Tomita M, Shimizu K, Takamiya M, Watanabe H.
    Rinsho Shinkeigaku; 1978 Oct; 18(10):593-600. PubMed ID: 709963
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  • 31. [Deafness as a symptom of neural muscular atrophy (Charcot-Marie-Tooth disease)].
    Laubert A.
    HNO; 1986 Oct; 34(10):434-7. PubMed ID: 3793530
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  • 32. [Family with hereditary polyneuropthy assoicated with pyramidal signs].
    Doi H, Shibasaki H, Goto I, Kuroiwa Y, Ohta M.
    Rinsho Shinkeigaku; 1976 Sep; 16(9):642-8. PubMed ID: 1034548
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  • 34. Deletion in the CMT1A locus on chromosome 17p11.2 in hereditary neuropathy with liability to pressure palsies.
    Verhalle D, Löfgren A, Nelis E, Dehaene I, Theys P, Lammens M, Dom R, Van Broeckhoven C, Robberecht W.
    Ann Neurol; 1994 Jun; 35(6):704-8. PubMed ID: 8210227
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  • 35. Hypertrophic interstitial neuropathy of Déjérine-Sottas.
    Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):103-4. PubMed ID: 5173113
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  • 37. [Hereditary spastic paraplegia associated with peroneal muscular atrophy].
    Laso FJ, Cacho J, Díez Jarilla JL, González Macías J.
    Med Clin (Barc); 1982 Apr 16; 78(8):329-31. PubMed ID: 7087602
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  • 38. Erythrocyte insulin binding in a family with hereditary motor sensory neuropathy (Charcot-Marie-Tooth) with superimposed insulin-dependent type I diabetes mellitus.
    Ivarsson SA, Bjerre I.
    Diabetes Res; 1989 Jan 16; 10(1):49-51. PubMed ID: 2667841
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  • 39. [Anatomo-clinical study of a neuronal form of Charcot-Marie-Tooth disease].
    Dupuis M, Brucher JM, Gonsette R.
    Rev Neurol (Paris); 1983 Jan 16; 139(11):643-9. PubMed ID: 6330834
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