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Journal Abstract Search

80 related items for PubMed ID: 5868071

  • 21. [Ataxia-areflexia-familial steatorrhea without abetalipoproteinemia or acanthocytosis].
    Larget-Piet L, Pouplard F.
    J Genet Hum; 1981 Sep; 29(3):249-51. PubMed ID: 7334347
    [No Abstract] [Full Text] [Related]

  • 22. [A family with Roussy-Levy syndrome].
    HAYNAL A, REGLI F.
    Confin Neurol; 1962 Sep; 22():128-40. PubMed ID: 13963587
    [No Abstract] [Full Text] [Related]

  • 23. Late-onset Friedreich ataxia: phenotypic analysis, magnetic resonance imaging findings, and review of the literature.
    Bhidayasiri R, Perlman SL, Pulst SM, Geschwind DH.
    Arch Neurol; 2005 Dec; 62(12):1865-9. PubMed ID: 16344344
    [Abstract] [Full Text] [Related]

  • 24. [Hereditary abnormalities of digestive enzymes. II. Malabsorption syndromes].
    Rey J.
    Rev Med Chir Mal Foie; 1971 Dec; 46(5):217-20. PubMed ID: 5159353
    [No Abstract] [Full Text] [Related]

  • 25. [An autopsy case of atypical Friedreich's ataxia with chronic idiopathic intestinal pseudo-obstruction].
    Nagata T, Aoki M, Hasegawa T, Shiga Y, Hayashi T, Higuchi J, Abe K, Tanno T, Konno H, Itoyama Y.
    Rinsho Shinkeigaku; 2001 Jul; 41(7):412-7. PubMed ID: 11808352
    [Abstract] [Full Text] [Related]

  • 26. A case of the Roussy-Levy syndrome family.
    Bartosik-Psujek H, Stelmasiak Z.
    Ann Univ Mariae Curie Sklodowska Med; 2001 Jul; 56():393-5. PubMed ID: 11977346
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  • 29. Chilaiditi's syndrome. Successful surgical correction by colopexy.
    Altomare DF, Rinaldi M, Petrolino M, Sallustio PL, Guglielmi A, Pannarale OC.
    Tech Coloproctol; 2001 Dec; 5(3):173-5. PubMed ID: 11875687
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  • 31. Masseter reflex potentials in olivo-ponto-cerebellar atrophy.
    Imai T, Matsumoto H, Ohmoto H, Chiba S, Kobayashi N.
    Electromyogr Clin Neurophysiol; 1998 Dec; 38(3):147-51. PubMed ID: 9637940
    [Abstract] [Full Text] [Related]

  • 32. [Cortical and peripheral responses evoked by stimulation of the nerve in pathology of the posterior funiculi].
    Bergamini L, Bergamasco B, Fra L, Gandiglio G, Mombelli AM, Mutani R.
    Rev Neurol (Paris); 1966 Jul; 115(1):99-112. PubMed ID: 5957655
    [No Abstract] [Full Text] [Related]

  • 33. A syndrome of microcephaly and retinal pigmentary abnormalities without mental retardation in a family with coincidental autosomal dominant hyperreflexia.
    Parke JT, Riccardi VM, Lewis RA, Ferrell RE.
    Am J Med Genet; 1984 Mar; 17(3):585-94. PubMed ID: 6711609
    [Abstract] [Full Text] [Related]

  • 34. [Otoneurologic study of Friedreich's ataxia by a multidisciplinary approach. Preliminary report].
    Cocchini F, Richichi M, Baiocco F, Formenti A, Finocchiaro G.
    Acta Otorhinolaryngol Ital; 1983 Mar; 3(5):491-501. PubMed ID: 6670541
    [No Abstract] [Full Text] [Related]

  • 35. [Heredo familial areflectoric dystasie. Roussy-Lévy-Syndrome (author's transl)].
    Coradello H, Lesigang C, Pollak A, Szilvassy J.
    Monatsschr Kinderheilkd (1902); 1976 Apr; 124(4):162-6. PubMed ID: 1264090
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  • 36. Familial ataxia, deaf-mutism, and muscular wasting.
    MATTHEWS WB.
    J Neurol Neurosurg Psychiatry; 1950 Nov; 13(4):307-11. PubMed ID: 14795246
    [No Abstract] [Full Text] [Related]

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  • 40. [Systemic mastocytosis and intestinal malabsorption].
    Barrière H, Dreno B, Pecquet C, Le Bodic MF, Bolze JL.
    Sem Hop; 1983 Nov 17; 59(42):2925-31. PubMed ID: 6318330
    [Abstract] [Full Text] [Related]

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