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196 related items for PubMed ID: 991874

  • 1. Laurence-Moon-Biedl syndrome (?) and Prader-Willi syndrome (?) in a single family.
    Endo M, Tasaka Y, Matsuura N, Matsuda I.
    Eur J Pediatr; 1976 Nov 03; 123(4):269-76. PubMed ID: 991874
    [Abstract] [Full Text] [Related]

  • 2. The Laurence-Moon-Bardet-Biedl-syndrome.
    Luz MF, Marques MN, Jorge E, Jacomini CZ, Ribero Z, Marques J.
    Metab Pediatr Syst Ophthalmol (1985); 1985 Nov 03; 8(2-3):15-20. PubMed ID: 3870940
    [Abstract] [Full Text] [Related]

  • 3. [Bardet-Biedl syndrome. Apropos of a family].
    Guízar-Vázquez JJ, Escobar-Morales BG, Valdés de Fromow ML, Salamanca-Gómez F.
    Bol Med Hosp Infant Mex; 1984 Aug 03; 41(8):442-6. PubMed ID: 6477712
    [No Abstract] [Full Text] [Related]

  • 4. [Genetic syndrome with obesity].
    Tsuda K, Seino Y.
    Nihon Rinsho; 1995 Jun 03; 53 Suppl():436-40. PubMed ID: 7563784
    [No Abstract] [Full Text] [Related]

  • 5. A family with the Bardet-Biedl syndrome and diabetes mellitus.
    Escallon F, Traboulsi EI, Infante R.
    Arch Ophthalmol; 1989 Jun 03; 107(6):855-7. PubMed ID: 2730406
    [Abstract] [Full Text] [Related]

  • 6. The cardinal manifestations of Bardet-Biedl syndrome, a form of Laurence-Moon-Biedl syndrome.
    Green JS, Parfrey PS, Harnett JD, Farid NR, Cramer BC, Johnson G, Heath O, McManamon PJ, O'Leary E, Pryse-Phillips W.
    N Engl J Med; 1989 Oct 12; 321(15):1002-9. PubMed ID: 2779627
    [Abstract] [Full Text] [Related]

  • 7. The possible relationship between Laurence-Moon-Biedl-Bardet syndrome and a schizophrenic-like psychosis.
    Weiss M, Meshulam B, Wijsenbeek H.
    J Nerv Ment Dis; 1981 Apr 12; 169(4):259-60. PubMed ID: 7217934
    [Abstract] [Full Text] [Related]

  • 8. Laurence-Moon-Biedl syndrome accompanied by congenital hepatic fibrosis.
    Nakamura F, Sasaki H, Kajihara H, Yamanoue M.
    J Gastroenterol Hepatol; 1990 Apr 12; 5(2):206-10. PubMed ID: 2103400
    [Abstract] [Full Text] [Related]

  • 9. Human obesity does not segregate with the chromosomal regions of Prader-Willi, Bardet-Biedl, Cohen, Borjeson or Wilson-Turner syndromes.
    Reed DR, Ding Y, Xu W, Cather C, Price RA.
    Int J Obes Relat Metab Disord; 1995 Sep 12; 19(9):599-603. PubMed ID: 8574268
    [Abstract] [Full Text] [Related]

  • 10. Dental abnormalities as a component of the Laurence-Moon-Bardet-Biedl syndrome.
    Kobrin JL, Ternand CL, Knobloch WH, Johnson DD.
    Ophthalmic Paediatr Genet; 1990 Dec 12; 11(4):299-303. PubMed ID: 2096358
    [Abstract] [Full Text] [Related]

  • 11. Seven hereditary syndromes with pigmentary retinopathy. A review and differential diagnosis.
    Cantani A, Bellioni P, Bamonte G, Salvinelli F, Bamonte MT.
    Clin Pediatr (Phila); 1985 Oct 12; 24(10):578-83. PubMed ID: 3896611
    [Abstract] [Full Text] [Related]

  • 12. [Prader-Willi syndrome and Laurence-Moon-Biedl syndrome].
    Takeshita K.
    Nihon Rinsho; 1978 May 12; Suppl():1490-1. PubMed ID: 691404
    [No Abstract] [Full Text] [Related]

  • 13. [Hereditary disease associated with obesity].
    Tsuda K, Imura H, Seino Y.
    Nihon Rinsho; 1988 Nov 12; 46(11):2471-6. PubMed ID: 3241373
    [No Abstract] [Full Text] [Related]

  • 14. Quadriparesis in the Laurence-Moon-Biedl-Bardet syndrome: case report.
    Nyska M, Mozes G, Howard C, Bar-Ziv J, Dekel S.
    Paraplegia; 1991 Jun 12; 29(5):350-4. PubMed ID: 1886735
    [Abstract] [Full Text] [Related]

  • 15. Laurence-Moon-Biedl syndrome: report of two cases.
    Lin HS, Lin TY.
    J Formos Med Assoc; 1993 Oct 12; 92(10):904-6. PubMed ID: 7908573
    [Abstract] [Full Text] [Related]

  • 16. [Considerations on a family with retinitis pigmentosa and Laurence-Moon-Bardet-Biedl syndrome].
    ROMEI L, IOLI-SPADA G.
    Acta Genet Med Gemellol (Roma); 1959 Oct 12; 8():487-92. PubMed ID: 14438605
    [No Abstract] [Full Text] [Related]

  • 17. Morbid obesity in an adolescent with Prader-Willi syndrome.
    Santos VM, Henrique de Paula F, Osterne EM, Nery NS, Turra TZ.
    Rev Med Chil; 2009 Feb 12; 137(2):264-8. PubMed ID: 19543650
    [Abstract] [Full Text] [Related]

  • 18. Endocrine dysfunction in Prader-Willi syndrome: a review with special reference to GH.
    Burman P, Ritzén EM, Lindgren AC.
    Endocr Rev; 2001 Dec 12; 22(6):787-99. PubMed ID: 11739333
    [Abstract] [Full Text] [Related]

  • 19. Assessment of ophthalmologic, endocrinologic and genetic findings in the Bardet-Biedl syndrome.
    Bergsma DR, Brown KS.
    Birth Defects Orig Artic Ser; 1975 Dec 12; 11(2):132-6. PubMed ID: 776244
    [Abstract] [Full Text] [Related]

  • 20. Cerebellar vermis hypoplasia in a patient with Bardet-Biedl syndrome.
    Baskin E, Kayiran SM, Oto S, Alehan F, Agildere AM, Saatçi U.
    J Child Neurol; 2002 May 12; 17(5):385-7. PubMed ID: 12150587
    [Abstract] [Full Text] [Related]

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