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Journal Abstract Search

166 related items for PubMed ID: 6068089

  • 1. Prader--Willi syndrome.
    Hoefnagel D, Costello PJ, Hatoum K.
    J Ment Defic Res; 1967 Mar; 11(1):1-11. PubMed ID: 6068089
    [No Abstract] [Full Text] [Related]

  • 2. Prader-Willi syndrome. (Hypotonia, obesity, hypogonadism, growth and mental retardation).
    Jancar J.
    J Ment Defic Res; 1971 Mar; 15(1):20-9. PubMed ID: 5581387
    [No Abstract] [Full Text] [Related]

  • 3. [Congenital asymmetry and nervous system disorders in the Prader-Labhart-Willi syndrome].
    Gaal K, Fazekas A, Vigvary L.
    Kinderarztl Prax; 1972 Oct; 40(10):453-60. PubMed ID: 4650217
    [No Abstract] [Full Text] [Related]

  • 4. Prader-Willi syndrome.
    Juul J, Dupont A.
    J Ment Defic Res; 1967 Mar; 11(1):12-22. PubMed ID: 6034523
    [No Abstract] [Full Text] [Related]

  • 5. [The Prader-Willi syndrome].
    Lydecken K.
    Duodecim; 1967 Mar; 83(22):1285-8. PubMed ID: 5594519
    [No Abstract] [Full Text] [Related]

  • 6. [Prader-Labhart-Willi syndrome diagnosed in a newborn].
    Ferenczy I, Péter J, Rixer G, Schaff Z.
    Orv Hetil; 1971 Jan 17; 112(3):137-40. PubMed ID: 5540532
    [No Abstract] [Full Text] [Related]

  • 7. [Clinical data on the Prader-Labhart-Willi syndrome. I. New aspects of bone and eye involvement].
    Fazekas A, Vígváry L, Nagy M, Bodnár L.
    Orv Hetil; 1971 Jul 18; 112(29):1687-90. PubMed ID: 5111511
    [No Abstract] [Full Text] [Related]

  • 8. [Prader-Labhardt-Willi syndrome].
    Bayart-Gennequin F, Poissonnier D, Farriaux JP, Fontaine G.
    Lille Med; 1970 Jul 18; 15(6):982-8. PubMed ID: 5454736
    [No Abstract] [Full Text] [Related]

  • 9. [H20 (hypotonia, hypomentia and obesity) syndrome].
    Ueda K, Sugawara S.
    Nihon Rinsho; 1969 May 18; 27(5):1510-1. PubMed ID: 5817515
    [No Abstract] [Full Text] [Related]

  • 10. [Prader-Willi-Labhardt syndrome in a girl with development of an insulinoprivic diabete].
    Battin J, Aubertin J, Alberty J, Fontan D.
    Bord Med; 1970 Oct 18; 3(10):2462. PubMed ID: 5480225
    [No Abstract] [Full Text] [Related]

  • 11. Hereditary deafness in man.
    Konigsmark BW.
    N Engl J Med; 1969 Oct 02; 281(14):774-8 contd. PubMed ID: 4185450
    [No Abstract] [Full Text] [Related]

  • 12. X-linked syndrome of congenital ichthyosis, hypogonadism, mental retardation and anosmia.
    Perrin JC, Idemoto JY, Sotos JF, Maurer WF, Steinberg AG.
    Birth Defects Orig Artic Ser; 1976 Oct 02; 12(5):267-74. PubMed ID: 182300
    [No Abstract] [Full Text] [Related]

  • 13. Hypogonadism in Prader-Willi syndrome.
    Wannarachue N, Ruvalcaba RH.
    Am J Ment Defic; 1975 Mar 02; 79(5):592-603. PubMed ID: 164772
    [Abstract] [Full Text] [Related]

  • 14. [Endocrine interrelations in diabetes mellitus in children].
    Barta L.
    Arch Kinderheilkd; 1969 May 02; 179(1):7-16. PubMed ID: 4240561
    [No Abstract] [Full Text] [Related]

  • 15. Forme fruste of the Prader-Willi syndrome (HHHO) and balanced D-E translocation.
    Schneider HJ, Zellweger H.
    Helv Paediatr Acta; 1968 Apr 02; 23(2):128-35. PubMed ID: 4387003
    [No Abstract] [Full Text] [Related]

  • 16. [Prader, Labhardt and Willi syndrome (study of 11 cases)].
    Gabilan JC, Royer P.
    Arch Fr Pediatr; 1968 Feb 02; 25(2):121-49. PubMed ID: 4386467
    [No Abstract] [Full Text] [Related]

  • 17. [Prader-Labhart-Willi syndrome. II. Neurologic implications].
    Gaál K.
    Orv Hetil; 1971 Aug 15; 112(33):1968-70. PubMed ID: 5166622
    [No Abstract] [Full Text] [Related]

  • 18. [Prader-Labhart-Wille-Fanconi syndrome].
    Schmuck L, Auerswald W, Oehlke W.
    Z Gesamte Inn Med; 1972 Jul 15; 27(14):627-30. PubMed ID: 5082878
    [No Abstract] [Full Text] [Related]

  • 19. [Report of case of Prader-Willi syndrome].
    Visco G, Ughi M, Trevenzoli G.
    Pediatr Med Chir; 1999 Jul 15; 21(3):149-50. PubMed ID: 10687166
    [Abstract] [Full Text] [Related]

  • 20. Hypogonadotropic hypogonadism, mental retardation, obesity and minor skeletal abnormalities: another new autosomal recessive syndrome from the Middle East.
    Teebi AS, Al-Awadi SA, Farag TI, Naguib KK.
    Am J Med Genet; 1986 Jun 15; 24(2):373-8. PubMed ID: 3717216
    [No Abstract] [Full Text] [Related]

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