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PUBMED FOR HANDHELDS

Journal Abstract Search

110 related items for PubMed ID: 5594519

  • 41. Bardet-Biedl syndrome.
    Keith CG.
    Aust J Ophthalmol; 1984 May; 12(2):143-8. PubMed ID: 6487184
    [Abstract] [Full Text] [Related]

  • 42. [Prader-Willi (H.H.H.O.) syndrome].
    Barta L, Sziklay L.
    Orv Hetil; 1970 Jul 19; 111(29):1710-1. PubMed ID: 5495296
    [No Abstract] [Full Text] [Related]

  • 43. Kleine-Levin syndrome in a boy with Prader-Willi syndrome.
    Gau SF, Soong WT, Liu HM, Hou JW, Tsai WY, Chiu YN, Yeh YC, Wang PJ, Wang TR.
    Sleep; 1996 Jan 19; 19(1):13-7. PubMed ID: 8650457
    [Abstract] [Full Text] [Related]

  • 44. 46 3q+ karyotype presenting as syndrome with obesity and hypogonadism.
    Raman PG, Shende A, Chakraborty D, Akolekar SS.
    J Assoc Physicians India; 2001 Apr 19; 49():481-4. PubMed ID: 11762626
    [No Abstract] [Full Text] [Related]

  • 45. Prader-Willi syndrome.
    Toledo-Pereyra LH, Valverde C, López-Amor E.
    Rev Invest Clin; 1970 Apr 19; 22(1):99-105. PubMed ID: 5513192
    [No Abstract] [Full Text] [Related]

  • 46. [Prader-Willi syndrome combined with Lobstein syndrome].
    Krajca K, Daniska J.
    Bratisl Lek Listy; 1973 Feb 19; 59(2):208-13. PubMed ID: 4689880
    [No Abstract] [Full Text] [Related]

  • 47. [Studies of palm and finger dermatoglyphics in the Prader-Labhardt-Willi syndrome].
    Dziuba P.
    Pediatr Pol; 1972 Jul 19; 47(7):879-82. PubMed ID: 5054577
    [No Abstract] [Full Text] [Related]

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  • 51. A new case of interstitial 6q16.2 deletion in a patient with Prader-Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity.
    Varela MC, Simões-Sato AY, Kim CA, Bertola DR, De Castro CI, Koiffmann CP.
    Eur J Med Genet; 2006 Jul 19; 49(4):298-305. PubMed ID: 16829351
    [Abstract] [Full Text] [Related]

  • 52. [Rud's syndrome].
    Predescu V, Christodorescu D, Alexianu M, Tudorache B, Ionescu R, Curelaru S, Constantinescu E.
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Neurol Psihiatr Neurochir; 1974 Jul 19; 19(5):421-7. PubMed ID: 4549650
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  • 54. [Prader Willi-like syndrome].
    Morgenstern H, Söltz-Szöts J.
    Z Haut Geschlechtskr; 1969 May 01; 44(9):Suppl:77-80. PubMed ID: 5793990
    [No Abstract] [Full Text] [Related]

  • 55. [Diagnosis and differential diagnosis of obesity in childhood].
    Crinò A, Greggio NA, Beccaria L, Schiaffini R, Pietrobelli A, Maffeis C.
    Minerva Pediatr; 2003 Oct 01; 55(5):461-70. PubMed ID: 14608269
    [Abstract] [Full Text] [Related]

  • 56. [Unusual forms of juvenile diabetes].
    Jean R, Bonnet H, Dumas R, Rieu D, Morel G.
    Arch Fr Pediatr; 1972 Nov 01; 29(9):957-64. PubMed ID: 4661883
    [No Abstract] [Full Text] [Related]

  • 57. [Chromosome abnormalities and child psychiatry].
    de Grouchy J.
    Rev Neuropsychiatr Infant; 1967 Nov 01; 15(4):263-73. PubMed ID: 5602320
    [No Abstract] [Full Text] [Related]

  • 58. The Prader-Willi syndrome with cardiorespiratory complications.
    Bianchine JW, Stambler AA, MacGregor MI.
    Birth Defects Orig Artic Ser; 1971 May 01; 7(6):301-2. PubMed ID: 5173184
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