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Journal Abstract Search

122 related items for PubMed ID: 1909490

  • 1. 46,XX gonadal dysgenesis with epibulbar dermoid.
    Quayle SA, Copeland KC.
    Am J Med Genet; 1991 Jul 01; 40(1):75-6. PubMed ID: 1909490
    [Abstract] [Full Text] [Related]

  • 2. Familial 46,XX gonadal dysgenesis.
    Portuondo JA, Neyro JL, Benito JA, de los Rios A, Barral A.
    Int J Fertil; 1987 Jul 01; 32(1):56-8. PubMed ID: 2880817
    [Abstract] [Full Text] [Related]

  • 3. 46,XX gonadal absence: a variant of the XX pure gonadal dysgenesis?
    Medina M, Kofman-Alfaro S, Pérez-Palacios G.
    Acta Endocrinol (Copenh); 1982 Apr 01; 99(4):585-7. PubMed ID: 6803492
    [Abstract] [Full Text] [Related]

  • 4. [The coincidence of gonadal dysgenesis and hyperprolactinemia].
    Rudolf K, Kunkel S, Smid I, Bazsa-Kassai Z.
    Zentralbl Gynakol; 1985 Apr 01; 107(14):889-93. PubMed ID: 3929498
    [Abstract] [Full Text] [Related]

  • 5. Management of phenotypic female patients with an XY karyotype.
    Portuondo JA, Neyro JL, Barral A, Gonzalez-Gorospe F, Benito JA.
    J Reprod Med; 1986 Jul 01; 31(7):611-5. PubMed ID: 3091820
    [Abstract] [Full Text] [Related]

  • 6. [The development of gonadotropic function in children with gonadal disorders].
    Lisá L, Dvorák P, Zizkovský V.
    Cesk Pediatr; 1987 Aug 01; 42(8):460-3. PubMed ID: 3117382
    [No Abstract] [Full Text] [Related]

  • 7. 46,XX gonadal dysgenesis, short stature, and recurrent metabolic acidosis in two sisters.
    Hisama FM, Zemel S, Cherniske EM, Vladutiu GD, Pober BR.
    Am J Med Genet; 2001 Jan 15; 98(2):121-4. PubMed ID: 11223846
    [Abstract] [Full Text] [Related]

  • 8. [Gonadal dysgenesis associated with gonadotropin and growth hormone deficiencies].
    Calle Fernández JR, Rubio Herrera MA, Gómez Pérez M, Herráiz Martínez MA, Faus Díaz JL.
    Rev Clin Esp; 1987 May 15; 180(8):435-7. PubMed ID: 3112873
    [No Abstract] [Full Text] [Related]

  • 9. Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of Malouf syndrome.
    Narahara K, Kamada M, Takahashi Y, Tsuji K, Yokoyama Y, Ninomiya S, Seino Y.
    Am J Med Genet; 1992 Oct 01; 44(3):369-73. PubMed ID: 1488988
    [Abstract] [Full Text] [Related]

  • 10. Plasma glycoprotein hormone alpha-subunit in the syndrome of gonadal dysgenesis: the effect of estrogen replacement in hypergonadotropic hypogonadism.
    Styne DM, Conte FA, Grumbach MM, Kaplan SL.
    J Clin Endocrinol Metab; 1980 Jun 01; 50(6):1049-52. PubMed ID: 6246142
    [No Abstract] [Full Text] [Related]

  • 11. [Diagnostic principles of gonadal dysgenesis in adolescents].
    Chipashvili MK, Kristesashvili DI, Chopikashvili NA, Kopaliani NSh.
    Georgian Med News; 2005 Nov 01; (128):24-8. PubMed ID: 16369057
    [Abstract] [Full Text] [Related]

  • 12. Familial ovarian dysgenesis in 46,XX females.
    Vesely DL, Bower RH, Kohler PO, Char F.
    Am J Med Sci; 1980 Nov 01; 280(3):157-66. PubMed ID: 6779629
    [Abstract] [Full Text] [Related]

  • 13. [Comparison of hormonal levels of LH and FSH with cytogenetic findings in patients with gonadal dysgenesis].
    Santavý J, Fingerová H, Knopová V, Fargasová I, Zenísek L.
    Bratisl Lek Listy; 1985 May 01; 83(5):485-92. PubMed ID: 3928097
    [No Abstract] [Full Text] [Related]

  • 14. Menstrual function and hirsutism in patients with gonadal dysgenesis.
    Rosen GF, Kaplan B, Lobo RA.
    Obstet Gynecol; 1988 May 01; 71(5):677-80. PubMed ID: 3128750
    [Abstract] [Full Text] [Related]

  • 15. [Clinical and hormonal studies in a male with karyotype 46,XX].
    Kumanow P, Beraha L.
    Andrologia; 1983 May 01; 15(5):426-30. PubMed ID: 6418027
    [Abstract] [Full Text] [Related]

  • 16. [Familial streak gonad syndrome with 46,XX karyotype (pure gonadal dysgenesis)].
    Tóth A, Gaál M, Bösze P, Komora V, László J.
    Orv Hetil; 1985 Mar 03; 126(9):527-9. PubMed ID: 3991192
    [No Abstract] [Full Text] [Related]

  • 17. Thyrotrophin and prolactin responses to thyrotrophin-releasing hormone in patients with streak gonad syndrome.
    Bösze P, Kóvacs Z, Egyed J, László J, Szilágyi G.
    Acta Endocrinol (Copenh); 1983 Feb 03; 102(2):179-84. PubMed ID: 6402863
    [Abstract] [Full Text] [Related]

  • 18. Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data.
    Simpson JL, Christakos AC, Horwith M, Silverman FS.
    Birth Defects Orig Artic Ser; 1971 May 03; 7(6):215-28. PubMed ID: 5173165
    [Abstract] [Full Text] [Related]

  • 19. Pure XX gonadal dysgenesis in identical twins.
    Youlton R, Michelsen H, Be C, Cruz-Coke R.
    Clin Genet; 1982 Apr 03; 21(4):262-5. PubMed ID: 6809371
    [Abstract] [Full Text] [Related]

  • 20. 46,XX pure gonadal dysgenesis with growth hormone deficiency and impaired 3 beta-hydroxysteroid dehydrogenase activity.
    Sills IN, Rapaport R, Skuza KA, Horlick MN.
    Am J Med Genet; 1992 Jan 01; 42(1):100-3. PubMed ID: 1339198
    [Abstract] [Full Text] [Related]

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