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Journal Abstract Search

103 related items for PubMed ID: 6609291

  • 21. A case of 17 alpha-hydroxylase deficiency syndrome associated with right adrenal tumor.
    Ogawa K, Hara A, Tanabe S, Tamori S, Yoshida H, Pak CH, Matsunaga M, Kawai C, Dodo H, Tanimura H.
    Clin Exp Hypertens A; 1984; 6(4):863-77. PubMed ID: 6609788
    [Abstract] [Full Text] [Related]

  • 22. Pubertal delay, hypokalemia, and hypertension caused by a rare form of congenital adrenal hyperplasia.
    Olson CA, Crudo DF.
    J Pediatr Adolesc Gynecol; 2011 Apr; 24(2):e29-31. PubMed ID: 21190871
    [Abstract] [Full Text] [Related]

  • 23. [Virilization caused by 21-hydroxylase deficiency and axillary sweat gland hyperplasia].
    Jourdain JC, Le Lorier B, Mourier C, Ploussard JP, Roussel F.
    Ann Dermatol Venereol; 1988 Apr; 115(11):1136-8. PubMed ID: 3266452
    [No Abstract] [Full Text] [Related]

  • 24. [Congenital adrenal hyperplasia as a result of 21-hydroxylase block. Review of 10 cases].
    Belhadj H, Ezzaouia G, Chammakhi S, Bouguerra R, Boukhris R.
    Tunis Med; 1986 Mar; 64(3):243-8. PubMed ID: 3490029
    [No Abstract] [Full Text] [Related]

  • 25. Late-onset 21-hydroxylase deficiency and polycystic ovary disease. A case report.
    Balkin MS, Altchek A.
    J Reprod Med; 1986 Jun; 31(6):517-9. PubMed ID: 3488399
    [Abstract] [Full Text] [Related]

  • 26. [Current concepts in the treatment of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    David M, Bertrand J, Kemlin I, François R.
    Pediatrie; 1981 Mar; 36(2):161-6. PubMed ID: 6972030
    [No Abstract] [Full Text] [Related]

  • 27. Combined 17 alpha-hydroxylase/17,20-lyase deficiency due to a stop codon in the N-terminal region of 17 alpha-hydroxylase cytochrome P-450.
    Yanase T, Kagimoto M, Matsui N, Simpson ER, Waterman MR.
    Mol Cell Endocrinol; 1988 Oct; 59(3):249-53. PubMed ID: 3263289
    [Abstract] [Full Text] [Related]

  • 28. [Research on hirsutism. Apropos of a case of partial 21-hydroxylase deficiency].
    Gheron G.
    Nouv Presse Med; 1981 Oct 24; 10(38):3163. PubMed ID: 6974855
    [No Abstract] [Full Text] [Related]

  • 29. Masculinizing operation for a female patient with congenital adrenocortical hyperplasia due to 21-hydroxylase deficiency.
    Okuyama A, Takiuchi H, Kajikawa H, Tada Y, Namiki M, Nakano E, Takaha M.
    Hinyokika Kiyo; 1985 Nov 24; 31(11):2003-5. PubMed ID: 3879104
    [Abstract] [Full Text] [Related]

  • 30. Steroid 11beta- hydroxylase deficiency congenital adrenal hyperplasia.
    Nimkarn S, New MI.
    Trends Endocrinol Metab; 2008 Apr 24; 19(3):96-9. PubMed ID: 18294861
    [Abstract] [Full Text] [Related]

  • 31. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F, Raffoux C, Gilgenkrantz S, Janot C, Streiff F, Pierson M.
    J Genet Hum; 1981 Mar 24; 29(1):103-13. PubMed ID: 6977617
    [No Abstract] [Full Text] [Related]

  • 32. A genetic male patient with 17 alpha-hydroxylase deficiency.
    Jones HW, Lee PA, Rock JA, Archer DF, Migeon CJ.
    Obstet Gynecol; 1982 Feb 24; 59(2):254-9. PubMed ID: 6979016
    [Abstract] [Full Text] [Related]

  • 33. [Aldosterone precursors and hypertension with hypokalemia and adrenal module non caused by primary hyperaldosteronism].
    Chamontin B, Blanchouin-Emeric N, Amar J, Khatibi F, Vernier I, Bennet A, Aupetit-Faisant B, Salvador M.
    Arch Mal Coeur Vaiss; 1996 Aug 24; 89(8):1055-8. PubMed ID: 8949378
    [Abstract] [Full Text] [Related]

  • 34. Hypokalemic myopathy associated with 17 alpha-hydroxylase deficiency: a case report.
    Yazaki K, Kuribayashi T, Yamamura Y, Kurihara T, Araki S.
    Neurology; 1982 Jan 24; 32(1):94-7. PubMed ID: 6976525
    [Abstract] [Full Text] [Related]

  • 35. [Report on 3 cases of 17 alpha-hydroxylase deficiency].
    Zhang ZJ.
    Zhonghua Nei Ke Za Zhi; 1983 Sep 24; 22(9):565-7. PubMed ID: 6606541
    [No Abstract] [Full Text] [Related]

  • 36. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency: diagnosis by gas chromatography--mass spectrometry.
    Burstein P, Marsh P, Fennessey P, Betz G.
    Obstet Gynecol; 1983 Mar 24; 61(3 Suppl):63S-68S. PubMed ID: 6296744
    [Abstract] [Full Text] [Related]

  • 37. [Cases of late onset and latent steroid-21-hydroxylase defect].
    Sólyom J, Kürti K.
    Orv Hetil; 1984 Jun 03; 125(23):1377-80, 83. PubMed ID: 6611530
    [No Abstract] [Full Text] [Related]

  • 38. Hypertension due to 17alpha-hydroxylase deficiency.
    Wang C, Yeung RT, Coghlan JP, Oddie CJ, Scoggins BA, Stockigt JR.
    Aust N Z J Med; 1978 Jun 03; 8(3):295-9. PubMed ID: 308800
    [Abstract] [Full Text] [Related]

  • 39. Clinical variability of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Rösler A, Leiberman E, Sack J, Landau H, Benderly A, Moses SW, Cohen T.
    Horm Res; 1982 Jun 03; 16(3):133-41. PubMed ID: 7049883
    [Abstract] [Full Text] [Related]

  • 40. [A case of 17 alpha-hydroxylase deficiency with long stature and epileptic cramps (author's transl)].
    Ono Y.
    Horumon To Rinsho; 1982 Apr 03; 30(4):353-7. PubMed ID: 6980065
    [No Abstract] [Full Text] [Related]

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