These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


102 related items for PubMed ID: 917571

  • 1. Hypergonadotrophic male pseudohermaphroditism due to complete 17-alpha-hyroxylase deficiency.
    Waldhäusl WK, Herkner K, Bratusch-Marrain P, Haydl H, Nowotny P.
    Padiatr Padol Suppl; 1977; (5):103-7. PubMed ID: 917571
    [Abstract] [Full Text] [Related]

  • 2. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    Yanase E, Nagai T, Kato M, Morimoto S.
    Jpn J Med; 1982 Apr; 21(2):128-34. PubMed ID: 6750188
    [Abstract] [Full Text] [Related]

  • 3. Male pseudohermaphroditism due to 17-hydroxylase deficiency.
    D'Alberton A, Reschini E, Motta T, Catania A.
    J Endocrinol Invest; 1989 Mar; 12(3):193-6. PubMed ID: 2786019
    [Abstract] [Full Text] [Related]

  • 4. Combined 17 alpha- and 18-hydroxylase deficiency associated with complete male pseudohermaphroditism and hypoaldosteronism.
    Waldhäusl W, Herkner K, Nowotny P, Bratusch-Marrain P.
    J Clin Endocrinol Metab; 1978 Feb; 46(2):236-46. PubMed ID: 312294
    [Abstract] [Full Text] [Related]

  • 5. Male pseudohermaphroditism due to multiple defects in steroid-biosynthetic microsomal mixed-function oxidases. A new variant of congenital adrenal hyperplasia.
    Peterson RE, Imperato-McGinley J, Gautier T, Shackleton C.
    N Engl J Med; 1985 Nov 07; 313(19):1182-91. PubMed ID: 2932643
    [Abstract] [Full Text] [Related]

  • 6. Male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency.
    New MI.
    J Clin Invest; 1970 Oct 07; 49(10):1930-41. PubMed ID: 5456802
    [Abstract] [Full Text] [Related]

  • 7. Female pseudohermaphroditism caused by maternal congenital adrenal hyperplasia.
    Kai H, Nose O, Iida Y, Ono J, Harada T, Yabuuchi H.
    J Pediatr; 1979 Sep 07; 95(3):418-20. PubMed ID: 469669
    [No Abstract] [Full Text] [Related]

  • 8. An autopsy case of 17 alpha-hydroxylase deficiency with malignant hypertension.
    Morimoto I, Maeda R, Izumi M, Ishimaru T, Nishimori I, Nagataki S.
    J Clin Endocrinol Metab; 1983 May 07; 56(5):915-9. PubMed ID: 6300176
    [Abstract] [Full Text] [Related]

  • 9. [Congenital adrenal hyperplasia].
    Stanić M, Nesović M.
    Med Pregl; 1999 May 07; 52(11-12):447-54. PubMed ID: 10748766
    [Abstract] [Full Text] [Related]

  • 10. Female phenotype in a male child due to 17-alpha-hydroxylase deficiency.
    Heremans GF, Moolenaar AJ, van Gelderen HH.
    Arch Dis Child; 1976 Sep 07; 51(9):721-3. PubMed ID: 999330
    [Abstract] [Full Text] [Related]

  • 11. Gynaecomastia in two prepubertal boys with congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency.
    Zadik Z, Pertzelan A, Kaufman H, Levin S, Laron Z.
    Helv Paediatr Acta; 1979 May 07; 34(2):185-7. PubMed ID: 457432
    [Abstract] [Full Text] [Related]

  • 12. Hypokalaemic paresis, hypertension, alkalosis and adrenal-dependent hyperadrenocorticism in a dog.
    Davies DR, Foster SF, Hopper BJ, Staudte KL, O'Hara AJ, Irwin PJ.
    Aust Vet J; 2008 Apr 07; 86(4):139-46. PubMed ID: 18363988
    [Abstract] [Full Text] [Related]

  • 13. Case report: 17 alpha-hydroxylase/17,20-lyase deficiency: a rare cause of endocrine hypertension.
    Hermans C, de Plaen JF, de Nayer P, Maiter D.
    Am J Med Sci; 1996 Sep 07; 312(3):126-9. PubMed ID: 8783679
    [Abstract] [Full Text] [Related]

  • 14. [A case of female pseudohermaphroditism caused by adrenal deficiency in 21-hydroxylase and 11-hydroxylase].
    ERNOULD HJ, TALMAS V, DECAMPS G.
    Rev Med Liege; 1961 Nov 15; 16():645-54. PubMed ID: 13890647
    [No Abstract] [Full Text] [Related]

  • 15. 19-Nor-corticosteroids in health, in hypertensive states in humans including 17 alpha-hydroxylase deficiency and in the spontaneously hypertensive rat (SHR).
    Melby JC, Dale SL, Holbrook M, Wilson TE, Griffing GT, Arison BH.
    Endocr Res; 1961 Nov 15; 10(3-4):591-607. PubMed ID: 6336061
    [Abstract] [Full Text] [Related]

  • 16. [Male pseudohermaphroditism caused by enzymatic deficiency of 17-alpha-hydroxylase. 1st case reported in Puerto Rico].
    Rosado A, Alegre M, Colón G.
    Bol Asoc Med P R; 1997 Nov 15; 89(10-12):197-9. PubMed ID: 9577056
    [Abstract] [Full Text] [Related]

  • 17. Psychosis in a male pseudohermaphrodite with 17-hydroxylase deficiency.
    Soundy TJ, Black JL, Peterson GC, Zimmerman D.
    Psychosomatics; 1992 Nov 15; 33(4):452-4. PubMed ID: 1461971
    [No Abstract] [Full Text] [Related]

  • 18. [The deficiency of 17-hydroxylase: a cause of growth and puberty retardation in the girl. One case].
    Feit JP, David L, Patricot MC, Macabéo V, Lebacq E, François R.
    Arch Fr Pediatr; 1978 Apr 15; 35(4):395-405. PubMed ID: 308359
    [Abstract] [Full Text] [Related]

  • 19. Male pseudohermaphroditism due to steroid 5-alpha-reductase deficiency.
    Peterson RE, Imperato-McGinley J, Gautier T, Sturla E.
    Am J Med; 1977 Feb 15; 62(2):170-91. PubMed ID: 835597
    [Abstract] [Full Text] [Related]

  • 20. Male pseudohermaphroditism with hypertension due to a 17alpha-hydroxylation deficiency.
    Tourniaire J, Audi-Parera L, Loras B, Blum J, Castelnovo P, Forest MG.
    Clin Endocrinol (Oxf); 1976 Jan 15; 5(1):53-61. PubMed ID: 174842
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 6.