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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

160 related articles for article (PubMed ID: 6300176)

  • 1. 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; 56(5):915-9. PubMed ID: 6300176
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Malignant arterial hypertension disclosing late congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency].
    Ribstein J; Sciolla JP; Barjon P; Sultan C; Forest M; de Peretti E
    Arch Mal Coeur Vaiss; 1988 Jun; 81 Spec No():93-5. PubMed ID: 3142437
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 313(19):1182-91. PubMed ID: 2932643
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 6. New studies of the 11 beta-hydroxylase and 18-hydroxylase enzymes in the hypertensive form of congenital adrenal hyperplasia.
    Levine LS; Rauh W; Gottesdiener K; Chow D; Gunczler P; Rapaport R; Pang S; Schneider B; New MI
    J Clin Endocrinol Metab; 1980 Feb; 50(2):258-63. PubMed ID: 6243663
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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; 5(1):53-61. PubMed ID: 174842
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Control of aldosterone in 17 alpha-hydroxylase deficiency.
    Saruta T; Kondo K; Saito I; Nagahama S; Suzuki H; Konishi K; Matsuki S
    Horm Res; 1980; 13(2):98-108. PubMed ID: 6262207
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency and hormonal profiles in the nuclear family.
    Rohmer V; Barbot N; Bertrand P; Nahoul K; Bigorgne JC; Forest MG
    J Clin Endocrinol Metab; 1990 Aug; 71(2):523-9. PubMed ID: 2166072
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Combined 21- and 11 beta-hydroxylase deficiency in familial congenital adrenal hyperplasia.
    Hurwitz A; Brautbar C; Milwidsky A; Vecsei P; Milewicz A; Navot D; Rösler A
    J Clin Endocrinol Metab; 1985 Apr; 60(4):631-8. PubMed ID: 2982904
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Two cases of 17 alpha-hydroxylase deficiency--one combined with complete gonadal agenesis.
    Tvedegaard E; Frederiksen V; Olgaard K; Nielsen MD; Starup J
    Acta Endocrinol (Copenh); 1981 Oct; 98(2):267-73. PubMed ID: 6270940
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Requirement of mineralocorticoid in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Hochberg Z; Benderly A; Kahana L; Zadik Z
    J Clin Endocrinol Metab; 1986 Jul; 63(1):36-40. PubMed ID: 3011843
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 14. A new variant of 17 alpha-hydroxylase deficiency with hyperaldosteronism in two Japanese sisters.
    Monno S; Takasu N
    Endocrinol Jpn; 1989 Apr; 36(2):315-23. PubMed ID: 2550210
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [A case of 21-hydroxylase deficiency and Bartter's syndrome associated with a balanced 6-9 translocation].
    Yabe R; Mizuno K; Ojima M; Ogawa S; Hashimoto S; Kunii N; Kishino K; Tani M; Niimura S; Watari H
    Nihon Naibunpi Gakkai Zasshi; 1986 Aug; 62(8):843-56. PubMed ID: 3491009
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 17 alpha-hydroxylase deficiency syndrome associated with bilateral streak gonads and impaired development of Müllerian ducts derivatives. Report of a case.
    de Gennes JL; Jambart S; Turpin G; Elkik F; Roger M
    Acta Endocrinol (Copenh); 1982 May; 100(1):68-76. PubMed ID: 6287777
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Dexamethasone-suppressible hypercorticosteronism in two 46,XX subjects with ambiguous genitalia and ovarian cysts. Partial defect of 17 alpha-hydroxylase or 17-20-desmolase.
    Roger M; Merceron RE; Girard F; Canlorbe P; Dehennin L; Konopka P; Seneze J; Toublanc JE
    Horm Res; 1982; 16(1):23-31. PubMed ID: 6279481
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe hypertension with absent secondary sex characteristics due to partial deficiency of steroid 17 alpha-hydroxylase activity.
    Fraser R; Brown JJ; Mason PA; Morton JJ; Lever AF; Robertson JI; Lee HA; Miller H
    J Hum Hypertens; 1987 Jun; 1(1):53-8. PubMed ID: 2854163
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Hypokalemic crisis simulating intestinal obstruction in a 4-year-old girl. A consequence of 17alpha-hydroxylase deficiency.
    Preeyasombat C; Pitchayayothin N; Viravekin A
    Am J Dis Child; 1976 Oct; 130(10):1143-5. PubMed ID: 973620
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.