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 *

127 related articles for article (PubMed ID: 2854163)

  • 1. 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]  

  • 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. 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; 8(3):295-9. PubMed ID: 308800
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. Direct evidence for a functional block in 18 oxidation in a patient with 17 alpha hydroxylase deficiency.
    Rovner DR; Gordon DL; Swisher SN
    Trans Assoc Am Physicians; 1978; 91():416-23. PubMed ID: 224555
    [No Abstract]   [Full Text] [Related]  

  • 7. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
    Holcombe JH; Keenan BS; Nichols BL; Kirkland RT; Clayton GW
    Pediatrics; 1980 Apr; 65(4):777-81. PubMed ID: 6966049
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [Primary amenorrhea and arterial hypertension in a case of 17 alpha-hydroxylase deficiency].
    Martin-Du Pan RC; Dahoun S; Stalberg A; Campana A
    J Gynecol Obstet Biol Reprod (Paris); 1994; 23(2):137-40. PubMed ID: 8040569
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Primary adrenal insufficiency with hypertension. A case report on partial primary adrenal insufficiency and partial 11-beta-hydroxylase deficiency.
    van Deijk WA; Blom PS; VD Vijver JC
    Neth J Med; 1979; 22(6):191-4. PubMed ID: 316501
    [No Abstract]   [Full Text] [Related]  

  • 11. [Deficiency of 17 alpha-hydroxylase. Presentation of 3 new cases].
    Gómez Sáez JM; Romero González R; Soler Ramón J; Bonnin Lafuenta R; Porta Martí M
    Med Clin (Barc); 1984 Mar; 82(9):407-9. PubMed ID: 6609291
    [No Abstract]   [Full Text] [Related]  

  • 12. A young woman with hypogonadism, hypertension and hypokalaemia.
    Toh VK; Yung CH
    Med J Malaysia; 2009 Sep; 64(3):242-3. PubMed ID: 20527279
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Partial deficiency of adrenal 11-hydroxylase. A possible cause of primary hypertension.
    de Simone G; Tommaselli AP; Rossi R; Valentino R; Lauria R; Scopacasa F; Lombardi G
    Hypertension; 1985; 7(2):204-10. PubMed ID: 2984117
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [A case of male pseudohermaphroditism due to 17 alpha-hydroxylase deficiency with high levels of plasma aldosterone and angiotensin II].
    Toyoda N; Murata K; Tanaka Y; Kawai Y; Yamamoto T; Nishiyama Y; Matsumoto T; Sugiyama Y
    Nihon Sanka Fujinka Gakkai Zasshi; 1986 Jul; 38(7):1162-5. PubMed ID: 3091739
    [No Abstract]   [Full Text] [Related]  

  • 16. 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]  

  • 17. Diagnosis and natural history of 17-hydroxylase deficiency in a newborn male.
    Dean HJ; Shackleton CH; Winter JS
    J Clin Endocrinol Metab; 1984 Sep; 59(3):513-20. PubMed ID: 6086702
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 17 alpha-hydroxylase deficiency: mineralocorticoid hormone profiles in an affected family.
    D'Armiento M; Reda G; Kater C; Shackleton CH; Biglieri EG
    J Clin Endocrinol Metab; 1983 Apr; 56(4):697-701. PubMed ID: 6300162
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.