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 *

150 related articles for article (PubMed ID: 2614011)

  • 1. Congenital adrenal hyperplasia due to combined 21- and 11 beta-hydroxylase deficiency.
    Penny R; Vecsei P
    J Endocrinol Invest; 1989 Nov; 12(10):723-8. PubMed ID: 2614011
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Extraadrenal steroid 21-hydroxylase activity in a woman with congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Winkel CA; Casey ML; Worley RJ; Madden JD; MacDonald PC
    J Clin Endocrinol Metab; 1983 Jan; 56(1):104-7. PubMed ID: 6600168
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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]  

  • 5. 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]  

  • 6. Increased plasma 21-deoxycorticosterone (21-DB) levels in late-onset adrenal 21-hydroxylase deficiency suggest a mild defect of the mineralocorticoid pathway.
    Fiet J; Gueux B; Raux-DeMay MC; Kuttenn F; Vexiau P; Brerault JL; Couillin P; Galons H; Villette JM; Julien R
    J Clin Endocrinol Metab; 1989 Mar; 68(3):542-7. PubMed ID: 2537337
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Apparent double defect in C11 beta and C21-steroid hydroxylation in congenital adrenal hyperplasia.
    Finkelstein M; Litvin Y; Mizrachi Y; Neiman G; Rösler A
    J Steroid Biochem; 1983 Jul; 19(1B):675-81. PubMed ID: 6310249
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Difficulties in the diagnosis of congenital adrenal hyperplasia in early infancy: the 11 beta-hydroxylase defect.
    Honour JW; Anderson JM; Shackleton CH
    Acta Endocrinol (Copenh); 1983 May; 103(1):101-9. PubMed ID: 6602444
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Hypertension in a neonate with 11 beta-hydroxylase deficiency.
    Mimouni M; Kaufman H; Roitman A; Morag C; Sadan N
    Eur J Pediatr; 1985 Jan; 143(3):231-3. PubMed ID: 3872797
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Serum 21-Deoxycortisol, 17-Hydroxyprogesterone, and 11-deoxycortisol in classic congenital adrenal hyperplasia: clinical and hormonal correlations and identification of patients with 11beta-hydroxylase deficiency among a large group with alleged 21-hydroxylase deficiency.
    Tonetto-Fernandes V; Lemos-Marini SH; Kuperman H; Ribeiro-Neto LM; Verreschi IT; Kater CE
    J Clin Endocrinol Metab; 2006 Jun; 91(6):2179-84. PubMed ID: 16551734
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Sex reassignment in a girl with 11 beta-hydroxylase deficiency.
    Bistritzer T; Sack J; Eshkol A; Zur H; Katznelson D
    Isr J Med Sci; 1984 Jan; 20(1):55-8. PubMed ID: 6607909
    [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. Salt loss in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Hochberg Z; Benderly A; Zadik Z
    Arch Dis Child; 1984 Nov; 59(11):1092-4. PubMed ID: 6334497
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Serum 17-hydroxypregnenolone and 17-hydroxypregnenolone sulfate concentrations in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Shimozawa K; Saisho S; Yata J; Kambegawa A
    Endocrinol Jpn; 1988 Feb; 35(1):11-8. PubMed ID: 3260857
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Bilateral testicular hypertrophy and congenital adrenal hyperplasia caused by 11-beta-hydroxylase deficiency].
    Khaldi F; Bennaceur B; Hamza M; Boudina T; Jafoura H; Hamza B
    Arch Fr Pediatr; 1987; 44(7):513-6. PubMed ID: 3501279
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Characterization of zona glomerulosa function in patients with classic and non-classic forms of congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Castro-Magana M; Angulo M; Canas JA; Mazur B; Sarrantonio M; Vitollo P; Palekar A; Fuentes B; Lee A
    J Pediatr Endocrinol Metab; 1995; 8(1):19-25. PubMed ID: 7584692
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. A case of congenital adrenal hyperplasia with concomitant abnormalities of steroid 21- and 11 beta-hydroxylase activities.
    Egusa G; Mori H; Yamane K; Okamura M; Oda K; Ishida S; Kado S; Hara H; Yamakido M
    Hiroshima J Med Sci; 1990 Dec; 39(4):145-7. PubMed ID: 2086566
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.