127 related items for PubMed ID: 6607909
1. 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
[Abstract] [Full Text] [Related]
2. [Causes of ambiguous external genitalia in neonates].
Zdravković D, Milenković T, Sedlecki K, Guć-Sćekić M, Rajić V, Banićević M.
Srp Arh Celok Lek; 2001 Jan; 129(3-4):57-60. PubMed ID: 11534268
[Abstract] [Full Text] [Related]
3. 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]
4. Neonatal salt loss in the hypertensive form of congenital adrenal hyperplasia.
Holcombe JH, Keenan BS, Nichols BL, Kirkland RT, Clayton GW.
Pediatrics; 1980 Apr 07; 65(4):777-81. PubMed ID: 6966049
[Abstract] [Full Text] [Related]
5. [Familial congenital adrenal hyperplasia caused by 11 beta-hydroxylase. Failure of prevention of sexual ambiguity and prenatal diagnosis].
Bouchard M, Forest MG, David M, Dechaud H, Juif JG.
Pediatrie; 1989 Apr 07; 44(8):637-40. PubMed ID: 2622705
[Abstract] [Full Text] [Related]
6. [Congenital virilizing adrenal hyperplasia due to 11 beta-hydroxylase deficiency. Study of eleven cases (author's transl)].
Dunand A, Roger M, Chaussain JL, Nocton F, Job JC.
Sem Hop; 1989 Apr 07; 57(33-36):1392-7. PubMed ID: 6270798
[Abstract] [Full Text] [Related]
7. [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 07; 81 Spec No():93-5. PubMed ID: 3142437
[Abstract] [Full Text] [Related]
8. [Medroxyprogesterone acetate. Contributive treatment in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in children].
La Selve H, Sempé M, Morel Y, Forest MG, de Peretti E, David M.
Arch Fr Pediatr; 1985 Jun 07; 42(7):511-6. PubMed ID: 2935112
[Abstract] [Full Text] [Related]
9. [A case of congenital adrenogenital syndrome].
Sumiya H, Kawamura K, Kataumi Z, Fuse H, Ito H, Shimazaki J.
Hinyokika Kiyo; 1985 Aug 07; 31(8):1433-9. PubMed ID: 3878668
[Abstract] [Full Text] [Related]
10. 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 07; 31(11):2003-5. PubMed ID: 3879104
[Abstract] [Full Text] [Related]
11. Obesity among children and adolescents with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Völkl TM, Simm D, Beier C, Dörr HG.
Pediatrics; 2006 Jan 07; 117(1):e98-105. PubMed ID: 16396852
[Abstract] [Full Text] [Related]
12. Occurrence of male phenotype in genotypic females with congenital virilizing adrenal hyperplasia.
Chan-Cua S, Freidenberg G, Jones KL.
Am J Med Genet; 1989 Nov 07; 34(3):406-12. PubMed ID: 2574534
[Abstract] [Full Text] [Related]
13. Early diagnosis of 11 beta-hydroxylase deficiency in two siblings confirmed by analysis of a novel steroid metabolite in newborn urine.
Hughes IA, Arisaka O, Perry LA, Honour JW.
Acta Endocrinol (Copenh); 1986 Mar 07; 111(3):349-54. PubMed ID: 3515819
[Abstract] [Full Text] [Related]
14. Steroid responsive hypertension secondary to 11-beta hydroxylase deficiency--a case report.
Isiavwe AR, Ekpebegh CO, Fasanmade OA, Ohwovoriole AE.
West Afr J Med; 2008 Jul 07; 27(3):182-5. PubMed ID: 19256327
[Abstract] [Full Text] [Related]
15. 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 07; 63(1):36-40. PubMed ID: 3011843
[Abstract] [Full Text] [Related]
16. Hypertension in a neonate with 11 beta-hydroxylase deficiency.
Mimouni M, Kaufman H, Roitman A, Morag C, Sadan N.
Eur J Pediatr; 1985 Jan 07; 143(3):231-3. PubMed ID: 3872797
[Abstract] [Full Text] [Related]
17. [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 20; 62(8):843-56. PubMed ID: 3491009
[Abstract] [Full Text] [Related]
18. Amniotic fluid levels of 17 alpha-hydroxyprogesterone during human pregnancy: pre-natal diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Wurster KG, Ranke MB, Heilbronner H, Gupta D.
Endokrinologie; 1982 Oct 20; 80(2):142-50. PubMed ID: 6984387
[Abstract] [Full Text] [Related]
19. Prenatal treatment of congenital adrenal hyperplasia resulting from 21-hydroxylase deficiency.
David M, Forest MG.
J Pediatr; 1984 Nov 20; 105(5):799-803. PubMed ID: 6334149
[Abstract] [Full Text] [Related]
20. [Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].
Liotta A, Cammarata M, Corsello G, Ferrara D, Giuffrè L.
Pediatr Med Chir; 1987 Nov 20; 9(3):309-10. PubMed ID: 2823235
[Abstract] [Full Text] [Related]
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