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 *

69 related articles for article (PubMed ID: 6980065)

  • 1. [A case of 17 alpha-hydroxylase deficiency with long stature and epileptic cramps (author's transl)].
    Ono Y
    Horumon To Rinsho; 1982 Apr; 30(4):353-7. PubMed ID: 6980065
    [No Abstract]   [Full Text] [Related]  

  • 2. [A case of 17 alpha-hydroxylase deficiency with bone anomalies (author's transl)].
    Itatsu T; Naitoh K; Matsuda N; Matsui N
    Nihon Naika Gakkai Zasshi; 1980 Aug; 69(8):960-6. PubMed ID: 6970788
    [No Abstract]   [Full Text] [Related]  

  • 3. [Short-term administration of dexamethasone in salt-losing 21-hydroxylase deficiency who showed sudden growth and pigmentation disorder under routine cortisol therapy].
    Kondo T; Ueda K; Horiuchi Y; Murakami T
    Horumon To Rinsho; 1983 Jun; 31 Suppl():116-8. PubMed ID: 6604596
    [No Abstract]   [Full Text] [Related]  

  • 4. Prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pang SY; Pollack MS; Marshall RN; Immken L
    N Engl J Med; 1990 Jan; 322(2):111-5. PubMed ID: 2403652
    [No Abstract]   [Full Text] [Related]  

  • 5. [Micro-filter paper method for 17 alpha-hydroxyprogesterone radioimmunoassay. Application for diagnosis of 21-hydroxylase deficiency (author's transl)].
    Shimozawa K; Tomita M; Nakagawa S; Saito Y; Sakurada N
    Horumon To Rinsho; 1979 Sep; 27(9):1048-53. PubMed ID: 316748
    [No Abstract]   [Full Text] [Related]  

  • 6. Comments about the need for prenatal treatment of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Migeon CJ
    J Clin Endocrinol Metab; 1990 Apr; 70(4):836-7. PubMed ID: 2318944
    [No Abstract]   [Full Text] [Related]  

  • 7. 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]  

  • 8. [Neglected congenital adrenogenital syndrome (AGS) in an adult. A case report (21-hydroxylase deficiency) with a summary of the current status of therapy with reference to adulthood].
    Mackenroth T
    Internist (Berl); 1986 Apr; 27(4):274-8. PubMed ID: 3519519
    [No Abstract]   [Full Text] [Related]  

  • 9. [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; 1981 Sep 18-25; 57(33-36):1392-7. PubMed ID: 6270798
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Congenital virilization in a newborn girl of a mother with adrenogenital syndrome due to 21-hydroxylase deficiency].
    Ferrante L
    Minerva Pediatr; 1976 Jun; 28(22):1443-4. PubMed ID: 986003
    [No Abstract]   [Full Text] [Related]  

  • 11. [A case of a simple virilizing form of 21-hydroxylase deficiency with schizophrenic symptoms, marked pigmentation and highly elevated plasma deoxycorticosterone].
    Suemaru S; Hashimoto K; Hattori T; Inoue H; Kageyama J; Ota Z
    Nihon Naika Gakkai Zasshi; 1987 Jan; 76(1):112-7. PubMed ID: 3033104
    [No Abstract]   [Full Text] [Related]  

  • 12. Growth and final height in classical and nonclassical 21-hydroxylase deficiency.
    New MI; Gertner JM; Speiser PW; del Balzo P
    Acta Paediatr Jpn; 1988; 30 Suppl():79-88. PubMed ID: 3146882
    [No Abstract]   [Full Text] [Related]  

  • 13. [Occurrence of severe striae in adolescents with congenital adrenal hyperplasia and 21-hydroxylation deficiency treated with dexamethasone].
    Guest G; Rappaport R; Philippe F; Thibaud E
    Arch Fr Pediatr; 1983; 40(6):453-6. PubMed ID: 6605132
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [Late diagnosis hyperandrogenism due to adrenal enzyme deficiency (author's transl)].
    Hazard J; Guilhaume B; Requeda E; Perlemuter L; Cenac A; Bernheim R
    Sem Hop; 1980 Dec 18-25; 56(47-68):1975-8. PubMed ID: 6256909
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. [Case of salt-losing congenital adrenal hyperplasia due to 21-hydroxylase deficiency and a short stature caused by early closure of epiphyseal lines in spite of steroid replacement therapy].
    Kondo T; Ueda K; Saito H; Horiuchi Y
    Horumon To Rinsho; 1983 Jul; 31(7):637-43. PubMed ID: 6605823
    [No Abstract]   [Full Text] [Related]  

  • 17. [Late discovery of female pseudo-hermaphroditism by complete blockade 21-hydroxylase (author's transl)].
    Heim J; Massart C; Lémée F; Amice-Chambon V
    Nouv Presse Med; 1981 Dec; 10(47):3841-3. PubMed ID: 6977130
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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; 44(8):637-40. PubMed ID: 2622705
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [17 alpha-hydroxylase deficiency].
    Kumagi R
    Nihon Rinsho; 1977; 35 Suppl 1():1096-7. PubMed ID: 306453
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 4.