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 *

68 related articles for article (PubMed ID: 948345)

  • 21. [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]  

  • 22. 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; 80(2):142-50. PubMed ID: 6984387
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Detection of heterozygote of 21-hydroxylase deficiency.
    Levine LS; Pang S; Dupont B; Pollack M; Lorenzen F; New MI
    Lancet; 1980 Mar; 1(8168 Pt 1):603-4. PubMed ID: 6102330
    [No Abstract]   [Full Text] [Related]  

  • 24. [Male pseudohermaphroditism caused by 17-alpha-hydroxylase deficiency. Personal case reports and a review of the literature].
    De Marinis L; Mancini A; Saporosi A; Calabrò F; Massari M; Moneta E; Menini E; Barbarino A
    Minerva Ginecol; 1989 Jul; 41(7):337-42. PubMed ID: 2691923
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Androgen metabolism in congenital adrenal hyperplasia due to 11 beta-hydroxylase deficiency.
    Frasier SD; Horton R; Ulstrom RA
    Pediatrics; 1969 Aug; 44(2):201-8. PubMed ID: 5806251
    [No Abstract]   [Full Text] [Related]  

  • 26. [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]  

  • 27. [Current concepts in the treatment of congenital adrenal hyperplasia caused by 21-hydroxylase deficiency].
    David M; Bertrand J; Kemlin I; François R
    Pediatrie; 1981 Mar; 36(2):161-6. PubMed ID: 6972030
    [No Abstract]   [Full Text] [Related]  

  • 28. [Clinical forms of congenital adrenal hyperplasia in the light of recent studies].
    Sendrail M; Gleizes L; Chkili T; Vassal D
    Maroc Med; 1971 Mar; 51(544):147-55. PubMed ID: 4934951
    [No Abstract]   [Full Text] [Related]  

  • 29. Steroid spectrum in human urine as revealed by gas chromatography. IV. Changes in the exception of 16-oxygenated neutral steroids by children with 21-hydroxylase deficiency during different stages of development.
    Kecskés L; Juricskay Z; Kosztoláni G; Szécsényi M
    Acta Biochim Biophys Acad Sci Hung; 1981; 16(1-2):57-75. PubMed ID: 6278806
    [No Abstract]   [Full Text] [Related]  

  • 30. [Male pseudohermaphroditism related to 17-alpha hydroxylase deficiency].
    Liotta A; Cammarata M; Corsello G; Ferrara D; Giuffrè L
    Pediatr Med Chir; 1987; 9(3):309-10. PubMed ID: 2823235
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Posterior fusion without clitoromegaly in a female with partial 21-hydroxylase deficiency.
    Wolff PB; Wilbois RP; Weldon VV; Haymond MW
    J Pediatr; 1977 Dec; 91(6):951-2. PubMed ID: 597374
    [No Abstract]   [Full Text] [Related]  

  • 32. Dynamics of adrenal steroidogenesis in childhood: changes in the excretion of 16-oxygenated- and 11-oxygenated-steroids by 21-hydroxylase deficient children at various ages.
    Kecskés L
    Endokrinologie; 1982 Oct; 80(2):151-7. PubMed ID: 6297879
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [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]  

  • 34. Late-onset type of 21-hydroxylase deficiency in childhood.
    Roitman A; Stivel M; Zamir R; Kaufman H; Pertzelan A; Laron Z
    Isr J Med Sci; 1982 Jul; 18(7):763-8. PubMed ID: 6980865
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [HLA and congenital genital adrenal syndrome caused by 21-hydroxylase deficiency].
    Colabucci F; Saraca S; Rossodivita A; Giordano P; Luciani G
    Minerva Pediatr; 1985 Sep; 37(18):696-7. PubMed ID: 3878454
    [No Abstract]   [Full Text] [Related]  

  • 36. [Hypoaldosteronism in twins. Probable 18-hydroxylase deficiency].
    Ravaussin JJ; de Martinville B; Lauras B; Chatelain P; Freycon F
    Pediatrie; 1977 Dec; 32(8):780-96. PubMed ID: 609505
    [No Abstract]   [Full Text] [Related]  

  • 37. Worldwide experience in newborn screening for classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Pang SY; Wallace MA; Hofman L; Thuline HC; Dorche C; Lyon IC; Dobbins RH; Kling S; Fujieda K; Suwa S
    Pediatrics; 1988 Jun; 81(6):866-74. PubMed ID: 3259306
    [TBL] [Abstract][Full Text] [Related]  

  • 38. [The deficiency of 17-hydroxylase: a cause of growth and puberty retardation in the girl. One case].
    Feit JP; David L; Patricot MC; Macabéo V; Lebacq E; François R
    Arch Fr Pediatr; 1978 Apr; 35(4):395-405. PubMed ID: 308359
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Late-onset 21-hydroxylase deficiency and polycystic ovary disease. A case report.
    Balkin MS; Altchek A
    J Reprod Med; 1986 Jun; 31(6):517-9. PubMed ID: 3488399
    [TBL] [Abstract][Full Text] [Related]  

  • 40. [Therapeutic problems in the adrenogenital syndrome caused by salt-losing 21-hydroxylase deficiency. Appearance of signs of corticoid overdosage at normally used doses].
    Iester A; Fasce L; Cambiaso P; Di Rocco M; Cordone G
    Minerva Pediatr; 1981 Apr; 33(8):367-73. PubMed ID: 6972480
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.