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 *

128 related articles for article (PubMed ID: 30591325)

  • 21. [Steroid 21-hydroxylase deficiencies and female infertility: pathophysiology and management].
    Robin G; Decanter C; Baffet H; Catteau-Jonard S; Dewailly D
    Gynecol Obstet Fertil; 2014 Jun; 42(6):422-8. PubMed ID: 24852906
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Late diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Müssig K; Kaltenbach S; Maser-Gluth C; Hartmann MF; Wudy SA; Horger M; Gallwitz B; Raue F; Häring HU; Schulze E
    Exp Clin Endocrinol Diabetes; 2006 Apr; 114(4):208-14. PubMed ID: 16705555
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Late diagnoses of 21-hydroxylase deficiencies in children (after the age of 3 years].
    Carel JC; Marrakchi Z; Roger M; Morel Y; Chaussain JL
    Ann Pediatr (Paris); 1993 Sep; 40(7):410-20. PubMed ID: 8239392
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Adrenocortical incidentaloma with uncertain prognosis associated with an inadequately treated congenital adrenal hyperplasia.
    Chevalier N; Carrier P; Piche M; Chevallier A; Wagner K; Tardy V; Benchimol D; Fénichel P
    Ann Endocrinol (Paris); 2010 Feb; 71(1):56-9. PubMed ID: 19942208
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Congenital adrenal hyperplasia apropos of 7 cases at the University Hospital Center of Dakar].
    Fall M; Sarr M; Sy HS; Ba M; Ould Cheikh A; Diack Mbaye A; Diouf S; Diagne I
    Dakar Med; 1989; 34(1-4):58-63. PubMed ID: 2491387
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Unusual phenotype of congenital adrenal hyperplasia (CAH) with a novel mutation of the CYP21A2 gene.
    Raisingani M; Contreras MF; Prasad K; Pappas JG; Kluge ML; Shah B; David R
    J Pediatr Endocrinol Metab; 2016 Jul; 29(7):867-71. PubMed ID: 27180336
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Adrenogenital syndrome with 21-hydroxylase deficiency].
    Dörr HG; Sippell WG
    Monatsschr Kinderheilkd; 1993 Jul; 141(7):609-21. PubMed ID: 8413342
    [No Abstract]   [Full Text] [Related]  

  • 28. A Case Report of Adrenocortical Adenoma Mimicking Congenital Adrenal Hyperplasia in a Young Girl.
    Sheng Q; Lv Z; Xu W; Liu J; Wu Y; Xi Z
    Medicine (Baltimore); 2015 Jun; 94(25):e1046. PubMed ID: 26107677
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Clinical and hormonal characteristics in heterozygote carriers of congenital adrenal hyperplasia.
    Guarnotta V; Niceta M; Bono M; Marchese S; Fabiano C; Indelicato S; Di Gaudio F; Garofalo P; Giordano C
    J Steroid Biochem Mol Biol; 2020 Apr; 198():105554. PubMed ID: 31805392
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Congenital adrenal hyperplasia owing to 21-hydroxylase deficiency presenting with erythrocytosis].
    Ramos I; Regadera A; Román P; Ezquieta B
    Med Clin (Barc); 2008 Nov; 131(16):638-9. PubMed ID: 19080859
    [No Abstract]   [Full Text] [Related]  

  • 31. Giant adrenal myelolipoma associated with 21-hydroxylase deficiency: unusual association mimicking an androgen-secreting adrenocortical carcinoma.
    Mermejo LM; Elias Junior J; Saggioro FP; Tucci Junior S; Castro Md; Moreira AC; Elias PC
    Arq Bras Endocrinol Metabol; 2010 Jun; 54(4):419-24. PubMed ID: 20625655
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche.
    Savas Erdeve S; Berberoglu M; Yurur-Kutlay N; Siklar Z; Hacihamdioglu B; Tukun A; Ocal G
    J Pediatr Endocrinol Metab; 2011; 24(11-12):965-70. PubMed ID: 22308849
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Basal levels of 17-hydroxyprogesterone can distinguish children with isolated precocious pubarche.
    Grandone A; Marzuillo P; Luongo C; Toraldo R; Mariani M; Miraglia Del Giudice E; Perrone L
    Pediatr Res; 2018 Oct; 84(4):533-536. PubMed ID: 29976972
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.
    Bulsari K; Falhammar H
    Endocrine; 2017 Jan; 55(1):19-36. PubMed ID: 27928728
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Congenital adrenal hyperplasia due to steroid 21-hydroxylase deficiency.
    Speiser PW; White PC
    Clin Endocrinol (Oxf); 1998 Oct; 49(4):411-7. PubMed ID: 9876336
    [No Abstract]   [Full Text] [Related]  

  • 36. Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Riepe FG; Sippell WG
    Rev Endocr Metab Disord; 2007 Dec; 8(4):349-63. PubMed ID: 17885806
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Growth and pubertal development in patients with congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency.
    Hochberg Z; Schechter J; Benderly A; Leiberman E; Rosler A
    Am J Dis Child; 1985 Aug; 139(8):771-6. PubMed ID: 3875277
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Nonclassic congenital adrenal hyperplasia: an overview.
    Van Ryzin C
    J Pediatr Nurs; 2009 Dec; 24(6):535-7. PubMed ID: 19946984
    [No Abstract]   [Full Text] [Related]  

  • 39. Peripheral precocious puberty with hypertension.
    Reddy S; Rao M; Rao MN
    Indian Pediatr; 1992 Jan; 29(1):109-11. PubMed ID: 1601479
    [No Abstract]   [Full Text] [Related]  

  • 40. Maturational deceleration after treatment of congenital adrenal hyperplasia.
    Bongiovanni AM; Moshang T; Parks JS
    Helv Paediatr Acta; 1973 May; 28(2):127-34. PubMed ID: 4706141
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.