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: 33744520)

  • 1. An unexpected finding in a 46,XX patient with congenital adrenal hyperplasia.
    Salle L; Lachâtre D; Galinat S
    J Gynecol Obstet Hum Reprod; 2021 Jun; 50(6):102113. PubMed ID: 33744520
    [No Abstract]   [Full Text] [Related]  

  • 2. Multiple tumors associated with late-onset congenital adrenal hyperplasia due to aberrant splicing of adrenal 21-hydroxylase gene.
    Boos CJ; Rumsby G; Matfin G
    Endocr Pract; 2002; 8(6):470-3. PubMed ID: 15251833
    [No Abstract]   [Full Text] [Related]  

  • 3. Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency detected by neonatal screening.
    Liu SY; Lee CT; Tung YC; Chien YH; Hwu WL; Tsai WY
    J Formos Med Assoc; 2018 Feb; 117(2):126-131. PubMed ID: 28392195
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Diagnosis of heterozygote carrier of mutant gene of 21-hydroxylase].
    Dzenis IG; Iudina TN; Brykova EK; Bakharev VA; Fanchenko ND
    Akush Ginekol (Mosk); 1995; (1):21-3. PubMed ID: 7762743
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Androglottia in a young female adolescent with congenital adrenal hyperplasia and 21-hydroxylase deficiency.
    Fürst-Recktenwald S; Dörr HG; Rosanowski F
    J Pediatr Endocrinol Metab; 2000; 13(7):959-62. PubMed ID: 10968487
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Comments to “A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency”.
    Concolino P; Mello E; Rossodivita A; Giardina B; Capoluongo E
    Gene; 2014 Jan; 534(2):449-450. PubMed ID: 24501745
    [No Abstract]   [Full Text] [Related]  

  • 7. Comments to "a rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency".
    Coeli-Lacchini FB; Turatti W; Elias PC; Elias LL; Martinelli CE; Moreira AC; Antonini SR; de Castro M
    Gene; 2014 Jan; 534(2):451-2. PubMed ID: 24100083
    [No Abstract]   [Full Text] [Related]  

  • 8. [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]  

  • 9. [Usefulness of molecular analysis in the differential diagnosis of congenital 21-hidroxylase deficiency detected in neonatal screening].
    Soriano Guillén L; Velázquez De Cuellar Paracchi M; Ezquieta B
    Med Clin (Barc); 2011 Mar; 136(7):313-4. PubMed ID: 19766262
    [No Abstract]   [Full Text] [Related]  

  • 10. [Adrenal hyperplasia as a result of 21-hydroxylase deficiency: prenatal diagnosis and treatment. Neonatal diagnosis].
    Lambotte C
    Rev Med Liege; 1986 Jan; 41(2):37-44. PubMed ID: 3006204
    [No Abstract]   [Full Text] [Related]  

  • 11. [Congenital adrenal hyperplasia].
    Bouvattier C; Chatelain P
    Rev Prat; 2008 May; 58(9):990-4. PubMed ID: 18672665
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Diagnosis and management of congenital adrenal hyperplasia.
    New MI
    Annu Rev Med; 1998; 49():311-28. PubMed ID: 9509266
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The value of time in assessing the effectiveness of newborn screening for congenital adrenal hyperplasia.
    Tarini BA
    JAMA Pediatr; 2014 Jun; 168(6):515-6. PubMed ID: 24733500
    [No Abstract]   [Full Text] [Related]  

  • 14. Does newborn screening have 100% sensitivity to detect salt wasting congenital adrenal hyperplasia?-Reply.
    Gidlöf S; Nordenström A
    JAMA Pediatr; 2014 Oct; 168(10):971. PubMed ID: 25285872
    [No Abstract]   [Full Text] [Related]  

  • 15. Does newborn screening have 100% sensitivity to detect salt-wasting congenital adrenal hyperplasia?: A word of caution.
    Grosse SD; Sarafoglou K
    JAMA Pediatr; 2014 Oct; 168(10):970-1. PubMed ID: 25285869
    [No Abstract]   [Full Text] [Related]  

  • 16. Glucocorticoid withdrawal - heterozygous carriers of congenital adrenal hyperplasia at risk?
    Brackmann F; Dörr HG; Bartram CR; Hinderhofer K; Holter W; Langer T
    Klin Padiatr; 2012 Oct; 224(6):392-3. PubMed ID: 22915453
    [No Abstract]   [Full Text] [Related]  

  • 17. 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]  

  • 18. Acne and non-classic congenital adrenal hyperplasia.
    Falhammar H
    N Z Med J; 2008 Jun; 121(1275):94-5. PubMed ID: 18551162
    [No Abstract]   [Full Text] [Related]  

  • 19. Successful pregnancy in a woman with rare compound heterozygoticity for congenital adrenal hyperplasia; case report.
    Kontoleon P; Ilias I; Papapetrou PD
    Clin Exp Obstet Gynecol; 2003; 30(4):263-4. PubMed ID: 14664429
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Nonclassic adrenal hyperplasia.
    Speiser PW
    Rev Endocr Metab Disord; 2009 Mar; 10(1):77-82. PubMed ID: 18690539
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.