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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

169 related items for PubMed ID: 2982907

  • 21. Salt wasting in simple virilizing congenital adrenal hyperplasia.
    Frisch H, Battelino T, Schober E, Baumgartner-Parzer S, Nowotny P, Vierhapper H.
    J Pediatr Endocrinol Metab; 2001; 14(9):1649-55. PubMed ID: 11795656
    [Abstract] [Full Text] [Related]

  • 22. Prenatal dexamethasone treatment in pregnancies at risk for congenital adrenal hyperplasia due to 21-hydroxylase deficiency: effect on midgestational amniotic fluid steroid levels.
    Dörr HG, Sippell WG.
    J Clin Endocrinol Metab; 1993 Jan; 76(1):117-20. PubMed ID: 8421074
    [Abstract] [Full Text] [Related]

  • 23. Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region.
    Boehm BO, Rosak C, Boehm TL, Kuehnl P, White PC, Schöffling K.
    Mol Biol Med; 1986 Oct; 3(5):437-48. PubMed ID: 2882404
    [Abstract] [Full Text] [Related]

  • 24. [A genetic and hormonal study of 5 patients with the nonclassical form of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Velasco FJ, Picó AM, Muñoz C, Mauri M, de la Sen ML.
    Med Clin (Barc); 1992 Jun 13; 99(3):81-6. PubMed ID: 1321317
    [Abstract] [Full Text] [Related]

  • 25. Isolated precocious pubarche: an approach.
    Balducci R, Boscherini B, Mangiantini A, Morellini M, Toscano V.
    J Clin Endocrinol Metab; 1994 Aug 13; 79(2):582-9. PubMed ID: 8045980
    [Abstract] [Full Text] [Related]

  • 26. [Detection of heterozygosity in congenital adrenal hyperplasia caused by 21-hydroxylase deficiency in the general population].
    Dumić M, Lukenda M, Plavsić V, Brkljacić L, Jovanović V, Kastelan A.
    Lijec Vjesn; 1990 Aug 13; 112(5-6):138-41. PubMed ID: 2172673
    [Abstract] [Full Text] [Related]

  • 27. Is salt-wasting in congenital adrenal hyperplasia due to the same gene as the fasciculata defect?
    Stoner E, Dimartino-Nardi J, Kuhnle U, Levine LS, Oberfield SE, New MI.
    Clin Endocrinol (Oxf); 1986 Jan 13; 24(1):9-20. PubMed ID: 3486728
    [Abstract] [Full Text] [Related]

  • 28. Adrenocorticotrophin stimulation and HLA polymorphisms suggest a high frequency of heterozygosity for steroid 21-hydroxylase deficiency in patients with Turner's syndrome and their families.
    Larizza D, Cuccia M, Martinetti M, Maghnie M, Dondi E, Salvaneschi L, Severi F.
    Clin Endocrinol (Oxf); 1994 Jan 13; 40(1):39-45. PubMed ID: 8306479
    [Abstract] [Full Text] [Related]

  • 29. Clinical and molecular characterization of a cohort of 161 unrelated women with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency and 330 family members.
    Bidet M, Bellanné-Chantelot C, Galand-Portier MB, Tardy V, Billaud L, Laborde K, Coussieu C, Morel Y, Vaury C, Golmard JL, Claustre A, Mornet E, Chakhtoura Z, Mowszowicz I, Bachelot A, Touraine P, Kuttenn F.
    J Clin Endocrinol Metab; 2009 May 13; 94(5):1570-8. PubMed ID: 19208730
    [Abstract] [Full Text] [Related]

  • 30. Molecular detection of genetic defects in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: a study of 27 families.
    Strumberg D, Hauffa BP, Horsthemke B, Grosse-Wilde H.
    Eur J Pediatr; 1992 Nov 13; 151(11):821-6. PubMed ID: 1361434
    [Abstract] [Full Text] [Related]

  • 31. Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination.
    Peter M, Sippell WG, Lorenzen F, Willig RP, Westphal E, Grosse-Wilde H.
    Lancet; 1990 Jun 02; 335(8701):1296-9. PubMed ID: 1971375
    [Abstract] [Full Text] [Related]

  • 32. Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia.
    Jaresch S, Kornely E, Kley HK, Schlaghecke R.
    J Clin Endocrinol Metab; 1992 Mar 02; 74(3):685-9. PubMed ID: 1311000
    [Abstract] [Full Text] [Related]

  • 33. Late onset congenital adrenal hyperplasia in a Puerto Rican family: hormonal and HLA typing.
    Hernán Martínez J, Riestra JL.
    Bol Asoc Med P R; 1986 Nov 02; 78(11):472-6. PubMed ID: 3026413
    [No Abstract] [Full Text] [Related]

  • 34. Impaired mineralocorticoid hormone responses to adrenocorticotropin stimulation: additional characterization of heterozygosity for the 21-hydroxylase deficiency type of congenital adrenal hyperplasia.
    Pardini DP, Kater CE, Vieira JG, Biglieri EG.
    J Clin Endocrinol Metab; 1983 Nov 02; 57(5):1061-6. PubMed ID: 6311859
    [Abstract] [Full Text] [Related]

  • 35. Congenital adrenal hyperplasia family studies using the short ACTH test.
    Kreutzmann DJ, Cowell CT, Howard NJ, De Souza M, Silink M.
    Aust Paediatr J; 1989 Dec 02; 25(6):340-5. PubMed ID: 2619637
    [Abstract] [Full Text] [Related]

  • 36. Follow-up of 68 children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: relevance of genotype for management.
    Pinto G, Tardy V, Trivin C, Thalassinos C, Lortat-Jacob S, Nihoul-Fékété C, Morel Y, Brauner R.
    J Clin Endocrinol Metab; 2003 Jun 02; 88(6):2624-33. PubMed ID: 12788866
    [Abstract] [Full Text] [Related]

  • 37. [Cortico-adrenal-genital syndrome. Diagnosis, therapy, follow-up].
    Gargantini L, Trifirò G, Bianchi C, Chiumello G.
    Pediatr Med Chir; 1985 Jun 02; 7(4):487-90. PubMed ID: 3016673
    [Abstract] [Full Text] [Related]

  • 38. The prevalence of non-classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency in Greek women with hirsutism and polycystic ovary syndrome.
    Trakakis E, Rizos D, Loghis C, Chryssikopoulos A, Spyropoulou M, Salamalekis E, Simeonides G, Vagopoulos V, Salamalekis G, Kassanos D.
    Endocr J; 2008 Mar 02; 55(1):33-9. PubMed ID: 18187875
    [Abstract] [Full Text] [Related]

  • 39. The incidence of late-onset congenital adrenal hyperplasia due to 21-hydroxylase deficiency among hirsute women.
    Chetkowski RJ, DeFazio J, Shamonki I, Judd HL, Chang RJ.
    J Clin Endocrinol Metab; 1984 Apr 02; 58(4):595-8. PubMed ID: 6321532
    [Abstract] [Full Text] [Related]

  • 40. Overdiagnosis of 21-hydroxylase late onset congenital adrenal hyperplasia: correlation of corticotropin test and human leukocyte antigen typing.
    Avivi I, Pollack S, Gideoni O, Linn S, Blumenfeld Z.
    Fertil Steril; 1996 Oct 02; 66(4):557-63. PubMed ID: 8816616
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 9.