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Journal Abstract Search

131 related items for PubMed ID: 25667374

  • 1. Genetic forms of adrenal insufficiency.
    Brett EM, Auchus RJ.
    Endocr Pract; 2015 Apr; 21(4):395-9. PubMed ID: 25667374
    [Abstract] [Full Text] [Related]

  • 2. Clinical features of congenital adrenal insufficiency including growth patterns and significance of ACTH stimulation test.
    Koh JW, Kim GH, Yoo HW, Yu J.
    J Korean Med Sci; 2013 Nov; 28(11):1650-6. PubMed ID: 24265530
    [Abstract] [Full Text] [Related]

  • 3. The classic and nonclassic concenital adrenal hyperplasias.
    Auchus RJ.
    Endocr Pract; 2015 Apr; 21(4):383-9. PubMed ID: 25536973
    [Abstract] [Full Text] [Related]

  • 4. Rare forms of genetic paediatric adrenal insufficiency: Excluding congenital adrenal hyperplasia.
    Hasenmajer V, Ferrigno R, Minnetti M, Pellegrini B, Isidori AM, Lenzi A, Salerno M, Cappa M, Chan L, De Martino MC, Savage MO.
    Rev Endocr Metab Disord; 2023 Apr; 24(2):345-363. PubMed ID: 36763264
    [Abstract] [Full Text] [Related]

  • 5. Mild adrenal insufficiency due to a NROB1 (DAX1) gene mutation in a boy presenting an association of hypogonadotropic hypogonadism, reduced final height and attention deficit disorder.
    Calliari LE, Rocha MN, Monte O, Longui CA.
    Arq Bras Endocrinol Metabol; 2013 Oct; 57(7):562-5. PubMed ID: 24232823
    [Abstract] [Full Text] [Related]

  • 6. X-linked Congenital Adrenal Hypoplasia with a Novel NR0B1/DAX Gene Mutation.
    Abraham MB, Shetty VB, McKenzie F, Curran J.
    Indian Pediatr; 2016 Jun 08; 53(6):529-31. PubMed ID: 27376611
    [Abstract] [Full Text] [Related]

  • 7. Congenital adrenal hypoplasia and hypogonadotropic hypogonadism: phenotypic variability of the DAX-1 gene R267P mutation.
    Sánchez-Pacheco M, Moreno-Pérez O, Sánchez-Ortiga R, Picó A, Moreno F.
    Endocrinol Nutr; 2012 Feb 08; 59(2):140-2. PubMed ID: 21925982
    [No Abstract] [Full Text] [Related]

  • 8. Adrenal hypoplasia congenita - an uncommon reason of primary adrenal insufficiency.
    Fichna M, Zurawek M, Gut P, Sowiński J, Nowak J.
    Ann Endocrinol (Paris); 2010 Sep 08; 71(4):309-13. PubMed ID: 20542258
    [Abstract] [Full Text] [Related]

  • 9. Primary adrenal insufficiency caused by a novel mutation in DAX1 gene.
    Evliyaoğlu O, Dokurel İ, Bucak F, Özcabı B, Ercan Ö, Ceylaner S.
    J Clin Res Pediatr Endocrinol; 2013 Sep 08; 5(1):55-7. PubMed ID: 23367499
    [Abstract] [Full Text] [Related]

  • 10. STAR mutations causing non‑classical lipoid adrenal hyperplasia manifested as familial glucocorticoid deficiency.
    Luo Y, Bai R, Wang Z, Zhu X, Xing J, Li X.
    Mol Med Rep; 2020 Aug 08; 22(2):681-686. PubMed ID: 32627004
    [Abstract] [Full Text] [Related]

  • 11. Delayed diagnosis of adrenal hypoplasia congenita in a patient with a new mutation in the NR0B1 gene.
    Esden-Tempska Z, Lewczuk A, Tobias ES, Borozdin W, Kohlhase J, Sworczak K.
    J Pediatr Endocrinol Metab; 2012 Aug 08; 25(1-2):147-8. PubMed ID: 22570964
    [Abstract] [Full Text] [Related]

  • 12. Primary Adrenal Insufficiency in Childhood: Data From a Large Nationwide Cohort.
    Capalbo D, Moracas C, Cappa M, Balsamo A, Maghnie M, Wasniewska MG, Greggio NA, Baronio F, Bizzarri C, Ferro G, Di Lascio A, Stancampiano MR, Azzolini S, Patti G, Longhi S, Valenzise M, Radetti G, Betterle C, Russo G, Salerno M.
    J Clin Endocrinol Metab; 2021 Mar 08; 106(3):762-773. PubMed ID: 33247909
    [Abstract] [Full Text] [Related]

  • 13.
    Feingold KR, Anawalt B, Blackman MR, Boyce A, Chrousos G, Corpas E, de Herder WW, Dhatariya K, Dungan K, Hofland J, Kalra S, Kaltsas G, Kapoor N, Koch C, Kopp P, Korbonits M, Kovacs CS, Kuohung W, Laferrère B, Levy M, McGee EA, McLachlan R, New M, Purnell J, Sahay R, Shah AS, Singer F, Sperling MA, Stratakis CA, Trence DL, Wilson DP, Kyritsi EM, Sertedaki A, Charmandari E, Chrousos GP.
    ; 2000 Mar 08. PubMed ID: 25905355
    [Abstract] [Full Text] [Related]

  • 14. Clinical and molecular characterization of thirty Chinese patients with congenital lipoid adrenal hyperplasia.
    Zhang T, Ma X, Wang J, Jia C, Wang W, Dong Z, Ye L, Sun S, Hu R, Ning G, Li C, Lu W.
    J Steroid Biochem Mol Biol; 2021 Feb 08; 206():105788. PubMed ID: 33227378
    [Abstract] [Full Text] [Related]

  • 15. NR0B1 (DAX1) mutations in patients affected by congenital adrenal hypoplasia with growth hormone deficiency as a new finding.
    Rojek A, Obara-Moszynska M, Malecka E, Slomko-Jozwiak M, Niedziela M.
    J Appl Genet; 2013 May 08; 54(2):225-30. PubMed ID: 23378245
    [No Abstract] [Full Text] [Related]

  • 16. Clinical and molecular genetic analysis of a Chinese family with congenital X-linked adrenal hypoplasia caused by novel mutation 1268delA in the DAX-1 gene.
    Zhang Z, Feng Y, Ye D, Li CJ, Dong FQ, Tong Y.
    J Zhejiang Univ Sci B; 2015 Nov 08; 16(11):963-8. PubMed ID: 26537215
    [Abstract] [Full Text] [Related]

  • 17. A de novo mutation of DAX1 in a boy with congenital adrenal hypoplasia without hypogonadotropic hypogonadism.
    Wang CL, Fen ZW, Liang L.
    J Pediatr Endocrinol Metab; 2014 Mar 08; 27(3-4):343-7. PubMed ID: 24197767
    [Abstract] [Full Text] [Related]

  • 18. Multiplex ligation-dependent probe amplification analysis of the NR0B1(DAX1) locus enables explanation of phenotypic differences in patients with X-linked congenital adrenal hypoplasia.
    Barbaro M, Bens S, Haake A, Peter M, Brämswig J, Holterhus PM, Lopez-Siguero JP, Menken U, Mix M, Sippell WG, Wedell A, Riepe FG.
    Horm Res Paediatr; 2012 Mar 08; 77(2):100-7. PubMed ID: 22456342
    [Abstract] [Full Text] [Related]

  • 19. Growth alterations in rare forms of primary adrenal insufficiency: a neglected issue in paediatric endocrinology.
    Ferrigno R, Cioffi D, Pellino V, Savanelli MC, Klain A.
    Endocrine; 2023 Apr 08; 80(1):1-9. PubMed ID: 36309634
    [Abstract] [Full Text] [Related]

  • 20. A novel DAX1/NR0B1 mutation in a patient with adrenal hypoplasia congenita and hypogonadotropic hypogonadism.
    Battistin C, Menezes Filho HC, Domenice S, Nishi MY, Della Manna T, Kuperman H, Steinmetz L, Dichtchekenian V, Setian N, Damiani D.
    Arq Bras Endocrinol Metabol; 2012 Nov 08; 56(8):496-500. PubMed ID: 23295288
    [Abstract] [Full Text] [Related]

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