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PUBMED FOR HANDHELDS

Journal Abstract Search


359 related items for PubMed ID: 9113619

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  • 44. [Are short boys disadvantaged as adults? Follow-up of 77 men with constitutional growth delay and (or) familial short stature].
    Holl RW, Schröder H, Heinze E.
    Dtsch Med Wochenschr; 1991 Jun 14; 116(24):928-34. PubMed ID: 2044460
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  • 45. Impact of hydrocortisone on adult height in congenital adrenal hyperplasia-the Minnesota cohort.
    Sarafoglou K, Addo OY, Turcotte L, Otten N, Wickremasinghe A, Pittock S, Kyllo J, Lteif AN, Himes JH, Miller BS.
    J Pediatr; 2014 May 14; 164(5):1141-1146.e1. PubMed ID: 24560184
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  • 49. Initial high dose hydrocortisone (HDC) treatment for 21-hydroxylase deficiency (21-OHD) does not affect linear growth during the first three years of life.
    Takasawa K, Ono M, Miyai K, Matsubara Y, Takizawa F, Onishi T, Kashimada K, Mizutani S.
    Endocr J; 2012 May 14; 59(11):1001-6. PubMed ID: 22785554
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  • 50. Final height in congenital adrenal hyperplasia: the dilemma of hypercortisolism versus hyperandrogenism.
    Cordeiro GV, Silva IN, Goulart EM, Chagas AJ, Kater CE.
    Arq Bras Endocrinol Metabol; 2013 Mar 14; 57(2):126-31. PubMed ID: 23525290
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  • 51. Growth in patients with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Dörr HG.
    Horm Res; 2007 Mar 14; 68 Suppl 5():93-9. PubMed ID: 18174719
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  • 52. Congenital adrenal hyperplasia due to 21-hydroxylase deficiency: alterations in cortisol pharmacokinetics at puberty.
    Charmandari E, Hindmarsh PC, Johnston A, Brook CG.
    J Clin Endocrinol Metab; 2001 Jun 14; 86(6):2701-8. PubMed ID: 11397874
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  • 53. Near-final height in 82 Chinese patients with congenital adrenal hyperplasia due to classic 21-hydroxylase deficiency: a single-center study from China.
    Juan L, Huamei M, Zhe S, Yanhong L, Hongshan C, Qiuli C, Jun Z, Song G, Minlian D.
    J Pediatr Endocrinol Metab; 2016 Jul 01; 29(7):841-8. PubMed ID: 27054598
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  • 56. Effect of growth hormone dose on bone maturation and puberty in children with idiopathic short stature.
    Crowe BJ, Rekers-Mombarg LT, Robling K, Wolka AM, Cutler GB, Wit JM, European Idiopathic Short Stature Group.
    J Clin Endocrinol Metab; 2006 Jan 01; 91(1):169-75. PubMed ID: 16263828
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  • 57. Bone mineral density and bone turnover in Romanian children and young adults with classical 21-hydroxylase deficiency are influenced by glucocorticoid replacement therapy.
    Zimmermann A, Sido PG, Schulze E, Al Khzouz C, Lazea C, Coldea C, Weber MM.
    Clin Endocrinol (Oxf); 2009 Oct 01; 71(4):477-84. PubMed ID: 19170706
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  • 58. Growth in disorders of adrenal hyperfunction.
    Savage MO, Scommegna S, Carroll PV, Ho JT, Monson JP, Besser GM, Grossman AB.
    Horm Res; 2002 Oct 01; 58 Suppl 1():39-43. PubMed ID: 12373013
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  • 59. Overestimation of final height prediction in patients with classical congenital adrenal hyperplasia using the Bayley and Pinneau method.
    Bonfig W, Schwarz HP.
    J Pediatr Endocrinol Metab; 2012 Oct 01; 25(7-8):645-9. PubMed ID: 23155688
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  • 60. Final height and pubertal development in children with growth hormone deficiency after long-term treatment.
    Frisch H, Birnbacher R.
    Horm Res; 1995 Oct 01; 43(4):132-4. PubMed ID: 7750913
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