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Journal Abstract Search

296 related items for PubMed ID: 18445675

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  • 44. Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?
    Dattani MT.
    Clin Endocrinol (Oxf); 2005 Aug; 63(2):121-30. PubMed ID: 16060904
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  • 46. Identification and functional analysis of the novel S179R POU1F1 mutation associated with combined pituitary hormone deficiency.
    Miyata I, Vallette-Kasic S, Saveanu A, Takeuchi M, Yoshikawa H, Tajima A, Tojo K, Reynaud R, Gueydan M, Enjalbert A, Tajima N, Eto Y, Brue T.
    J Clin Endocrinol Metab; 2006 Dec; 91(12):4981-7. PubMed ID: 16968807
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  • 47. Symptomatic heterozygotes and prenatal diagnoses in a nonconsanguineous family with syndromic combined pituitary hormone deficiency resulting from two novel LHX3 mutations.
    Sobrier ML, Brachet C, Vié-Luton MP, Perez C, Copin B, Legendre M, Heinrichs C, Amselem S.
    J Clin Endocrinol Metab; 2012 Mar; 97(3):E503-9. PubMed ID: 22238406
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  • 48. Classical and non-classical causes of GH deficiency in the paediatric age.
    Di Iorgi N, Morana G, Allegri AE, Napoli F, Gastaldi R, Calcagno A, Patti G, Loche S, Maghnie M.
    Best Pract Res Clin Endocrinol Metab; 2016 Dec; 30(6):705-736. PubMed ID: 27974186
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  • 49. Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea.
    Choi JH, Jung CW, Kang E, Kim YM, Heo SH, Lee BH, Kim GH, Yoo HW.
    Yonsei Med J; 2017 May; 58(3):527-532. PubMed ID: 28332357
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  • 51. Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes.
    Kırkgöz T, Gürsoy S, Acar S, Nalbantoğlu Ö, Özkaya B, Anıl Korkmaz H, Hazan F, Özkan B.
    Arch Endocrinol Metab; 2023 Nov 10; 68():e220254. PubMed ID: 37948564
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  • 53. Magnetic resonance imaging of the hypothalamus-pituitary unit in childrensuspected of hypopituitarism: who, how and when toinvestigate.
    Maghnie M, Ghirardello S, Genovese E.
    J Endocrinol Invest; 2004 May 10; 27(5):496-509. PubMed ID: 15279086
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  • 54. A novel mutation in the LIM homeobox 3 gene is responsible for combined pituitary hormone deficiency, hearing impairment, and vertebral malformations.
    Kriström B, Zdunek AM, Rydh A, Jonsson H, Sehlin P, Escher SA.
    J Clin Endocrinol Metab; 2009 Apr 10; 94(4):1154-61. PubMed ID: 19126629
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  • 55. Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD.
    Sobrier ML, Tsai YC, Pérez C, Leheup B, Bouceba T, Duquesnoy P, Copin B, Sizova D, Penzo A, Stanger BZ, Cooke NE, Liebhaber SA, Amselem S.
    Hum Mol Genet; 2016 Feb 01; 25(3):472-83. PubMed ID: 26612202
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  • 56. [Transcription factors of the anterior pituitary and combined hypopituitarism].
    Vallette S, Pellegrini-Bouiller I, Jaquet P, Enjalbert A, Brue T.
    Ann Endocrinol (Paris); 1999 Sep 01; 60(3):216-23. PubMed ID: 10520413
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