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PUBMED FOR HANDHELDS

Journal Abstract Search


321 related items for PubMed ID: 18174732

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  • 44. [Congenital hypopituitarism: when should transcription factor gene screenings be performed?].
    Reynaud R, Barlier A, Chadli-Chaieb M, Saveanu A, Simonin G, Enjalbert A, Brue T.
    Presse Med; 2004 Mar 27; 33(6):400-5. PubMed ID: 15105786
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  • 45. Identification of genetic variants and phenotypic characterization of a large cohort of patients with congenital hypopituitarism and related disorders.
    Gregory LC, Cionna C, Cerbone M, Dattani MT.
    Genet Med; 2023 Sep 27; 25(9):100881. PubMed ID: 37165954
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  • 46. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.
    Baş F, Uyguner ZO, Darendeliler F, Aycan Z, Çetinkaya E, Berberoğlu M, Şiklar Z, Öcal G, Darcan Ş, Gökşen D, Topaloğlu AK, Yüksel B, Özbek MN, Ercan O, Evliyaoğlu O, Çetinkaya S, Şen Y, Atabek E, Toksoy G, Aydin BK, Bundak R.
    Endocrine; 2015 Jun 27; 49(2):479-91. PubMed ID: 25500790
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  • 49. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia.
    Rainbow LA, Rees SA, Shaikh MG, Shaw NJ, Cole T, Barrett TG, Kirk JM.
    Clin Endocrinol (Oxf); 2005 Feb 27; 62(2):163-8. PubMed ID: 15670191
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  • 50. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations.
    Madeira JL, Nishi MY, Nakaguma M, Benedetti AF, Biscotto IP, Fernandes T, Pequeno T, Figueiredo T, Franca MM, Correa FA, Otto AP, Abrão M, Miras MB, Santos S, Jorge AA, Costalonga EF, Mendonca BB, Arnhold IJ, Carvalho LR.
    Clin Endocrinol (Oxf); 2017 Dec 27; 87(6):725-732. PubMed ID: 28734020
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  • 56. Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency.
    Avbelj Stefanija M, Kotnik P, Bratanič N, Žerjav Tanšek M, Bertok S, Bratina N, Battelino T, Trebušak Podkrajšek K.
    Horm Res Paediatr; 2015 Dec 27; 84(3):153-8. PubMed ID: 26111865
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