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Journal Abstract Search

367 related items for PubMed ID: 19337183

  • 21. [Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].
    Halász Z.
    Orv Hetil; 2011 Feb 06; 152(6):221-32. PubMed ID: 21278027
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  • 25. PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.
    Lemos MC, Gomes L, Bastos M, Leite V, Limbert E, Carvalho D, Bacelar C, Monteiro M, Fonseca F, Agapito A, Castro JJ, Regateiro FJ, Carvalheiro M.
    Clin Endocrinol (Oxf); 2006 Oct 06; 65(4):479-85. PubMed ID: 16984240
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  • 27. Molecular analysis of LHX3 and PROP-1 in pituitary hormone deficiency patients with posterior pituitary ectopia.
    Sloop KW, Walvoord EC, Showalter AD, Pescovitz OH, Rhodes SJ.
    J Clin Endocrinol Metab; 2000 Aug 06; 85(8):2701-8. PubMed ID: 10946868
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  • 28. [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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  • 30. A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.
    Castinetti F, Saveanu A, Reynaud R, Quentien MH, Buffin A, Brauner R, Kaffel N, Albarel F, Guedj AM, El Kholy M, Amin M, Enjalbert A, Barlier A, Brue T.
    J Clin Endocrinol Metab; 2008 Jul 27; 93(7):2790-9. PubMed ID: 18445675
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  • 31. Clinical characteristics and molecular analysis of PIT1, PROP1,LHX3, and HESX1 in combined pituitary hormone deficiency patients with abnormal pituitary MR imaging.
    Kim SS, Kim Y, Shin YL, Kim GH, Kim TU, Yoo HW.
    Horm Res; 2003 Jul 27; 60(6):277-83. PubMed ID: 14646405
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  • 36. 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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  • 37. 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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  • 38. Mutations in LHX3 result in a new syndrome revealed by combined pituitary hormone deficiency.
    Netchine I, Sobrier ML, Krude H, Schnabel D, Maghnie M, Marcos E, Duriez B, Cacheux V, Moers Av, Goossens M, Grüters A, Amselem S.
    Nat Genet; 2000 Jun 27; 25(2):182-6. PubMed ID: 10835633
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  • 40. Pituitary development: a complex, temporal regulated process dependent on specific transcriptional factors.
    de Moraes DC, Vaisman M, Conceição FL, Ortiga-Carvalho TM.
    J Endocrinol; 2012 Nov 27; 215(2):239-45. PubMed ID: 22872762
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