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Journal Abstract Search

174 related items for PubMed ID: 26781211

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  • 2. 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; 84(3):153-8. PubMed ID: 26111865
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  • 5. Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without features of septo-optic dysplasia.
    Corneli G, Vivenza D, Prodam F, Di Dio G, Vottero A, Rapa A, Bellone S, Bernasconi S, Bona G.
    J Endocrinol Invest; 2008 Aug; 31(8):689-93. PubMed ID: 18852528
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  • 7. Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency.
    Cruz JB, Nunes VS, Clara SA, Perone D, Kopp P, Nogueira CR.
    Arq Bras Endocrinol Metabol; 2010 Aug; 54(5):482-7. PubMed ID: 20694410
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  • 8. Enhanced repression by HESX1 as a cause of hypopituitarism and septooptic dysplasia.
    Cohen RN, Cohen LE, Botero D, Yu C, Sagar A, Jurkiewicz M, Radovick S.
    J Clin Endocrinol Metab; 2003 Oct; 88(10):4832-9. PubMed ID: 14557462
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  • 9. A novel homozygous HESX1 mutation causes panhypopituitarism without midline defects and optic nerve anomalies.
    Durmaz B, Cogulu O, Dizdarer C, Stobbe H, Pfaeffle R, Ozkinay F.
    J Pediatr Endocrinol Metab; 2011 Oct; 24(9-10):779-82. PubMed ID: 22145475
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  • 10. HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.
    McNay DE, Turton JP, Kelberman D, Woods KS, Brauner R, Papadimitriou A, Keller E, Keller A, Haufs N, Krude H, Shalet SM, Dattani MT.
    J Clin Endocrinol Metab; 2007 Feb; 92(2):691-7. PubMed ID: 17148560
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  • 12. Panhypopituitarism: genetic versus acquired etiological factors.
    Coya R, Vela A, Pérez de Nanclares G, Rica I, Castaño L, Busturia MA, Martul P, GEDPIT group.
    J Pediatr Endocrinol Metab; 2007 Jan; 20(1):27-36. PubMed ID: 17315526
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  • 19. 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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