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Journal Abstract Search

174 related items for PubMed ID: 26781211

  • 21. Ectopic posterior pituitary lobe and periventricular heterotopia: cerebral malformations with the same underlying mechanism?
    Mitchell LA, Thomas PQ, Zacharin MR, Scheffer IE.
    AJNR Am J Neuroradiol; 2002 Oct; 23(9):1475-81. PubMed ID: 12372734
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  • 24. Identification of Novel PROP1 and POU1F1 Mutations in Patients with Combined Pituitary Hormone Deficiency.
    Birla S, Khadgawat R, Jyotsna VP, Jain V, Garg MK, Bhalla AS, Sharma A.
    Horm Metab Res; 2016 Dec; 48(12):822-827. PubMed ID: 27756091
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  • 28. Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
    Turton JP, Mehta A, Raza J, Woods KS, Tiulpakov A, Cassar J, Chong K, Thomas PQ, Eunice M, Ammini AC, Bouloux PM, Starzyk J, Hindmarsh PC, Dattani MT.
    Clin Endocrinol (Oxf); 2005 Jul; 63(1):10-8. PubMed ID: 15963055
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  • 30. Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities.
    Sobrier ML, Maghnie M, Vié-Luton MP, Secco A, di Iorgi N, Lorini R, Amselem S.
    J Clin Endocrinol Metab; 2006 Nov; 91(11):4528-36. PubMed ID: 16940453
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  • 31. Growth without growth hormone and similar dysmorphic features in three patients with sporadic combined pituitary hormone deficiencies.
    Gat-Yablonski G, Lazar L, Bar M, de Vries L, Weintrob N, Phillip M.
    Horm Res; 2009 Nov; 72(5):302-9. PubMed ID: 19844116
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  • 32. [Genetic aspects of growth hormone deficiency].
    Reynaud R, Castinetti F, Galon-Faure N, Albarel-Loy F, Saveanu A, Quentien MH, Jullien N, Khammar A, Enjalbert A, Barlier A, Brue T.
    Arch Pediatr; 2011 Jun; 18(6):696-706. PubMed ID: 21497494
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  • 33. Genetic screening of regulatory regions of pituitary transcription factors in patients with idiopathic pituitary hormone deficiencies.
    Elizabeth M, Hokken-Koelega ACS, Schuilwerve J, Peeters RP, Visser TJ, de Graaff LCG.
    Pituitary; 2018 Feb; 21(1):76-83. PubMed ID: 29255988
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  • 34. [Clinical and genetic aspects of combined pituitary hormone deficiencies].
    Castinetti F, Reynaud R, Saveanu A, Quentien MH, Albarel F, Barlier A, Enjalbert A, Brue T.
    Ann Endocrinol (Paris); 2008 Feb; 69(1):7-17. PubMed ID: 18291347
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  • 36. 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 Feb; 60(6):277-83. PubMed ID: 14646405
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  • 37. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe.
    Melo ME, Marui S, Carvalho LR, Arnhold IJ, Leite CC, Mendonça BB, Knoepfelmacher M.
    Clin Endocrinol (Oxf); 2007 Jan; 66(1):95-102. PubMed ID: 17201807
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  • 38. Combined pituitary hormone deficiency caused by PROP1 mutations: update 20 years post-discovery.
    Correa FA, Nakaguma M, Madeira JLO, Nishi MY, Abrão MG, Jorge AAL, Carvalho LR, Arnhold IJP, Mendonça BB.
    Arch Endocrinol Metab; 2019 May 13; 63(2):167-174. PubMed ID: 31090814
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  • 40. HESX1: a novel gene implicated in a familial form of septo-optic dysplasia.
    Dattani MT, Martinez-Barbera JP, Thomas PQ, Brickman JM, Gupta R, Wales JK, Hindmarsh PC, Beddington RS, Robinson IC.
    Acta Paediatr Suppl; 1999 Dec 13; 88(433):49-54. PubMed ID: 10626545
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