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Journal Abstract Search

177 related items for PubMed ID: 10084575

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  • 4. Suprasellar mass mimicking a hypothalamic glioma in a patient with a complete PROP1 deletion.
    Akcay A, Ulucan K, Taskin N, Boyraz M, Akcay T, Zurita O, Gomez A, Heath KE, Campos-Barros A.
    Eur J Med Genet; 2013 Aug; 56(8):445-51. PubMed ID: 23831233
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  • 6. Adrenocorticotropin deficiency in combined pituitary hormone deficiency patients homozygous for a novel PROP1 deletion.
    Agarwal G, Bhatia V, Cook S, Thomas PQ.
    J Clin Endocrinol Metab; 2000 Dec; 85(12):4556-61. PubMed ID: 11134108
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  • 8. Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism?
    Voutetakis A, Sertedaki A, Livadas S, Xekouki P, Bossis I, Dacou-Voutetakis C, Argyropoulou MI.
    J Endocrinol Invest; 2006 May; 29(5):462-6. PubMed ID: 16794371
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  • 9. High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency.
    Navardauskaite R, Dusatkova P, Obermannova B, Pfaeffle RW, Blum WF, Adukauskiene D, Smetanina N, Cinek O, Verkauskiene R, Lebl J.
    J Clin Endocrinol Metab; 2014 Jan; 99(1):299-306. PubMed ID: 24178788
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  • 11. Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1.
    Osorio MG, Kopp P, Marui S, Latronico AC, Mendonca BB, Arnhold IJ.
    J Clin Endocrinol Metab; 2000 Aug; 85(8):2779-85. PubMed ID: 10946881
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  • 14. 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; 65(4):479-85. PubMed ID: 16984240
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  • 15. Clinical and biochemical phenotype of familial anterior hypopituitarism from mutation of the PROP1 gene.
    Rosenbloom AL, Almonte AS, Brown MR, Fisher DA, Baumbach L, Parks JS.
    J Clin Endocrinol Metab; 1999 Jan; 84(1):50-7. PubMed ID: 9920061
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  • 16. 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 Jan; 60(6):277-83. PubMed ID: 14646405
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  • 18. A novel PROP1 gene mutation (157delA) in Japanese siblings with combined anterior pituitary hormone deficiency.
    Tatsumi KI, Kikuchi K, Tsumura K, Amino N.
    Clin Endocrinol (Oxf); 2004 Nov; 61(5):635-40. PubMed ID: 15521968
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  • 19. A novel missense mutation (P366T) of the LHX4 gene causes severe combined pituitary hormone deficiency with pituitary hypoplasia, ectopic posterior lobe and a poorly developed sella turcica.
    Tajima T, Hattori T, Nakajima T, Okuhara K, Tsubaki J, Fujieda K.
    Endocr J; 2007 Aug; 54(4):637-41. PubMed ID: 17527005
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  • 20. "Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.
    Deladoëy J, Flück C, Büyükgebiz A, Kuhlmann BV, Eblé A, Hindmarsh PC, Wu W, Mullis PE.
    J Clin Endocrinol Metab; 1999 May; 84(5):1645-50. PubMed ID: 10323394
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