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Journal Abstract Search

201 related items for PubMed ID: 12153609

  • 1. A unique case of combined pituitary hormone deficiency caused by a PROP1 gene mutation (R120C) associated with normal height and absent puberty.
    Arroyo A, Pernasetti F, Vasilyev VV, Amato P, Yen SS, Mellon PL.
    Clin Endocrinol (Oxf); 2002 Aug; 57(2):283-91. PubMed ID: 12153609
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  • 2. Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C).
    Flück C, Deladoey J, Rutishauser K, Eblé A, Marti U, Wu W, Mullis PE.
    J Clin Endocrinol Metab; 1998 Oct; 83(10):3727-34. PubMed ID: 9768691
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  • 8. 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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  • 9. Longitudinal hormonal and pituitary imaging changes in two females with combined pituitary hormone deficiency due to deletion of A301,G302 in the PROP1 gene.
    Mendonca BB, Osorio MG, Latronico AC, Estefan V, Lo LS, Arnhold IJ.
    J Clin Endocrinol Metab; 1999 Mar; 84(3):942-5. PubMed ID: 10084575
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  • 10. 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. Congenital combined pituitary hormone deficiency attributable to a novel PROP1 mutation (467insT).
    Nose O, Tatsumi K, Nakano Y, Amino N.
    J Pediatr Endocrinol Metab; 2006 Apr; 19(4):491-8. PubMed ID: 16759034
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  • 12. Central hypocortisolism as part of combined pituitary hormone deficiency due to mutations of PROP-1 gene.
    Asteria C, Oliveira JH, Abucham J, Beck-Peccoz P.
    Eur J Endocrinol; 2000 Sep; 143(3):347-52. PubMed ID: 11022176
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  • 13. 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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