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Journal Abstract Search

137 related items for PubMed ID: 10946881

  • 1. 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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  • 3. Longitudinal imaging reveals pituitary enlargement preceding hypoplasia in two brothers with combined pituitary hormone deficiency attributable to PROP1 mutation.
    Riepe FG, Partsch CJ, Blankenstein O, Mönig H, Pfäffle RW, Sippell WG.
    J Clin Endocrinol Metab; 2001 Sep; 86(9):4353-7. PubMed ID: 11549674
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  • 4. 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; 85(8):2701-8. PubMed ID: 10946868
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  • 5. [Evaluation of pituitary imaging in patients with prop-1 gene mutation].
    Tkacenko N, Lasiene D, Jakstiene S, Basevicius A, Verkauskiene R.
    Medicina (Kaunas); 2009 Aug; 45(9):693-8. PubMed ID: 19834305
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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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  • 11. Four novel mutations of the LHX3 gene cause combined pituitary hormone deficiencies with or without limited neck rotation.
    Pfaeffle RW, Savage JJ, Hunter CS, Palme C, Ahlmann M, Kumar P, Bellone J, Schoenau E, Korsch E, Brämswig JH, Stobbe HM, Blum WF, Rhodes SJ.
    J Clin Endocrinol Metab; 2007 May; 92(5):1909-19. PubMed ID: 17327381
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  • 15. Magnetic resonance imaging of the hypothalamus-pituitary unit in childrensuspected of hypopituitarism: who, how and when toinvestigate.
    Maghnie M, Ghirardello S, Genovese E.
    J Endocrinol Invest; 2004 May; 27(5):496-509. PubMed ID: 15279086
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  • 16. A recessive mutation resulting in a disabling amino acid substitution (T194R) in the LHX3 homeodomain causes combined pituitary hormone deficiency.
    Bechtold-Dalla Pozza S, Hiedl S, Roeb J, Lohse P, Malik RE, Park S, Durán-Prado M, Rhodes SJ.
    Horm Res Paediatr; 2012 May; 77(1):41-51. PubMed ID: 22286346
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  • 17. Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.
    Osorio MG, Marui S, Jorge AA, Latronico AC, Lo LS, Leite CC, Estefan V, Mendonca BB, Arnhold IJ.
    J Clin Endocrinol Metab; 2002 Nov; 87(11):5076-84. PubMed ID: 12414875
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  • 19. 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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  • 20. A mutational hot spot in the Prop-1 gene in Russian children with combined pituitary hormone deficiency.
    Fofanova OV, Takamura N, Kinoshita E, Parks JS, Brown MR, Peterkova VA, Evgrafov OV, Goncharov NP, Bulatov AA, Dedov II, Yamashita S.
    Pituitary; 1998 Apr; 1(1):45-9. PubMed ID: 11081182
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