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Journal Abstract Search

197 related items for PubMed ID: 22286346

  • 1. 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; 77(1):41-51. PubMed ID: 22286346
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  • 3. A novel mutation of LHX3 is associated with combined pituitary hormone deficiency including ACTH deficiency, sensorineural hearing loss, and short neck-a case report and review of the literature.
    Bonfig W, Krude H, Schmidt H.
    Eur J Pediatr; 2011 Aug; 170(8):1017-21. PubMed ID: 21249393
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  • 7. Clinical case seminar: a novel LHX3 mutation presenting as combined pituitary hormonal deficiency.
    Bhangoo AP, Hunter CS, Savage JJ, Anhalt H, Pavlakis S, Walvoord EC, Ten S, Rhodes SJ.
    J Clin Endocrinol Metab; 2006 Mar; 91(3):747-53. PubMed ID: 16394081
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  • 9. Hypopituitarism oddities: congenital causes.
    Kelberman D, Dattani MT.
    Horm Res; 2007 Mar; 68 Suppl 5():138-44. PubMed ID: 18174732
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  • 10. LHX3 transcription factor mutations associated with combined pituitary hormone deficiency impair the activation of pituitary target genes.
    Sloop KW, Parker GE, Hanna KR, Wright HA, Rhodes SJ.
    Gene; 2001 Mar 07; 265(1-2):61-9. PubMed ID: 11255008
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  • 13. Model of pediatric pituitary hormone deficiency separates the endocrine and neural functions of the LHX3 transcription factor in vivo.
    Colvin SC, Malik RE, Showalter AD, Sloop KW, Rhodes SJ.
    Proc Natl Acad Sci U S A; 2011 Jan 04; 108(1):173-8. PubMed ID: 21149718
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  • 15. PROP1, HESX1, POU1F1, LHX3 and LHX4 mutation and deletion screening and GH1 P89L and IVS3+1/+2 mutation screening in a Dutch nationwide cohort of patients with combined pituitary hormone deficiency.
    de Graaff LC, Argente J, Veenma DC, Drent ML, Uitterlinden AG, Hokken-Koelega AC.
    Horm Res Paediatr; 2010 Jan 04; 73(5):363-71. PubMed ID: 20389107
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