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7. Rare Frequency of Mutations in Pituitary Transcription Factor Genes in Combined Pituitary Hormone or Isolated Growth Hormone Deficiencies in Korea. Choi JH; Jung CW; Kang E; Kim YM; Heo SH; Lee BH; Kim GH; Yoo HW Yonsei Med J; 2017 May; 58(3):527-532. PubMed ID: 28332357 [TBL] [Abstract][Full Text] [Related]
8. Novel Mutations in HESX1 and PROP1 Genes in Combined Pituitary Hormone Deficiency. Avbelj Stefanija M; Kotnik P; Bratanič N; Žerjav Tanšek M; Bertok S; Bratina N; Battelino T; Trebušak Podkrajšek K Horm Res Paediatr; 2015; 84(3):153-8. PubMed ID: 26111865 [TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations with three novel mutations. Madeira JL; Nishi MY; Nakaguma M; Benedetti AF; Biscotto IP; Fernandes T; Pequeno T; Figueiredo T; Franca MM; Correa FA; Otto AP; Abrão M; Miras MB; Santos S; Jorge AA; Costalonga EF; Mendonca BB; Arnhold IJ; Carvalho LR Clin Endocrinol (Oxf); 2017 Dec; 87(6):725-732. PubMed ID: 28734020 [TBL] [Abstract][Full Text] [Related]
10. Long-term follow-up of combined pituitary hormone deficiency in two siblings with a Prophet of Pit-1 gene mutation. Georgopoulos NA; Katsikis I; Giamalis P; Koika V; Adonakis G; Kourtis A; Kourounis G; Panidis D Gynecol Endocrinol; 2006 Dec; 22(12):704-9. PubMed ID: 17162714 [TBL] [Abstract][Full Text] [Related]
11. 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 [TBL] [Abstract][Full Text] [Related]
12. Frequency of mutations in PROP-1 gene in Turkish children with combined pituitary hormone deficiency. Kandemir N; Vurallı D; Taşkıran E; Gönç N; Özön A; Alikaşifoğlu A; Yılmaz E Turk J Pediatr; 2012; 54(6):570-5. PubMed ID: 23692781 [TBL] [Abstract][Full Text] [Related]
13. Comparison of clinical characteristics of a pediatric cohort with combined pituitary hormone deficiency caused by mutation of the PROP1 gene or of other origins. Zygmunt-Górska A; Wójcik M; Gilis-Januszewska A; Starmach A; Bik-Multanowski M; Starzyk JB Hormones (Athens); 2024 Mar; 23(1):69-79. PubMed ID: 38147295 [TBL] [Abstract][Full Text] [Related]
14. Mutation analysis of POUF-1, PROP-1 and HESX-1 show low frequency of mutations in children with sporadic forms of combined pituitary hormone deficiency and septo-optic dysplasia. Rainbow LA; Rees SA; Shaikh MG; Shaw NJ; Cole T; Barrett TG; Kirk JM Clin Endocrinol (Oxf); 2005 Feb; 62(2):163-8. PubMed ID: 15670191 [TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of PROP1, PIT1, HESX1, LHX3, and LHX4 shows high frequency of PROP1 mutations in patients with familial forms of combined pituitary hormone deficiency. Vieira TC; Boldarine VT; Abucham J Arq Bras Endocrinol Metabol; 2007 Oct; 51(7):1097-103. PubMed ID: 18157385 [TBL] [Abstract][Full Text] [Related]
16. 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 [TBL] [Abstract][Full Text] [Related]
17. 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; 73(5):363-71. PubMed ID: 20389107 [TBL] [Abstract][Full Text] [Related]