286 related articles for article (PubMed ID: 14646405)
1. 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; 60(6):277-83. PubMed ID: 14646405
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Molecular analysis of the PROP1 and HESX1 genes in patients with septo-optic dysplasia and/or pituitary hormone deficiency.
Cruz JB; Nunes VS; Clara SA; Perone D; Kopp P; Nogueira CR
Arq Bras Endocrinol Metabol; 2010; 54(5):482-7. PubMed ID: 20694410
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.
Baş F; Uyguner ZO; Darendeliler F; Aycan Z; Çetinkaya E; Berberoğlu M; Şiklar Z; Öcal G; Darcan Ş; Gökşen D; Topaloğlu AK; Yüksel B; Özbek MN; Ercan O; Evliyaoğlu O; Çetinkaya S; Şen Y; Atabek E; Toksoy G; Aydin BK; Bundak R
Endocrine; 2015 Jun; 49(2):479-91. PubMed ID: 25500790
[TBL] [Abstract][Full Text] [Related]
9. 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
[TBL] [Abstract][Full Text] [Related]
10. Panhypopituitarism: genetic versus acquired etiological factors.
Coya R; Vela A; Pérez de Nanclares G; Rica I; Castaño L; Busturia MA; Martul P;
J Pediatr Endocrinol Metab; 2007 Jan; 20(1):27-36. PubMed ID: 17315526
[TBL] [Abstract][Full Text] [Related]
11. Hormonal, pituitary magnetic resonance, LHX4 and HESX1 evaluation in patients with hypopituitarism and ectopic posterior pituitary lobe.
Melo ME; Marui S; Carvalho LR; Arnhold IJ; Leite CC; Mendonça BB; Knoepfelmacher M
Clin Endocrinol (Oxf); 2007 Jan; 66(1):95-102. PubMed ID: 17201807
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Mutations within the transcription factor PROP1 are rare in a cohort of patients with sporadic combined pituitary hormone deficiency (CPHD).
Turton JP; Mehta A; Raza J; Woods KS; Tiulpakov A; Cassar J; Chong K; Thomas PQ; Eunice M; Ammini AC; Bouloux PM; Starzyk J; Hindmarsh PC; Dattani MT
Clin Endocrinol (Oxf); 2005 Jul; 63(1):10-8. PubMed ID: 15963055
[TBL] [Abstract][Full Text] [Related]
15. Hypopituitarism oddities: congenital causes.
Kelberman D; Dattani MT
Horm Res; 2007; 68 Suppl 5():138-44. PubMed ID: 18174732
[TBL] [Abstract][Full Text] [Related]
16. Mutations Within the Transcription Factor
Bulut FD; Özdemir Dilek S; Kotan D; Mengen E; Gürbüz F; Yüksel B
J Clin Res Pediatr Endocrinol; 2020 Sep; 12(3):261-268. PubMed ID: 31948187
[TBL] [Abstract][Full Text] [Related]
17. 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
[TBL] [Abstract][Full Text] [Related]
18. Sporadic heterozygous frameshift mutation of HESX1 causing pituitary and optic nerve hypoplasia and combined pituitary hormone deficiency in a Japanese patient.
Tajima T; Hattorri T; Nakajima T; Okuhara K; Sato K; Abe S; Nakae J; Fujieda K
J Clin Endocrinol Metab; 2003 Jan; 88(1):45-50. PubMed ID: 12519827
[TBL] [Abstract][Full Text] [Related]
19. Mutations in PROP1 cause familial combined pituitary hormone deficiency.
Wu W; Cogan JD; Pfäffle RW; Dasen JS; Frisch H; O'Connell SM; Flynn SE; Brown MR; Mullis PE; Parks JS; Phillips JA; Rosenfeld MG
Nat Genet; 1998 Feb; 18(2):147-9. PubMed ID: 9462743
[TBL] [Abstract][Full Text] [Related]
20. Genetic screening of combined pituitary hormone deficiency: experience in 195 patients.
Reynaud R; Gueydan M; Saveanu A; Vallette-Kasic S; Enjalbert A; Brue T; Barlier A
J Clin Endocrinol Metab; 2006 Sep; 91(9):3329-36. PubMed ID: 16735499
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]