161 related articles for article (PubMed ID: 9745452)
21. 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]
22. 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]
23. 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
[TBL] [Abstract][Full Text] [Related]
24. 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
[TBL] [Abstract][Full Text] [Related]
25. [Genetic background of inherited multiple pituitary hormone deficiency. Mutations of PROP1 gene in Hungary].
Halász Z
Orv Hetil; 2011 Feb; 152(6):221-32. PubMed ID: 21278027
[TBL] [Abstract][Full Text] [Related]
26. 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]
27. Combined pituitary hormone deficiency (CPHD) due to a complete PROP1 deletion.
Abrão MG; Leite MV; Carvalho LR; Billerbeck AE; Nishi MY; Barbosa AS; Martin RM; Arnhold IJ; Mendonca BB
Clin Endocrinol (Oxf); 2006 Sep; 65(3):294-300. PubMed ID: 16918947
[TBL] [Abstract][Full Text] [Related]
28. Conserved amino acid sequences confer nuclear localization upon the Prophet of Pit-1 pituitary transcription factor protein.
Guy JC; Hunter CS; Showalter AD; Smith TP; Charoonpatrapong K; Sloop KW; Bidwell JP; Rhodes SJ
Gene; 2004 Jul; 336(2):263-73. PubMed ID: 15246537
[TBL] [Abstract][Full Text] [Related]
29. Functional SNPs within the intron 1 of the PROP1 gene contribute to combined growth hormone deficiency (CPHD).
Godi M; Mellone S; Tiradani L; Marabese R; Bardelli C; Salerno M; Prodam F; Bellone S; Petri A; Momigliano-Richiardi P; Bona G; Giordano M
J Clin Endocrinol Metab; 2012 Sep; 97(9):E1791-7. PubMed ID: 22745233
[TBL] [Abstract][Full Text] [Related]
30. Two new PROP1 gene mutations responsible for compound pituitary hormone deficiency.
Paracchini R; Giordano M; Corrias A; Mellone S; Matarazzo P; Bellone J; Momigliano-Richiardi P; Bona G
Clin Genet; 2003 Aug; 64(2):142-7. PubMed ID: 12859410
[TBL] [Abstract][Full Text] [Related]
31. 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
[TBL] [Abstract][Full Text] [Related]
32. Mutation and gene copy number analyses of six pituitary transcription factor genes in 71 patients with combined pituitary hormone deficiency: identification of a single patient with LHX4 deletion.
Dateki S; Fukami M; Uematsu A; Kaji M; Iso M; Ono M; Mizota M; Yokoya S; Motomura K; Kinoshita E; Moriuchi H; Ogata T
J Clin Endocrinol Metab; 2010 Aug; 95(8):4043-7. PubMed ID: 20534763
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. A critical functional missense mutation (H173R) in the bovine PROP1 gene significantly affects growth traits in cattle.
Pan C; Wu C; Jia W; Xu Y; Lei C; Hu S; Lan X; Chen H
Gene; 2013 Dec; 531(2):398-402. PubMed ID: 24029076
[TBL] [Abstract][Full Text] [Related]
35. 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]
36. Identification of a Novel PROP1 Mutation in a Patient with Combined Pituitary Hormone Deficiency and Enlarged Pituitary.
Penta L; Bizzarri C; Panichi M; Novelli A; Lepri FR; Cappa M; Esposito S
Int J Mol Sci; 2019 Apr; 20(8):. PubMed ID: 30988269
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. 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]
39. PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency.
Vallette-Kasic S; Barlier A; Teinturier C; Diaz A; Manavela M; Berthezène F; Bouchard P; Chaussain JL; Brauner R; Pellegrini-Bouiller I; Jaquet P; Enjalbert A; Brue T
J Clin Endocrinol Metab; 2001 Sep; 86(9):4529-35. PubMed ID: 11549703
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
