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2. Pituitary magnetic resonance imaging in 15 patients with Prop1 gene mutations: pituitary enlargement may originate from the intermediate lobe. Voutetakis A; Argyropoulou M; Sertedaki A; Livadas S; Xekouki P; Maniati-Christidi M; Bossis I; Thalassinos N; Patronas N; Dacou-Voutetakis C J Clin Endocrinol Metab; 2004 May; 89(5):2200-6. PubMed ID: 15126542 [TBL] [Abstract][Full Text] [Related]
3. 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 [TBL] [Abstract][Full Text] [Related]
4. MR imaging of the pituitary gland in children and young adults with congenital combined pituitary hormone deficiency associated with PROP1 mutations. Fofanova O; Takamura N; Kinoshita E; Vorontsov A; Vladimirova V; Dedov I; Peterkova V; Yamashita S AJR Am J Roentgenol; 2000 Feb; 174(2):555-9. PubMed ID: 10658742 [TBL] [Abstract][Full Text] [Related]
5. Impaired adrenocorticotropin-adrenal axis in combined pituitary hormone deficiency caused by a two-base pair deletion (301-302delAG) in the prophet of Pit-1 gene. Pernasetti F; Toledo SP; Vasilyev VV; Hayashida CY; Cogan JD; Ferrari C; Lourenço DM; Mellon PL J Clin Endocrinol Metab; 2000 Jan; 85(1):390-7. PubMed ID: 10634415 [TBL] [Abstract][Full Text] [Related]
6. 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 [TBL] [Abstract][Full Text] [Related]
7. Mutations and pituitary morphology in a series of 82 patients with PROP1 gene defects. Obermannova B; Pfaeffle R; Zygmunt-Gorska A; Starzyk J; Verkauskiene R; Smetanina N; Bezlepkina O; Peterkova V; Frisch H; Cinek O; Child CJ; Blum WF; Lebl J Horm Res Paediatr; 2011; 76(5):348-54. PubMed ID: 22024773 [TBL] [Abstract][Full Text] [Related]
8. High prevalence of PROP1 defects in Lithuania: phenotypic findings in an ethnically homogenous cohort of patients with multiple pituitary hormone deficiency. Navardauskaite R; Dusatkova P; Obermannova B; Pfaeffle RW; Blum WF; Adukauskiene D; Smetanina N; Cinek O; Verkauskiene R; Lebl J J Clin Endocrinol Metab; 2014 Jan; 99(1):299-306. PubMed ID: 24178788 [TBL] [Abstract][Full Text] [Related]
9. PROP1 mutations cause progressive deterioration of anterior pituitary function including adrenal insufficiency: a longitudinal analysis. Böttner A; Keller E; Kratzsch J; Stobbe H; Weigel JF; Keller A; Hirsch W; Kiess W; Blum WF; Pfäffle RW J Clin Endocrinol Metab; 2004 Oct; 89(10):5256-65. PubMed ID: 15472232 [TBL] [Abstract][Full Text] [Related]
10. 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]
14. 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]
15. 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]
16. 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]
17. Auxological and endocrine phenotype in a population-based cohort of patients with PROP1 gene defects. Lebl J; Vosáhlo J; Pfaeffle RW; Stobbe H; Cerná J; Novotná D; Zapletalová J; Kalvachová B; Hána V; Weiss V; Blum WF Eur J Endocrinol; 2005 Sep; 153(3):389-96. PubMed ID: 16131601 [TBL] [Abstract][Full Text] [Related]
18. Long-Term Outcomes, Genetics, and Pituitary Morphology in Patients with Isolated Growth Hormone Deficiency and Multiple Pituitary Hormone Deficiencies: A Single-Centre Experience of Four Decades of Growth Hormone Replacement. Rohayem J; Drechsel H; Tittel B; Hahn G; Pfaeffle R; Huebner A Horm Res Paediatr; 2016; 86(2):106-116. PubMed ID: 27487097 [TBL] [Abstract][Full Text] [Related]
19. [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]