These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

126 related articles for article (PubMed ID: 22024773)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. PROP1 gene analysis in Portuguese patients with combined pituitary hormone deficiency.
    Lemos MC; Gomes L; Bastos M; Leite V; Limbert E; Carvalho D; Bacelar C; Monteiro M; Fonseca F; Agapito A; Castro JJ; Regateiro FJ; Carvalheiro M
    Clin Endocrinol (Oxf); 2006 Oct; 65(4):479-85. PubMed ID: 16984240
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. 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]  

  • 8. [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]  

  • 9. [Evaluation of pituitary imaging in patients with prop-1 gene mutation].
    Tkacenko N; Lasiene D; Jakstiene S; Basevicius A; Verkauskiene R
    Medicina (Kaunas); 2009; 45(9):693-8. PubMed ID: 19834305
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pituitary size fluctuation in long-term MR studies of PROP1 deficient patients: A persistent pathophysiological mechanism?
    Voutetakis A; Sertedaki A; Livadas S; Xekouki P; Bossis I; Dacou-Voutetakis C; Argyropoulou MI
    J Endocrinol Invest; 2006 May; 29(5):462-6. PubMed ID: 16794371
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. 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]  

  • 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. Case seminar: a young female with acute hyponatremia and a sellar mass.
    Pekic S; Doknic M; Miljic D; Saveanu A; Reynaud R; Barlier A; Brue T; Popovic V
    Endocrine; 2011 Dec; 40(3):325-31. PubMed ID: 21863341
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. High prevalence of PROP1 gene mutations in Hungarian patients with childhood-onset combined anterior pituitary hormone deficiency.
    Halász Z; Toke J; Patócs A; Bertalan R; Tömböl Z; Sallai A; Hosszú E; Muzsnai A; Kovács L; Sólyom J; Fekete G; Rácz K
    Endocrine; 2006 Dec; 30(3):255-60. PubMed ID: 17526936
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.