BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

141 related articles for article (PubMed ID: 15126542)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. 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]  

  • 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. 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]  

  • 10. 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]  

  • 11. 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]  

  • 12. Pituitary magnetic resonance imaging and function in patients with growth hormone deficiency with and without mutations in GHRH-R, GH-1, or PROP-1 genes.
    Osorio MG; Marui S; Jorge AA; Latronico AC; Lo LS; Leite CC; Estefan V; Mendonca BB; Arnhold IJ
    J Clin Endocrinol Metab; 2002 Nov; 87(11):5076-84. PubMed ID: 12414875
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 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. 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]  

  • 16. Thickened pituitary stalk on magnetic resonance imaging in children with central diabetes insipidus.
    Leger J; Velasquez A; Garel C; Hassan M; Czernichow P
    J Clin Endocrinol Metab; 1999 Jun; 84(6):1954-60. PubMed ID: 10372693
    [TBL] [Abstract][Full Text] [Related]  

  • 17. "Hot spot" in the PROP1 gene responsible for combined pituitary hormone deficiency.
    Deladoëy J; Flück C; Büyükgebiz A; Kuhlmann BV; Eblé A; Hindmarsh PC; Wu W; Mullis PE
    J Clin Endocrinol Metab; 1999 May; 84(5):1645-50. PubMed ID: 10323394
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Relationship between the morphological evaluation of the pituitary and the growth hormone (GH) response to GH-releasing hormone Plus arginine in children and adults with congenital hypopituitarism.
    Maghnie M; Salati B; Bianchi S; Rallo M; Tinelli C; Autelli M; Aimaretti G; Ghigo E
    J Clin Endocrinol Metab; 2001 Apr; 86(4):1574-9. PubMed ID: 11297586
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.