BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

518 related articles for article (PubMed ID: 21497494)

  • 1. [Genetic aspects of growth hormone deficiency].
    Reynaud R; Castinetti F; Galon-Faure N; Albarel-Loy F; Saveanu A; Quentien MH; Jullien N; Khammar A; Enjalbert A; Barlier A; Brue T
    Arch Pediatr; 2011 Jun; 18(6):696-706. PubMed ID: 21497494
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Clinical and genetic aspects of combined pituitary hormone deficiencies].
    Castinetti F; Reynaud R; Saveanu A; Quentien MH; Albarel F; Barlier A; Enjalbert A; Brue T
    Ann Endocrinol (Paris); 2008 Feb; 69(1):7-17. PubMed ID: 18291347
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Growth hormone deficiency and combined pituitary hormone deficiency: does the genotype matter?
    Dattani MT
    Clin Endocrinol (Oxf); 2005 Aug; 63(2):121-30. PubMed ID: 16060904
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Hypopituitarism oddities: congenital causes.
    Kelberman D; Dattani MT
    Horm Res; 2007; 68 Suppl 5():138-44. PubMed ID: 18174732
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Genetic forms of hypopituitarism and their manifestation in the neonatal period.
    Alatzoglou KS; Dattani MT
    Early Hum Dev; 2009 Nov; 85(11):705-12. PubMed ID: 19762173
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. LHX3 and LHX4 transcription factors in pituitary development and disease.
    Colvin SC; Mullen RD; Pfaeffle RW; Rhodes SJ
    Pediatr Endocrinol Rev; 2009 Jan; 6 Suppl 2():283-90. PubMed ID: 19337183
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Classical and non-classical causes of GH deficiency in the paediatric age.
    Di Iorgi N; Morana G; Allegri AE; Napoli F; Gastaldi R; Calcagno A; Patti G; Loche S; Maghnie M
    Best Pract Res Clin Endocrinol Metab; 2016 Dec; 30(6):705-736. PubMed ID: 27974186
    [TBL] [Abstract][Full Text] [Related]  

  • 13. A novel dysfunctional LHX4 mutation with high phenotypical variability in patients with hypopituitarism.
    Castinetti F; Saveanu A; Reynaud R; Quentien MH; Buffin A; Brauner R; Kaffel N; Albarel F; Guedj AM; El Kholy M; Amin M; Enjalbert A; Barlier A; Brue T
    J Clin Endocrinol Metab; 2008 Jul; 93(7):2790-9. PubMed ID: 18445675
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Pituitary hormone deficiencies due to transcription factor gene alterations.
    Reynaud R; Saveanu A; Barlier A; Enjalbert A; Brue T
    Growth Horm IGF Res; 2004 Dec; 14(6):442-8. PubMed ID: 15519252
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort.
    Jullien N; Saveanu A; Vergier J; Marquant E; Quentien MH; Castinetti F; Galon-Faure N; Brauner R; Marrakchi Turki Z; Tauber M; El Kholy M; Linglart A; Rodien P; Fedala NS; Bergada I; Cortet-Rudelli C; Polak M; Nicolino M; Stuckens C; Barlier A; Brue T; Reynaud R;
    Clin Endocrinol (Oxf); 2021 Feb; 94(2):277-289. PubMed ID: 33098107
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Growth hormone deficiency (GHD) and small for gestational age (SGA): genetic alterations.
    Jancevska A; Gucev ZS; Tasic V; Pop-Jordanova N
    Prilozi; 2009 Dec; 30(2):33-55. PubMed ID: 20087248
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Role of transcription factors in midline central nervous system and pituitary defects.
    Kelberman D; Dattani MT
    Endocr Dev; 2009; 14():67-82. PubMed ID: 19293576
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism.
    Fritez N; Sobrier ML; Iraqi H; Vié-Luton MP; Netchine I; El Annas A; Pantel J; Collot N; Rose S; Piterboth W; Legendre M; Chraibi A; Amselem S; Kadiri A; Hilal L
    Clin Endocrinol (Oxf); 2015 Jun; 82(6):876-84. PubMed ID: 25557026
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 26.