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PUBMED FOR HANDHELDS

Journal Abstract Search


526 related items for PubMed ID: 21497494

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  • 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
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  • 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
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  • 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
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  • 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
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  • 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
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  • 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, Genhypopit Network.
    Clin Endocrinol (Oxf); 2021 Feb; 94(2):277-289. PubMed ID: 33098107
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  • 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
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  • 18. Role of transcription factors in midline central nervous system and pituitary defects.
    Kelberman D, Dattani MT.
    Endocr Dev; 2009 Feb; 14():67-82. PubMed ID: 19293576
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