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PUBMED FOR HANDHELDS

Journal Abstract Search


226 related items for PubMed ID: 17438671

  • 1. The role of transcription factors implicated in anterior pituitary development in the aetiology of congenital hypopituitarism.
    Kelberman D, Dattani MT.
    Ann Med; 2006; 38(8):560-77. PubMed ID: 17438671
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  • 2. Hypothalamic and pituitary development: novel insights into the aetiology.
    Kelberman D, Dattani MT.
    Eur J Endocrinol; 2007 Aug; 157 Suppl 1():S3-14. PubMed ID: 17785694
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  • 3. Developmental disorders of the hypothalamus and pituitary gland associated with congenital hypopituitarism.
    Mehta A, Dattani MT.
    Best Pract Res Clin Endocrinol Metab; 2008 Feb; 22(1):191-206. PubMed ID: 18279788
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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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  • 5. Role of transcription factors in midline central nervous system and pituitary defects.
    Kelberman D, Dattani MT.
    Endocr Dev; 2009 Aug; 14():67-82. PubMed ID: 19293576
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  • 6. 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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  • 7. Hypopituitarism oddities: congenital causes.
    Kelberman D, Dattani MT.
    Horm Res; 2007 Nov; 68 Suppl 5():138-44. PubMed ID: 18174732
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  • 9. [Congenital hypopituitarism: when should transcription factor gene screenings be performed?].
    Reynaud R, Barlier A, Chadli-Chaieb M, Saveanu A, Simonin G, Enjalbert A, Brue T.
    Presse Med; 2004 Mar 27; 33(6):400-5. PubMed ID: 15105786
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  • 10. Genetic causes of isolated and combined pituitary hormone deficiency.
    Giordano M.
    Best Pract Res Clin Endocrinol Metab; 2016 Dec 27; 30(6):679-691. PubMed ID: 27974184
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  • 13. Genetic disorders of the pituitary.
    Cohen LE.
    Curr Opin Endocrinol Diabetes Obes; 2012 Feb 27; 19(1):33-9. PubMed ID: 22157402
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  • 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 27; 62(2):163-8. PubMed ID: 15670191
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  • 16. Genetics of septo-optic dysplasia.
    Kelberman D, Dattani MT.
    Pituitary; 2007 Feb 27; 10(4):393-407. PubMed ID: 17587179
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  • 20. The role of the sonic hedgehog signalling pathway in patients with midline defects and congenital hypopituitarism.
    Gregory LC, Gaston-Massuet C, Andoniadou CL, Carreno G, Webb EA, Kelberman D, McCabe MJ, Panagiotakopoulos L, Saldanha JW, Spoudeas HA, Torpiano J, Rossi M, Raine J, Canham N, Martinez-Barbera JP, Dattani MT.
    Clin Endocrinol (Oxf); 2015 May 27; 82(5):728-38. PubMed ID: 25327282
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