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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
13. Genetic disorders of the pituitary. Cohen LE. Curr Opin Endocrinol Diabetes Obes; 2012 Feb 27; 19(1):33-9. PubMed ID: 22157402 [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 27; 62(2):163-8. PubMed ID: 15670191 [Abstract] [Full Text] [Related]