These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

245 related items for PubMed ID: 22715480

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Genetic screening of regulatory regions of pituitary transcription factors in patients with idiopathic pituitary hormone deficiencies.
    Elizabeth M, Hokken-Koelega ACS, Schuilwerve J, Peeters RP, Visser TJ, de Graaff LCG.
    Pituitary; 2018 Feb; 21(1):76-83. PubMed ID: 29255988
    [Abstract] [Full Text] [Related]

  • 31. [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
    [Abstract] [Full Text] [Related]

  • 32. Combined pituitary hormone deficiency in Australian children: clinical and genetic correlates.
    McLennan K, Jeske Y, Cotterill A, Cowley D, Penfold J, Jones T, Howard N, Thomsett M, Choong C.
    Clin Endocrinol (Oxf); 2003 Jun; 58(6):785-94. PubMed ID: 12780757
    [Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. 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
    [Abstract] [Full Text] [Related]

  • 35.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 36. 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
    [Abstract] [Full Text] [Related]

  • 37. Gradual loss of ACTH due to a novel mutation in LHX4: comprehensive mutation screening in Japanese patients with congenital hypopituitarism.
    Takagi M, Ishii T, Inokuchi M, Amano N, Narumi S, Asakura Y, Muroya K, Hasegawa Y, Adachi M, Hasegawa T.
    PLoS One; 2012 Feb; 7(9):e46008. PubMed ID: 23029363
    [Abstract] [Full Text] [Related]

  • 38. Genetic causes of isolated and combined pituitary hormone deficiency.
    Giordano M.
    Best Pract Res Clin Endocrinol Metab; 2016 Dec; 30(6):679-691. PubMed ID: 27974184
    [Abstract] [Full Text] [Related]

  • 39. 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
    [Abstract] [Full Text] [Related]

  • 40. A novel OTX2 gene frameshift mutation in a child with microphthalmia, ectopic pituitary and growth hormone deficiency.
    Lonero A, Delvecchio M, Primignani P, Caputo R, Bargiacchi S, Penco S, Mauri L, Andreucci E, Faienza MF, Cavallo L.
    J Pediatr Endocrinol Metab; 2016 May 01; 29(5):603-5. PubMed ID: 26974134
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 13.