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

219 related items for PubMed ID: 18852528

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 6. A novel mutation in HESX1 causes combined pituitary hormone deficiency without septo optic dysplasia phenotypes.
    Takagi M, Takahashi M, Ohtsu Y, Sato T, Narumi S, Arakawa H, Hasegawa T.
    Endocr J; 2016 Apr 25; 63(4):405-10. PubMed ID: 26781211
    [Abstract] [Full Text] [Related]

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Analysis of mouse models carrying the I26T and R160C substitutions in the transcriptional repressor HESX1 as models for septo-optic dysplasia and hypopituitarism.
    Sajedi E, Gaston-Massuet C, Signore M, Andoniadou CL, Kelberman D, Castro S, Etchevers HC, Gerrelli D, Dattani MT, Martinez-Barbera JP.
    Dis Model Mech; 2008 Apr 25; 1(4-5):241-54. PubMed ID: 19093031
    [Abstract] [Full Text] [Related]

  • 12. Septo-optic dysplasia complex: a heterogeneous malformation syndrome.
    Polizzi A, Pavone P, Iannetti P, Manfré L, Ruggieri M.
    Pediatr Neurol; 2006 Jan 25; 34(1):66-71. PubMed ID: 16376284
    [Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. [Natural course of septo-optic dysplasia: retrospective analysis of 20 cases].
    León-Gonzalez M, García-Peñas JJ, Puertas-Bordallo D, López-Pino MA, Argente-Oliver J, Cantarín-Extremera V.
    Rev Neurol; 2012 Mar 16; 54(6):321-31. PubMed ID: 22403144
    [Abstract] [Full Text] [Related]

  • 16. Ectopic posterior pituitary lobe and periventricular heterotopia: cerebral malformations with the same underlying mechanism?
    Mitchell LA, Thomas PQ, Zacharin MR, Scheffer IE.
    AJNR Am J Neuroradiol; 2002 Oct 16; 23(9):1475-81. PubMed ID: 12372734
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Structural pituitary abnormalities associated with CHARGE syndrome.
    Gregory LC, Gevers EF, Baker J, Kasia T, Chong K, Josifova DJ, Caimari M, Bilan F, McCabe MJ, Dattani MT.
    J Clin Endocrinol Metab; 2013 Apr 16; 98(4):E737-43. PubMed ID: 23526466
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. A homozygous mutation in HESX1 is associated with evolving hypopituitarism due to impaired repressor-corepressor interaction.
    Carvalho LR, Woods KS, Mendonca BB, Marcal N, Zamparini AL, Stifani S, Brickman JM, Arnhold IJ, Dattani MT.
    J Clin Invest; 2003 Oct 16; 112(8):1192-201. PubMed ID: 14561704
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.