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

246 related items for PubMed ID: 22920836

  • 1. Hippocampal volume reduction in chromosome 22q11.2 deletion syndrome (22q11.2DS): a longitudinal study of morphometry and symptomatology.
    Flahault A, Schaer M, Ottet MC, Debbané M, Eliez S.
    Psychiatry Res; 2012 Jul 30; 203(1):1-5. PubMed ID: 22920836
    [Abstract] [Full Text] [Related]

  • 2. Hippocampal volume reduction in 22q11.2 deletion syndrome.
    Debbané M, Schaer M, Farhoumand R, Glaser B, Eliez S.
    Neuropsychologia; 2006 Jul 30; 44(12):2360-5. PubMed ID: 16787654
    [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.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

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

  • 9. Cingulate gyral reductions are related to low executive functioning and psychotic symptoms in 22q 11.2 deletion syndrome.
    Dufour F, Schaer M, Debbané M, Farhoumand R, Glaser B, Eliez S.
    Neuropsychologia; 2008 Oct 30; 46(12):2986-92. PubMed ID: 18616958
    [Abstract] [Full Text] [Related]

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

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome.
    Prasad SE, Howley S, Murphy KC.
    Dev Disabil Res Rev; 2008 Oct 30; 14(1):26-34. PubMed ID: 18636634
    [Abstract] [Full Text] [Related]

  • 14. Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study.
    Gothelf D, Penniman L, Gu E, Eliez S, Reiss AL.
    Schizophr Res; 2007 Nov 30; 96(1-3):72-81. PubMed ID: 17804201
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 20. Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
    Gothelf D, Law AJ, Frisch A, Chen J, Zarchi O, Michaelovsky E, Ren-Patterson R, Lipska BK, Carmel M, Kolachana B, Weizman A, Weinberger DR.
    Biol Psychiatry; 2014 Mar 01; 75(5):406-13. PubMed ID: 23992923
    [Abstract] [Full Text] [Related]

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