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Results: 1 to 20 of 43

1.

Children with chromosome 22q11.2 deletion syndrome exhibit impaired spatial working memory.

Wong LM, Riggins T, Harvey D, Cabaral M, Simon TJ.

Am J Intellect Dev Disabil. 2014 Mar;119(2):115-32. doi: 10.1352/1944-7558-119.2.115.

PMID:
24679349
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Structural abnormalities in cortical volume, thickness, and surface area in 22q11.2 microdeletion syndrome: Relationship with psychotic symptoms.

Jalbrzikowski M, Jonas R, Senturk D, Patel A, Chow C, Green MF, Bearden CE.

Neuroimage Clin. 2013 Oct 14;3:405-15. doi: 10.1016/j.nicl.2013.09.013. eCollection 2013.

PMID:
24273724
[PubMed]
Free PMC Article
3.

Typical and atypical brain development: a review of neuroimaging studies.

Dennis EL, Thompson PM.

Dialogues Clin Neurosci. 2013 Sep;15(3):359-84. Review.

PMID:
24174907
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Divergent structural brain abnormalities between different genetic subtypes of children with Prader-Willi syndrome.

Lukoshe A, White T, Schmidt MN, van der Lugt A, Hokken-Koelega AC.

J Neurodev Disord. 2013 Oct 22;5(1):31. doi: 10.1186/1866-1955-5-31.

PMID:
24144356
[PubMed]
Free PMC Article
5.

Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome.

Kikinis Z, Makris N, Finn CT, Bouix S, Lucia D, Coleman MJ, Tworog-Dube E, Kikinis R, Kucherlapati R, Shenton ME, Kubicki M.

Brain Imaging Behav. 2013 Sep;7(3):316-25. doi: 10.1007/s11682-013-9232-5.

PMID:
23612843
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Shared deficits in space, time, and quantity processing in childhood genetic disorders.

Vicario CM, Yates MJ, Nicholls ME.

Front Psychol. 2013 Feb 7;4:43. doi: 10.3389/fpsyg.2013.00043. eCollection 2013. No abstract available.

PMID:
23405055
[PubMed]
Free PMC Article
7.

Proximal femoral density distribution and structure in relation to age and hip fracture risk in women.

Carballido-Gamio J, Harnish R, Saeed I, Streeper T, Sigurdsson S, Amin S, Atkinson EJ, Therneau TM, Siggeirsdottir K, Cheng X, Melton LJ 3rd, Keyak J, Gudnason V, Khosla S, Harris TB, Lang TF.

J Bone Miner Res. 2013 Mar;28(3):537-46. doi: 10.1002/jbmr.1802.

PMID:
23109068
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Converging levels of analysis on a genomic hotspot for psychosis: insights from 22q11.2 deletion syndrome.

Schreiner MJ, Lazaro MT, Jalbrzikowski M, Bearden CE.

Neuropharmacology. 2013 May;68:157-73. doi: 10.1016/j.neuropharm.2012.09.012. Epub 2012 Oct 23. Review.

PMID:
23098994
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Epilepsy in Muenke syndrome: FGFR3-related craniosynostosis.

Agochukwu NB, Solomon BD, Gropman AL, Muenke M.

Pediatr Neurol. 2012 Nov;47(5):355-61. doi: 10.1016/j.pediatrneurol.2012.07.004. Review.

PMID:
23044018
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

A cross-sectional study of the development of volitional control of spatial attention in children with chromosome 22q11.2 deletion syndrome.

Shapiro HM, Takarae Y, Harvey DJ, Cabaral MH, Simon TJ.

J Neurodev Disord. 2012 Feb 15;4(1):5. doi: 10.1186/1866-1955-4-5.

PMID:
22958432
[PubMed]
Free PMC Article
11.

Altered development of the dorsolateral prefrontal cortex in chromosome 22q11.2 deletion syndrome: an in vivo proton spectroscopy study.

Shashi V, Veerapandiyan A, Keshavan MS, Zapadka M, Schoch K, Kwapil TR, Hooper SR, Stanley JA.

Biol Psychiatry. 2012 Oct 15;72(8):684-91. doi: 10.1016/j.biopsych.2012.04.023. Epub 2012 May 25.

PMID:
22633947
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

MicroRNA dysregulation in neuropsychiatric disorders and cognitive dysfunction.

Xu B, Hsu PK, Karayiorgou M, Gogos JA.

Neurobiol Dis. 2012 May;46(2):291-301. doi: 10.1016/j.nbd.2012.02.016. Epub 2012 Mar 3. Review.

PMID:
22406400
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Conceptualizing neurodevelopmental disorders through a mechanistic understanding of fragile X syndrome and Williams syndrome.

Fung LK, Quintin EM, Haas BW, Reiss AL.

Curr Opin Neurol. 2012 Apr;25(2):112-24. doi: 10.1097/WCO.0b013e328351823c. Review.

PMID:
22395002
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders.

Hunsaker MR.

Prog Neurobiol. 2012 Feb;96(2):220-41. doi: 10.1016/j.pneurobio.2011.12.001. Epub 2012 Jan 13. Review.

PMID:
22266125
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Computerized neurocognitive profile in young people with 22q11.2 deletion syndrome compared to youths with schizophrenia and at-risk for psychosis.

Goldenberg PC, Calkins ME, Richard J, McDonald-McGinn D, Zackai E, Mitra N, Emanuel B, Devoto M, Borgmann-Winter K, Kohler C, Conroy CG, Gur RC, Gur RE.

Am J Med Genet B Neuropsychiatr Genet. 2012 Jan;159B(1):87-93. doi: 10.1002/ajmg.b.32005. Epub 2011 Dec 13.

PMID:
22170773
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

White matter microstructure in 22q11 deletion syndrome: a pilot diffusion tensor imaging and voxel-based morphometry study of children and adolescents.

Sundram F, Campbell LE, Azuma R, Daly E, Bloemen OJ, Barker GJ, Chitnis X, Jones DK, van Amelsvoort T, Murphy KC, Murphy DG.

J Neurodev Disord. 2010 Jun;2(2):77-92. doi: 10.1007/s11689-010-9043-6. Epub 2010 Mar 5.

PMID:
22127856
[PubMed]
Free PMC Article
17.

Proline and COMT status affect visual connectivity in children with 22q11.2 deletion syndrome.

Magnée MJ, Lamme VA, de Sain-van der Velden MG, Vorstman JA, Kemner C.

PLoS One. 2011;6(10):e25882. doi: 10.1371/journal.pone.0025882. Epub 2011 Oct 5.

PMID:
21998713
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Clues to the foundations of numerical cognitive impairments: evidence from genetic disorders.

Simon TJ.

Dev Neuropsychol. 2011;36(6):788-805. doi: 10.1080/87565641.2010.549879. Review.

PMID:
21761998
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Discordance in Diagnoses and Treatment of Psychiatric Disorders in Children and Adolescents with 22q11.2 Deletion Syndrome.

Young AS, Shashi V, Schoch K, Kwapil T, Hooper SR.

Asian J Psychiatr. 2011 Jun 1;4(2):119-124.

PMID:
21743818
[PubMed]
Free PMC Article
20.

Visuospatial working memory in children and adolescents with 22q11.2 deletion syndrome; an fMRI study.

Azuma R, Daly EM, Campbell LE, Stevens AF, Deeley Q, Giampietro V, Brammer MJ, Glaser B, Ambery FZ, Morris RG, Williams SC, Owen MJ, Murphy DG, Murphy KC.

J Neurodev Disord. 2009 Mar;1(1):46-60. doi: 10.1007/s11689-009-9008-9. Epub 2009 Mar 5.

PMID:
21547621
[PubMed]
Free PMC Article

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