Eliez S - Search Results

1

Face processing in 22q11.2 deletion syndrome: atypical development and visual scanning alterations.

Zaharia A, Schneider M, Glaser B, Franchini M, Menghetti S, Schaer M, Debbané M, Eliez S. Zaharia A, et al. Among authors: eliez s. J Neurodev Disord. 2018 Aug 29;10(1):26. doi: 10.1186/s11689-018-9245-x. J Neurodev Disord. 2018. PMID: 30157749 Free PMC article.

2

Neurobehavioral phenotype in carriers of the fragile X premutation.

Johnston C, Eliez S, Dyer-Friedman J, Hessl D, Glaser B, Blasey C, Taylor A, Reiss A. Johnston C, et al. Among authors: eliez s. Am J Med Genet. 2001 Nov 1;103(4):314-9. Am J Med Genet. 2001. PMID: 11746012

3

Language skills in children with velocardiofacial syndrome (deletion 22q11.2).

Glaser B, Mumme DL, Blasey C, Morris MA, Dahoun SP, Antonarakis SE, Reiss AL, Eliez S. Glaser B, et al. Among authors: eliez s. J Pediatr. 2002 Jun;140(6):753-8. doi: 10.1067/mpd.2002.124774. J Pediatr. 2002. PMID: 12072882

4

Factors associated with parenting stress in mothers of children with fragile X syndrome.

Johnston C, Hessl D, Blasey C, Eliez S, Erba H, Dyer-Friedman J, Glaser B, Reiss AL. Johnston C, et al. Among authors: eliez s. J Dev Behav Pediatr. 2003 Aug;24(4):267-75. doi: 10.1097/00004703-200308000-00008. J Dev Behav Pediatr. 2003. PMID: 12915799

5

From research to practice: teacher and pediatrician awareness of phenotypic traits in neurogenetic syndromes.

Lee TH, Blasey CM, Dyer-Friedman J, Glaser B, Reiss AL, Eliez S. Lee TH, et al. Among authors: eliez s. Am J Ment Retard. 2005 Mar;110(2):100-6. doi: 10.1352/0895-8017(2005)110<100:FRTPTA>2.0.CO;2. Am J Ment Retard. 2005. PMID: 15762820

6

Temporal perception in velo-cardio-facial syndrome.

Debbané M, Glaser B, Gex-Fabry M, Eliez S. Debbané M, et al. Among authors: eliez s. Neuropsychologia. 2005;43(12):1754-62. doi: 10.1016/j.neuropsychologia.2005.02.006. Epub 2005 Mar 24. Neuropsychologia. 2005. PMID: 16154451

7

Decreased anterior cingulate volume in combat-related PTSD.

Woodward SH, Kaloupek DG, Streeter CC, Martinez C, Schaer M, Eliez S. Woodward SH, et al. Among authors: eliez s. Biol Psychiatry. 2006 Apr 1;59(7):582-7. doi: 10.1016/j.biopsych.2005.07.033. Epub 2005 Sep 13. Biol Psychiatry. 2006. PMID: 16165099

8

Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study.

Schaer M, Schmitt JE, Glaser B, Lazeyras F, Delavelle J, Eliez S. Schaer M, et al. Among authors: eliez s. Psychiatry Res. 2006 Jan 30;146(1):1-11. doi: 10.1016/j.pscychresns.2005.10.002. Epub 2006 Jan 4. Psychiatry Res. 2006. PMID: 16388934

9

No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.

Glaser B, Debbane M, Hinard C, Morris MA, Dahoun SP, Antonarakis SE, Eliez S. Glaser B, et al. Among authors: eliez s. Am J Psychiatry. 2006 Mar;163(3):537-9. doi: 10.1176/appi.ajp.163.3.537. Am J Psychiatry. 2006. PMID: 16513880

10

Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications.

Debbané M, Glaser B, David MK, Feinstein C, Eliez S. Debbané M, et al. Among authors: eliez s. Schizophr Res. 2006 Jun;84(2-3):187-93. doi: 10.1016/j.schres.2006.01.019. Epub 2006 Mar 20. Schizophr Res. 2006. PMID: 16545541

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