SEARCH

SEARCH BY CITATION

References

  • 1
    Tezenas Du Montcel S, Mendizabai H, Ayme S, Levy A, Philip N. Prevalence of 22q11 microdeletion. J Med Genet 1996; 33: 719.
  • 2
    Simon TJ, Ding L, Bish JP, McDonald-McGinn DM, Zackai EH, Gee J. Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study. Neuroimage 2005; 25: 16980.
  • 3
    Eliez S, Schmitt JE, White CD, Reiss AL. Children and adolescents with velocardiofacial syndrome: a volumetric MRI study. Am J Psychiatry 2000; 157: 40915.
  • 4
    Kates WR, Burnette CP, Jabs EW, et al. Regional cortical white matter reductions in velocardiofacial syndrome: a volumetric MRI analysis. Biol Psychiatry 2001; 49: 67784.
  • 5
    Gerdes M, Solot C, Wang PP, et al. Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion. Am J Med Genet 1999; 85: 12733.
  • 6
    Bingham PM, Zimmerman RA, McDonald-McGinn D, Driscoll D, Emanuel BS, Zackai E. Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11. Am J Med Genet 1997; 74: 53843.
  • 7
    Schaer M, Schmitt JE, Glaser B, Lazeyras F, Delavelle J, Eliez S. Abnormal patterns of cortical gyrification in velo-cardio-facial syndrome (deletion 22q11.2): an MRI study. Psychiatry Res 2006; 146: 111.
  • 8
    Schaer M, Cuadra MB, Tamarit L, Lazeyras F, Eliez S, Thiran JP. A surface-based approach to quantify local cortical gyrification. IEEE Trans Med Imaging 2008; 27: 16170.
  • 9
    McDonald-McGinn DM, Kirschner R, Goldmuntz E, et al. The Philadelphia story: the 22q11.2 deletion: report on 250 patients. Genet Couns 1999; 10: 1124.
  • 10
    Glauser TA, Rorke LB, Weinberg PM, Clancy RR. Congenital brain anomalies associated with the hypoplastic left heart syndrome. Pediatrics 1990; 85: 98490.
  • 11
    Miller SP, McQuillen PS. Neurology of congenital heart disease: insight from brain imaging. Arch Dis Child Fetal Neonatal Ed 2007; 92: F43537.
  • 12
    Bearden CE, Van Erp TG, Dutton RA, et al. Mapping cortical thickness in children with 22q11.2 deletions. Cereb Cortex 2007; 17: 188998.
  • 13
    Achenbach TM. Manual for the Child Behavior Checklist 4-18 and 1991 Profile. Burlington, VT: University of Vermont, Department of Psychiatry, 1991.
  • 14
    Achenbach TM. Manual for the Youth Self-Report Form and Profile. Burlington, VT: University of Vermont, Department of Psychiatry, 1991.
  • 15
    Achenbach TM, Rescorla LA. Manual for the ASEBA adults forms and profile. Burlington, VT: University of Vermont, Department of Psychiatry, 2003.
  • 16
    Swillen A, Devriendt K, Legius E, et al. The behavioural phenotype in velo-cardio-facial syndrome (VCFS): from infancy to adolescence. Genet Couns 1999; 10: 7988.
  • 17
    Fischl B, Liu A, Dale AM. Automated manifold surgery: constructing geometrically accurate and topologically correct models of the human cerebral cortex. IEEE Trans Med Imaging 2001; 20: 7080.
  • 18
    Zilles K, Armstrong E, Schleicher A, Kretschmann HJ. The human pattern of gyrification in the cerebral cortex. Anat Embryol (Berl) 1988; 179: 17379.
  • 19
    Genovese CR, Lazar NA, Nichols T. Thresholding of statistical maps in functional neuroimaging using the false discovery rate. Neuroimage 2002; 15: 87078.
  • 20
    Rakic P. Radial unit hypothesis of neocortical expansion. Novartis Found Symp 2000; 228: 3042; discussion p 52.
  • 21
    Eliez S, Blasey CM, Menon V, White CD, Schmitt JE, Reiss AL. Functional brain imaging study of mathematical reasoning abilities in velocardiofacial syndrome (del22q11.2). Genet Med 2001; 3: 4955.
  • 22
    Barnea-Goraly N, Menon V, Krasnow B, Ko A, Reiss A, Eliez S. Investigation of white matter structure in velocardiofacial syndrome: a diffusion tensor imaging study. Am J Psychiatry 2003; 160: 186369.
  • 23
    Gothelf D, Presburger G, Levy D, et al. Genetic, developmental, and physical factors associated with attention deficit hyperactivity disorder in patients with velocardiofacial syndrome. Am J Med Genet B Neuropsychiatr Genet. 2004; 126: 11621.
  • 24
    Dufour F, Schaer M, Debbane M, Farhoumand R, Glaser B, Eliez S. Cingulate gyral reductions are related to low executive functioning and psychotic symptoms in 22q11.2 deletion syndrome. Neuropsychologia 2008; 46: 298692.
  • 25
    Van Aken K, De Smedt B, Van Roie A, et al. Motor development in school-aged children with 22q11 deletion (velocardiofacial/DiGeorge syndrome). Dev Med Child Neurol 2007; 49: 21013.
  • 26
    Scambler PJ. The 22q11 deletion syndromes. Hum Mol Genet. 2000; 9: 242126.
  • 27
    Robin NH, Taylor CJ, McDonald-McGinn DM, et al. Polymicrogyria and deletion 22q11.2 syndrome: window to the etiology of a common cortical malformation. Am J Med Genet A 2006; 140: 241625.
  • 28
    Barkovich AJ, Rowley H, Bollen A. Correlation of prenatal events with the development of polymicrogyria. AJNR Am J Neuroradiol 1995; 16 (Suppl. 4): 82227.
  • 29
    Gothelf D, Penniman L, Gu E, Eliez S, Reiss AL. Developmental trajectories of brain structure in adolescents with 22q11.2 deletion syndrome: a longitudinal study. Schizophr Res 2007; 96: 7281.
  • 30
    Lindsay EA, Vitelli F, Su H, et al. Tbx1 haploinsufficieny in the DiGeorge syndrome region causes aortic arch defects in mice. Nature 2001; 410: 97101.
  • 31
    Donofrio MT, Bremer YA, Schieken RM, et al. Autoregulation of cerebral blood flow in fetuses with congenital heart disease: the brain sparing effect. Pediatr Cardiol 2003; 24: 43643.
  • 32
    Kiehl TR, Chow EW, Mikulis DJ, George SR, Bassett AS. Neuropathologic Features in Adults with 22q11.2 Deletion Syndrome. Cereb Cortex 2009; 19: 15364.
  • 33
    Momjian-Mayor I, Baron JC. The pathophysiology of watershed infarction in internal carotid artery disease: review of cerebral perfusion studies. Stroke 2005; 36: 56777.