An fMRI study of facial emotion processing in children and adolescents with 22q11.2 deletion syndrome

被引:0
|
作者
Rayna Azuma
Quinton Deeley
Linda E Campbell
Eileen M Daly
Vincent Giampietro
Michael J Brammer
Kieran C Murphy
Declan GM Murphy
机构
[1] Waseda University,School of International Liberal Studies
[2] Institute of Psychiatry,Department of Forensic and Neurodevelopmental Science
[3] King’s College London,National Autism Unit, Bethlem Royal Hospital
[4] SLAM NHS Foundation Trust,School of Psychology
[5] University of Newcastle,Department of Neuroimaging
[6] Institute of Psychiatry,Department of Psychiatry, Royal College of Surgeons in Ireland
[7] King’s College London,Institute of Psychiatry
[8] Beaumont Hospital,undefined
[9] Sackler Institute for Translational Neurodevelopment,undefined
[10] King’s College London,undefined
来源
Journal of Neurodevelopmental Disorders | 2015年 / 7卷
关键词
Velo-cardio-facial syndrome (VCFS); 22q11.2 deletion syndrome (22q11DS); Emotion; fMRI; Children; Social cognition;
D O I
暂无
中图分类号
学科分类号
摘要
引用
收藏
相关论文
共 50 条
  • [21] Molecular genetics of 22q11.2 deletion syndrome
    Morrow, Bernice E.
    McDonald-McGinn, Donna M.
    Emanuel, Beverly S.
    Vermeesch, Joris R.
    Scambler, Peter J.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (10) : 2070 - 2081
  • [22] Clinical Manifestations of 22q11.2 Deletion Syndrome
    Cirillo, Annapaola
    Lioncino, Michele
    Maratea, Annachiara
    Passariello, Annalisa
    Fusco, Adelaide
    Fratta, Fiorella
    Monda, Emanuele
    Caiazza, Martina
    Signore, Giovanni
    Esposito, Augusto
    Baban, Anwar
    Versacci, Paolo
    Putotto, Carolina
    Marino, Bruno
    Pignata, Claudio
    Cirillo, Emilia
    Giardino, Giuliana
    Sarubbi, Berardo
    Limongelli, Giuseppe
    Russo, Maria Giovanna
    HEART FAILURE CLINICS, 2022, 18 (01) : 155 - 164
  • [23] Deletion Syndrome 22q11.2: A Systematic Review
    Cortes-Martin, Jonathan
    Lopez Penuela, Nuria
    Carlos Sanchez-Garcia, Juan
    Montiel-Troya, Maria
    Diaz-Rodriguez, Lourdes
    Rodriguez-Blanque, Raquel
    CHILDREN-BASEL, 2022, 9 (08):
  • [24] Abnormal development of early auditory processing in 22q11.2 Deletion Syndrome
    Cantonas, Lucia-Manuela
    Tomescu, Miralena I.
    Biria, Marjan
    Jan, Reem K.
    Schneider, Maude
    Eliez, Stephan
    Rihs, Tonia A.
    Michel, Christoph M.
    TRANSLATIONAL PSYCHIATRY, 2019, 9 (1)
  • [25] Chromatin Modifications in 22q11.2 Deletion Syndrome
    Zhang, Zhe
    Shi, LiHua
    Song, Li
    Maurer, Kelly
    Zhao, Xue
    Zackai, Elaine H.
    McGinn, Daniel E.
    Crowley, T. Blaine
    McGinn, Donna M. McDonald
    Sullivan, Kathleen E.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2021, 41 (08) : 1853 - 1864
  • [26] Impaired multiple object tracking in children with chromosome 22q11.2 deletion syndrome
    Cabaral, Margarita H.
    Beaton, Elliott A.
    Stoddard, Joel
    Simon, Tony J.
    JOURNAL OF NEURODEVELOPMENTAL DISORDERS, 2012, 4
  • [27] Neurologic challenges in 22q11.2 deletion syndrome
    Hopkins, Sarah E.
    Chadehumbe, Madeline
    Crowley, Terrence Blaine
    Zackai, Elaine H.
    Bilaniuk, Larissa T.
    McDonald-McGinn, Donna M.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (10) : 2140 - 2145
  • [28] Musical auditory processing, cognition, and psychopathology in 22q11.2 deletion syndrome
    Gao, Lucy
    Tang, Sunny X.
    Yi, James J.
    McDonald-McGinn, Donna M.
    Zackai, Elaine H.
    Emanuel, Beverly S.
    Gur, Ruben C.
    Calkins, Monica E.
    Gur, Raquel E.
    AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS, 2018, 177 (08) : 765 - 773
  • [29] FISH Diagnosis of 22q11.2 Deletion Syndrome
    Miller, Kimberley A.
    NEWBORN AND INFANT NURSING REVIEWS, 2008, 8 (01) : E11 - E19
  • [30] Otorhinologic Disorders in 22q11.2 Deletion Syndrome
    Lu, Nathan
    Kacin, Alexa J. J.
    Shaffer, Amber D. D.
    Stapleton, Amanda L. L.
    OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 2023, 169 (04) : 1012 - 1019