Cognition and brain in children with 22q11.2 deletion syndrome

被引：0
|
作者：
Campbell, L. E. [1 ]
Stevens, A. F. [1 ]
Azuma, R. [1 ]
Morris, R. G. [1 ]
Murphy, D. G. M. [1 ]
Murphy, K. C. [1 ]
机构：
[1] Univ Newcastle, Ctr Mental Hlth, Inst Psychiat, Univ London Kings Coll, Newcastle, NSW 2308, Australia
来源：
AUSTRALIAN AND NEW ZEALAND JOURNAL OF PSYCHIATRY | 2006年 / 40卷
关键词：
D O I：
暂无
中图分类号：
R749 [精神病学];
学科分类号：
100205 ;
摘要：
引用
收藏
页码：A121 / A121
页数：1
相关论文
共 50 条
  • [41] Clozapine Use in 22q11.2 Deletion Syndrome
    Colijn, Mark Ainsley
    JOURNAL OF CLINICAL PSYCHOPHARMACOLOGY, 2024, 44 (02) : 168 - 178
  • [42] Otolaryngologic manifestations of the 22q11.2 deletion syndrome
    Dyce, O
    McDonald-McGinn, D
    Kirschner, RE
    Zackai, E
    Young, K
    Jacobs, IN
    ARCHIVES OF OTOLARYNGOLOGY-HEAD & NECK SURGERY, 2002, 128 (12) : 1408 - 1412
  • [43] 22q11.2 deletion syndrome: an anaesthetic perspective
    Kemp, N.
    SOUTHERN AFRICAN JOURNAL OF ANAESTHESIA AND ANALGESIA, 2021, 27 (05) : 206 - 210
  • [44] Developmental trajectories in 22q11.2 deletion syndrome
    Swillen, Ann
    McDonald-McGinn, Donna
    AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2015, 169 (02) : 172 - 181
  • [45] Olfactory deficits in deletion syndrome 22q11.2
    Romanos, Marcel
    Schecklmann, Martin
    Kraus, Katharina
    Fallgatter, Andreas J.
    Warnke, Andreas
    Lesch, Klaus-Peter
    Gerlach, Manfred
    SCHIZOPHRENIA RESEARCH, 2011, 129 (2-3) : 220 - 221
  • [46] Labyrinthine malformation in the 22q11.2 deletion syndrome
    Hopsu, Erkki
    Markkola, Antti
    Pitkaranta, Anne
    CLINICAL DYSMORPHOLOGY, 2007, 16 (01) : 67 - 68
  • [47] 22q11.2 deletion syndrome in diverse populations
    Kruszka, Paul
    Addissie, Yonit A.
    McGinn, Daniel E.
    Porras, Antonio R.
    Biggs, Elijah
    Share, Matthew
    Crowley, T. Blaine
    Chung, Brian H. Y.
    Mok, Gary T. K.
    Mak, Christopher C. Y.
    Muthukumarasamy, Premala
    Thong, Meow-Keong
    Sirisena, Nirmala D.
    Dissanayake, Vajira H. W.
    Paththinige, C. Sampath
    Prabodha, L. B. Lahiru
    Mishra, Rupesh
    Shotelersuk, Vorasuk
    Ekure, Ekanem Nsikak
    Sokunbi, Ogochukwu Jidechukwu
    Kalu, Nnenna
    Ferreira, Carlos R.
    Duncan, Jordann-Mishael
    Patil, Siddaramappa Jagdish
    Jones, Kelly L.
    Kaplan, Julie D.
    Abdul-Rahman, Omar A.
    Uwineza, Annette
    Mutesa, Leon
    Moresco, Angelica
    Gabriela Obregon, Maria
    Richieri-Costa, Antonio
    Gil-da-Silva-Lopes, Vera L.
    Adeyemo, Adebowale A.
    Summar, Marshall
    Zackai, Elaine H.
    McDonald-McGinn, Donna M.
    Linguraru, Marius George
    Muenke, Maximilian
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2017, 173 (04) : 879 - 888
  • [48] Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndrome
    Lima, Kari
    Abrahamsen, Tore G.
    Wolff, Anette Boe
    Husebye, Eystein
    Alimohammadi, Mohammad
    Kampe, Olle
    Folling, Ivar
    EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2011, 165 (02) : 345 - 352
  • [49] Immunodeficiency and autoimmunity in 22q11.2 deletion syndrome
    McLean-Tooke, A.
    Spickett, G. P.
    Gennery, A. R.
    SCANDINAVIAN JOURNAL OF IMMUNOLOGY, 2007, 66 (01) : 1 - 7
  • [50] Opitz GBBB syndrome and the 22q11.2 deletion
    Lacassie, Y
    Arriaza, MI
    AMERICAN JOURNAL OF MEDICAL GENETICS, 1996, 62 (03): : 318 - 318
12345