COVID-19, Substance Use, Anorexia Nervosa, 22q11.2 Deletion Syndrome, and Stress

被引：1
|
作者：
Kalin, Ned H. [1 ]
机构：
[1] Univ Wisconsin, Dept Psychiat, Sch Med & Publ Hlth, Madison, WI 53706 USA
来源：
AMERICAN JOURNAL OF PSYCHIATRY | 2020年 / 177卷 / 07期
关键词：
D O I：
10.1176/appi.ajp.2020.20050685
中图分类号：
R749 [精神病学];
学科分类号：
100205 ;
摘要：
[No abstract available]
引用
收藏
页码：561 / 563
页数：3
相关论文
共 50 条
  • [11] Schizophrenia and 22q11.2 deletion syndrome
    Bassett A.S.
    Chow E.W.C.
    Current Psychiatry Reports, 2008, 10 (2) : 148 - 157
  • [12] 22q11.2 deletion syndrome: Introduction
    Lajiness-O'Neill, R
    CHILD NEUROPSYCHOLOGY, 2005, 11 (01) : 1 - 3
  • [13] Tonsillectomy in Children with 22q11.2 Deletion Syndrome
    Arganbright, Jill M.
    Hankey, Paul Bryan
    Tracy, Meghan
    Narayanan, Srivats
    Noel-MacDonnell, Janelle
    Ingram, David
    GENES, 2022, 13 (12)
  • [14] 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
  • [15] 22q11.2 deletion syndrome: an anaesthetic perspective
    Kemp, N.
    SOUTHERN AFRICAN JOURNAL OF ANAESTHESIA AND ANALGESIA, 2021, 27 (05) : 206 - 210
  • [16] Labyrinthine malformation in the 22q11.2 deletion syndrome
    Hopsu, Erkki
    Markkola, Antti
    Pitkaranta, Anne
    CLINICAL DYSMORPHOLOGY, 2007, 16 (01) : 67 - 68
  • [17] 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
  • [18] 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
  • [19] 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
  • [20] 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
12345