Olfactory deficits in deletion syndrome 22q11.2.

作者信息

Romanos Marcel, Schecklmann Martin, Kraus Katharina, Fallgatter Andreas J, Warnke Andreas, Lesch Klaus-Peter, Gerlach Manfred

出版信息

Schizophr Res. 2011 Jul;129(2-3):220-1. doi: 10.1016/j.schres.2010.12.015. Epub 2011 Feb 1.

DOI:10.1016/j.schres.2010.12.015

PMID:21282042

Abstract

摘要

相似文献

Olfactory deficits in deletion syndrome 22q11.2.

Schizophr Res. 2011 Jul;129(2-3):220-1. doi: 10.1016/j.schres.2010.12.015. Epub 2011 Feb 1.

[Scoliosis in children with chromosome 22q11.2 deletion syndrome].

Ned Tijdschr Geneeskd. 2012;156(4):A4298.

[Graves disease and IgA deficiency as manifestations of 22q11.2 deletion syndrome].

Arq Bras Endocrinol Metabol. 2010 Aug;54(6):572-7. doi: 10.1590/s0004-27302010000600011.

Disseminated Mycobacterial Disease in a Patient with 22q11.2 Deletion Syndrome: Case Report and Review of the Literature.

J Clin Immunol. 2019 Oct;39(7):743-746. doi: 10.1007/s10875-019-00678-5. Epub 2019 Aug 5.

Auxological evaluation in patients with a 22q11.2 microdeletion syndrome: normal prevalence of obesity and neonatal length and gender influence on body mass index evolution.

Horm Res Paediatr. 2011;76(3):172-7. doi: 10.1159/000328454. Epub 2011 Aug 5.

Mutation of TNFRSF13B in a child with 22q11 deletion syndrome associated with granulomatous lymphoproliferation.

J Allergy Clin Immunol. 2015 Feb;135(2):559-61. doi: 10.1016/j.jaci.2014.07.025. Epub 2014 Aug 28.

Lymphoproliferative disorder with polyautoimmunity and hypogammaglobulinemia: An unusual presentation of 22q11.2 deletion syndrome.

Clin Immunol. 2020 Nov;220:108590. doi: 10.1016/j.clim.2020.108590. Epub 2020 Sep 11.

[22q11.2 deletion syndrome diagnosed in an adult male].

Ned Tijdschr Geneeskd. 2011;155(40):A3644.

Nonverbal and verbal learning: a comparative study of children and adolescents with 22q11 deletion syndrome, non-syndromal Nonverbal Learning Disorder and memory disorder.

Neurocase. 2011 Dec;17(6):480-90. doi: 10.1080/13554794.2010.536954. Epub 2011 May 23.

Dilated cardiomyopathy in a patient with 22q11.2 microdeletion syndrome.

Genet Couns. 2013;24(2):235-8.

引用本文的文献

Salivary α-Synuclein as a Candidate Biomarker of Parkinsonism in 22q11.2 Deletion Syndrome.

Mov Disord Clin Pract. 2024 Jul;11(7):808-813. doi: 10.1002/mdc3.14046. Epub 2024 Apr 25.

22q11.2 Deletion Syndrome-Associated Parkinson's Disease.

Mov Disord Clin Pract. 2018 Nov 9;6(1):11-16. doi: 10.1002/mdc3.12687. eCollection 2019 Jan.

Olfactory deficits and psychosis-spectrum symptoms in 22q11.2 deletion syndrome.

Schizophr Res. 2018 Dec;202:113-119. doi: 10.1016/j.schres.2018.07.012. Epub 2018 Jul 11.

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2.

Neurology. 2018 Jun 5;90(23):e2059-e2067. doi: 10.1212/WNL.0000000000005660. Epub 2018 May 11.

Spectrum of Clinical and Associated MR Imaging Findings in Children with Olfactory Anomalies.

AJNR Am J Neuroradiol. 2016 Aug;37(8):1541-8. doi: 10.3174/ajnr.A4738. Epub 2016 Mar 17.

A systematic review on olfaction in child and adolescent psychiatric disorders.

J Neural Transm (Vienna). 2013 Jan;120(1):121-30. doi: 10.1007/s00702-012-0855-2. Epub 2012 Jul 19.

Olfaction in child and adolescent anorexia nervosa.

J Neural Transm (Vienna). 2012 Jun;119(6):721-8. doi: 10.1007/s00702-011-0752-0. Epub 2011 Dec 20.

Effects of the val(158)met catechol-O-methyltransferase gene polymorphism on olfactory processing in schizophrenia.

Behav Neurosci. 2012 Feb;126(1):209-215. doi: 10.1037/a0026466. Epub 2011 Dec 12.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验