Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Movement disorders and other motor abnormalities in adults with 22q11.2 deletion syndrome

Published:2015-02-13 Issue:3 Volume:167 Page:639-645
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Boot Erik¹²³⁴,Butcher Nancy J⁵⁶,van Amelsvoort Thérèse AMJ⁷,Lang Anthony E⁶⁸⁹¹⁰¹¹,Marras Connie⁸¹¹,Pondal Margarita¹¹,Andrade Danielle M⁸¹²,Fung Wai Lun Alan¹³⁴⁵¹³,Bassett Anne S¹³⁴⁵¹⁴

Affiliation:

1. The Dalglish Family Hearts and Minds Clinic for Adults with 22q11.2 Deletion Syndrome; Toronto Ontario Canada

2. Department of Nuclear Medicine; Academic Medical Centre; Amsterdam The Netherlands

3. Department of Psychiatry; University Health Network; Toronto Ontario Canada

4. Department of Psychiatry; University of Toronto; Toronto Ontario Canada

5. Clinical Genetics Research Program; Centre for Addiction and Mental Health; Toronto Ontario Canada

6. Institute of Medical Science; University of Toronto; Toronto Ontario Canada

7. Department of Psychiatry and Psychology; School of Mental Health and Neuroscience; Maastricht University Medical Centre; Maastricht The Netherlands

8. Department of Medicine; Division of Neurology; University of Toronto; Toronto Ontario Canada

9. Department of Medicine; Tanz Centre for Research in Neurodegenerative Diseases; University of Toronto; Toronto Ontario Canada

10. Toronto Western Hospital Research Institute; University Health Network; Toronto Ontario Canada

11. Morton and Gloria Shulman Movement Disorder Centre and the Edmond J. Safra Program in Parkinson's Disease; Toronto Western Hospital; University Health Network and University of Toronto; Toronto Ontario Canada

12. Epilepsy Genetics Program; Toronto Western Hospital; University Health Network and University of Toronto; Toronto Ontario Canada

13. Toronto General Research Institute; University Health Network; Toronto Ontario Canada

14. Institute of Medical Science; University of Toronto; Toronto Ontario Canada. Toronto General Research Institute; University Health Network; Toronto Ontario Canada. Department of Medicine; Division of Cardiology; University Health Network; Toronto Ontario Canada

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference29 articles.

1. Practical guidelines for managing patients with 22q11.2 deletion syndrome;Bassett;J Pediatr,2011

2. Olanzapine-induced tardive oculogyric crises;Bavle;Indian J Psychol Med,2013

3. Co-occurrence of early-onset Parkinson disease and 22q11.2 deletion syndrome: Potential role for dopamine transporter imaging;Booij;Am J Med Genet A,2010

4. Association between early-onset Parkinson disease and 22q11.2 deletion syndrome: Identification of a novel genetic form of Parkinson disease and its clinical implications;Butcher;JAMA Neurol,2013

5. Response to clozapine in a clinically identifiable subtype of schizophrenia: 22q11 .2 deletions mediate side effect risk and dosage;Butcher;Br J Psychiatry

Cited by 53 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neuroanatomical Correlates of Cognitive Dysfunction in 22q11.2 Deletion Syndrome;Genes;2024-03-30

2. The effectiveness and tolerability of pharmacotherapy for psychosis in 22q11.2 Deletion Syndrome: A systematic review;Australian & New Zealand Journal of Psychiatry;2024-02-21

3. Clozapine Use in 22q11.2 Deletion Syndrome;Journal of Clinical Psychopharmacology;2024-02-10

4. The Relationship between Motor Symptoms, Signs, and Parkinsonism with Facial Emotion Recognition Deficits in Individuals with 22q11.2 Deletion Syndrome at High Genetic Risk for Psychosis;Acta Neurologica Scandinavica;2023-03-28

5. Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndrome;Genetics in Medicine;2023-03