Psychiatric Aspects of Wilson Disease

S Munjal, PC Zimbrean - Management of Wilson Disease: A Pocket Guide, 2018 - Springer
Psychiatric disturbances represent an important diagnostic and therapeutic issue in Wilson
disease (WD). They represent a significant part of the clinical presentation of WD and can …

Long-term mood disorder antedating the diagnosis of Wilson's disease

TC Vale, P Caramelli, AL Teixeira - Brazilian Journal of Psychiatry, 2011 - SciELO Brasil
Dear Editor, We evaluated a young patient with a long history of psychiatric symptoms and
misdiagnosis. After nine years of receiving many ineffective symptomatic therapies, she was …

Treatment of Wilson's disease–an update

T Litwin, P Dusek, M Skowrońska… - Expert Opinion on …, 2019 - Taylor & Francis
Introduction: Wilson's disease (WD) is one of the few genetic disorders that can be
successfully treated if diagnosed early and treated correctly. Currently, two groups of drugs …

Fenomenología depresiva al inicio de enfermedades neuropediátricas

J Narbona - 2014 - dadun.unav.edu
Introducción. La depresión, en sus diversas formas, afecta al 8-10% de niños y
adolescentes y en la mayor parte de casos su origen es primario, siguiendo el modelo …

Acute movement disorders in the medical setting: A case series, neurophysiological model, and literature review

I Zawar, MA Caro, L Feldman… - … International Journal of …, 2016 - journals.sagepub.com
Objective Psychosomatic medicine psychiatrists are often tasked with the evaluation and
treatment of complex neuropsychiatric states which may be motoric in phenotype. Little …

Primarily depression manifestation of Wilson's disease—Case report

A Kułak-Bejda, N Waszkiewicz, B Galińska-Skok… - Clinical Neurology and …, 2020 - Elsevier
Wilson's disease is an inherited autosomal-recessive disorder of biliary copper excretion. It
is characterized by hepatic, neurological and ophthalmic manifestations related to the …

以精神障碍为首发症状的肝豆状核变性1 例报告

崔园园, 杨以良, 王莎莎, 华瑞 - 临床肝胆病杂志, 2016 - lcgdbzz.org
< 正> 肝豆状核变性是一种常染色体隐性单基因遗传病, 是位于13q14. 3 的ATP7B 基因突变,
导致铜蓝蛋白合成障碍, 引起细胞内铜离子的跨膜转运障碍, 过量的铜沉积在肝脏, 肾脏, 大脑 …

Movement disorders in childhood metabolic diseases

E Fernandez-Alvarez, A Roubertie - Movement Disorders in …, 2014 - books.google.com
Group 3: Disorders involving complex molecules. This group involves cellular organelles
and cellular trafficking and processing of complex molecules; it includes lysosomal …

[引用][C] KF 环自动检测系统设计

苑玮琦, 常乐 - 光学精密工程, 2016

[引用][C] 肝豆状核变性合并精神障碍研究述要

董文文, 杨文明, 刘丹青 - 中医药临床杂志, 2014