Mirja Nicolas,Diana Schneider,Fabian Fritz et al.
Mirja Nicolas et al.
Wissenschaftliche Bewertung von Methoden für den Nachweis von „Post-/Long-COVID-Syndromen“ und ihrer Überlappung mit „ME/CFS“ : Kurzfassung der Stellungnahme der Deutschen Gesellschaft für Neurowissenschaftliche Begutachtung (DGNB) [0.03%]
德国神经科学鉴定协会(DGNB)关于“长新冠”诊断方法及其与“肌痛性脑脊髓炎/慢性疲劳综合症(ME/CFS)”重叠情况的评估意见概述
F Erbguth,M Tegenthoff,C Böwering-Möllenkamp et al.
F Erbguth et al.
[From feeblemindedness to intellectual deficiency : Some comments from the forensic-psychiatric perspective on the replacement of the juridical term in the German Criminal Code (the criminal liability paragraph 20 StGB)] [0.03%]
《从白痴到智能缺陷——兼论德意志刑法典中刑事责任能力第20条用语置换的法医精神病学视角》
Dieter Seifert
Dieter Seifert
Mark Mühlbacher,Rebecca Schennach,Robert Birk et al.
Mark Mühlbacher et al.
Pathological hoarding is an independent psychological disorder characterized by persistent difficulties in discarding possessions, excessive accumulation and a functionally relevant impairment of living conditions and daily functioning. The...
[Dextromethorphan-bupropion for the treatment of agitation in Alzheimer's disease] [0.03%]
右美沙芬-安非他酮治疗阿尔茨海默病激越失眠
Michael Paulzen
Michael Paulzen
[Late-onset manifestation of Tay-Sachs disease-A disease of the cerebellum and motor neurons with psychiatric sequelae] [0.03%]
晚发型泰-萨克斯病的一种表现形式-一种累及小脑和运动神经元并伴有精神症状的疾病
Karl Eugen Mengel,Grecia Mendoza,Latha Mani et al.
Karl Eugen Mengel et al.
Data on the manifestation and progression of neurological and psychiatric symptoms in adult patients with late-onset Tay-Sachs (LOTS) disease after the age of 2 years are scarce and not available for Germany. In this cross-sectional study d...
[Neuropsychiatric manifestations of sex chromosome aberrations-Clinical and therapeutic aspects of neuropsychiatric care] [0.03%]
性染色体异常的精神神经学表现-性染色体异常患者的临床和治疗方面精神神经照护概述
Heiko Paland,Alexandra Philipsen,Eva C Schulte
Heiko Paland
Background: Sex chromosome aberrations affect approximately 1.5 per 1000 individuals, although somatically inconspicuous phenotypes can remain undetected. Even when diagnosed, the elevated risk of neuropsychiatric manifes...
[Associations Between Genetic Causes of Psychiatric Disorders and Rare Monogenic Epilepsies] [0.03%]
[精神疾病遗传病因与罕见遗传性癫痫的关系]
Caroline Baumgartner,Tobias Baumgartner,Alexandra Philipsen et al.
Caroline Baumgartner et al.
Psychiatric disorders are more common in people with epilepsy and vice versa psychiatric patients have an increased risk of epilepsy. Psychosocial factors, medication effects, peri-ictal or interictal symptoms play a role as do shared genet...
[From the diagnostic category "mental deficiency" (ICD-6) to the diagnostic category "disorder of intellectual development" (ICD-11)] [0.03%]
从第6版国际疾病分类的“精神发育不全”到第11版国际疾病分类的“智力发展障碍”
Michael Seidel
Michael Seidel
The diagnostic category Disorder of Intellectual Development in the International Classification of Diseases (ICD)-11 had precursors in all previous ICD versions from ICD‑6 onwards. In the successive ICD versions up to ICD-11, there have b...
[New interdisciplinary S3 guidelines on deletion syndrome 22q11.2, a genetic disease predisposing to neuropsychiatric morbidity] [0.03%]
[新的跨学科S3指南：22q11.2缺失综合征的诊治（一种易患神经精神疾病的遗传病）]
Franziska Radtke,Carina Sauter
Franziska Radtke
The deletion syndrome 22q11.2 is one of the most frequent genetic syndromes in humans, with a prevalence of 1:2500 [1]. The syndrome is particularly relevant for neurology, psychiatry and child and adolescent psychiatry due to a massive gen...