Practice parameters for psychologists in addictive disorders

1995 ◽  
Keyword(s):  
Addictive Disorders ◽  
Practice Parameters

Suchterkrankungen im Diagnostischen und Statistischen Manual Psychischer Störungen DSM-5

2015 ◽  
Vol 12 (02) ◽  
pp. 110-117
Author(s):  
O. Pogarell ◽  
G. Koller
Keyword(s):  
Addictive Disorders ◽  
Dsm 5 ◽  
Icd 10 ◽  
Dsm Iv

Zusammenfassung Hintergrund: Im Jahr 2014 wurde das DSM-IV durch die fünfte Version des Diagnostischen und Statistischen Manuals Psychischer Störungen (DSM-5) abgelöst. In der vorliegenden Übersicht soll auf die Darstellung der Abhängigkeitserkrankungen im DSM-5 (Kapitel: Substance Related and Addictive Disorders, in der Übersetzung: Störungen im Zusammenhang mit psychotropen Substanzen und abhängige Verhaltensweisen) eingegangen werden. Ziel: Nach einem Überblick über die neue Systematik werden die entsprechenden Änderungen und Besonderheiten gegenüber DSM-IV und ICD-10 erläutert, sowie die Rezeption im deutschsprachigen Raum dargestellt.

Antipsychotics Management in Addictive Disorders

2014 ◽  
Vol 2 (3) ◽  
pp. 212-217
Author(s):  
Pierre Geoffroy ◽  
Benjamin Rolland ◽  
Vincent Laprevote ◽  
Olivier Cottencin
Keyword(s):  
Addictive Disorders

scholarly journals FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring

2021 ◽  
Vol 13 (1) ◽  
Author(s):  
Reymundo Lozano ◽  
Catherine Gbekie ◽  
Paige M. Siper ◽  
Shubhika Srivastava ◽  
Jeffrey M. Saland ◽  
...  
Keyword(s):  
Neurodevelopmental Disorder ◽  
Autism Spectrum ◽  
Medical Assessment ◽  
Forkhead Box ◽  
Organ Systems ◽  
Practice Parameters ◽  
Assessment And Monitoring ◽  
Multidisciplinary Group ◽  
The Brain

AbstractFOXP1 syndrome is a neurodevelopmental disorder caused by mutations or deletions that disrupt the forkhead box protein 1 (FOXP1) gene, which encodes a transcription factor important for the early development of many organ systems, including the brain. Numerous clinical studies have elucidated the role of FOXP1 in neurodevelopment and have characterized a phenotype. FOXP1 syndrome is associated with intellectual disability, language deficits, autism spectrum disorder, hypotonia, and congenital anomalies, including mild dysmorphic features, and brain, cardiac, and urogenital abnormalities. Here, we present a review of human studies summarizing the clinical features of individuals with FOXP1 syndrome and enlist a multidisciplinary group of clinicians (pediatrics, genetics, psychiatry, neurology, cardiology, endocrinology, nephrology, and psychology) to provide recommendations for the assessment of FOXP1 syndrome.

Clinical and biological predictors of psychedelic response in the treatment of psychiatric and addictive disorders: A systematic review

2021 ◽  
Vol 137 ◽  
pp. 273-282
Author(s):  
Bruno Romeo ◽  
Marianne Hermand ◽  
Amélie Pétillion ◽  
Laurent Karila ◽  
Amine Benyamina
Keyword(s):  
Systematic Review ◽  
Addictive Disorders
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