Results 21 to 30 of about 4,356 (249)

Psychosocial Treatment for the Infant with Stereotypic Movement Disorder : The treatment in Children's home

, 2010
There have been very few reports on treatment for the infant with Stereotypic Movement Disorder who lives in children’s home. Then, this paper reports the treatment method and process (psychosocial Treatment) for the infant with Stereotypic Movement ...
安田, 勉, ヤスダ, ツトム, Yasuda, Tsutomu   +2 more
core   +2 more sources

Developmental profile and diagnoses in children presenting with motor stereotypies

Frontiers in Pediatrics, 2016
Introduction: Motor stereotypies represent a typical example of the difficulty in distinguishing non-clinical behaviors (physiological and transient) from symptoms or among different disorders (primary stereotypies, associated with Autistic Spectrum ...
Francesco Cardona, Francesca Valente, Daniela Miraglia, Caterina D'Ardia, Valentina Baglioni, Flavia Chiarotti   +5 more
doaj   +1 more source

Comparative Efficacy of Antipsychotic Medication for Stereotypic Behavior in Autism Spectrum Disorder: A Systematic Review and Meta-analysis

Journal of Psychiatry Spectrum
Background: Stereotypic movements in autism form core symptoms under the rubric of repetitive and restricted patterns of behavior. Aim: The systematic review was aimed to find which antipsychotic has better efficacy in treating stereotypic behavior in ...
Shivanand Kattimani, Sandhiya Selvarajan, Natarajan Varadharajan, Prabhavaty Gopalakrishnan   +3 more
doaj   +1 more source

Formulation and Effectiveness of Neuro Exuberant Proliferation Therapy on Developmental Indicators and Symptoms of Children with Autism Spectrum Disorder [PDF]

Ravānshināsī-i Afrād-i Istis̠nāyī
The formulation of a therapeutic model centered on neurology can be crucial for the effective treatment of neurodevelopmental disorders. This research investigates the development and evaluation of an innovative "Neuro-Exuberant Proliferation Therapy" as
Sara Rouhani, Mohammad Narimani, Nader Hajloo, REZA Farzizadeh   +3 more
doaj   +1 more source

Eye Movement Disorder in Infancy: Stereotypic vs. Tic?

, 2022
Paroxysmal events such as stereotypic movement disorder and provisional tic disorder are common motor behaviors in childhood; differentiating between the two is difficult, particularly in infancy.
Kayla Schusterman; Julianne Lee; Isabella Canut; Gerry Maitland
core  

Silver Russell syndrome: A suspected syndromic child in Sri Lanka presenting with recurrent head-banging associated with force-feeding

Sri Lanka Journal of Psychiatry
No abstract ...
P. Vidyatilake, D. Kodikaraarachchi, M. Chandradasa, S. Wijetunge   +3 more
doaj   +1 more source

Baseline Regional Cholinergic Denervation Predicts Cognitive Trajectories in Moderate Parkinson Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Cognitive decline is a disabling and variable feature of Parkinson disease (PD). While cholinergic system degeneration is linked to cognitive impairments in PD, most prior research reported cross‐sectional associations. We aimed to fill this gap by investigating whether baseline regional cerebral vesicular acetylcholine transporter ...
Taylor Brown, Giulia Carli, Prabesh Kanel, Stiven Roytman, Jaimie Barr, Nicolaas I. Bohnen, Roger L. Albin   +6 more
wiley   +1 more source

Prominent Movement Disorders in RNU2‐2‐Related Spliceosomopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Pediatric movement disorders often overlap with neurodevelopmental diseases, suggesting shared molecular mechanisms. Variants in small nuclear RNA (snRNA) genes encoding spliceosome components have recently been associated with neurodevelopmental disorders, termed “RNUopathies.” We analyzed genome sequencing data from 14 patients with ...
Magdalena Krygier, Ugo Sorrentino, Matias Wagner, Marta Zawadzka, Anna Lemska, Maria Mazurkiewicz‐Bełdzińska, Michael Zech   +6 more
wiley   +1 more source

A 57‐Year‐Old Male With Behavioral Variant Frontotemporal Dementia and MATR3 and NOS3 Mutations

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT This report presents a case of behavioral variant frontotemporal dementia caused by mutations in the MATR3 and NOS3 genes, aiming to analyze its clinical manifestations and genetic characteristics. For a case presenting with personality changes and gait abnormalities as the initial symptoms, this study conducted a comprehensive analysis of its
Feifei Lin, Saie Huang
wiley   +1 more source

Patient advocacy and DSM-5

, 2015
The revision of the Diagnostic and Statistical Manual of Mental Disorders (DSM) provides a useful opportunity to revisit debates about the nature of psychiatric classification.
Stein, Dan J, Phillips, Katharine A
core   +1 more source