Results 1 to 10 of about 12,103 (259)

Developmental Motor Profile in Preschool Children with Primary Stereotypic Movement Disorder. [PDF]

open access: yesBiomed Res Int, 2019
Aim. Different neuropsychological dysfunctions have been described in children with primary Stereotypic Movement Disorder (SMD), mainly attention or motor coordination problems.
Valente F   +6 more
europepmc   +6 more sources

Stereotyped movement disorder in ICD-11 [PDF]

open access: yesBrazilian Journal of Psychiatry, 2014
According to current proposals for ICD-11, stereotyped movement disorder will be classified in the grouping of neurodevelopmental disorders, with a qualifier to indicate whether self-injury is present, similar to the classification of stereotypic ...
Dan J. Stein, Douglas W. Woods
doaj   +4 more sources

Evaluation of functional mobility of patients with stroke sequela after treatment in hydrotherapy pool using the Timed Up and Go Test [PDF]

open access: yesEinstein (São Paulo), 2011
Objective: To evaluate the functional mobility of patients with stroke over 12 sessions of hydrotherapy. Methods: Ten stroke patients aged between 5 and 85 years were evaluated by means of the Timed Up and Go test, which contains some items, such as ...
Daniel Gonçalves dos Santos   +5 more
doaj   +3 more sources

Effects of a multimodal physical exercise program on physical and mental health indicators in males with substance use disorder

open access: yesABCS Health Sciences, 2021
Introduction: Substance use disorder (SUD) is seen as a serious and growing public safety and health problem worldwide. Long-term sequelae may involve permanent damage to physical fitness, body balance, and coordination skills, with a severe motor ...
Bruno Marson Malagodi   +4 more
doaj   +1 more source

Chronic stress promotes basal ganglia disinhibition by increasing the excitatory drive of direct-pathway neurons

open access: yesNeurobiology of Stress, 2023
Chronic stress (CS) is a well-recognized triggering factor in obsessive-compulsive disorder (OCD) and Tourette's syndrome (TS), two neuropsychiatric disorders characterized by the presence of stereotypic motor symptoms.
Diana Rodrigues, Patricia Monteiro
doaj   +1 more source

Prevalence, comorbidities, and profiles of neurodevelopmental disorders according to the DSM-5-TR in children aged 6 years old in a European region

open access: yesFrontiers in Psychiatry, 2023
BackgroundThere are no studies that measure the prevalence and real comorbidities of neurodevelopmental disorders (NDDs) according to the DSM-5-TR in 6-year-old children in population and clinical samples or studies that measure them as a whole. The data
Lorena Francés   +14 more
doaj   +1 more source

Stereotypic Movements in Case of Sporadic Creutzfeldt-Jakob Disease: Possible Role of Anti-NMDA Receptor Antibodies

open access: yesCase Reports in Neurology, 2012
Sporadic Creutzfeldt-Jakob disease (sCJD) and anti-NMDA receptor antibody encephalitis (NMDAE) can both produce a rapidly progressive dementia with resulting state of catatonia or akinetic mutism. Both are associated with movement disorders. In published
Michelle Molina, Robert Fekete
doaj   +1 more source

Quantification of abnormal repetitive behaviour in captive European starlings (Sturnus vulgaris). [PDF]

open access: yes, 2009
Stereotypies are repetitive, unvarying and goalless behaviour patterns that are often considered indicative of poor welfare in captive animals. Quantifying stereotypies can be difficult, particularly during the early stages of their development when ...
Asher, L   +4 more
core   +2 more sources

Impairments in motor coordination without major changes in cerebellar plasticity in the Tc1 mouse model of Down syndrome [PDF]

open access: yes, 2009
Down syndrome (DS) is a genetic disorder arising from the presence of a third copy of human chromosome 21 (Hsa21). Recently, O’Doherty et al. [An aneuploid mouse strain carrying human chromosome 21 with Down syndrome phenotypes. Science 309 (2005) 2033–
Bliss, T.V.P.   +7 more
core   +3 more sources

First case report of Rett syndrome in the Azeri Turkish population and brief review of the literature

open access: yesEpilepsy and Behavior Case Reports, 2015
Rett syndrome is a dominant X-linked male-lethal disorder largely caused by mutations in the gene encoding methyl-CpG binding protein 2 (MECP2). Clinical manifestations include neurodevelopmental disorder characterized by early-onset intractable seizures,
Jalal Gharesouran   +3 more
doaj   +1 more source

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