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1526 search results for:

Stereotypic Movement Disorder 

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  1. 01-08-2007 | OriginalPaper

    Trichotillomania, stereotypic movement disorder, and related disorders

    Trichotillomania is currently classified as an impulse control disorder not otherwise classified, whereas body-focused behaviors other than hair-pulling may be diagnosed as stereotypic movement disorder. A number of disorders characterized by …

  2. Open Access 29-09-2023 | Stereotypic Movement Disorder | ReviewPaper

    Co-morbid tics and stereotypies: a systematic literature review

    Tics and stereotypies are the most common hyperkinetic movement disorders occurring during the developmental period [ 1 ]. The current edition of the DSM [ 2 ] lists tic disorders and stereotypic movement disorder alongside developmental …

  3. Open Access 04-01-2024 | Stereotypic Movement Disorder | EditorialNotes

    Body-focused Repetitive Behavior: Towards a Better Understanding of this Prevalent but Undertreated Disorder

  4. Open Access 16-05-2024 | Online First

    41st Meeting of the Pediatric Section of the German Society of Trauma Surgeons

    Kongress für Kinder in Orthopädie und Unfallchirurgie 2023 41. Jahrestagung der SKT 36. Jahrestagung der VKO 19. – 20. Mai 2023 Garmisch-Partenkirchen
  5. 21-11-2023 | Levodopa | ReviewPaper

    A video-atlas of levodopa-induced dyskinesia in Parkinson’s disease: terminology matters

    Dyskinesia is a common complication of long-term levodopa therapy in patients with Parkinson’s disease (PD), which often worsens the quality of life. It is usually dose-dependent and emerges possibly due to pulsatile stimulation of dopamine …

  6. Open Access 05-03-2024 | Dystonia | BriefCommunication

    CHD8-related disorders redefined: an expanding spectrum of dystonic phenotypes

    Human CHD8 is located on chromosomal region 14q11.2. Its main transcript comprises 38 exons encoding for a 290-kDa Chromodomain-Helicase-DNA-binding protein, which acts as an ATP-dependent chromatin remodeler [ 1 ]. Through its dynamic interaction …

  7. Open Access 06-11-2023 | ReviewPaper

    A close look at sociality in DSM criteria

    Over the course of the history of psychiatric classification, mental disorders have been alternatively defined either as individual biological dysfunctions or as functional reactions to a dysfunctional environment. Mental disorders as individual …

  8. 22-02-2024 | Valproate | OriginalPaper

    Expanding the clinical and genetic landscape of (developmental) epileptic encephalopathy with spike-and-wave activation in sleep: results from studies of a Turkish cohort

    The terms developmental epileptic encephalopathy with spike-and-wave activation in sleep (DEE-SWAS) and epileptic encephalopathy with spike-and-wave activation in sleep (EE-SWAS) designate a spectrum of conditions that are typified by different …

  9. Open Access 01-12-2024 | Autism Spectrum Disorder | OriginalPaper

    Phenotypic and genetic analysis of children with unexplained neurodevelopmental delay and neurodevelopmental comorbidities in a Chinese cohort using trio-based whole-exome sequencing

    Neurodevelopmental delay (NDD) is a group of common neurological diseases with high clinical heterogeneity during childhood [ 1 ] and affects approximately 1%–3% of children worldwide, resulting in an average lifetime cost of $1 million to support …

  10. Open Access 19-03-2024 | Movement Disorder | Review

    An Evidence-Based Update on Anticholinergic Use for Drug-Induced Movement Disorders

    Drug-induced movement disorders (DIMDs) are associated with use of dopamine receptor blocking agents (DRBAs), including antipsychotics.

  11. Open Access 01-04-2024 | Huntington's Disease | Online First

    Safety of Deutetrabenazine for the Treatment of Tardive Dyskinesia and Chorea Associated with Huntington Disease

    Tardive dyskinesia (TD) and Huntington disease (HD) are hyperkinetic movement disorders that negatively impact quality of life and can be socially stigmatizing [ 1 – 3 ]. TD is caused by dopamine receptor antagonists (DRAs). The estimated frequency …

  12. Open Access 01-12-2024 | Autism Spectrum Disorder | OriginalPaper

    Dietary intake and gastrointestinal symptoms are altered in children with Autism Spectrum Disorder: the relative contribution of autism-linked traits

    Autism spectrum disorder (ASD) is a heterogeneous neurodevelopmental disorder characterized by persistent deficits in social communication and interactions and the presence of restricted, repetitive behaviors (RRBs), interests, or activities …

  13. Open Access 01-12-2024 | Rett Syndrome | OriginalPaper

    Rett syndrome in Ireland: a demographic study

    Rett syndrome, originally described in the 1960’s by Andreas Rett, is an X-linked rare neurodevelopmental condition with specific clinical features [ 1 ]. It affects brain function and development, with global prevalence ranging from 5–10 cases …

  14. Open Access 01-12-2024 | Disorders of Intellectual Development | OriginalPaper

    The spectrum of neurological presentation in individuals affected by TBL1XR1 gene defects

    Neurodevelopmental disorders such as autism spectrum disorder (ASD), intellectual disability (ID), and developmental delay, are common neurological conditions affecting the typical developmental trajectory [ 1 ]. With the rise of readily available …

  15. Open Access 01-02-2024 | OriginalPaper

    Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory Disease

    TLR7 recognizes pathogen-derived single-stranded RNA (ssRNA), a function integral to the innate immune response to viral infection. Notably, TLR7 can also recognize self-derived ssRNA, with gain-of-function mutations in human TLR7 recently …

  16. 02-03-2024 | Tremor | Online First

    Differential patterns of functional connectivity in tremor dominant Parkinson’s disease and essential tremor plus

    Tremor dominant Parkinson’s disease (TDPD) and essential tremor plus (ETP) syndrome are commonly encountered tremor dominant neurological disorders. Although the basal ganglia thalamocortical (BGTC) and cerebello thalamocortical (CTC) networks are …

  17. Open Access 01-12-2024 | Alzheimer's Disease | ReviewPaper

    Updates on mouse models of Alzheimer’s disease

    Alzheimer’s disease (AD) is the most common neurodegenerative disease in the United States (US). Animal models, specifically mouse models have been developed to better elucidate disease mechanisms and test therapeutic strategies for AD. A large …

  18. Open Access 01-12-2024 | Rett Syndrome | OriginalPaper

    Safety and efficacy of trofinetide in Rett syndrome: a systematic review and meta-analysis of randomized controlled trials

    Rett syndrome is a genetic neurodevelopmental disorder that predominantly affects females, with a prevalence ranging from 1:10,000 to 1:23,000 female live births [ 1 ]. A recent systematic review and meta-analysis by Petriti et al. (2023) reported …

  19. 08-04-2024 | Cataract | Online First

    Atypical phenotypes and novel OCRL variations in southern Chinese patients with Lowe syndrome

    The oculocerebrorenal syndrome of Lowe (Lowe syndrome, OMIM #309000) is an X-linked recessive disorder that impacts multiple systems and is estimated to affect approximately 1 in 500,000 individuals [ 1 ]. The characteristic features of Lowe …

  20. Open Access 20-02-2024 | Rett Syndrome | BriefCommunication

    Managing Gastrointestinal Symptoms Resulting from Treatment with Trofinetide for Rett Syndrome: Caregiver and Nurse Perspectives

    Rett syndrome (RTT) is a rare genetic neurodevelopmental disorder mainly affecting female individuals. Trofinetide was recently approved as the first treatment for RTT, largely on the basis of results from the phase 3 LAVENDER trial, in which …

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