Pediatric movement disorders

TD Sanger - Current Opinion in Neurology, 2003 - journals.lww.com
Pediatric movement disorders : Current Opinion in Neurology Pediatric movement disorders :
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Mitochondrial modulation with leriglitazone as a potential treatment for Rett syndrome

U Musokhranova, C Grau, C Vergara… - Journal of Translational …, 2023 - Springer
Background Rett syndrome is a neuropediatric disease occurring due to mutations in
MECP2 and characterized by a regression in the neuronal development following a normal …

Preserved navigation abilities and spatio‐temporal memory in individuals with autism spectrum disorder

C Laidi, N Neu, A Watilliaux… - Autism …, 2023 - Wiley Online Library
Cerebellar abnormalities have been reported in autism spectrum disorder (ASD). Beyond its
role in hallmark features of ASD, the cerebellum and its connectivity with forebrain structures …

Primary complex motor stereotypies are associated with de novo damaging DNA coding mutations that identify KDM5B as a risk gene

TV Fernandez, ZP Williams, T Kline, S Rajendran… - Plos one, 2023 - journals.plos.org
Motor stereotypies are common in children with autism spectrum disorder (ASD), intellectual
disability, or sensory deprivation, as well as in typically developing children (“primary” …

Toward understanding autism heterogeneity: Identifying clinical subgroups and neuroanatomical deviations.

J Meijer, B Hebling Vieira, C Elleaume… - … and Clinical Science, 2024 - psycnet.apa.org
Abstract Autism spectrum disorder (“autism”) is a neurodevelopmental condition
characterized by substantial behavioral and neuroanatomical heterogeneity. This poses …

Insight into the function of a unique voltage-sensor protein (TMEM266) and its short form in mouse cerebellum

T Kawai, H Narita, K Konno, S Akter… - Biochemical …, 2022 - portlandpress.com
Voltage-sensing proteins generally consist of voltage-sensor domains and pore-gate
domains, forming the voltage-gated ion channels. However, there are several …

Deficiency of the histone lysine demethylase KDM5B causes autism-like phenotypes via increased NMDAR signalling

L Pérez-Sisqués, SU Bhatt, A Caruso, MU Ahmed… - bioRxiv, 2024 - biorxiv.org
Loss-of-function mutations in genes encoding lysine methyltransferases (KMTs) and
demethylases (KDMs) responsible for regulating the trimethylation of histone 3 on lysine 4 …

The neurodevelopmental movement disorders: tics and stereotypies

SL Dean - Capute and Accardo's Neurodevelopmental …, 2025 - Elsevier
Abnormal movements are common features of neurodevelopmental disabilities and also
occur as isolated movement disorders. The two most common developmental movement …

[PDF][PDF] Influence of sociodemographic characteristics on right-wing authoritarianism

JD Nikolov - Specijalna edukacija i rehabilitacija, 2024 - casopis.fasper.bg.ac.rs
160 while others were specified as predictors. The Right-Wing Authoritarianism (RWA)
scale, consisting of 12 questions and measured at an interval level, was used to assess right …

The mouse at the popcorn stage of development

R Lalonde, C Strazielle - International Journal of …, 2022 - Wiley Online Library
In mice, rats, and rabbits, vigorous jumping and hyperexcitability occur at the popcorn stage
of postnatal development. In view of subcortical structures appearing before cortical ones …