Results 91 to 100 of about 258,614 (316)
PLoS ONE, 2018 BackgroundBotulinum toxin type A (BoNT-A) is generally considered safe and is widely used to treat a variety of clinical conditions involving muscle hyperactivity and for cosmetic purposes.
Ge-Fei Li +15 more
doaj +1 more source
Cerebellar defects in Pdss2 conditional knockout mice during embryonic development and in adulthood
Neurobiology of Disease, 2012 PDSS2 is a gene that encodes one of the two subunits of trans-prenyl diphosphate synthase that is essential for ubiquinone biosynthesis. It is known that mutations in PDSS2 can cause primary ubiquinone deficiency in humans and a similar disease in mice ...
Song Lu +6 more
doaj +1 more source
A Depolarizing Leak in Sodium Bicarbonate Cotransporter NBCe1 Causes Brain Edema
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objectives SLC4A4 encodes electrogenic sodium bicarbonate cotransporter NBCe1, prominently expressed in kidney and brain. Recessive loss‐of‐function variants in SLC4A4 cause proximal renal tubular acidosis, no brain edema. In the brain, NBCe1 is expressed by astrocytes, where it regulates pH and mediates astrocyte volume changes.
Quinty Bisseling +16 more
wiley +1 more source
, 2023 In recent decades, the consensus has been reached about the role of the cerebellum in social cognition. In addition to its well-known role in emotional processing, the specific involvement of the cerebellum in modulating theory of mind (ToM) abilities ...
Leggio M., Olivito G., Siciliano L.
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SPG4 and Dementia: Expanding the Clinical Spectrum
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Relationship Between Neurologic Symptoms and Signs and FMR1 Genotype in Premutation Carriers
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background and Objectives Fragile X‐associated Tremor/Ataxia Syndrome (FXTAS) is the most severe late‐onset condition caused by a premutation in the FMR1 gene, characterized by expanded CGG triplet repeats of 55–200. Clinical presentations of FXTAS, including gait ataxia, kinetic tremor, cognitive decline, and rare Parkinsonism, are linked to ...
Flora Tassone +8 more
wiley +1 more source
The influence of expertise on brain activation of the Action Observation Network during anticipation of tennis and volleyball serves [PDF]
, 2014 In many daily activities, and especially in sport, it is necessary to predict the effects of others’ actions in order to initiate appropriate responses.
Kindermann, S +35 more
core +1 more source
Cerebellum, Embodied Emotions, and Psychological Traits
, 2022 This chapter addresses how the embodiment approach may represent a unifying perspective for examining the cerebellar role in emotional behavior and psychological traits.
Cutuli, Debora +3 more
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Ibn Al-Haitham Journal for Pure and Applied Sciences, 2017 A histological study was conducted to examine the structure of rhombencephalon (Cerebellum) in Columba livia gaddi (Gmeiin, 1789). The result showed that the cerebellum is aportion of the brain lying behind the cerebrum, the surface of the ...
W. B. Abid, A. B. Abid
doaj
Morphological and Metabolic Alteration of Cerebellum in Patients with Post-Stroke Depression
Cellular Physiology and Biochemistry, 2016 Background: To study morphological and metabolic changes of cerebellum with multimodality magnetic resonance imaging (MRI) and proton magnetic resonance spectroscopy (1H-MRS), respective, to explore correlation between cerebellum alteration and severity ...
Ling Zhang +3 more
doaj +1 more source