Anti-N-methyl D-aspartate receptor (NMDAR) encephalitis is an autoimmune encephalitis
caused by the binding of antibodies to extracellular epitopes of cell-surface proteins of the …

Individuals with neurodevelopmental disabilities (NDDs) may be at increased risk for
catatonia, which can be an especially challenging condition to diagnose and treat. There …

Attention Deficit Hyperactivity Disorder (ADHD) is a childhood-onset neurodevelopmental
disorder, whose etiology and pathogenesis are still largely unknown. In order to uncover …

We were very pleased to read the excellent umbrella review (UR) by van der Burg et al.[1]
who highlighted genetic factors associated with drug-related movement disorders (DRMD) …

Lithium (Li) is a medication long-used to treat bipolar disorder. It is currently under
investigation for multiple nervous system disorders, including Alzheimer's disease (AD) …

Aberrant mitochondrial phenotypes are common to many central nervous system (CNS)
disorders, including neurodegenerative and neurodevelopmental diseases. Mitochondrial …

The coordinated interaction between mitochondria and lysosomes, mainly manifested by
mitophagy, mitochondria‐derived vesicles, and direct physical contact, is essential for …

DNA methylation is an epigenetic alteration that plays a fundamental part in governing gene
regulatory processes. The DNA methylation mechanism affixes methyl groups to distinct …

Catatonia is a rare, underdiagnosed syndrome in children. ‍ We report the case of a 4-year-
old child admitted for recent social withdrawal alternating with psychomotor excitement …

Uterine carcinosarcoma (UCS) is a highly invasive malignant tumor that originated from the
uterine epithelium. Many studies suggested that the abnormal changes of alternative …