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Genetic alterations, such as CDKN2A mutation, RPLP1-C19MC fusion, and chromosomal changes like 1p loss and 7q gain, highlight the molecular heterogeneity of MNTI and its possible overlap with other embryonal tumors, like neuroblastoma (Almomani and Rentea 2021)
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Uncovering ferroptosis in Parkinsons disease via bioinformatics and machine learning, and reversed deducing potential therapeutic natural products
Since many autistic children have a co-occurring diagnosis of ADHD, primary caregivers completed the Conners-3(K.C., n.d.-a) or Conners-4(K.C., n.d.-b) assessment to evaluate symptoms and impairments associated with ADHD using dimensional measures within this cohort