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Beyond ventral and dorsal streams: thalamo-cortical connections for subcortical language integration 

Dorothee Saur

doi : 10.1093/brain/awae152

Volume 147, Issue 6, June 2024

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The brain’s arbitration system and obsessive-compulsive disorder

doi : 10.1093/brain/awae133

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Targeting excitatory:inhibitory network imbalance in Alzheimer’s disease

doi : 10.1093/brain/awae146

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The implications of amyloid-β pathology: only time will tell

doi : 10.1093/brain/awae147

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The basal forebrain cholinergic system as target for cell replacement therapy in Parkinson’s disease

doi : 10.1093/brain/awae026

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A neuroanatomical and cognitive model of impaired social behaviour in frontotemporal dementia

doi : 10.1093/brain/awae040

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Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant

doi : 10.1093/brain/awae057

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Lesion network of oculogyric crises maps to brain dopaminergic transcriptomic signature

doi : 10.1093/brain/awae094

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Broadening the clinical spectrum: molecular mechanisms and new phenotypes of ANO3-dystonia

doi : 10.1093/brain/awad412

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Genetic analysis and natural history of Parkinson’s disease due to the LRRK2 G2019S variant

doi : 10.1093/brain/awae073

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Huntington’s disease affects mitochondrial network dynamics predisposing to pathogenic mitochondrial DNA mutations

doi : 10.1093/brain/awae007

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Neurodevelopmental and synaptic defects in DNAJC6 parkinsonism, amenable to gene therapy

doi : 10.1093/brain/awae020

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Motor network gamma oscillations in chronic home recordings predict dyskinesia in Parkinson’s disease

doi : 10.1093/brain/awae004

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Mitigation of TDP-43 toxic phenotype by an RGNEF fragment in amyotrophic lateral sclerosis models

doi : 10.1093/brain/awae078

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Imbalanced mitochondrial dynamics contributes to the pathogenesis of X-linked adrenoleukodystrophy

doi : 10.1093/brain/awae038

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Neuropathy target esterase activity defines phenotypes among PNPLA6 disorders

doi : 10.1093/brain/awae055

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Toxic effects of mutant huntingtin in axons are mediated by its proline-rich domain

doi : 10.1093/brain/awad280

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Morc2a variants cause hydroxyl radical-mediated neuropathy and are rescued by restoring GHKL ATPase

doi : 10.1093/brain/awae017

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Maf1 loss regulates spinogenesis and attenuates cognitive impairment in Alzheimer’s disease

doi : 10.1093/brain/awae015

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Characterizing brain tau and cognitive decline along the amyloid timeline in Alzheimer’s disease

doi : 10.1093/brain/awae116

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Plasma VEGFA and PGF impact longitudinal tau and cognition in preclinical Alzheimer’s disease

doi : 10.1093/brain/awae034

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Seizures exacerbate excitatory: inhibitory imbalance in Alzheimer’s disease and 5XFAD mice

doi : 10.1093/brain/awae126

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Disease-linked mutations in Munc18-1 deplete synaptic Doc2

doi : 10.1093/brain/awae019

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Localization of stuttering based on causal brain lesions

doi : 10.1093/brain/awae059

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Macroscopic changes in aquaporin-4 underlie blast traumatic brain injury-related impairment in glymphatic function

doi : 10.1093/brain/awae065

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Neurocomputational model of compulsivity: deviating from an uncertain goal-directed system

doi : 10.1093/brain/awae102

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Multimodal study of multilevel pulvino-temporal connections: a new piece in the puzzle of lexical retrieval networks

doi : 10.1093/brain/awae021

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