Evidence‐based review and frontiers of migraine therapy
Abstract Background Cyclic vomiting syndrome (CVS) is identified as one of the “episodic syndromes that may be associated with migraine,” along with benign paroxysmal torticollis, benign paroxysmal vertigo, and abdominal migraine. It has been proposed that CVS and migraine may share pathophysiologic mechanisms of hypothalamic activation and altered ...
Kaitlin A. Greene+2 more
wiley +1 more source
Sodium Channels and Dendritic Spike Initiation at Excitatory Synapses in Globus Pallidus Neurons [PDF]
Jesse E. Hanson+2 more
openalex +1 more source
Cognitive profile in burning mouth syndrome versus mild cognitive impairment: A comparative study
Abstract Objectives This study aims to assess and contrast cognitive and psychological aspects of patients with burning mouth syndrome (BMS‐MCI) and geriatric patients (G‐MCI) with mild cognitive impairment, focusing on potential predictors like pain, mood disorders, blood biomarkers, and age‐related white matter changes (ARWMCs).
Grazia Daniela Femminella+15 more
wiley +1 more source
HCN2 and HCN1 Channels Govern the Regularity of Autonomous Pacemaking and Synaptic Resetting in Globus Pallidus Neurons [PDF]
C. Savio Chan+3 more
openalex +1 more source
Neuronal loss drives differentially expressed protein-pathways in the PSP globus pallidus. [PDF]
Dick F, Johanson GS, Tzoulis C.
europepmc +1 more source
Main Points CoPAN affects CoA biosynthesis and leads to iron dyshomeostasis. CoPAN d‐astrocytes show ferroptosis, iron accumulation, senescence, lipid peroxidation, mitochondrial damage and tubulin acetylation loss. Astrocytes recapitulate CoPAN disease.
Anna Cozzi+8 more
wiley +1 more source
Linear high intensity area along the medial margin of the internal segment of the globus pallidus in Machado-Joseph disease patients [PDF]
Sayaka Yamada
openalex +1 more source
Selective encoding of reward predictions and prediction errors by globus pallidus subpopulations. [PDF]
Farries MA+3 more
europepmc +1 more source
MTSS2 ‐Related Disorder: Refining the Phenotype in Four New Cases and Literature Review
ABSTRACT MTSS2 encodes a protein highly expressed in the central nervous system, with a crucial role in neurodevelopment. The de novo recurrent variant c.2011C>T (p.Arg671Trp) was first identified in 2022 as cause of Intellectual Developmental Disorder with ocular anomalies and distinctive facial features (OMIM#620086).
Angela De Dominicis+12 more
wiley +1 more source