Results 251 to 260 of about 117,087 (348)

Neuron-specific modulation of SLC30A10 identifies dopaminergic and glutamatergic neurons as targets of manganese-induced motor disease. [PDF]

Proc Natl Acad Sci U S A
Grant SM, Melkote A, Bernstein MX, Jursa T, Taylor CA, Hutchens S, Shawlot W, Zweifel LS, Gonzales RA, Smith DR, Mukhopadhyay S.   +10 more
europepmc   +1 more source

The association between neural crest‐derived glia and melanocyte lineages throughout development and disease

Developmental Dynamics, EarlyView.
Abstract Neural crest cells are a transient cell population that emerges from the dorsal neural tube during neurulation and migrates extensively throughout the embryo. Among their diverse derivatives, glial cells (such as Schwann and satellite ganglionic cells) and melanocytes represent two major lineages. In vitro studies suggested they share a common
Chaya Kalcheim
wiley   +1 more source

Incidental Diagnosis of Fahr's Disease Following Severe Traumatic Brain Injury: A Case Report. [PDF]

Clin Case Rep
Ebrahimi H, Holakoo A, Hejazian SE, Ahmadian H, Zohrevand AH, Sharifzadeh M.   +5 more
europepmc   +1 more source

Role of SoxE transcription factors in development and disease

Developmental Dynamics, EarlyView.
Abstract Sox8, Sox9, and Sox10 arose by multiple rounds of genome duplications from a single SoxE gene in ancestral vertebrates. In this review, we will briefly discuss the molecular structure and function of SoxE transcription factors and their evolutionary origin. We will then discuss their expression, function, and developmental disorders.
Merin Lawrence, Gerhard Schlosser
wiley   +1 more source

Principal axis of primate basal ganglia in processing cognitive flexibility and habitual stability. [PDF]

Brain
Kim HF.
europepmc   +1 more source

Basal ganglia chronic hypoxic ischaemic disease

, 2020
openaire   +1 more source

Electro‐clinical features of Mowat–Wilson syndrome: A retrospective study of 31 children in mainland China

Epileptic Disorders, EarlyView.
Abstract Objective To summarize the electro‐clinical and genetic characteristics of children with Mowat–Wilson syndrome (MWS). Methods This study is a hospital‐based case series analyzing clinical data from 31 pediatric patients with MWS and epilepsy treated at Peking University First Hospital between June 2020 and December 2024.
Yi Ju, Tao‐yun Ji
wiley   +1 more source

Verdict: No Evidence of Increased Parkinsonism Risk With Macrocyclic Gadolinium-Based Contrast Agents. [PDF]

Korean J Radiol
Moon WJ.
europepmc   +1 more source

Crossed cerebellar diaschisis in status epilepticus: A systematic review of the literature

Epileptic Disorders, EarlyView.
Abstract Objective Crossed cerebellar diaschisis is a neuroimaging phenomenon observed in various neurological conditions, including status epilepticus. This systematic review aims to summarize the clinical and radiological characteristics of patients developing crossed cerebellar diaschisis following status epilepticus and to discuss potential ...
Payam Tabaee Damavandi, Pilar Bosque‐Varela, Helena Barbosa Horta Santos, Bassam Al‐Fatly, Lukas Machegger, Eugen Trinka, Giorgi Kuchukhidze   +6 more
wiley   +1 more source