Results 201 to 210 of about 2,173,247 (301)

Cellular expression domains of type 3 deiodinase in the meninges, choroid plexus, tanycytes and barrier tissues of the brain. [PDF]

Front Endocrinol (Lausanne)
Liu Y, Ng L, Liu H, Forrest D.
europepmc   +1 more source

Eye‐Brain Neuroimmune Axis Enables Long‐Term Survival in Glioblastoma by Modulating Brain Immune Surveillance and Neuronal Excitability

Advanced Science, Volume 13, Issue 52, 18 September 2026.
The eye–brain neuroimmune axis triggers immune activation and disrupts pathological neuronal connectivity to extend glioblastoma survival. ABSTRACT As an anatomical extension of the central nervous system (CNS), the eye harbors rich neural and immune interfaces with the brain. However, the integrated immunological and neurological nexus between the eye
Mingyue Cui, Lulu Qian, Binbin Chu, Xuan Qin, Menglin Wu, Minke Wu, Tongyu He, Baochuan Zhang, Bin Song, Yao He   +9 more
wiley   +1 more source

Choroidal microcirculation in pediatric craniopharyngioma: postoperative alterations in choroidal thickness. [PDF]

Front Pediatr
Rakusiewicz-Krasnodębska K, Bogusz-Wójcik A, Moszczyńska E, Jaworski M, Kowalczyk P, Hautz W.   +5 more
europepmc   +1 more source

Clinical, Behavioral and Neuroradiological Phenotype in an Italian Cohort of Patients With Xia Gibbs Syndrome: A Multicenter Cross‐Sectional Study and Systematic Literature Review

American Journal of Medical Genetics Part A, Volume 200, Issue 9, Page 2067-2079, September 2026.
ABSTRACT Heterozygous variants in the AHDC1 gene are associated with Xia Gibbs Syndrome (XGS), a genetic disorder with a highly variable phenotype. Cognitive impairment, motor delay, language delay, neonatal hypotonia, and sleep apnea are considered “cardinal” signs of the disease.
Giulia Cinelli, Stefania Della Vecchia, Patrizia Bergonzini, Elisa Caramaschi, Elisabetta Spezia, Claudia Parenti, Simona Filomena Madeo, Laura Lucaccioni, Cavalleri Francesca, Marisa Pugliese, Federico Raviglione, Clara Colonna, Olga Calabrese, Ilaria Stanghellini, Maria Carmen Marongiu, Enrico Biagioni, Anna Rita Ferrari, Roberta Battini, Lorenzo Iughetti   +18 more
wiley   +1 more source

A meta‐refined human Alzheimer's disease‐associated gene subset shows partial mouse‐model pathway correspondence and limited cross‐cohort machine‐learning transportability

Alzheimer's &Dementia, Volume 22, Issue 9, September 2026.
Abstract INTRODUCTION Common Alzheimer's disease (AD) mouse models are widely used, but their molecular correspondence with human AD remains uncertain. METHODS We analyzed 15 post mortem human brain datasets, four human non‐brain or in vitro sensitivity datasets, and nine AD‐related mouse‐model molecular‐profiling datasets; GSE222494 was analyzed ...
Linsong Chai, Yunshi Huang, Jinglei Ni, Shuang Zuo, Jia Huang, Bingbing Lin   +5 more
wiley   +1 more source

Abnormal Glycaemic Fluctuations Associated With Early Microvascular Changes in the Retina and Choroid of Nondiabetic Adults. [PDF]

Diabetes Obes Metab
Jiang Y, Gu L, Ma Y, Qu Y, Wan H, Lv K, Zhu Q, Zhou H, Sun J, Lu F, Li X, Wang Y, Zhou J, Liu K, Wang Y, Shen Y.   +15 more
europepmc   +1 more source

Distinct ocular microvascular alterations in Alzheimer's disease and cerebral small vessel disease

Alzheimer's &Dementia, Volume 22, Issue 9, September 2026.
Abstract INTRODUCTION While both Alzheimer's disease (AD) and cerebral small vessel disease (CSVD) involve vascular dysfunction, the ocular microvascular differences between them remain largely underinvestigated. METHODS This cross‐sectional study included 650 participants (149 AD, 276 CSVD, and 225 cognitively unimpaired individuals).
Ziyi Zhang, Le Cao, Peng Liu, Shiyun Yang, Yuying Yan, William Robert Kwapong, Ying He, Mingyuan Yang, Hang Wang, Youjie Wang, Zijuan Feng, Jingyu Zhou, Ming Liu, Peng Lei, Bo Wu, Shuting Zhang   +15 more
wiley   +1 more source

Potential of Fenofibric Acid as Topical Eye Drops for Management of Dry Eye Syndrome. [PDF]

Pharmaceutics
Tan G, Chen M, Xie P, Bian C, Wang W, Wu S, Jin Y, Cheng L.   +7 more
europepmc   +1 more source

Congenital encephalomeningocele presenting as a giant orbital mass in a neonate: a case report. [PDF]

BMC Ophthalmol
Chen X, Ni Y, Zhan C.
europepmc   +1 more source

Aggressive Periodontitis and Palmoplantar Keratoderma: Papillon–Lefèvre Syndrome in an 11‐Year‐Old Nepalese Girl

Clinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Papillon–Lefèvre syndrome is a rare autosomal recessive disorder characterized by palmoplantar keratoderma and aggressive periodontitis. We report an 11‐year‐old Nepalese girl presenting with severe periodontal destruction and characteristic cutaneous manifestations. Clinical and radiographic findings established the diagnosis.
Jenisha Bhattarai, Sanish Pokhrel, Yogendra Poudel, Ujjwal Rimal   +3 more
wiley   +1 more source