Results 201 to 210 of about 79,800 (306)

Dropped jaw as a feature of suspected nutritional encephalopathy in a cat

Veterinary Record Case Reports, Volume 14, Issue 1, February 2026.
Abstract A 3‐year‐1‐month‐old female neutered domestic shorthair cat was presented for reluctance to jump over 3 months. Neurological and orthopaedic examinations, laboratory tests and cerebrospinal fluid analysis were unremarkable. Magnetic resonance imaging revealed mild bilateral symmetrical intra‐axial changes in the caudal brainstem.
Eleftheria Skovola, Oliver Williams, Serena Maini, Abbe Crawford   +3 more
wiley   +1 more source

Dementia of Frontal Type and Dementias with Subcortical Gliosis

, 1998
David M. A. Mann
openalex   +2 more sources

A versatile 3D culture model facilitates monitoring of astrocytes undergoing reactive gliosis [PDF]

, 2009
Emma East, Jon P. Golding, James B. Phillips   +2 more
openalex   +1 more source

HYPK‐Related Neurodevelopmental Syndrome: Case Report of Intellectual Disability, Developmental Delay, and Dysmorphic Features

Clinical Genetics, Volume 109, Issue 2, Page 352-355, February 2026.
We present the first published case of HYPK‐related neurodevelopmental disorder in a male proband with atypical facies, developmental delay, and autism spectrum disorder– like features. HYPK is a part of the NatA complex, like NAA10 and NAA15, with dysfunction leading to similar but milder features to those of Ogden Syndrome.
Rahi Patel, Rikhil Makwana, Elaine Marchi, Ziyi Fan, Erin Falsey, Beatriz Menendez, Philip Giampietro, Ingrid M. Wentzensen, Tzung‐Chien Hsieh, Shu‐ou Shan, Gholson J. Lyon   +10 more
wiley   +1 more source

Evaluation of CSF biomarkers for axonal and neuronal degeneration, gliosis, and beta-amyloid metabolism in Alzheimer's disease

, 2001
Nancy C. Andreasen
openalex   +1 more source

Maternal cafeteria diet exposure primes depression-like behavior in the offspring evoking lower brain volume related to changes in synaptic terminals and gliosis

, 2020
Luis A. Trujillo-Villarreal, Viktor J. Romero-Díaz, Iván Alberto Marino-Martínez, Lizbeth Fuentes-Mera, Marco Antonio Ponce-Camacho, Gabriel A. Devenyi, M. Mallar Chakravarty, Alberto Camacho‐Morales, Eduardo A. Garza‐Villarreal   +8 more
openalex   +2 more sources

Modeling cerebral palsy in animals

Developmental Medicine &Child Neurology, Volume 68, Issue 2, Page 158-174, February 2026.
Abstract Advancements in the treatment of cerebral palsy depend on animal research. Yet, most animal models have not been fully evaluated for spasticity and dystonia using clinically relevant measures of altered tone or movement patterns, which form the basis for diagnosing people with the condition.
Katharina A. Quinlan, Emily J. Reedich, Elvia Mena Avila, Brendan C. Moline, Landon T. Genry, Megan R. Detloff, Benjamin R. Katholi, Deborah Gaebler‐Spira, Bhooma R. Aravamuthan   +8 more
wiley   +1 more source

Autism-associated CHD8 controls reactive gliosis and neuroinflammation via remodeling chromatin in astrocytes

Platon Megagiannis, Mei Yuan, Rachel Yan, Yuan Lin, Jonathan J. Wilde, Hailey Eckersberg, Rahul Suresh, Xinzhu Tan, Hong Chen, W. Todd Farmer, Kuwook Cha, Phuong Uyen Le, Hélène Catoire, Daniel Rochefort, Tony Kwan, Brian A. Yee, Patrick A. Dion, Arjun Krishnaswamy, Jean‐François Cloutier, Stefano Stifani, Kevin Petrecca, G Yeo, Keith K. Murai, Guoping Feng, Guy A. Rouleau, Trey Ideker, Neville E. Sanjana, Yang Zhou   +27 more
openalex   +1 more source

Pleiotrophin/Midkine Pathway Is Dysregulated in a TDP‐43A315T Mouse Model of Amyotrophic Lateral Sclerosis (ALS)

Neuropathology, Volume 46, Issue 1, February 2026.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a fatal motor neuron disease (MND) characterized by progressive degeneration of both upper and lower motor neurons, along with skeletal muscles innervated by them. The identification of key molecules involved in disease pathology remains crucial for ALS, as no curative treatment is currently available ...
Paloma Martínez‐Alesón, Cristina Benito‐Casado, Carmen María Fernández‐Martos, María José Polanco Mora   +3 more
wiley   +1 more source

Familial ALS With p. L127S (L126S) Variant of the Cu/Zn SOD1 Gene: A Report of Two New Cases and Literature Review. [PDF]

Neuropathology
Inoue K, Toyooka K, Fujimura H, Ueda K, Kaido M, Yamamoto Y, Izumi Y.   +6 more
europepmc   +1 more source