Results 151 to 160 of about 6,134,485 (406)

Exosome Proteomics of SOD1D90A Mutation Suggest Early Disease Mechanisms, and FN1 as a Biomarker

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Amyotrophic lateral sclerosis (ALS) is a neuromuscular disease. Super oxide dismutase 1 (SOD1) gene mutations cause ALS, and the D90A mutation is associated with primarily upper motor neuron (UMN) loss. Objective Our goal is to reveal the early cellular events in ALS pathology and identify potential pharmacokinetic biomarkers, using well ...
Mukesh Gautam, Ali Laith, Aslihan Gunel, Melda Yilmaz, Nazli Basak, Halil Idrisoglu, P. Hande Ozdinler   +6 more
wiley   +1 more source

NAD(P)H : quinone Oxidoreductase 1 Deficiency and Increased Susceptibility to 7,12-Dimethylbenz[a]-anthracene-Induced Carcinogenesis in Mouse Skin [PDF]

, 2001
Delwin J. Long, Rebekah L. Waikel, Xia Wang, Dennis R. Roop, Anil K. Jaiswal   +4 more
openalex   +1 more source

Isospin Diffusion in Heavy-Ion Collisions and the Neutron Skin Thickness of Lead

, 2005
The correlation between the thickness of the neutron skin in Pb-208, and the degree of isospin diffusion in heavy-ion collisions is examined. The same equation of state is used to compute the degree of isospin diffusion in an isospin-depedent transport ...
Li, Bao-An, Steiner, Andrew W.
core   +1 more source

Scoliosis Surgery in a Patient With Advanced Friedreich's Ataxia—It Is Not Too Late

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Friedreich's ataxia is a multisystem disorder with scoliosis being the most common non‐neurological manifestation. While scoliosis surgery is typically performed in adolescent, ambulatory patients, few data exist on surgical outcomes in patients with advanced disease.
Kathrin Reetz, Stella A. Lischewski, Jörg B. Schulz, Maximilian Praster, Miguel Pishnamaz, on behalf of the FACROSS study group, Imis Dogan, Sandro Romanzetti, Ravi Dadsena, Kerstin Konrad, Thomas Clavel, Vera Jankowski, Joachim Jankowski, Oliver Pabst, Nikolaus Marx, Julia Moellmann, Malte Jacobsen, Katharina Marx‐Schütt, Juergen Dukart, Simon Eickhoff, Ralf‐Dieter Hilgers   +20 more
wiley   +1 more source

Longitudinal Observational Study on Quality of Life in Patients with Chronic Wounds Using DLQI and EQ-5D

Medicina
Background and Objectives: Chronic wounds severely impair patients’ quality of life (QoL), impacting physical, emotional, and functional well-being.
David Palomar-Albert, Jorge Zamora-Ortiz, Federico Palomar-Llatas, Marta Escudero-Martínez, Alba Naranjo-Cuellar, Maria Isabel Pastor-Orduña   +5 more
doaj   +1 more source

Evaluating the Repeatability of Friction Coefficient Measurements and Tactile Perceptions in Skin–Textile Interactions Across Body Regions [PDF]

, 2022
Mevra Temel, A. Johnson, Alex Lloyd
openalex   +1 more source

Impact of Stress‐Induced Hyperglycemia on In‐Hospital Medical Complications in Patients With Acute Stroke: From a Large‐Scale Nationwide Longitudinal Registry

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Aims This study aimed to explore the relationship between stress‐induced hyperglycemia (SIH) and in‐hospital medical complications in patients with acute stroke. Methods We enrolled 865,765 patients with acute stroke from the Chinese Stroke Center Alliance cohort.
Xintong Song, Yi Ju, Hongqiu Gu, Zhikai Zhu, Zixiao Li, Qian Zhang, Xingquan Zhao   +6 more
wiley   +1 more source

Particulate matter‐induced atmospheric skin aging is aggravated by UVA and inhibited by a topical l‐ascorbic acid compound

, 2021
Soomin Kim, Jihee Kim, Young In Lee, Seulgi Jang, Seung Yong Song, Won Jai Lee, Ju Hee Lee   +6 more
openalex   +2 more sources

Microsecretory adenocarcinoma of the skin, a novel type of sweat gland carcinoma: Report of three additional cases [PDF]

, 2023
Sofia Bogiatzi, Ángela Estenaga, Baptiste Louveau, Amélie Osio, Lydia Deschamps, Samia Mourah, Brigitte Poirot, Jacqueline Lehmann‐Che, B. Cribier, Maxime Battistella   +9 more
openalex   +1 more source

Autosomal Recessive Spastic Ataxia of Charlevoix‐Saguenay in Two Half‐Siblings

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Autosomal recessive spastic ataxia of Charlevoix‐Saguenay (ARSACS) is caused by biallelic pathogenic variants in the SACS gene. We report the clinical, radiologic and neurophysiologic features of a pair of half‐siblings who presented with progressive cerebellar ataxia, peripheral neuropathy and upper motor neuron signs.
Dennis Yeow, Matthew Katz, Jonathan Rodgers, Mark Davis, Thomas Robertson, R. J. McKinlay Gardner, Pamela A. McCombe   +6 more
wiley   +1 more source