Results 211 to 220 of about 1,760,110 (357)

Relationship of cognitive decline with glucocerebrosidase activity and amyloid‐beta 42 in DLB and PD

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Objective Dementia with Lewy bodies (DLB) and Parkinson's disease (PD) share clinical, pathological, and genetic risk factors, including GBA1 and APOEε4 mutations. Biomarkers associated with the pathways of these mutations, such as glucocerebrosidase enzyme (GCase) activity and amyloid‐beta 42 (Aβ42) levels, may hold potential as predictive ...
Maria Camila Gonzalez, Linn Oftedal, Johannes Lange, Diego Alejandro Tovar‐Rios, Ole‐Bjørn Tysnes, Claire Paquet, Marta Marquié, Mercè Boada, Daniel Alcolea, Konrad Rejdak, Ewa Papuc, Jakub Hort, Cristian Falup‐Pecurariu, Dag Aarsland, Guido Alves, Jodi Maple‐Grødem   +15 more
wiley   +1 more source

Exploring the diagnostic potential: magnetic particle imaging for brain diseases. [PDF]

Mil Med Res
Guo LS, An Y, Zhang ZY, Ma CB, Li JQ, Dong Z, Tian J, Liu ZY, Liu JG.   +8 more
europepmc   +1 more source

On Serous Effusion from the Membranes and into the Ventricles of the Brain, and its Connection with Apoplexy and other Diseases of the Brain [PDF]

John R. Sims
openalex   +1 more source

Lipid studies in the blood and brain in multiple sclerosis and motor neurone disease [PDF]

, 1965
J. N. Cumings, R. C. Shortman, THOMAS R. SKRBIC   +2 more
openalex   +1 more source

CT in equine brain diseases [PDF]

, 2013
Crijns, Casper, Gielen, Ingrid
core   +1 more source

LINC00323 variant is associated with increased risk of essential tremor

Annals of Clinical and Translational Neurology, EarlyView.
Abstract Essential tremor (ET) is a common adult movement disorder, with accumulating evidence suggesting that genetic factors primarily account for ET risk. However, replication studies on the genetic variants have yielded inconsistent results. In our case–control study, we show that the LINC00323 variant, identified in a European GWAS study, is ...
Brendan Tan, Ebonne Ng, Qiao Yang Sun, Aaron Mai, Ling‐Ling Chan, Thomas Welton, Kumar M. Prakash, Kay Yaw Tay, Wing Lok Au, Louis C.S. Tan, Eng‐King Tan, Bin Xiao   +11 more
wiley   +1 more source

Investigation of the role of miRNA variants in neurodegenerative brain diseases. [PDF]

Front Genet
Frydas A, Cacace R, van der Zee J, Van Broeckhoven C, Wauters E.   +4 more
europepmc   +1 more source

Reversibility of Tumor-like Lesions: Meticulous Diagnosis for Treatable Brain Diseases. [PDF]

Neurol Clin Pract, 2023
Hsieh ST.
europepmc   +1 more source

UDP‐glucose dehydrogenase variants cause dystroglycanopathy

Annals of Clinical and Translational Neurology, EarlyView.
Abstract UDP‐glucose dehydrogenase (UGDH) variants have been associated with hypotonia, developmental delay, and epilepsy. We report the first pathologic evidence of dystroglycanopathy in siblings with UGDH variants. Both presented around 6 months with developmental delay and elevated creatinine kinase.
Anna M. Reelfs, Carrie M. Stephan, Theresa M. Czech, Mary O. Cox, Soumya Joseph, Benjamin W. Darbro, Steven A. Moore, Kevin P. Campbell, Katherine D. Mathews   +8 more
wiley   +1 more source

A realistic human head phantom for electromagnetic detection of brain diseases. [PDF]

PeerJ
Bai Z, Chen D, Ma K, Jin G, Qiu J, Li Q, Li H, Chen M.   +7 more
europepmc   +1 more source