Results 201 to 210 of about 1,108,914 (332)

Long-read genome sequencing enhances diagnostics of pediatric neurological disorders. [PDF]

Genome Med
Ek M, Kvarnung M, Ten Berk de Boer E, La Fleur L, Ljöstad L, Lyander A, Faergeman SL, Drue SO, Thonberg H, Nordgren A, Soller MJ, Wirta V, Eisfeldt J, Lindstrand A.   +13 more
europepmc   +1 more source

Decreased content of ascorbic acid (vitamin C) in the brain of knockout mouse models of Na+,K+-ATPase-related neurologic disorders

, 2021
Keiko Ikeda, Adriana A. Tienda, Fiona E. Harrison, Kiyoshi Kawakami   +3 more
openalex   +1 more source

Bayesian Estimation Improves Prediction of Outcomes After Epilepsy Surgery

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT We estimated the statistical power of studies predicting seizure freedom after epilepsy surgery. We extracted data from a Cochrane meta‐analysis. The median power across all studies was 14%. Studies with a median sample size or less (n ≤ 56) and a statistically significant result exaggerated the true effect size by a factor of 5.4, while the ...
Adam S. Dickey, Vineet Reddy, Ammar A. Rashied, Nigel P. Pedersen, Robert T. Krafty   +4 more
wiley   +1 more source

Complement activation in immunological neurological disorders: mechanisms and therapeutic strategies. [PDF]

Front Neurol
Chen JY, Sanghani N, Palmer K, Li Y, Lin F, Abbatemarco JR.   +5 more
europepmc   +1 more source

Genetics of hereditary neurological disorders in children.

, 2014
Yue Huang, Sui Yu, Zhanhe Wu, Beisha Tang   +3 more
openalex   +1 more source

Factors predictive of abnormal results for computed tomography of the head in horses affected by neurologic disorders: 57 cases (2001–2007) [PDF]

, 2009
Cristina Sogaro-Robinson, Véronique A. Lacombe, Stephen M. Reed, Rajesh Balkrishnan   +3 more
openalex   +1 more source

Developmental, Neuroanatomical and Cellular Expression of Genes Causing Dystonia

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Dystonia is one of the most common movement disorders, with variants in multiple genes identified as causative. However, an understanding of which developmental stages, brain regions, and cell types are most relevant is crucial for developing relevant disease models and therapeutics.
Darren Cameron, Nicholas E. Clifton, Daniel Cabezas de la Fuente, Peter Holmans, Nicholas J. Bray, Kathryn J. Peall   +5 more
wiley   +1 more source

Sexual Health After Neurological Disorders: A Comprehensive Umbrella Review of Treatment Evidence. [PDF]

Med Sci (Basel)
Manuli A, Calderone A, Latella D, Quattrini F, Pucciarelli G, Calabrò RS.   +5 more
europepmc   +1 more source

Functional neurological disorder and gut microbiome: Casual or causal relationship?

Alejandro Borrego-Ruiz, Juan J. Borrego
openalex   +1 more source

An Out‐of‐Place Etiology: Recognizing FMR1 Premutation in the Memory Clinic

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The FMR1 gene premutation (55–200 CGG repeats) is usually associated with a wide range of symptoms and phenotypes within the Fragile X‐tremor/ataxia syndrome (FXTAS), but may also manifest as predominant or isolated cognitive decline. We describe three male patients referred for progressive cognitive impairment and behavioral changes. Standard
Guido Greco, Caterina Motta, Enrica Marchionni, Maria Rosaria D'Apice, Carlangelo Carrese, Giuseppe Novelli, Alessandro Martorana, Chiara Giuseppina Bonomi   +7 more
wiley   +1 more source