Results 291 to 300 of about 1,092,875 (381)

A Novel Mixed Convolution Transformer Model for the Fast and Accurate Diagnosis of Glioma Subtypes

Advanced Intelligent Systems, EarlyView.
The mixed convolutional transformer model represents a novel approach for the accurate and rapid diagnosis of glioma subtypes. This model employs advanced, complex layers and functions, establishing its uniqueness and enhancing its ability to deliver precise outcomes in glioma subtype detection.
S. M. Nuruzzaman Nobel, S. M. Masfequier Rahman Swapno, Md Babul Islam, AKM Azad, Salem A. Alyami, Md Alamin, Pietro Liò, Mohammad Ali Moni   +7 more
wiley   +1 more source

Editorial: NeuroCOVID. Insights into the clinical manifestations and pathophysiology. [PDF]

Front Neurol
González-Quevedo A, Valdés Sosa PA, Machado Curbelo C, Gutiérrez Gil J.   +3 more
europepmc   +1 more source

Clinical and radiological characteristics of parenchymal and meningeal spinal tuberculosis. [PDF]

BMC Infect Dis
Shan QL, Zhang L, Fu XW, Qi M, Wei JL, Gan W, Li X, Shen LJ.   +7 more
europepmc   +1 more source

Peripherin, A New Promising Biomarker in Neurological Disorders. [PDF]

Eur J Neurosci
Manco C, Righi D, Primiano G, Romano A, Luigetti M, Leonardi L, De Stefano N, Plantone D.   +7 more
europepmc   +1 more source

Levels of DEFA1, Progranulin, and NRG4 in Patients with Autonomic Neuropathy: Potential Biomarkers for Diagnosis and Prognosis. [PDF]

Metabolites
Nikolova D, Kamenov Z, Hristova J, Gateva AT.   +3 more
europepmc   +1 more source

Clinical Insights Into Nabais Sá‐De Vries Syndrome due to a Novel SPOP Mutation: Neuromotor, Cognitive, Adaptive, Behavioral, and Neurovisual Features

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Nabais Sá‐De Vries syndrome (NSDVS) is an extremely rare autosomal dominant disorder caused by SPOP mutations. To date, only 10 cases have been described presenting with intellectual disability, neurological signs and symptoms, and a variable association of dysmorphic features.
Jessica Galli, Erika Loi, Federica Zanardini, Giovanna Baldoni, Francesca Novara, Serena Panigada, Roberto Ciccone, Maria Rosa Cutrì, Alice Bertoletti, Lorenzo Pinelli, Elisa Fazzi   +10 more
wiley   +1 more source

Editorial: Nervous regeneration and functional recovery in the central and peripheral nervous systems: diagnostic methods, gene/cell therapies, and interventions. [PDF]

Front Mol Neurosci
Natarajan D, Hotta R, Fujiwara N, Perin S.   +3 more
europepmc   +1 more source

Peripheral versus central nervous system APOE in Alzheimer’s disease: Interplay across the blood-brain barrier

, 2019
Dustin Chernick, Stephanie Ortiz‐Valle, Angela Jeong, Wenhui Qu, Ling Li   +4 more
openalex   +2 more sources

Natural History and Diagnostic Findings in an Adult Man Diagnosed With Attenuated Krabbe Disease

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Krabbe disease (KD), or globoid cell leukodystrophy, is a rare autosomal recessive lysosomal storage disorder caused by a deficiency in galactocerebrosidase (GALC), leading to psychosine (galactosylsphingosine) accumulation and myelin damage.
Eamon P. McCarron, Andrew Oldham, Amit Herwadkar, Sarah Jenkinson, Christopher Campbell, Kate Neal, Heather J. Church, James A. Cooper, Karolina M. Stepien   +8 more
wiley   +1 more source

Abnormal DNA Methylation Profile Suggests the Extension of the Clinical Spectrum of the SETD2‐Related Disorders to a Syndromic Multiple Tumor Phenotype

American Journal of Medical Genetics Part A, EarlyView.
ABSTRACT SETD2 has an essential role in epigenetic regulation. SETD2 pathogenic variants cause neurodevelopmental disorders (SETD2‐NDDs) that most commonly include various degrees of intellectual disability and behavioral disorders, macrocephaly, brain malformations, and generalized overgrowth.
Marie Lucain, Antonio Vitobello, Bekim Sadikovic, Juliette Albuisson, Léa Gaudillat, Martin Chevarin, Julien Maraval, Christel Thauvin‐Robinet, Jennifer Kerkhof, Christophe Philippe, Sophie Nambot, Laurence Faivre   +11 more
wiley   +1 more source