Results 201 to 210 of about 9,722 (294)
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source
ERP systems introduction time: factors, analysis and application of projects management techniques [PDF]
Thais Cássia Cabral Padilha +3 more
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Techniques for Improving the Readability of Information and Images Projected onto Documents
Taiichiro Nakayama +2 more
openalex +2 more sources
Prediction Model for Etiologic Differentiation of Isolated Vestibular Syndrome in Emergency Settings
ABSTRACT Objective This study aimed to develop and validate a predictive model for differentiating central from peripheral etiologies in patients with isolated vestibular syndrome (VS). Methods In this multicenter retrospective cohort study, 506 patients with isolated VS from five hospitals were divided into derivation (n = 301) and validation (n = 205)
Guo Wenting +12 more
wiley +1 more source
New quantum LDPC codes based on projective geometry. [PDF]
Tang C, Bai C, Feng Y.
europepmc +1 more source
ABSTRACT Introduction Neuronal pentraxin 2 (NPTX2) is a synaptic protein involved in synaptic plasticity and regulation of neuronal excitability. Lower baseline cerebrospinal fluid (CSF) NPTX2 levels have been shown to be associated with an earlier onset of mild cognitive impairment (MCI), a pre‐dementia syndrome, even after CSF Alzheimer's Disease (AD)
Juan P. Vazquez +12 more
wiley +1 more source
Quantum error correction of qudits beyond break-even. [PDF]
Brock BL +7 more
europepmc +1 more source
ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun +95 more
wiley +1 more source
Neurodynamic robust adaptive UWB localization algorithm with NLOS mitigation. [PDF]
Liu Y, Hu E, Chen Y, Guo C.
europepmc +1 more source
The scientific status of projective techniques in discussion [PDF]
Anna Elisa de Villemor-Amaral +1 more
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