INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano +27 more
wiley +1 more source
Fitness, Weight Status and Executive Functions in Adolescents: A Cluster Analysis. [PDF]
Scand J Med Sci SportsGrao-Cruces A +5 more
europepmc +1 more source
On the Analysis of Covid-19 Transmission in Wuhan, Diamond Princess and Jakarta-cluster
, 2020 Edy Soewono
openalex +2 more sources
Clustering Analysis of Stock Volume and Price Relationship based on Gaussian Mixture Model [PDF]
, 2014 Yaohui Bai, Jianwu Dang
openalex +1 more source
Modern Algorithms of Cluster Analysis
, 2018 M. Klopotek, S. Wierzchon
semanticscholar +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Natalizumab (NTZ) is a highly effective therapy for multiple sclerosis (MS); however, its use is limited by the risk of a rare potentially severe opportunistic brain infection, progressive multifocal leukoencephalopathy (PML). Alternative dosing strategies are evaluated to reduce PML risk while still maintaining efficacy, which ...
Regina Berkovich +10 more
wiley +1 more source
Sex-specific sleep profiles in Spanish adults: cross-sectional actigraphy-PSQI study with cluster analysis in Salamanca and Ávila. [PDF]
BMJ OpenJiménez-Vaquero C +7 more
europepmc +1 more source
Spatial Clustering Analysis with Spectral Imaging-based Single-Step Multiplex Immunofluorescence (SISS-mIF) for Assisting Histological Diagnosis [PDF]
T. Nakamura +10 more
openalex +1 more source
Visualization in stylometry: Cluster analysis using networks
Digital Scholarship in the Humanities, 2017 Maciej Eder
semanticscholar +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
Annals of Clinical and Translational Neurology, EarlyView.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