• A review of core myopathy: central core disease, multiminicore disease, dusty core disease, and core-rod myopathy
• Accelerating Hyperparameter Tuning in Machine Learning for Alzheimer's Disease With High Performance Computing
• An Embedded Multi-Core Real-Time Simulation Platform of Basal Ganglia for Deep Brain Stimulation
• An integration-free iPSC line SDQLCHi025-A from a girl with multiminicore disease carrying compound heterozygote mutations in RYR1 gene
• Association between obesity and frequency of high-grade prostate cancer on biopsy in men: A single-center retrospective study
• Automated picking of amyloid fibrils from cryo-EM images for helical reconstruction with RELION
• Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a <em>De Novo</em> Seven-Octapeptide Repeat Insertion
• CIDACS-RL: a novel indexing search and scoring-based record linkage system for huge datasets with high accuracy and scalability
• Congenital myopathy with a novel SELN missense mutation and the challenge to differentiate it from congenital muscular dystrophy
• Core myopathies - a short review
• Cored in the act: the use of models to understand core myopathies
• Design and Development of Gold-Loaded and Boron-Attached Multicore Manganese Ferrite Nanoparticles as a Potential Agent in Biomedical Applications
• Design of functionalized magnetic silica multi-core composite nanoparticles for synergistic magnetic hyperthermia/radiotherapy in cancer cells
• First report on multidrug-resistant non-encapsulated Streptococcus pneumoniae isolated from a patient with pneumonia
• Gene Panel Sequencing Identifies a Novel <em>RYR1</em> p.Ser2300Pro Variant as Candidate for Malignant Hyperthermia with Multi-Minicore Myopathy
• gpuZoo: Cost-effective estimation of gene regulatory networks using the Graphics Processing Unit
• Hardware Acceleration of the STRIKE String Kernel Algorithm for Estimating Protein to Protein Interactions
• Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum
• Hyperparameter Tuning with High Performance Computing Machine Learning for Imbalanced Alzheimer's Disease Data
• Motor function performance in individuals with RYR1-related myopathies
• New Compound Heterozygous Splice Site Mutations of the Skeletal Muscle Ryanodine Receptor (<em>RYR1</em>) Gene Manifest Fetal Akinesia: A Linkage with Congenital Myopathies
• Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
• Nutil: A Pre- and Post-processing Toolbox for Histological Rodent Brain Section Images
• ParRADMeth: Identification of Differentially Methylated Regions on Multicore Clusters
• PyGNA: a unified framework for geneset network analysis
• Quantitative reduction of RyR1 protein caused by a single-allele frameshift mutation in RYR1 ex36 impairs the strength of adult skeletal muscle fibres
• Recessive mutations in muscle-specific isoforms of FXR1 cause congenital multi-minicore myopathy
• Recessive mutations in proximal I-band of TTN gene cause severe congenital multi-minicore disease without cardiac involvement
• Significance of Asymptomatic Hyper Creatine-Kinase Emia
• Structural Basis for a Dual Function ATP Grasp Ligase That Installs Single and Bicyclic ω-Ester Macrocycles in a New Multicore RiPP Natural Product