[(11)C]PK11195-PET Brain Imaging of the Mitochondrial Translocator Protein in Mitochondrial Disease.

Final results of a phase 1 study of loncastuximab tesirine in relapsed/refractory B-cell non-Hodgkin lymphoma.

Autoantibody Detection for Diagnosis in Direct Immunofluorescence-Negative Mucous Membrane Pemphigoid: Ocular and Other Sites Compared.

A plasmid DNA-launched SARS-CoV-2 reverse genetics system and coronavirus toolkit for COVID-19 research.

Fatal and Nonfatal Events Within 14 days After Early, Intensive Mobilization Poststroke.

Differentiating Solutes with Precise Nanofiltration for Next Generation Environmental Separations: A Review.

Effectiveness and Reach of the Primary Palliative Care for Emergency Medicine (PRIM-ER) Pilot Study: a Qualitative Analysis.

Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDL.

The contribution of X-linked coding variation to severe developmental disorders.

NxGen evidence: Redesigning the Agency for Healthcare Research and Quality Effective Health Care website to promote engagement, interactivity, and usability of systematic reviews.

Comparative host-coronavirus protein interaction networks reveal pan-viral disease mechanisms.

De Novo VPS4A Mutations Cause Multisystem Disease with Abnormal Neurodevelopment.

Identification of UBAP1 mutations in juvenile hereditary spastic paraplegia in the 100,000 Genomes Project.

Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS.

Clinical, neuropathological, and genetic characterization of STUB1 variants in cerebellar ataxias: a frequent cause of predominant cognitive impairment.