Objectives Early, accurate diagnosis is crucial for the prognosis of patients with soft tissue
sarcomas. To this end, standardization of imaging algorithms, technical requirements, and …

Werner syndrome (WS) is a heritable autosomal recessive human disorder characterized by
the premature onset of several age-associated pathologies including cancer. The protein …

Werner syndrome (WS) is a premature aging disorder caused by mutations in a RecQ-family
DNA helicase, WRN. Mice lacking part of the helicase domain of the WRN orthologue exhibit …

The aim of this study was to explore the application value of transvaginal color Doppler
ultrasound based on the improved mean shift algorithm in the diagnosis of idiopathic …

Significance: Werner syndrome (WS) is a rare autosomal recessive malady typified by a pro-
oxidant/proinflammatory status, genetic instability, and by the early onset of numerous age …

Werner syndrome (WS), also known as adult progeria, is a rare autosomal recessive
inherited progeroid syndrome characterised by multiple features consistent with accelerated …

Werner syndrome (WS) is an autosomal recessive syndrome characterized by genomic
instability that affects multiple body systems. The characteristic features of the disease …

Human variation is a cornerstone of biomedical science and patient care. In a first-year
anatomy course, medical students at one dissection table had difficulty finding the piriformis …

el síndrome de Werner es una patología poco frecuente, de herencia autosómica recesiva,
caracterizado por signos de envejecimiento prematuro y tendencia a desarrollar tumores …

Werner syndrome (WS) is a rare autosomal recessive disorder characterized by genomic
instability and the premature onset of several age-associated phenotypes. The protein …