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期刊名:Nature reviews disease primers

缩写:NAT REV DIS PRIMERS

ISSN:2056-676X

e-ISSN:2056-676X

IF/分区:60.6/Q1

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Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
VEXAS syndrome [0.03%]
David B Beck,Sophie Georgin-Lavialle,Yohei Kirino et al. David B Beck et al.
VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a disorder discovered in 2020 that bridges haematology, immunology and genetics. VEXAS syndrome arises from somatic mutations in UBA1, which encodes an E1 ubiquiti...
Kai Spiegelhalder,Chiara Baglioni,Charles M Morin et al. Kai Spiegelhalder et al.
Insomnia disorder (ID) causes both night-time and daytime symptoms. Night-time symptoms include subjective difficulties initiating and maintaining sleep and early morning awakenings, whereas fatigue, perceived impairments in cognitive funct...
Franc Strle,Klemen Strle,Adriana Marques et al. Franc Strle et al.
Lyme borreliosis is the most common tick-borne disease in the northern hemisphere. It is a zoonosis caused by several species of Borrelia burgdorferi sensu lato and transmitted by the bite of infected ticks of the Ixodes ricinus complex. Ly...
Melanie J Davies,Soo Lim,Tommy Slater et al. Melanie J Davies et al.
Type 2 diabetes mellitus (T2DM) is a chronic, progressive disease driven by a complex interplay of genetic, biological, behavioural and social factors. The epidemiology of T2DM has shifted considerably, largely attributable to increasing ob...
Kellen Winden,E Martina Bebin,Shafali Jeste et al. Kellen Winden et al.
Tuberous sclerosis complex (TSC) is a rare genetic disease caused by heterozygous loss-of-function variants in TSC1 or TSC2. Patients present with benign tumours known as hamartomas in the brain, eyes, lungs, kidneys, heart and skin. Many h...