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| http://dx.doi.org/10.1097/CM9.0000000000003379 | DOI Listing |
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World J Pediatr
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The First Hospital of Peking University, Beijing, China.
Background: Glucose transporter 1 deficiency syndrome (Glut1DS) was initially reported by De Vivo and colleagues in 1991. This disease arises from mutations in the SLC2A1 and presents with a broad clinical spectrum. It is a treatable neuro-metabolic condition, where prompt diagnosis and initiation of ketogenic dietary therapy can markedly enhance the prognosis.
View Article and Find Full Text PDF[Clinical Impact of Current Variants in COVID-19 Patients: Clinical Characteristics in Variant EG.5].
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University of Health Sciences, Ankara Bilkent City Health Application and Research Center, Clinic of Medical Microbiology, Ankara, Türkiye.
The severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) virus has mutated at a high rate since the beginning of the pandemic, leading to the formation of different variants. Alpha, Beta, Gamma, Delta and Omicron have emerged as concerning variants identified by the World Health Organization (WHO). The Omicron variant and its sublineages became dominant worldwide in 2022.
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Nursing Practice Development Unit, Princess Alexandra Hospital, Woolloongabba, Queensland, Australia.
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Laryngoscope
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Institute of Health Policy, Management, and Evaluation, University of Toronto, Toronto, Ontario, Canada.
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