Treatment outcomes for patients with Middle Eastern Respiratory Syndrome Coronavirus (MERS CoV) infection at a coronavirus referral center in the Kingdom of Saudi ArabiaResearch Article Published on 2016-04-212022-10-28 Journal: BMC Infectious Diseases [Category] Coronavirus, MERS, [키워드] Abnormalities Administered Admission age Alanine ALT Analysis Anemia Characteristics chest X-ray clearance clinical feature Confounding Coronary artery disease coronavirus CoV creatinine CXR death determine Diagnosis disease effect of treatment Efficacy elevated evaluate evaluated Gender healthcare worker hypertension Hypoxemia increased survival independent Infection interferon beta Kingdom Laboratory Leukocytosis lung male MERS MERS CoV MERS-CoV middle Middle Eastern respiratory syndrome coronavirus Most patient multivariate logistic regression outcome overall mortality Patient PCR polymerase chain predictor randomized trial reduced renal respiratory respiratory rate Result retrospective retrospective cohort Saudi Arabia severity severity of illness survival the patient Treatment Treatment outcome treatment regimen Univariate analysis vomiting was performed was reduced [DOI] 10.1186/s12879-016-1492-4 PMC 바로가기 [Article Type] Research Article
Disruption of Mouse Cenpj, a Regulator of Centriole Biogenesis, Phenocopies Seckel Syndrome중심소체 생합성, Phenocopies Seckel 증후군의 조절자인 마우스 Cenpj의 교란Research Article Published on 2012-11-152022-09-06 Journal: PLoS Genetics [Category] Communicable Disease, [키워드] Abnormalities addition allele Apoptosis Author Birth Brain cause Cell cell death CENPJ centriole characteristic chromosomal abnormalities chromosomal abnormality chromosome chromosomes clinical feature Clinical features clinical manifestations compared conserved contribute CPAP damaged disorder Disruption DNA damage dwarfism elevated Embryo embryonic embryonic development exhibited expresse expressed feature fibroblast found Frequency Gene genomic growth growth failure hypomorphic immunohistochemistry impairment in addition to Increased J gene lead majority mechanism memory memory impairment Mental mental retardation mice microcephaly mitotic mono mouse Mutation ocular phenocopy proliferation Protein reduced reduction in regulator Seckel Seckel syndrome Signaling skeletal specific mutation specific mutations syndrome wild-type cells [DOI] 10.1371/journal.pgen.1003022 PMC 바로가기 [Article Type] Research Article