Leukocyte adhesion deficiency type-1 is frequently associated with otorhinolaryngological manifestations,most notably a high prevalence of otitis media.Although multiple case reports have documented an increased preva...
Objective To monitor the subtype distributions and drug resistance mutations of human immunodeficiency virus(HIV)-1 in people with human immunodeficiency virus-1(PLWH)who had not experienced anti-retroviral therapy(AR...
Objective To analyze the confirmation rate of human immunodeficiency virus(HIV),the clinical epidemiological characteristics of confirmed HIV-infected individuals,and the performance of HIV screening reagents,so that ...
Objective To analyze the influencing factors of genotypic drug resistance mutations in people with human immunodeficiency virus and acquired immunodeficiency syndrome(PLWHA)who failed anti-retroviral therapy(ART)in He...
supported by the Capital’s Funds for Health Improvement and Research(CFH:2024-2G-4402).
1.Background,Forty years have passed since the initial discovery and isolation of the human immunodeficiency virus(HIV)in 1984.[1,2]At the end of 2022,approximately 85.6 million people had been infected with the virus...
人类免疫缺陷病毒感染者的孤立性夜间高血压:一项横断面研究Zanuzzi MG,López SM,Cattaneo MJ,Pérez-Maure MA,Lahiri CD,Romero CA.Isolated nocturnal hypertension in people living with human immunodeficiency virus:a cross-se...
In this editorial,we discuss the clinical implications of the article by Zhang et al.Pulmonary alveolar proteinosis(PAP)is a rare lung disease characterized by excessive surfactant accumulation in the alveoli.It is cl...
National Natural Science Foundation of China(81873761,81571178,81371399);National 13th Five-Year Plan Major Science and Technology Project(2018ZX10302104).
The spread of AIDS and increasing use of immunosuppressive therapy have led to a yearly increase in the incidence of immunodeficiency-associated pneumonia(IAP).The pathogenic spectrum,clinical features,and prognosis o...
Background: DiGeorge syndrome (also known as velo-cardio-facial syndrome) is a rare multisystem genetic disorder occurring in approximately 1 in 4000 to 1 in 6000 live births [1]. Although advances in genetic screenin...