Results 21 to 30 of about 41,788 (191)

Rubella immunity among pregnant women aged 15–44 years, Namibia, 2010

open access: yesInternational Journal of Infectious Diseases, 2016
Background: The level of rubella susceptibility among women of reproductive age in Namibia is unknown. Documenting the risk of rubella will help estimate the potential burden of disease in Namibian women and the risk of congenital rubella syndrome (CRS ...
Anna Jonas   +14 more
doaj   +1 more source

Case based rubella surveillance in Abia State, South East Nigeria, 2007–2011 [PDF]

open access: yesPeerJ, 2014
Introduction. Rubella infection has the potential of causing severe fetal birth defects collectively called congenital rubella syndrome (CRS) if the mother is infected early in pregnancy.
Chukwuemeka Anthony Umeh   +1 more
doaj   +2 more sources

Development and evaluation of a next-generation sequencing methodology for measles virus using Oxford Nanopore Technology

open access: yesJournal of Clinical Microbiology
We report the development of a bench protocol and evaluation of bioinformatics pipelines for the whole genome sequence (WGS) of measles virus (MeV) genotype D8. We established a bench protocol using 1 kb amplicons tiling the MeV WGS.
Vanessa Zubach   +5 more
doaj   +1 more source

Vaccine-induced neutralizing antibodies bind to the H protein of a historical measles virus

open access: yesInternational Journal of Medical Microbiology
Measles is a highly contagious airborne viral disease. It can lead to serious complications and death and is preventable by vaccination. The live-attenuated measles vaccine (LAMV) derived from a measles virus (MV) isolated in 1954 has been in use ...
Anne Zemella   +16 more
doaj   +1 more source

Updating Standard Procedures for Diagnosis and Treatment of Congenital Rubella Case

open access: yesLa Pediatria Medica e Chirurgica, 2013
Congenital Rubella is the dramatic consequence of rubella during gestation. A combined strategy of Measles and Rubella universal vaccination on children and selective vaccination of susceptible women has been shown effective in the elimination of ...
W. Buffolano   +4 more
doaj   +1 more source

Factors Predicting Rubella Vaccination and Antibody in Pregnant Women in Japan: A Report from Pregnant Women Health Initiative

open access: yesVaccines, 2022
This study aimed to identify the factors predicting rubella vaccination status based on self-reported data and the presence of sufficient rubella antibody titers in pregnant women in Japan.
Akiko Iwata   +6 more
doaj   +1 more source

SINDROM RUBELLA KONGENITAL

open access: yesAverrous: Jurnal Kedokteran dan Kesehatan Malikussaleh, 2018
Congenital Rubella Syndrome (CRS) adalah suatu kumpulan gejala penyakit terdiri dari katarak, penyakit jantung bawaan, gangguan pendengaran, dan keterlambatan perkembangan.
Julia Fitriany, Yulia Husna
doaj   +1 more source

PD‐L1‐Binding Antigen Presenters: Redirecting Vaccine‐Induced Antibodies for Cancer Immunotherapy

open access: yesAdvanced Science, EarlyView.
The PBAP‐gE complex anchors gE antigen to PD‐L1 on tumor cells. Vaccine‐induced anti‐gE antibodies simultaneously engage FcγRIIIa on NK cells and tumor‐bound PBAP‐gE, triggering NK cell activation and antibody‐dependent cellular cytotoxicity, thereby selectively eliminating PD‐L1–expressing tumor cells.
Huixin Gao   +24 more
wiley   +1 more source

Reliability of CMV-IgG kinetics in the diagnosis of CMV primary infection: sensitivity, specificity, and clinical implications

open access: yesMicrobiology Spectrum
Diagnosis of cytomegalovirus (CMV) primary infection (PI) during pregnancy relies on serology (CMV-IgG, IgM, and IgG avidity). However, as for toxoplasmosis, subsequent serology testing 3–5 weeks later is often performed to confirm the diagnosis. In this
Vincent Portet Sulla   +8 more
doaj   +1 more source

Atypical Clinical Course of Griscelli Syndrome Type 2 With Primarily Neurologic Presentation and Adult‐Onset in a 46‐Year‐Old Male

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Griscelli Syndrome Type 2 (GS2) is a rare autosomal recessive disorder caused by pathogenic mutations in the RAB27A gene. Typically, it is characterized by cutaneous hypopigmentation, immunodeficiency, with or without neurological abnormalities secondary to hemophagocytic lymphohistiocytosis (HLH). Without treatment, GS2 often results in fatal
Dzhoy Papingi   +6 more
wiley   +1 more source

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