Results 201 to 210 of about 314,751 (339)

New insights into applications of base editor in hereditary disorders

Interdisciplinary Medicine, EarlyView.
Abstract Hereditary disorders are a group of diseases caused by genetic mutations or chromosomal variations. Although the incidence of each genetic disorder is relatively low, patients affected by the disease generally experience a range of severe symptoms, including blindness, disability, and even premature death. In addition, the available treatments
Maoping Cai, Linhui Zhang, Liqing Li, Yue Liu, Canbin Lv, Yan Shi, Jianyuan Zhao, Dingwei Ye, Yuanyuan Qu   +8 more
wiley   +1 more source

Relationship between adenovirus infection and intussusception via pathological evidence confirms. [PDF]

J Clin Pathol
Lin LH, Huang CJ, Lo CY, Lee YH, Chen YC.   +4 more
europepmc   +1 more source

Isolation of adenovirus-associated viruses from man. [PDF]

, 1967
Neil R. Blacklow, M D Hoggan, Wallace P. Rowe   +2 more
openalex   +1 more source

No apparent increase in cases of severe acute hepatitis of unknown etiology with fulminant liver failure in children in Germany, 2022

JPGN Reports, EarlyView.
Abstract Objectives In April 2022, the United Kingdom and the United States reported alarming increases in cases of severe acute hepatitis of unknown etiology in children, indicating a multicountry outbreak. We aimed to determine if Germany was affected by the outbreak.
Anna‐Lisa Behnke, Achim Dörre, Julia Enkelmann, Birgit Knoppke, Working Group for Pediatric Liver Transplantation of the German Society for Pediatric Gastroenterology and Nutrition (GPGE), Ruth Zimmermann, Mirko Faber   +6 more
wiley   +1 more source

Human adenovirus in Taiwan, 2019-2023. [PDF]

Arch Virol
Yang SL, Tsai WJ, Li CH, Cheng YH, Lin SW, Liu MT, Wu FT.   +6 more
europepmc   +1 more source

STRUCTURE OF TYPE 5 ADENOVIRUS [PDF]

, 1963
Wesley C. Wilcox, Harold S. Ginsberg
openalex   +1 more source

A case of autoimmune hepatitis in a patient with inflammatory bowel disease and significant lymphadenopathy in the porta hepatis

JPGN Reports, EarlyView.
Abstract The diagnosis of autoimmune hepatitis (AIH) is supported by the presence of elevated transaminases, hypergammaglobulinemia, liver biopsy consistent with AIH, and the presence of AIH autoantibodies. In this case presentation, we highlight the challenges associated with diagnosing AIH in a patient with inflammatory bowel disease (IBD) who ...
Benjamin J. Malamet, Shannon Joerger, Karen Caudill, Mai He, Juan Reyes Genere, Janis Stoll   +5 more
wiley   +1 more source

TXNIP mediates ferroptosis in a bronchopulmonary dysplasia mouse model by regulating the SLC7A11/GPX4 pathway. [PDF]

Sci Rep
Chen D, Yin F, Yang P, Xia W, Huang Y, Feng Y, Yang L, Lin S, Zhang Q.   +8 more
europepmc   +1 more source

A CORRELATIVE STUDY BY ELECTRON AND LIGHT MICROSCOPY OF THE DEVELOPMENT OF TYPE 5 ADENOVIRUS [PDF]

, 1960
Gabriel C. Godman, Councilman Morgan, Peter M. Breitenfeld, Harry M. Rose   +3 more
openalex   +1 more source

DOCK8 deficiency presenting with sclerosing cholangitis, raised immunoglobulin E, and bronchiectasis: A fatal pediatric case report

JPGN Reports, EarlyView.
Abstract Dedicator of cytokinesis 8 (DOCK8) deficiency is a rare autosomal recessive primary immunodeficiency. Patients with DOCK8 deficiency typically present at early age with allergic manifestations, cutaneous and respiratory infections, raised immunoglobulin E, and they have an increased risk of developing malignancies.
Natalia Nedelkopoulou, Kelechi Ugonna, Stephen Hughes, Sanjay Rajwal, Marumbo Mtegha   +4 more
wiley   +1 more source