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International Journal of Molecular Sciences|October 14, 2022
Comparison of Homologous and Heterologous Booster SARS-CoV-2 Vaccination in Autoimmune Rheumatic and Musculoskeletal PatientsDániel Honfi, Nikolett Gémes, Enikő Szabó, et al.
L'Encephale|December 1, 2023
High average daily temperature in summer and the incidence of thrombolytic treatment for acute ischemic strokeAndrás Folyovich, Réka Mátis, Dávid Biczó, et al.
Frontiers in Immunology|April 18, 2022
Humoral and Cellular Immunogenicity and Safety of Five Different SARS-CoV-2 Vaccines in Patients With Autoimmune Rheumatic and Musculoskeletal Diseases in Remission or With Low Disease Activity and in Healthy Controls: A Single Center StudyGábor J Szebeni, Nikolett Gémes, Dániel Honfi, et al.
BMC Medical Genetics|November 21, 2014
A study of genes encoding cytokines (IL6, IL10, TNF), cytokine receptors (IL6R, IL6ST), and glucocorticoid receptor (NR3C1) and susceptibility to bronchopulmonary dysplasiaJohanna M Huusko, Minna K Karjalainen, Mari Mahlman, et al.
Pediatric Pulmonology|March 11, 2014
Polymorphisms of the gene encoding Kit ligand are associated with bronchopulmonary dysplasiaJohanna M Huusko, Mari Mahlman, Minna K Karjalainen, et al.
Case Reports in Medicine|November 12, 2020
Epileptic Seizure Provoked by Bone Metastasis of Chronic Lymphoid Leukemia and Merkel Cell CarcinomaAndrás Folyovich, Angéla Majoros, Tamás Jarecsny, et al.
Seminars in Immunopathology|November 24, 2025
The microbiome's hidden influence: preclinical insights into inflammatory responses in necrotizing enterocolitisBriana M Peterson, Ina Rudloff, Nadia S Deen, et al.
NPJ Genomic Medicine|November 8, 2024
Benchmarking nanopore sequencing and rapid genomics feasibility: validation at a quaternary hospital in New ZealandDenis M Nyaga, Peter Tsai, Clare Gebbie, et al.
American Journal of Hematology|September 1, 2021
Recommendations for diagnosis and treatment of methemoglobinemiaAchille Iolascon, Paola Bianchi, Immacolata Andolfo, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 20, 2020
Pseudouridylation defect due to <i>DKC1</i> and <i>NOP10</i> mutations causes nephrotic syndrome with cataracts, hearing impairment, and enterocolitisEszter Balogh, Jennifer C Chandler, Máté Varga, et al.
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