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The Journal of Infectious Diseases|November 4, 2019
Risk of Severe Influenza Among Adults With Chronic Medical ConditionsTiffany A Walker, Ben Waite, Mark G Thompson, et al.
Vaccines|October 28, 2025
Neutralisation of the Immunoglobulin-Cleaving Activity of <i>Streptococcus equi</i> Subspecies <i>equi</i> IdeE by Blood Sera from Ponies Vaccinated with a Multicomponent Protein VaccineFrancesco Righetti, Karina Hentrich, Margareta Flock, et al.
Equine Veterinary Journal|January 9, 2022
Conservation of vaccine antigen sequences encoded by sequenced strains of Streptococcus equi subsp. equiSara Frosth, Ellen Ruth A Morris, Hayley Wilson, et al.
Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|December 12, 2025
Extended influenza seasons in Australia and New Zealand in 2025 due to the emergence of influenza A(H3N2) subclade K virusesClyde Dapat, Heidi Peck, Lauren Jelley, et al.
Human Mutation|August 13, 2021
Molecular basis of mucopolysaccharidosis IVA (Morquio A syndrome): A review and classification of GALNS gene variants and reporting of 68 novel variantsAlessandra Zanetti, Francesca D'Avanzo, Moeenaldeen AlSayed, et al.
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology|May 27, 2025
Cone beam CT dose optimisation: A review and expert consensus by the 2022 ESTRO Physics Workshop IGRT working groupLydia J Wilson, Andria Hadjipanteli, Daniella E Østergaard, et al.
Human Molecular Genetics|September 6, 2022
Functional assessment of homozygous ALDH18A1 variants reveals alterations in amino acid and antioxidant metabolismMaxwell B Colonna, Tonya Moss, Sneha Mokashi, et al.
Clinical Chemistry|October 3, 2015
A Novel N-Tetrasaccharide in Patients with Congenital Disorders of Glycosylation, Including Asparagine-Linked Glycosylation Protein 1, Phosphomannomutase 2, and Mannose Phosphate Isomerase DeficienciesWenyue Zhang, Philip M James, Bobby G Ng, et al.
Molecular Genetics and Metabolism|November 1, 2020
Expanding the clinical and metabolic phenotype of DPM2 deficient congenital disorders of glycosylationSilvia Radenkovic, Taylor Fitzpatrick-Schmidt, Seul Kee Byeon, et al.
Mitochondrion|October 16, 2024
An integrated multi-omics approach allowed ultra-rapid diagnosis of a deep intronic pathogenic variant in PDHX and precision treatment in a neonate critically ill with lactic acidosisRodrigo T Starosta, Austin A Larson, Naomi J L Meeks, et al.
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