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Listeria: an Australian perspective (2001-2010).
Popovic I, Heron B, Covacin C. Popovic I, et al. Among authors: heron b. Foodborne Pathog Dis. 2014 Jun;11(6):425-32. doi: 10.1089/fpd.2013.1697. Epub 2014 Apr 3. Foodborne Pathog Dis. 2014. PMID: 24697613 Review.
Implementation of routine genomic surveillance provided insights into a locally acquired outbreak caused by a rare clade of Salmonella enterica serovar Enteritidis in Queensland, Australia.
Rathnayake IU, Graham RMA, Bayliss J, Staples M, Micalizzi G, Ariotti L, Cover L, Heron B, Graham T, Stafford R, Rubenach S, D'Addona A, Jennison AV. Rathnayake IU, et al. Among authors: heron b. Microb Genom. 2023 Jul;9(7):mgen001059. doi: 10.1099/mgen.0.001059. Microb Genom. 2023. PMID: 37459172 Free PMC article.
A predominant and virulent Legionella pneumophila serogroup 1 strain detected in isolates from patients and water in Queensland, Australia, by an amplified fragment length polymorphism protocol and virulence gene-based PCR assays.
Huang B, Heron BA, Gray BR, Eglezos S, Bates JR, Savill J. Huang B, et al. Among authors: heron ba. J Clin Microbiol. 2004 Sep;42(9):4164-8. doi: 10.1128/JCM.42.9.4164-4168.2004. J Clin Microbiol. 2004. PMID: 15365006 Free PMC article.
Corrigendum: 'Implementation of routine genomic surveillance provided insights into a locally acquired outbreak caused by a rare clade of Salmonella enterica serovar Enteritidis in Queensland, Australia'.
Rathnayake IU, Graham RMA, Bayliss J, Staples M, Micalizzi G, Ariotti L, Cover L, Heron B, Graham T, Stafford R, Rubenach S, D'Addona A, Jennison AV. Rathnayake IU, et al. Among authors: heron b. Microb Genom. 2023 Aug;9(8):mgen001096. doi: 10.1099/mgen.0.001096. Microb Genom. 2023. PMID: 37589550 Free PMC article. No abstract available.
Recurrent "outsider" intronic variation in the SLC5A6 gene causes severe mixed axonal and demyelinating neuropathy, cyclic vomiting and optic atrophy in 3 families from Maghreb.
Mansour-Hendili L, Gitiaux C, Harion M, Latouche C, Heron B, Stojkovic T, Rama M, Smol T, Sophie Jourdain A, Mention K, Nadjar Y, Schiff M, Lemale J, Ghoumid J, Gottrand F, Talbotec C, Rötig A, Funalot B, Desguerre I. Mansour-Hendili L, et al. Among authors: heron b. Front Genet. 2024 Jan 29;15:1352006. doi: 10.3389/fgene.2024.1352006. eCollection 2024. Front Genet. 2024. PMID: 38348452 Free PMC article.
De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity.
Tessarech M, Friocourt G, Marguet F, Lecointre M, Le Mao M, Díaz RM, Mignot C, Keren B, Héron B, De Bie C, Van Gassen K, Loisel D, Delorme B, Syrbe S, Klabunde-Cherwon A, Jamra RA, Wegler M, Callewaert B, Dheedene A, Zidane-Marinnes M, Guichet A, Bris C, Van Bogaert P, Biquard F, Lenaers G, Marcorelles P, Ferec C, Gonzalez B, Procaccio V, Vitobello A, Bonneau D, Laquerriere A, Khiati S, Colin E. Tessarech M, et al. Among authors: heron b. Genet Med. 2024 May;26(5):101087. doi: 10.1016/j.gim.2024.101087. Epub 2024 Jan 27. Genet Med. 2024. PMID: 38288683 Free article.
136 results