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1
289 Hereditary spherocytosis associated with Gilbert syndrome – a case report
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289 Hereditary spherocytosis associated with Gilbert syndrome – a case report

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A122-A123 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2021-europaediatrics.289

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2
217 Hyperosmolar hyperglycemic state in a 7-year-old boy with newly diagnosed type 1 diabetes mellitus
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Article
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217 Hyperosmolar hyperglycemic state in a 7-year-old boy with newly diagnosed type 1 diabetes mellitus

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A91-A92 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2021-europaediatrics.217

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3
274 Screening for celiac disease among first-grade pupils using rapid point-of-care test, a prospective study
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Article
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274 Screening for celiac disease among first-grade pupils using rapid point-of-care test, a prospective study

Archives of disease in childhood, 2021-10, Vol.106 (Suppl 2), p.A116-A116 [Peer Reviewed Journal]

Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;2021 Author(s) (or their employer(s)) 2021. No commercial re-use. See rights and permissions. Published by BMJ. ;ISSN: 0003-9888 ;EISSN: 1468-2044 ;DOI: 10.1136/archdischild-2021-europaediatrics.274

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