Clinical and laboratory profile of hereditary spherocytosis

Autor: Larisa Gaikovaya, Marina N. Zenina, Nataliya Yu. Chernysh, Tatevik T. Asatryan

Publikováno v: Vestnik severo-zapadnogo gosudarstvennogo medicinskogo universiteta im. I.I. Mečnikova, Vol 11, Iss 1, Pp 65-72 (2019)

Diagnostics of hereditary spherocytosis is usually based on clinical picture, family history and laboratory tests. The list of laboratory tests includes osmotic fragility test, a glycerol lysis test, an eosin-5-maleimide binding test and others. None

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9169f59e6eae63e8ea1d56ae4a1bff3a
https://journals.eco-vector.com/vszgmu/article/viewFile/10724/9258