Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Petronilla Vanzanelli"'
Autor:
Chiara Marraccini, Barbara Iotti, Petronilla Vanzanelli, Elisa Bedeschi, Enrico Farnetti, Davide Nicoli, Pamela Berni, Agnese Razzoli, Eleonora Maurizi, Gaia Gavioli, Angela Mazzi, Roberto Baricchi, Lucia Merolle, Davide Schiroli
Publikováno v:
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.
Several ABO gene mutations are known to determine rare subgroups: these ABO variants are often responsible for weak or null phenotypes and may cause an incorrect determination of the serotype. Here we describe for the first time the phenotypic discre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887bf10aff5fa2e00c2ee76863bb650a
https://pubmed.ncbi.nlm.nih.gov/36535828
https://pubmed.ncbi.nlm.nih.gov/36535828
Autor:
Claudia Fiorani, Goretta Bonacorsi, Stefano Sacchi, Ilaria Castelli, Paola Temperani, Petronilla Vanzanelli, Stefania Tonelli
Publikováno v:
Leukemia Research. 24:877-879
We describe a case of persistent polyclonal B-cell lymphocytosis (PPBL) studied by morphological, immunological, cytogenetic and molecular analysis. PPBL is a rare lymphoproliferative disorder with an unclear natural history. Although a few cases of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac2e7d61489077489e70974658fd9ec5
https://doi.org/10.1016/s0145-2126(00)00069-2
https://doi.org/10.1016/s0145-2126(00)00069-2