Vanessa Nivaggioni

A mutation in the Gardos channel is associated with hereditary xerocytosis

Raphaël Rapetti‐Mauss, Caroline Lacoste, Véronique Picard et al. · Blood · 2015 · 119 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

A new approach for diagnosing chronic myelomonocytic leukemia using structural parameters of Sysmex XN^TM analyzers in routine laboratory practice

Françoise Schillinger, Élise Sourdeau, Marouane Boubaya et al. · Scandinavian Journal of Clinical and Laboratory Investigation · 2018 · 25 citations · Full text

Medicine, Hematology, Pathology +17

Detection of Minimal Residual Disease in B Cell Acute Lymphoblastic Leukemia Using an Eight‐Color Tube with Dried Antibody Reagents

Lakhdar Bouriche, Denis Bernot, Vanessa Nivaggioni et al. · Cytometry Part B Clinical Cytometry · 2019 · 22 citations · Full text

Medicine, Hematology, Pathology +16

Early (Day 15 Post Diagnosis) Peripheral Blood Assessment of Measurable Residual Disease in Flow Cytometry is a Strong Predictor of Outcome in Childhood B‐Lineage Lymphoblastic Leukemia

Marie Loosveld, Vanessa Nivaggioni, Isabelle Arnoux et al. · Cytometry Part B Clinical Cytometry · 2019 · 15 citations · Full text

Medicine, Hematology, Pediatrics +17

Use of Sysmex XN‐10 red blood cell parameters for screening of hereditary red blood cell diseases and iron deficiency anaemia

Vanessa Nivaggioni, Lakhdar Bouriche, Sylvie Coito et al. · International Journal of Laboratory Hematology · 2020 · 13 citations · Full text

Medicine, Hematology, Iron Metabolism Disorders +16