Suchergebnisse - "Cristina Vercellati"

1

Effect of primary lesions in cytoskeleton proteins on red cell membrane stability in patients with hereditary spherocytosis

von: Cristina Vercellati

2022, in: Frontiers in Physiology

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2

Cytokine polymorphisms in patients with autoimmune hemolytic anemia

von: Anna Zaninoni

2023, in: Frontiers in Immunology

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3

Congenital Hemolytic Anemias: Is There a Role for the Immune System?

von: Anna Zaninoni

2020, in: Frontiers in Immunology

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4

Case report: Transfusion independence and abolition of extravascular hemolysis in a PNH patient treated with pegcetacoplan

von: Bruno Fattizzo

2022, in: Frontiers in Immunology

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5

Use of Laser Assisted Optical Rotational Cell Analyzer (LoRRca MaxSis) in the Diagnosis of RBC Membrane Disorders, Enzyme Defects, and Congenital Dyserythropoietic Anemias: A Monocentric Study on 202 Patients

von: Anna Zaninoni

2018, in: Frontiers in Physiology

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6

PB1990: GLYCOLYTIC ACTIVITY AND EFFECT OF EX-VIVO TREATMENT WITH THE PYRUVATE KINASE (PK) ACTIVATOR AG-946 IN RED BLOOD CELLS FROM LOW-RISK MYELODYSPLASTIC SYNDROMES PATIENTS: A PROOF-OF-CONCEPT STUDY

von: Bruno Fattizzo

2023, in: HemaSphere

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7

Hereditary Xerocytosis due to Mutations in PIEZO1 Gene Associated with Heterozygous Pyruvate Kinase Deficiency and Beta-Thalassemia Trait in Two Unrelated Families

von: Elisa Fermo

2017, in: Case Reports in Hematology

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8

Clinical and Molecular Spectrum of Glucose-6-Phosphate Isomerase Deficiency. Report of 12 New Cases

von: Elisa Fermo

2019, in: Frontiers in Physiology

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9

Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study

von: Elisa Fermo

2021, in: Frontiers in Physiology

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10

Evaluation of the main regulators of systemic iron homeostasis in pyruvate kinase deficiency

von: Anna Zaninoni

2023, in: Scientific Reports

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11

PB2546: DIAGNOSTIC POWER OF ERYTHROCYTE AND RETICULOCYTE AUTOMATIC PARAMETERS IN THE SCREENING FOR CONGENITAL HEMOLYTIC ANEMIAS

von: Paola Bianchi

2023, in: HemaSphere

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12

‘Gardos Channelopathy’: a variant of hereditary Stomatocytosis with complex molecular regulation

von: Elisa Fermo

2017, in: Scientific Reports

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