A. Marcello

发表

Diagnostic power of laboratory tests for hereditary spherocytosis: a comparison study in 150 patients grouped according to molecular and clinical characteristics

A. Zanella, P. Bianchi, A. Cortelezzi, 2012, Haematologica.

Triose phosphate isomerase deficiency associated with two novel mutations in TPI gene

A. Zanella, P. Bianchi, D. Rees, 2010, European journal of haematology.

Blood p50 evaluation enhances diagnostic definition of isolated erythrocytosis

M. Cazzola, F. Passamonti, L. Arcaini, 2009, Journal of internal medicine.

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

A. Zanella, N. Mirra, P. Bianchi, 2017, Case reports in hematology.

A new variant of phosphoglycerate kinase deficiency (p.I371K) with multiple tissue involvement: molecular and functional characterization.

A. Zanella, L. Chiarelli, P. Bianchi, 2012, Molecular Genetics and Metabolism.

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

A. Zanella, L. Kaestner, N. Mirra, 2017, Scientific Reports.

A new variant of adenylate kinase (delG138) associated with severe hemolytic anemia.

A. Zanella, P. Bianchi, E. Fermo, 2004, Blood cells, molecules & diseases.

Pyruvate Kinase Deficiency: Current Challenges and Future Prospects

C. Vercellati, A. Marcello, W. Barcellini, 2022, Journal of blood medicine.

Hereditary red cell membrane defects: diagnostic and clinical aspects.

A. Zanella, P. Bianchi, E. Fermo, 2011, Blood transfusion = Trasfusione del sangue.

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

P. Bianchi, E. Fermo, C. Vercellati, 2020, Frontiers in Immunology.

Rasburicase-induced Methemoglobinemia: A Case Report and Literature Review.

A. Giambona, P. D’Angelo, P. Farruggia, 2020, Journal of pediatric hematology/oncology.

Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene

A. Zanella, P. Righetti, P. Bianchi, 2009, Human mutation.

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

D. Consonni, A. Iolascon, R. Russo, 2021, Scientific Reports.

Detection of red blood cell antibodies in mitogen‐stimulated cultures from patients with hereditary spherocytosis

A. Zanella, P. Bianchi, A. Cortelezzi, 2015, Transfusion.

Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defect

A. Zanella, E. Fermo, P. Pedotti, 2008, Haematologica.

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

A. Zanella, P. Bianchi, E. Fermo, 2019, Front. Physiol..

Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years

A. Zanella, P. Bianchi, E. Fermo, 2022, British journal of haematology.

Iron overload in congenital haemolytic anaemias: role of hepcidin and cytokines and predictive value of ferritin and transferrin saturation

M. Cappellini, P. Bianchi, E. Fermo, 2019, British journal of haematology.

Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase gene.

A. Zanella, P. Bianchi, E. Fermo, 2008, Blood cells, molecules & diseases.

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

S. Perrotta, A. Zanella, E. Keskin, 2021, Frontiers in Physiology.

A case of hereditary spherocytosis misdiagnosed as pyruvate kinase deficient hemolytic anemia.

A. Zanella, P. Bianchi, E. Fermo, 2013, Clinical laboratory.

Gardos channelopathy: functional analysis of a novel KCNN4 variant.

G. Bouyer, L. Kaestner, G. Graziadei, 2020, Blood advances.

Gardos Channel Mutation Is Associated with Hereditary Dehydrate Stomatocytosis: a Complex Channelopathy

A. Zanella, N. Mirra, A. Makhro, 2015 .

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

P. Bianchi, E. Fermo, C. Vercellati, 2022, Frontiers in Physiology.

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

D. Consonni, A. Zanella, P. Bianchi, 2018, Front. Physiol..

CDAII presenting as hydrops foetalis: molecular characterization of two cases.

A. Zanella, P. Bianchi, L. Notarangelo, 2010, Blood cells, molecules & diseases.

A Case With Pyruvate Kinase Deficiency Remarkably Sensitive to Heat.

P. Bianchi, E. Fermo, N. Özbek, 2018, Journal of pediatric hematology/oncology.

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

A. Zanella, L. Kaestner, N. Mirra, 2017, Scientific Reports.

Overhydrated hereditary stomatocytosis: A rare cause of familiar persistent macrocytosis due to SLC4A1 variants

P. Bianchi, E. Fermo, F. Ferrua, 2023, Pediatric blood & cancer.

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

D. Consonni, A. Iolascon, R. Russo, 2023, Scientific Reports.

Use of Next Generation Sequencing Panel to Clarify Undiagnosed Cases of Hereditary Hemolytic Anemias

S. Perrotta, A. Zanella, E. Keskin, 2017 .

A case of congenital red cell pyruvate kinase deficiency associated with hereditary stomatocytosis.

A. Zanella, P. Bianchi, E. Fermo, 2008, Blood cells, molecules & diseases.

When alpha spectrin null alleles meet low expression alpha spectrin polymorphisms

P. Bianchi, E. Fermo, C. Vercellati, 2023, British journal of haematology.

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

C. Vercellati, A. Marcello, W. Barcellini, 2022, Frontiers in Immunology.