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Fingerprint Dive into the research topics where Cristina Vercellati is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 11 Similar Profiles
Mutation Medicine & Life Sciences
Hereditary Spherocytosis Medicine & Life Sciences
Hemolytic Anemia Medicine & Life Sciences
Genes Medicine & Life Sciences
Erythrocytes Medicine & Life Sciences
Congenital Dyserythropoietic Anemia Medicine & Life Sciences
Pyruvate Kinase Medicine & Life Sciences
Methemoglobinemia Medicine & Life Sciences

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Research Output 1996 2019

  • 704 Citations
  • 16 h-Index
  • 40 Article
1 Citation (Scopus)

Clinical and molecular spectrum of glucose-6-phosphate isomerase deficiency. Report of 12 new cases

Fermo, E., Vercellati, C., Marcello, A. P., Zaninoni, A., Aytac, S., Cetin, M., Capolsini, I., Casale, M., Paci, S., Zanella, A., Barcellini, W. & Bianchi, P., Jan 1 2019, In : Frontiers in Physiology. 10, MAY, 467.

Research output: Contribution to journalArticle

Open Access
Glucose-6-Phosphate Isomerase

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

Barcellini, W., Zaninoni, A., Gregorini, A. I., Soverini, G., Duca, L., Fattizzo, B., Giannotta, J. A., Pedrotti, P., Vercellati, C., Marcello, A. P., Fermo, E., Bianchi, P. & Cappellini, M. D., May 1 2019, In : British Journal of Haematology. 185, 3, p. 523-531 9 p.

Research output: Contribution to journalArticle

Congenital Hemolytic Anemia
Iron Overload
7 Citations (Scopus)
Congenital Dyserythropoietic Anemia
Hemolytic Anemia
Hereditary Elliptocytosis
Hereditary Spherocytosis
Glucose-6-Phosphate Isomerase

Cyanosis due to methemoglobinemia induced by topical anesthesia in a premature infant

Eleftheriou, G., Butera, R., Varsalone, F., Nociforo, F. & Vercellati, C., Apr 1 2017, In : Current Drug Therapy. 12, 1, p. 73-76 4 p.

Research output: Contribution to journalArticle

Cytochrome-B(5) Reductase
Premature Infants
26 Citations (Scopus)

'Gardos Channelopathy': A variant of hereditary Stomatocytosis with complex molecular regulation

Fermo, E., Bogdanova, A., Petkova-Kirova, P., Zaninoni, A., Marcello, A. P., Makhro, A., Hänggi, P., Hertz, L., Danielczok, J., Vercellati, C., Mirra, N., Zanella, A., Cortelezzi, A., Barcellini, W., Kaestner, L. & Bianchi, P., Dec 1 2017, In : Scientific Reports. 7, 1, 1744.

Research output: Contribution to journalArticle

Hemolytic Anemia