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

  • 9 Similar Profiles
Hereditary Spherocytosis Medicine & Life Sciences
Hemolytic Anemia Medicine & Life Sciences
Mutation Medicine & Life Sciences
Congenital Dyserythropoietic Anemia Medicine & Life Sciences
Genes Medicine & Life Sciences
Congenital Hemolytic Anemia Medicine & Life Sciences
Glucose-6-Phosphate Isomerase Medicine & Life Sciences
Pyruvate Kinase Medicine & Life Sciences

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Research Output 2004 2019

  • 458 Citations
  • 9 h-Index
  • 18 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
Mutation
Glycolysis
Anemia
Glucose-6-Phosphate

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
Hepcidins
Iron Overload
Transferrin
Ferritins

A Case with Pyruvate Kinase Deficiency Remarkably Sensitive to Heat

Aksu, T., Yarali, N., Fermo, E., Marcello, A., Hacisalihoǧlu, Ş., Bianchi, P. & Özbek, N. Y., Oct 1 2018, In : Journal of Pediatric Hematology/Oncology. 40, 7, p. e458-e460

Research output: Contribution to journalArticle

Pyruvate Kinase
Hot Temperature
Congenital Hemolytic Anemia
Babesia
Glucuronosyltransferase
7 Citations (Scopus)
Congenital Dyserythropoietic Anemia
Hemolytic Anemia
Hereditary Elliptocytosis
Hereditary Spherocytosis
Glucose-6-Phosphate Isomerase
25 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

Channelopathies
Mutation
Exome
Erythroblasts
Hemolytic Anemia