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2. A New Homozygous Mutation (c.393-394del TA/c.393-394del TA) in the NT5C3 Gene Associated With Pyrimidine-5′-Nucleotidase Deficiency: A Case Report. Issue 8 (November 2019)

4. Addressing the diagnostic gaps in pyruvate kinase deficiency: Consensus recommendations on the diagnosis of pyruvate kinase deficiency. Issue 1 (28th November 2018)

5. Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype‐phenotype correlations. (29th July 2016)

7. Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years. (11th March 2022)

9. Detection of red blood cell antibodies in mitogen‐stimulated cultures from patients with hereditary spherocytosis. Issue 12 (10th August 2015)

10. Discrepancies between bone marrow histopathology and clinical phenotype in BCR-ABL1-negative myeloproliferative neoplasms associated with splanchnic vein thrombosis. Issue 5 (May 2015)