Michaela Calvillo

Genoa, 16147, Italy

Last Updated: 09/26/2026

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Found 22 publications

Chromosomal Deletion Involving ANKRD26 Leads to Expression of a Fusion Protein Responsible for ANKRD26-Related Thrombocytopenia.

Chromosomal Deletion Involving ANKRD26 Leads to Expression of a Fusion Protein Responsible for ANKRD26-Related Thrombocytopenia.

Journal: International journal of molecular sciences

Published: June 17, 2025

Severe Lactic Acidosis Caused by Thiamine Deficiency in a Child with Relapsing Acute Lymphoblastic Leukemia: A Case Report.

Severe Lactic Acidosis Caused by Thiamine Deficiency in a Child with Relapsing Acute Lymphoblastic Leukemia: A Case Report.

Journal: Children (Basel, Switzerland)

Published: August 18, 2023

Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?

Autoimmune Lymphoproliferative Syndrome (ALPS) Disease and ALPS Phenotype: Are They Two Distinct Entities?

Journal: HemaSphere

Published: July 01, 2022

Underlying CTLA4 Deficiency in a Patient With Juvenile Idiopathic Arthritis and Autoimmune Lymphoproliferative Syndrome Features Successfully Treated With Abatacept-A Case Report.

Underlying CTLA4 Deficiency in a Patient With Juvenile Idiopathic Arthritis and Autoimmune Lymphoproliferative Syndrome Features Successfully Treated With Abatacept-A Case Report.

Journal: Journal of pediatric hematology/oncology

Published: October 21, 2020

Unusual Late-onset Enteropathy in a Patient With Lipopolysaccharide-responsive Beige-like Anchor Protein Deficiency.

Unusual Late-onset Enteropathy in a Patient With Lipopolysaccharide-responsive Beige-like Anchor Protein Deficiency.

Journal: Journal of pediatric hematology/oncology

Published: December 27, 2019

Thrombotic thrombocytopenic purpura and defective apoptosis due to CASP8/10 mutations: the role of mycophenolate mofetil.

Thrombotic thrombocytopenic purpura and defective apoptosis due to CASP8/10 mutations: the role of mycophenolate mofetil.

Journal: Blood advances

Published: June 13, 2019

FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene.

FAS-mediated apoptosis impairment in patients with ALPS/ALPS-like phenotype carrying variants on CASP10 gene.

Journal: British journal of haematology

Published: April 17, 2019

Sirolimus as a rescue therapy in children with immune thrombocytopenia refractory to mycophenolate mofetil.

Sirolimus as a rescue therapy in children with immune thrombocytopenia refractory to mycophenolate mofetil.

Journal: American journal of hematology

Published: April 05, 2018

Clinical features and therapeutic challenges of cytopenias belonging to alps and alps-related (ARS) phenotype.

Clinical features and therapeutic challenges of cytopenias belonging to alps and alps-related (ARS) phenotype.

Journal: British journal of haematology

Published: March 13, 2018

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.

Hypomorphic FANCA mutations correlate with mild mitochondrial and clinical phenotype in Fanconi anemia.

Journal: Haematologica

Published: July 12, 2017

Long-term use of pegfilgrastim in children with severe congenital neutropenia: clinical and pharmacokinetic data.

Long-term use of pegfilgrastim in children with severe congenital neutropenia: clinical and pharmacokinetic data.

Journal: Blood

Published: September 14, 2016

Mycophenolate mofetil and Sirolimus as second or further line treatment in children with chronic refractory Primitive or Secondary Autoimmune Cytopenias: a single centre experience.

Mycophenolate mofetil and Sirolimus as second or further line treatment in children with chronic refractory Primitive or Secondary Autoimmune Cytopenias: a single centre experience.

Journal: British journal of haematology

Published: March 11, 2015

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Last Updated: 09/26/2026