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Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel

Haematologica (Roma), 2014-05, Vol.99 (5), p.811

2014

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A Novel Germline Mutation of ADA2 Gene in Two “Discordant” Homozygous Female Twins Affected by Adenosine Deaminase 2 Deficiency: Description of the Bone-Related Phenotype

International journal of molecular sciences, 2021-08, Vol.22 (15), p.8331

2021

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CAN A THIRD HAEMATOPOIETIC STEM CELL TRANSPLANTATION BE A VIABLE OPTION FOR JMML RELAPSE? A CASE REPORT

EJC paediatric oncology, 2023-12, Vol.2, p.100099, Article 100099

2023

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The role of HLA matching in unrelated donor hematopoietic stem cell transplantation for sickle cell disease in Europe

Bone marrow transplantation (Basingstoke), 2020-10, Vol.55 (10), p.1946-1954

2020

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Isolated leukopenia in children and adolescents referred to a Pediatric Hematology Clinic

Journal of pediatric and neonatal individualized medicine, 2023-04, Vol.12 (1), p.e120108-e120108

2023

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Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency

Frontiers in immunology, 2022-09, Vol.13

2022

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Neutropenia, hypogammaglobulinemia, and pneumonia: A case of WHIM syndrome

Pediatrics international, 2018-03, Vol.60 (3), p.318-319

2018

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Finding balance between mature and immature neutrophils: The effects of empagliflozin in GSD‐Ib

EJHaem, 2023-05, Vol.4 (2), p.551-554

2023

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Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis

Frontiers in immunology, 2021-04, Vol.12, p.673487

2021

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Risk factors and severe outcome in thrombotic microangiopathy after allogeneic hematopoietic stem cell transplantation

Transplantation, 2006-09, Vol.82 (5), p.638

2006

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Pediatric immune myelofibrosis (PedIMF) as a novel and distinct clinical pathological entity

Frontiers in pediatrics, 2022-11, Vol.10, p.1031687-1031687

2022

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A COUNTRYWIDE STUDY OF GATA2 DEFICIENCY IN ITALY REVEALS NOVEL SYMPTOMS AND GENOTYPE-PHENOTYPE CORRELATION

EJC paediatric oncology, 2023-12, Vol.2, p.100057, Article 100057

2023

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The chemerin/CMKLR1 axis regulates intestinal graft-versus-host disease

JCI insight, 2023-03, Vol.8 (5)

2023

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Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia

Haematologica (Roma), 2010-01, Vol.95 (1), p.168-169

2010

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Extracorporeal Photochemotherapy for the Treatment of Chronic Graft-Versus-Host Disease: Trend for a Possible Cell Dose-Related Effect?

Therapeutic apheresis and dialysis, 2007-04, Vol.11 (2), p.85-93

2007

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Empagliflozin Modifies Neutrophils' Subsets in Patients with Glycogen Storage Disease Type Ib By Increasing Mature Neutrophils and Decreasing Immature Neutrophils

Blood, 2022-11, Vol.140 (Supplement 1), p.2614-2616

2022

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Treosulfan Therapeutic Drug Monitoring: Optimizing Conditioning Therapy in Pediatric Hematopoietic Stem Cell Transplantation

Blood, 2022-11, Vol.140 (Supplement 1), p.12854-12855

2022

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Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond‐like syndrome

British journal of haematology, 2020-05, Vol.189 (4), p.e171-e174

2020

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Minimal residual disease before and after transplantation for childhood acute lymphoblastic leukaemia: is there any room for intervention?

British journal of haematology, 2014-02, Vol.164 (3), p.396-408

2014

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Safety and efficacy of narsoplimab in pediatric and adult patients with transplant-associated thrombotic microangiopathy: a real-world experience

Bone marrow transplantation (Basingstoke), 2024-08, Vol.59 (8), p.1161-1168

2024

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Hepatic focal nodular hyperplasia after pediatric hematopoietic stem cell transplantation: The impact of hormonal replacement therapy and iron overload

Pediatric blood & cancer, 2020-04, Vol.67 (4), p.e28137-n/a

2020

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Cytokine release syndrome after CAR infusion in pediatric patients with refractory/relapsed B-ALL: is there a role for diclofenac?

Tumori, 2022-12, Vol.108 (6), p.556-562

2022

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Diagnosis and management of neutropenia in children: The approach of the Study Group on Neutropenia and Marrow Failure Syndromes of the Pediatric Italian Hemato‐Oncology Association (Associazione Italiana Emato‐Oncologia Pediatrica ‐ AIEOP)

Pediatric blood & cancer, 2022-06, Vol.69 (6), p.e29599-n/a

2022

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Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel

Absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy in folliculin-interacting protein 1 deficiency

A Novel Germline Mutation of ADA2 Gene in Two “Discordant” Homozygous Female Twins Affected by Adenosine Deaminase 2 Deficiency: Description of the Bone-Related Phenotype

CAN A THIRD HAEMATOPOIETIC STEM CELL TRANSPLANTATION BE A VIABLE OPTION FOR JMML RELAPSE? A CASE REPORT

The role of HLA matching in unrelated donor hematopoietic stem cell transplantation for sickle cell disease in Europe

Isolated leukopenia in children and adolescents referred to a Pediatric Hematology Clinic

Diagnosis and management of acquired aplastic anemia in childhood. Guidelines from the Marrow Failure Study Group of the Pediatric Haemato-Oncology Italian Association (AIEOP)

Case Report: Consistent disease manifestations with a staggered time course in two identical twins affected by adenosine deaminase 2 deficiency

Neutropenia, hypogammaglobulinemia, and pneumonia: A case of WHIM syndrome

Finding balance between mature and immature neutrophils: The effects of empagliflozin in GSD‐Ib

Case Report: Hypomorphic Function and Somatic Reversion in DOCK8 Deficiency in One Patient With Two Novel Variants and Sclerosing Cholangitis

Risk factors and severe outcome in thrombotic microangiopathy after allogeneic hematopoietic stem cell transplantation

Pediatric immune myelofibrosis (PedIMF) as a novel and distinct clinical pathological entity

A COUNTRYWIDE STUDY OF GATA2 DEFICIENCY IN ITALY REVEALS NOVEL SYMPTOMS AND GENOTYPE-PHENOTYPE CORRELATION

The chemerin/CMKLR1 axis regulates intestinal graft-versus-host disease

Novel HAX1 gene mutations associated to neurodevelopment abnormalities in two Italian patients with severe congenital neutropenia

Extracorporeal Photochemotherapy for the Treatment of Chronic Graft-Versus-Host Disease: Trend for a Possible Cell Dose-Related Effect?

Empagliflozin Modifies Neutrophils' Subsets in Patients with Glycogen Storage Disease Type Ib By Increasing Mature Neutrophils and Decreasing Immature Neutrophils

Treosulfan Therapeutic Drug Monitoring: Optimizing Conditioning Therapy in Pediatric Hematopoietic Stem Cell Transplantation

Intermittent granulocyte maturation arrest, hypocellular bone marrow, and episodic normal neutrophil count can be associated with SRP54 mutations causing Shwachman–Diamond‐like syndrome

Minimal residual disease before and after transplantation for childhood acute lymphoblastic leukaemia: is there any room for intervention?

Safety and efficacy of narsoplimab in pediatric and adult patients with transplant-associated thrombotic microangiopathy: a real-world experience

Hepatic focal nodular hyperplasia after pediatric hematopoietic stem cell transplantation: The impact of hormonal replacement therapy and iron overload

Cytokine release syndrome after CAR infusion in pediatric patients with refractory/relapsed B-ALL: is there a role for diclofenac?

Diagnosis and management of neutropenia in children: The approach of the Study Group on Neutropenia and Marrow Failure Syndromes of the Pediatric Italian Hemato‐Oncology Association (Associazione Italiana Emato‐Oncologia Pediatrica ‐ AIEOP)

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