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Posttransplant complications in patients with marrow failure syndromes: are we improving long-term outcomes?

Hematology, 2023-12, Vol.2023 (1), p.141-148

2023

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The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy

Blood, 2016-02, Vol.127 (8), p.989-996

2016

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Diagnosis, Treatment, and Molecular Pathology of Shwachman-Diamond Syndrome

Hematology/oncology clinics of North America, 2018-08, Vol.32 (4), p.687-700

2018

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A new paradigm: Diagnosis and management of HSCT-associated thrombotic microangiopathy as multi-system endothelial injury

Blood reviews, 2015-05, Vol.29 (3), p.191-204

2015

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Complement blockade for TA-TMA: lessons learned from a large pediatric cohort treated with eculizumab

Blood, 2020-03, Vol.135 (13), p.1049-1057

2020

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Variable Clinical Presentation of Shwachman–Diamond Syndrome: Update from the North American Shwachman–Diamond Syndrome Registry

The Journal of pediatrics, 2014-04, Vol.164 (4), p.866-870

2014

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Somatic mutations and clonal hematopoiesis in congenital neutropenia

Blood, 2018-01, Vol.131 (4), p.408-416

2018

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Pulmonary Complications After Pediatric Stem Cell Transplant

Frontiers in oncology, 2021-10, Vol.11, p.755878-755878

2021

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Diagnostic and risk criteria for HSCT-associated thrombotic microangiopathy: a study in children and young adults

Blood, 2014-07, Vol.124 (4), p.645-653

2014

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Gonadal function in pediatric Fanconi anemia patients treated with hematopoietic stem cell transplant

Haematologica (Roma), 2023-09

2023

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Infrequent fractures and resilient bone mineral density: bone health in patients with Fanconi anemia

Haematologica (Roma), 2024-10, Vol.109 (10), p.3435-3438

2024

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Mouse models of neutropenia reveal progenitor-stage-specific defects

Nature (London), 2020-06, Vol.582 (7810), p.109-114

2020

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Azithromycin does not increase hematologic relapse in pediatric hematopoietic cell transplant recipients

Bone marrow transplantation (Basingstoke), 2022-10, Vol.57 (10), p.1589-1591

2022

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A case of co‐occurring acute myeloid leukemia and relapsed diffuse large B‐cell lymphoma in a young adult with Shwachman–Diamond syndrome

Pediatric blood & cancer, 2024-08, Vol.71 (8), p.e31137-n/a

2024

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A Complete Histologic Approach to Gastrointestinal Biopsy From Hematopoietic Stem Cell Transplant Patients With Evidence of Transplant-Associated Gastrointestinal Thrombotic Microangiopathy

Archives of pathology & laboratory medicine (1976), 2017-11, Vol.141 (11), p.1558-1566

2017

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Pre‐transplant glomerular hyperfiltration is not a risk factor for increased renal morbidity and mortality in pediatric stem cell transplant patients

Pediatric blood & cancer, 2024-04, Vol.71 (4), p.e30853-n/a

2024

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Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update

Hematology/oncology clinics of North America, 2013-02, Vol.27 (1), p.117-128

2013

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New approaches in the diagnosis, pathophysiology, and treatment of pediatric hematopoietic stem cell transplantation-associated thrombotic microangiopathy

Transfusion and apheresis science, 2016-04, Vol.54 (2), p.181-190

2016

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Testicular thrombotic microangiopathy: An unrecognized complication

Pediatric blood & cancer, 2021-08, Vol.68 (8), p.e29128-n/a

2021

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Phenotypes of adults with Fanconi anaemia

British journal of haematology, 2023-04, Vol.201 (1), p.133-139

2023

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Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency

Genetics in medicine, 2021-09, Vol.23 (9), p.1705-1714

2021

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On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology

Nature biomedical engineering, 2020-04, Vol.4 (4), p.394-406

2020

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Coronavirus disease 2019 and vaccination in patients with Shwachman‐Diamond syndrome

Pediatric blood & cancer, 2022-05, Vol.69 (5), p.e29647-n/a

2022

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Ruxolitinib for the Treatment of Chronic GVHD and Overlap Syndrome in Children and Young Adults

Transplantation, 2022-02, Vol.106 (2), p.412-419

2022

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Thinking Beyond HLH: Clinical Features of Patients with Concurrent Presentation of Hemophagocytic Lymphohistiocytosis and Thrombotic Microangiopathy

Journal of clinical immunology, 2020-07, Vol.40 (5), p.699-707

2020

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Posttransplant complications in patients with marrow failure syndromes: are we improving long-term outcomes?

The genetic fingerprint of susceptibility for transplant-associated thrombotic microangiopathy

Diagnosis, Treatment, and Molecular Pathology of Shwachman-Diamond Syndrome

A new paradigm: Diagnosis and management of HSCT-associated thrombotic microangiopathy as multi-system endothelial injury

Complement blockade for TA-TMA: lessons learned from a large pediatric cohort treated with eculizumab

Variable Clinical Presentation of Shwachman–Diamond Syndrome: Update from the North American Shwachman–Diamond Syndrome Registry

Somatic mutations and clonal hematopoiesis in congenital neutropenia

Pulmonary Complications After Pediatric Stem Cell Transplant

Diagnostic and risk criteria for HSCT-associated thrombotic microangiopathy: a study in children and young adults

Gonadal function in pediatric Fanconi anemia patients treated with hematopoietic stem cell transplant

Infrequent fractures and resilient bone mineral density: bone health in patients with Fanconi anemia

Mouse models of neutropenia reveal progenitor-stage-specific defects

Azithromycin does not increase hematologic relapse in pediatric hematopoietic cell transplant recipients

A case of co‐occurring acute myeloid leukemia and relapsed diffuse large B‐cell lymphoma in a young adult with Shwachman–Diamond syndrome

A Complete Histologic Approach to Gastrointestinal Biopsy From Hematopoietic Stem Cell Transplant Patients With Evidence of Transplant-Associated Gastrointestinal Thrombotic Microangiopathy

Pre‐transplant glomerular hyperfiltration is not a risk factor for increased renal morbidity and mortality in pediatric stem cell transplant patients

Clinical and molecular pathophysiology of Shwachman-Diamond syndrome: an update

New approaches in the diagnosis, pathophysiology, and treatment of pediatric hematopoietic stem cell transplantation-associated thrombotic microangiopathy

Testicular thrombotic microangiopathy: An unrecognized complication

Phenotypes of adults with Fanconi anaemia

Neutropenia and intellectual disability are hallmarks of biallelic and de novo CLPB deficiency

On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology

Coronavirus disease 2019 and vaccination in patients with Shwachman‐Diamond syndrome

Ruxolitinib for the Treatment of Chronic GVHD and Overlap Syndrome in Children and Young Adults

Thinking Beyond HLH: Clinical Features of Patients with Concurrent Presentation of Hemophagocytic Lymphohistiocytosis and Thrombotic Microangiopathy

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