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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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The phenotype of human STK4 deficiency

Blood, 2012-04, Vol.119 (15), p.3450-3457

2012

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Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome

Blood, 2018-09, Vol.132 (12), p.1318-1331

2018

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Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia

Blood, 2012-05, Vol.119 (22), p.5071-5077

2012

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The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy

Blood, 2006-06, Vol.107 (12), p.4628-4635

2006

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The spectrum of Evans syndrome in adults: new insight into the disease based on the analysis of 68 cases

Blood, 2009-10, Vol.114 (15), p.3167-3172

2009

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Selective inhibition of nuclear export with selinexor in patients with non-Hodgkin lymphoma

Blood, 2017-06, Vol.129 (24), p.3175-3183

2017

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Neutrophil elastase in cyclic and severe congenital neutropenia

Blood, 2007-03, Vol.109 (5), p.1817-1824

2007

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How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome

Blood, 2017-12, Vol.130 (23), p.2491-2498

2017

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Efficacy of transfusion with granulocytes from G-CSF/dexamethasone–treated donors in neutropenic patients with infection

Blood, 2015-10, Vol.126 (18), p.2153-2161

2015

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Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor

Blood, 2020-08, Vol.136 (9), p.1033-1043

2020

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G-CSF and its receptor in myeloid malignancy

Blood, 2010-06, Vol.115 (25), p.5131-5136

2010

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Heterozygous variants of CLPB are a cause of severe congenital neutropenia

Blood, 2022-02, Vol.139 (5), p.779-791

2022

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How we evaluate and treat neutropenia in adults

Blood, 2014-08, Vol.124 (8), p.1251-1258

2014

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Lenalidomide therapy in myelofibrosis with myeloid metaplasia

Blood, 2006-08, Vol.108 (4), p.1158-1164

2006

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Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-β–deficient neutrophils in a congenital neutropenia syndrome

Blood, 2010-10, Vol.116 (15), p.2783-2792

2010

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Severe chronic primary neutropenia in adults: report on a series of 108 patients

Blood, 2015-10, Vol.126 (14), p.1643-1650

2015

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Mutations of the ELA2 gene found in patients with severe congenital neutropenia induce the unfolded protein response and cellular apoptosis

Blood, 2007-12, Vol.110 (13), p.4179-4187

2007

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An open-label, single-arm phase 2 trial of valemetostat for relapsed or refractory adult T-cell leukemia/lymphoma

Blood, 2023-03, Vol.141 (10), p.1159-1168

2023

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GM-CSF stimulates granulopoiesis in a congenital neutropenia patient with loss-of-function biallelic heterozygous CSF3R mutations

Blood, 2015-10, Vol.126 (15), p.1865-1867

2015

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Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register

Blood, 2004-06, Vol.103 (11), p.4119-4125

2004

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Somatic mutations and clonal hematopoiesis in congenital neutropenia

The phenotype of human STK4 deficiency

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond–like syndrome

Sequential gain of mutations in severe congenital neutropenia progressing to acute myeloid leukemia

The incidence of leukemia and mortality from sepsis in patients with severe congenital neutropenia receiving long-term G-CSF therapy

The spectrum of Evans syndrome in adults: new insight into the disease based on the analysis of 68 cases

Selective inhibition of nuclear export with selinexor in patients with non-Hodgkin lymphoma

Cooperativity of RUNX1 and CSF3R mutations in severe congenital neutropenia: a unique pathway in myeloid leukemogenesis

Neutrophil elastase in cyclic and severe congenital neutropenia

Stem cell transplantation in severe congenital neutropenia: an analysis from the European Society for Blood and Marrow Transplantation

How I treat warts, hypogammaglobulinemia, infections, and myelokathexis syndrome

Long-term follow-up of MCL patients treated with single-agent ibrutinib: updated safety and efficacy results

Efficacy of transfusion with granulocytes from G-CSF/dexamethasone–treated donors in neutropenic patients with infection

Treating neutropenia and neutrophil dysfunction in glycogen storage disease type Ib with an SGLT2 inhibitor

A randomized phase 3 study of tipifarnib compared with best supportive care, including hydroxyurea, in the treatment of newly diagnosed acute myeloid leukemia in patients 70 years or older

G-CSF and its receptor in myeloid malignancy

Heterozygous variants of CLPB are a cause of severe congenital neutropenia

How we evaluate and treat neutropenia in adults

Lenalidomide therapy in myelofibrosis with myeloid metaplasia

Lack of glucose recycling between endoplasmic reticulum and cytoplasm underlies cellular dysfunction in glucose-6-phosphatase-β–deficient neutrophils in a congenital neutropenia syndrome

Severe chronic primary neutropenia in adults: report on a series of 108 patients

Mutations of the ELA2 gene found in patients with severe congenital neutropenia induce the unfolded protein response and cellular apoptosis

An open-label, single-arm phase 2 trial of valemetostat for relapsed or refractory adult T-cell leukemia/lymphoma

GM-CSF stimulates granulopoiesis in a congenital neutropenia patient with loss-of-function biallelic heterozygous CSF3R mutations

Mutations in the ELA2 gene correlate with more severe expression of neutropenia: a study of 81 patients from the French Neutropenia Register

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