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Red cell membrane disorders: structure meets function

Blood, 2020-09, Vol.136 (11), p.1250-1261

2020

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Warm antibody autoimmune hemolytic anemia

Hematology, 2016-12, Vol.2016 (1), p.690-697

Kalfa, Theodosia A

2016

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Diagnosis and clinical management of red cell membrane disorders

Hematology, 2021-12, Vol.2021 (1), p.331-340

Kalfa, Theodosia A

2021

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Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management

Hematology/oncology clinics of North America, 2019-06, Vol.33 (3), p.373-392

2019

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Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis

Blood, 2017-10, Vol.130 (16), p.1845-1856

2017

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Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease

Blood, 2013-03, Vol.121 (11), p.2099-2107

2013

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Immunosuppressive CD71+ erythroid cells compromise neonatal host defence against infection

Nature (London), 2013-12, Vol.504 (7478), p.158-162

2013

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Autoimmune Hemolytic Anemia in the Pediatric Setting

Journal of clinical medicine, 2021-01, Vol.10 (2), p.216

2021

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Navigating the marrow sea towards erythromyeloblastic islands under normal and inflammatory conditions

Current opinion in hematology, 2023-05, Vol.30 (3), p.80

2023

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Crosstalk between terminal erythropoiesis and granulopoiesis within their common niche: the erythromyeloblastic island

Current opinion in hematology, 2023-07, Vol.30 (4), p.99-105

2023

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Unraveling Macrophage Heterogeneity in Erythroblastic Islands

Frontiers in immunology, 2017-09, Vol.8, p.1140-1140

2017

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Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia—TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial

The Lancet (British edition), 2016-02, Vol.387 (10019), p.661-670

2016

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Signaling and cytoskeletal requirements in erythroblast enucleation

Blood, 2012-06, Vol.119 (25), p.6118-6127

2012

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Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients

Scientific reports, 2021-04, Vol.11 (1), p.7909-7909, Article 7909

2021

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VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects

American journal of human genetics, 2020-12, Vol.107 (6), p.1149-1156

2020

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Etavopivat, a Pyruvate Kinase Activator in Red Blood Cells, for the Treatment of Sickle Cell Disease

The Journal of pharmacology and experimental therapeutics, 2022-03, Vol.380 (3), p.210-219

2022

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Rapid measurement of hemoglobin-oxygen dissociation by leveraging Bohr effect and Soret band bathochromic shift

Analyst (London), 2024-04, Vol.149 (9), p.2561-2572

2024

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Erythroblastic islands foster granulopoiesis in parallel to terminal erythropoiesis

Blood, 2022-10, Vol.140 (14), p.1621-1634

2022

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Rho GTPases in hematopoiesis and hemopathies

Blood, 2010-02, Vol.115 (5), p.936-947

2010

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M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling

Scientific reports, 2022-01, Vol.12 (1), p.1235-1235, Article 1235

2022

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ER-to-Golgi transport and SEC23-dependent COPII vesicles regulate T cell alloimmunity

The Journal of clinical investigation, 2021-01, Vol.131 (2), p.1-13

2021

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Rho GTPases in erythroid maturation

Current opinion in hematology, 2014-05, Vol.21 (3), p.165-171

2014

Volltextzugriff (PDF)

Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III

Haematologica (Roma), 2023-02, Vol.108 (2), p.581-587

2023

Volltextzugriff (PDF)

Loss of TBC1D2B causes a progressive neurological disorder with gingival overgrowth

European journal of human genetics : EJHG, 2024-05, Vol.32 (5), p.558-566

2024

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Red cell membrane disorders: structure meets function

Warm antibody autoimmune hemolytic anemia

Diagnosis and clinical management of red cell membrane disorders

Rare Hereditary Hemolytic Anemias: Diagnostic Approach and Considerations in Management

Base editing of haematopoietic stem cells rescues sickle cell disease in mice

Novel mechanisms of PIEZO1 dysfunction in hereditary xerocytosis

Erythrocyte NADPH oxidase activity modulated by Rac GTPases, PKC, and plasma cytokines contributes to oxidative stress in sickle cell disease

Immunosuppressive CD71+ erythroid cells compromise neonatal host defence against infection

Autoimmune Hemolytic Anemia in the Pediatric Setting

Navigating the marrow sea towards erythromyeloblastic islands under normal and inflammatory conditions

Crosstalk between terminal erythropoiesis and granulopoiesis within their common niche: the erythromyeloblastic island

Unraveling Macrophage Heterogeneity in Erythroblastic Islands

Hydroxycarbamide versus chronic transfusion for maintenance of transcranial doppler flow velocities in children with sickle cell anaemia—TCD With Transfusions Changing to Hydroxyurea (TWiTCH): a multicentre, open-label, phase 3, non-inferiority trial

Signaling and cytoskeletal requirements in erythroblast enucleation

Characterizing bulk rigidity of rigid red blood cell populations in sickle-cell disease patients

VPS4A Mutations in Humans Cause Syndromic Congenital Dyserythropoietic Anemia due to Cytokinesis and Trafficking Defects

Etavopivat, a Pyruvate Kinase Activator in Red Blood Cells, for the Treatment of Sickle Cell Disease

Rapid measurement of hemoglobin-oxygen dissociation by leveraging Bohr effect and Soret band bathochromic shift

Erythroblastic islands foster granulopoiesis in parallel to terminal erythropoiesis

Rho GTPases in hematopoiesis and hemopathies

M-CSF supports medullary erythropoiesis and erythroid iron demand following burn injury through its activity on homeostatic iron recycling

ER-to-Golgi transport and SEC23-dependent COPII vesicles regulate T cell alloimmunity

Rho GTPases in erythroid maturation

Mutations in the RACGAP1 gene cause autosomal recessive congenital dyserythropoietic anemia type III

Loss of TBC1D2B causes a progressive neurological disorder with gingival overgrowth

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