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Journal Articles

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

Blood (2021) 137 (4): 493–499.

https://doi.org/10.1182/blood.2020006441

Published: 2021

Includes: Supplemental data

Journal Articles

A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H

Blood (2020) 136 (15): 1789–1793.

https://doi.org/10.1182/blood.2020005934

Published: 2020

Includes: Supplemental data

Journal Articles

Changes in gene expression of granulocytes during in vivo granulocyte colony-stimulating factor/dexamethasone mobilization for transfusion purposes

Agata Drewniak, Bram J. van Raam, Judy Geissler, Anton T.J. Tool, Olaf R.F. Mook, Timo K. van den Berg, Frank Baas, Taco W. Kuijpers

Blood (2009) 113 (23): 5979–5998.

https://doi.org/10.1182/blood-2008-10-182147

Published: 2009

Includes: Supplemental data

Journal Articles

LAD-1/variant syndrome is caused by mutations in FERMT3

Taco W. Kuijpers, Edith van de Vijver, Marian A. J. Weterman, Martin de Boer, Anton T. J. Tool, Timo K. van den Berg, Markus Moser, Marja E. Jakobs, Karl Seeger, Özden Sanal, Sule Ünal, Mualla Çetin, Dirk Roos, Arthur J. Verhoeven, Frank Baas

Blood (2009) 113 (19): 4740–4746.

https://doi.org/10.1182/blood-2008-10-182154

Published: 2009

Journal Articles

Response: Adherence to the LAD variant form

Taco Kuijpers, Frank Baas, Marian Weterman, Anton Tool, Dirk Roos

Blood (2007) 110 (12): 4129–4130.

https://doi.org/10.1182/blood-2007-06-093815

Published: 2007

Journal Articles

Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis

Taco W. Kuijpers, Nikolai A. Maianski, Anton T. J. Tool, Kolja Becker, Barbara Plecko, Fredoen Valianpour, Ron J. A. Wanders, Rob Pereira, Johan Van Hove, Arthur J. Verhoeven, Dirk Roos, Frank Baas, Peter G. Barth

Blood (2004) 103 (10): 3915–3923.

https://doi.org/10.1182/blood-2003-11-3940

Published: 2004

NARROW

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

A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H

Changes in gene expression of granulocytes during in vivo granulocyte colony-stimulating factor/dexamethasone mobilization for transfusion purposes

LAD-1/variant syndrome is caused by mutations in FERMT3

Response: Adherence to the LAD variant form

Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis

Email alerts

ASH Publications

American Society of Hematology

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

A new gene associated with a β-thalassemia phenotype: the observation of variants in SUPT5H

Changes in gene expression of granulocytes during in vivo granulocyte colony-stimulating factor/dexamethasone mobilization for transfusion purposes

LAD-1/variant syndrome is caused by mutations in FERMT3

Response: Adherence to the LAD variant form

Neutrophils in Barth syndrome (BTHS) avidly bind annexin-V in the absence of apoptosis

Email alerts

ASH Publications

American Society of Hematology

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