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Journal Articles

Plateletpheresis-associated lymphopenia in frequent platelet donors

Blood (2019) 133 (6): 605–614.

https://doi.org/10.1182/blood-2018-09-873125

Published: 2019

Includes: Supplemental data

Journal Articles

Flexible migration program regulates γδ T-cell involvement in humoral immunity

Marlène Brandes, Katharina Willimann, Alois B. Lang, Ki-Hoan Nam, Chenggang Jin, Michael B. Brenner, Craig T. Morita, Bernhard Moser

Blood (2003) 102 (10): 3693–3701.

https://doi.org/10.1182/blood-2003-04-1016

Published: 2003

Includes: Supplemental data

Journal Articles

Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosis

B Brenner, A Zivelin, N Lanir, JS Greengard, JH Griffin, U Seligsohn

Blood (1996) 88 (3): 877–880.

https://doi.org/10.1182/blood.V88.3.877.877

Published: 1996

Journal Articles

Variant Bernard-Soulier syndrome associated with a homozygous mutation in the leucine-rich domain of glycoprotein IX

JM Clemetson, PA Kyrle, B Brenner, KJ Clemetson

Blood (1994) 84 (4): 1124–1131.

https://doi.org/10.1182/blood.V84.4.1124.1124

Published: 1994

Journal Articles

Rapid neonatal diagnosis of type IIB von Willebrand disease using the polymerase chain reaction [letter]

C Mannhalter, PA Kyrle, B Brenner, K Lechner

Blood (1991) 77 (11): 2539–2540.

https://doi.org/10.1182/blood.V77.11.2539.2539

Published: 1991

NARROW

Plateletpheresis-associated lymphopenia in frequent platelet donors

Flexible migration program regulates γδ T-cell involvement in humoral immunity

Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosis

Variant Bernard-Soulier syndrome associated with a homozygous mutation in the leucine-rich domain of glycoprotein IX

Rapid neonatal diagnosis of type IIB von Willebrand disease using the polymerase chain reaction [letter]

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ASH Publications

American Society of Hematology

Plateletpheresis-associated lymphopenia in frequent platelet donors

Flexible migration program regulates γδ T-cell involvement in humoral immunity

Venous thromboembolism associated with double heterozygosity for R506Q mutation of factor V and for T298M mutation of protein C in a large family of a previously described homozygous protein C-deficient newborn with massive thrombosis

Variant Bernard-Soulier syndrome associated with a homozygous mutation in the leucine-rich domain of glycoprotein IX

Rapid neonatal diagnosis of type IIB von Willebrand disease using the polymerase chain reaction [letter]

Email alerts

ASH Publications

American Society of Hematology

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