L. Carlsson

发表

Heparin-induced thrombocytopenia: new insights into the impact of the FcgammaRIIa-R-H131 polymorphism.

A. Greinacher, J. V. D. van de Winkel, J. G. Winkel, 1998, Blood.

Very low platelet counts in post-transfusion purpura falsely diagnosed as heparin-induced thrombocytopenia. Report of four cases and review of literature.

A. Greinacher, P. Eichler, N. Lubenow, 2000, Thrombosis research.

Heparin-Induced Thrombocytopenia : New Insights Into the Impact of the Fc g RIIa-RH 131 Polymorphism

A. Greinacher, J. G. Winkel, P. Eichler, 1998 .

Polymorphisms of the human platelet antigens HPA-1, HPA-2, HPA-3, and HPA-5 on the platelet receptors for fibrinogen (GPIIb/IIIa), von Willebrand factor (GPIb/IX), and collagen (GPIa/IIa) are not correlated with an increased risk for stroke.

C. Kessler, A. Greinacher, L. Carlsson, 1997, Stroke.

The 2 Gene Coding Sequence T807/A873 of the Platelet Collagen Receptor Integrin 2β1 Might Be a Genetic Risk Factor for the Development of Stroke in Younger Patients

C. Kessler, A. Greinacher, S. Santoso, 1999 .

The alpha2 gene coding sequence T807/A873 of the platelet collagen receptor integrin alpha2beta1 might be a genetic risk factor for the development of stroke in younger patients.

C. Kessler, A. Greinacher, S. Santoso, 1999, Blood.

Polymorphisms of Fcγ-receptors RIIa, RIIIa, and RIIIb in patients with adult periodontal diseases

A. Greinacher, T. Kocher, P. Meisel, 2001, Genes and Immunity.

Impact of Genetic Polymorphisms on the Smoking-related Risk of Periodontal Disease: the Population-based Study SHIP

U. John, C. Schwahn, T. Kocher, 2003, Tobacco induced diseases.

Impact of Genetic Polymorphisms on the Smoking-related Risk of Periodontal Disease: the Population-based Study SHIP

U. John, C. Schwahn, T. Kocher, 2003, Tobacco Induced Diseases.

The FcγRIIa Polymorphism in Children with Atopic Diseases

A. Pawlik, B. Gawrońska-Szklarz, P. Meisel, 2004, International Archives of Allergy and Immunology.

Nonmuscle myosin heavy chain IIA mutations define a spectrum of autosomal dominant macrothrombocytopenias: May-Hegglin anomaly and Fechtner, Sebastian, Epstein, and Alport-like syndromes.

J. White, C. Epstein, J. Martignetti, 2001, American journal of human genetics.

MYH9 spectrum of autosomal‐dominant giant platelet syndromes: Unexpected association with fibulin‐1 variant‐D inactivation

C. Epstein, J. Martignetti, N. Amariglio, 2003, American journal of hematology.

Autosomal-dominant giant platelet syndromes: a hint of the same genetic defect as in Fechtner syndrome owing to a similar genetic linkage to chromosome 22q11-13.

C. Epstein, N. Amariglio, G. Rechavi, 2000, Blood.

Iron deficiency anaemia in young women

S. Hempel, A. Greinacher, L. Carlsson, 2002, European Journal of Haematology.

Integrin a2b1 Might Be a Genetic Risk Factor for the Development of Stroke in Younger Patients

C. Kessler, A. Greinacher, S. Santoso, 1999 .

Heparin-induced thrombocytopenia: temporal pattern of thrombocytopenia in relation to initial use or reexposure to heparin.

A. Greinacher, P. Eichler, N. Lubenow, 2002, Chest.

Polymorphisms of Fc gamma-receptors RIIa, RIIIa, and RIIIb in patients with adult periodontal diseases.

A. Greinacher, T. Kocher, P. Meisel, 2001, Genes and immunity.

Platelet receptor and clotting factor polymorphisms as genetic risk factors for thromboembolic complications in heparin-induced thrombocytopenia.

A. Greinacher, F. Herrmann, P. Eichler, 2003, Pharmacogenetics.