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Gynaecological and obstetrical morbidity in women with type I von Willebrand disease: results of a patient survey

Haemophilia : the official journal of the World Federation of Hemophilia, 2000-11, Vol.6 (6), p.643-648

2000

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Signal Pathway Regulation of Interleukin-8-Induced Actin Polymerization in Neutrophils

Blood, 1993-10, Vol.82 (8), p.2546-2551

1993

Volltextzugriff (PDF)

Infections affecting blood cell morphology

American journal of hematology, 1998-11, Vol.59 (3), p.238-241

1998

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Management of hereditary hemochromatosis

Blood reviews, 1994-12, Vol.8 (4), p.193-198

1994

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Protein kinase C modulates actin conformation in human T lymphocytes

The Journal of immunology (1950), 1988-11, Vol.141 (9), p.2929

1988

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Screening for hemochromatosis in primary care settings

Annals of internal medicine, 1998-12, Vol.129 (11), p.962

1998

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Hepatic iron index: how useful is it?

Gastroenterology (New York, N.Y. 1943), 1998-05, Vol.114 (5), p.1112-1112

1998

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Disorders that resemble lymphomas

American journal of hematology, 1997-09, Vol.56 (1), p.63-68

1997

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Screening for hemochromatosis: Additional considerations

Gastroenterology (New York, N.Y. 1943), 1996-02, Vol.110 (2), p.653-654

1996

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Asymptomatic hemochromatosis subjects: genotypic and phenotypic profiles

Blood, 2000-12, Vol.96 (12), p.3707-3711

2000

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Hematologic neoplasia and the central nervous system

American journal of hematology, 1999-12, Vol.62 (4), p.234-238

1999

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Correlation Between Genotype and Phenotype in Hereditary Hemochromatosis: Analysis of 61 Cases

Blood cells, molecules, & diseases, 1997-08, Vol.23 (2), p.314-320

1997

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Unusual anemias

American journal of hematology, 1997-03, Vol.54 (3), p.249-252

1997

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Functional characteristics of mature granulocytes in a patient with acute promyelocytic leukemia treated with all- trans retinoic acid

Leukemia research, 1995-08, Vol.19 (8), p.505-511

1995

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Serum ferritin level predicts advanced hepatic fibrosis among U.S. patients with phenotypic hemochromatosis

Annals of internal medicine, 2003-04, Vol.138 (8), p.627

2003

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Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features

Blood cells, molecules, & diseases, 2005-03, Vol.34 (2), p.157-161

2005

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Fatal thrombotic thrombocytopenic purpura (TTP) presenting concurrently with metastatic multiple endocrine neoplasia (MEN) type I

Hematopathology and molecular hematology, 1996, Vol.10 (3), p.161

1996

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Mutation Analysis in Hereditary Hemochromatosis

Blood cells, molecules, & diseases, 1996, Vol.22 (2), p.187-194

1996

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Functional properties of HL60 cells matured with all- trans-retinoic acid and DMSO: Differences in response to interleukin-8 and fMLP

Leukemia research, 1995, Vol.19 (1), p.1-6

1995

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Engagement of the T-cell antigen receptor by anti-CD3 monoclonal antibody causes a rapid increase in lymphocyte F-actin

Journal of cellular physiology, 1994-05, Vol.159 (2), p.365-370

1994

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Isolated splenic blastic transformation of idiopathic myelofibrosis and response to splenectomy

Leukemia research, 1997-03, Vol.21 (3), p.255-257

1997

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Reversible drug‐induced interstitial pneumonitis following imatinib mesylate therapy

American journal of hematology, 2005-05, Vol.79 (1), p.80-81

2005

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Association of heterozygous hemochromatosis C282Y gene mutation with hand osteoarthritis

Journal of rheumatology, 2003-01, Vol.30 (1), p.121

2003

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Localization of the Hemochromatosis Disease Gene: Linkage Disequilibrium Analysis Using an American Patient Collection

Blood cells, molecules, & diseases, 1996, Vol.22 (1), p.36-46

1996

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The Effect of Dexamethasone on Functional Properties of HL60 Cells During All- trans Retinoic Acid Induced Differentiation. Are There Implications for the Retinoic Acid Syndrome?

Blood cells, molecules, & diseases, 1996, Vol.22 (2), p.139-149

1996

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Gynaecological and obstetrical morbidity in women with type I von Willebrand disease: results of a patient survey

Signal Pathway Regulation of Interleukin-8-Induced Actin Polymerization in Neutrophils

Infections affecting blood cell morphology

Management of hereditary hemochromatosis

Protein kinase C modulates actin conformation in human T lymphocytes

Screening for hemochromatosis in primary care settings

Hepatic iron index: how useful is it?

Disorders that resemble lymphomas

Screening for hemochromatosis: Additional considerations

Asymptomatic hemochromatosis subjects: genotypic and phenotypic profiles

Hematologic neoplasia and the central nervous system

Correlation Between Genotype and Phenotype in Hereditary Hemochromatosis: Analysis of 61 Cases

Unusual anemias

Functional characteristics of mature granulocytes in a patient with acute promyelocytic leukemia treated with all- trans retinoic acid

Serum ferritin level predicts advanced hepatic fibrosis among U.S. patients with phenotypic hemochromatosis

Autosomal dominant hereditary hemochromatosis associated with a novel ferroportin mutation and unique clinical features

Fatal thrombotic thrombocytopenic purpura (TTP) presenting concurrently with metastatic multiple endocrine neoplasia (MEN) type I

Mutation Analysis in Hereditary Hemochromatosis

Functional properties of HL60 cells matured with all- trans-retinoic acid and DMSO: Differences in response to interleukin-8 and fMLP

Engagement of the T-cell antigen receptor by anti-CD3 monoclonal antibody causes a rapid increase in lymphocyte F-actin

Isolated splenic blastic transformation of idiopathic myelofibrosis and response to splenectomy

Reversible drug‐induced interstitial pneumonitis following imatinib mesylate therapy

Association of heterozygous hemochromatosis C282Y gene mutation with hand osteoarthritis

Localization of the Hemochromatosis Disease Gene: Linkage Disequilibrium Analysis Using an American Patient Collection

The Effect of Dexamethasone on Functional Properties of HL60 Cells During All- trans Retinoic Acid Induced Differentiation. Are There Implications for the Retinoic Acid Syndrome?

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