André P. Abbes

Novel molecular defect in the platelet ADP receptor P2Y12 of a patient with haemorrhagic diathesis

Jasper A. Remijn, Martin J. W. IJsseldijk, Annuska Strunk et al. · Clinical Chemistry and Laboratory Medicine (CCLM) · 2007 · 55 citations

Medicine, Hematology, Pharmacology +14

Reliable Genotyping of the G-20210-A Mutation of Coagulation Factor II (Prothrombin)

Jan Danneberg, André P. Abbes, Ben J M Bruggeman et al. · Clinical Chemistry · 1998 · 41 citations · Full text

Medicine, Genetics, Hematology +17

The Expression of Transferrin Receptors on Erythroblasts in Anaemia of Chronic Disease, Myelodysplastic Syndromes and Iron Deficiency

P.A. Kuiper‐Kramer, Christian Huisman, Van der Molen-Sinke et al. · Acta Haematologica · 2009 · 38 citations

Medicine, Hematology, Pathology +17

Familial Neurohypophysial Diabetes Insipidus in a Large Dutch Kindred: Effect of the Onset of Diabetes on Growth in Children and Cell Biological Defects of the Mutant Vasopressin Prohormone¹

Marga Nijenhuis, Erica L T van den Akker, Robbert Zalm et al. · The Journal of Clinical Endocrinology & Metabolism · 2001 · 36 citations · Full text

Medicine, Endocrinology, Molecular Genetics +13

Minor disturbances in central nervous system function in familial neurohypophysial diabetes insipidus

J. Bruins, Gábor L. Kovaćs, André P. Abbes et al. · Psychoneuroendocrinology · 2005 · 23 citations

Medicine, Endocrinology, Neuroscience +12