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Publications by K. Wulff
Variability of Clinical Manifestation of Factor VII-deficiency in Homozygous and Heterozygous Subjects of the European F7 Gene Mutation A294V
Haematologica
Hematology
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Variability in Clinical Phenotypes of Heterozygous and Homozygous Cases ofParkin-related Parkinson's Disease
International Journal of Neuroscience
Medicine
Neuroscience
Clinical Studies and Thrombin Generation in Patients Homozygous or Heterozygous for the G20210A Mutation in the Prothrombin Gene
Arteriosclerosis, Thrombosis, and Vascular Biology
Cardiovascular Medicine
Cardiology
Phenotype and Genotype Report on Homozygous and Heterozygous Patients With Congenital Factor X Deficiency
Haematologica
Hematology
Phenotypic Expression of Heterozygous Lipoprotein Lipase Deficiency in the Extended Pedigree of a Proband Homozygous for a Missense Mutation.
Journal of Clinical Investigation
Medicine
Spontaneous Thrombosis in a Patient With Factor XI Deficiency Homozygous for the p.Cys398Tyr Mutation
Cumhuriyet Medical Journal
Medicine
Clinical and Biochemical Characteristics and Bone Mineral Density of Homozygous, Compound Heterozygous and Heterozygous Carriers of Three novelIGFALSmutations
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Familial Association of Hypoplasminogenemia and Heterozygous Factor v Deficiency
Clinical and Applied Thrombosis/Hemostasis
Medicine
Hematology
Coagulant Activity of Recombinant Human Factor VII Produced by Lentiviral Human F7 Gene Transfer in Immortalized Hepatocyte-Like Cell Line
PLoS ONE
Multidisciplinary
Clinical Significance of Prothrombin G20210A Mutation in Homozygous Patients
American Journal of Hematology
Hematology
