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Publications by F. H. Herrmann
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
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Clinical Studies and Thrombin Generation in Patients Homozygous or Heterozygous for the G20210A Mutation in the Prothrombin Gene
Arteriosclerosis, Thrombosis, and Vascular Biology
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Phenotype and Genotype Report on Homozygous and Heterozygous Patients With Congenital Factor X Deficiency
Haematologica
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Phenotypic Expression of Heterozygous Lipoprotein Lipase Deficiency in the Extended Pedigree of a Proband Homozygous for a Missense Mutation.
Journal of Clinical Investigation
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Spontaneous Thrombosis in a Patient With Factor XI Deficiency Homozygous for the p.Cys398Tyr Mutation
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Clinical and Biochemical Characteristics and Bone Mineral Density of Homozygous, Compound Heterozygous and Heterozygous Carriers of Three novelIGFALSmutations
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Familial Association of Hypoplasminogenemia and Heterozygous Factor v Deficiency
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Coagulant Activity of Recombinant Human Factor VII Produced by Lentiviral Human F7 Gene Transfer in Immortalized Hepatocyte-Like Cell Line
PLoS ONE
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Clinical Significance of Prothrombin G20210A Mutation in Homozygous Patients
American Journal of Hematology
Hematology
