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المصدر: Haberichter, S L, Castaman, G, Budde, U, Peake, I, Goodeve, A, Rodeghiero, F, Federici, A B, Batlle, J, Meyer, D, Mazurier, C, Goudemand, J, Eikenboom, J, Schneppenheim, R, Ingerslev, J, Vorlova, Z, Habart, D, Holmberg, L, Lethagen, S, Pasi, J, Hill, F G H & Montgomery, R R 2008, ' Identification of type 1 von Willebrand disease patients with reduced von Willebrand factor survival by assay of the VWF propeptide in the European study: molecular and clinical markers for the diagnosis and management of type 1 VWD (MCMDM-1VWD) ', Blood, vol. 111, no. 10, pp. 4979-85 . https://doi.org/10.1182/blood-2007-09-110940Test

مصطلحات موضوعية: medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Immunology, Biochemistry, Hemostasis, Thrombosis, and Vascular Biology, Von Willebrand factor, Predictive Value of Tests, von Willebrand Disease, Internal medicine, hemic and lymphatic diseases, von Willebrand Factor, Von Willebrand disease, medicine, Humans, In patient, Deamino Arginine Vasopressin, Protein Precursors, Protein precursor, Desmopressin, Survival analysis, Hematology, biology, business.industry, Cell Biology, Plasma levels, medicine.disease, Survival Analysis, Europe, von Willebrand Diseases, Endocrinology, Treatment Outcome, Mutation, biology.protein, cardiovascular system, Biological Markers, business, Biomarkers, medicine.drug, circulatory and respiratory physiology, Half-Life

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2da860dbc846a5d06939c1c9bc086dc2Test
https://europepmc.org/articles/PMC2384129Test/

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Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD)

المصدر: Budde, U, Schneppenheim, R, Eikenboom, J, Goodeve, A, Will, K, Drewke, E, Castaman, G, Rodeghiero, F, Federici, A B, Batlle, J, Pérez, A, Meyer, D, Mazurier, C, Goudemand, J, Ingerslev, J, Habart, D, Vorlova, Z, Holmberg, L, Lethagen, S, Pasi, J, Hill, F & Peake, I 2008, ' Detailed von Willebrand factor multimer analysis in patients with von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 von Willebrand disease (MCMDM-1VWD) ', Journal of Thrombosis and Haemostasis, vol. 6, no. 5, pp. 762-71 . https://doi.org/10.1111/j.1538-7836.2008.02945.xTest

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Genotype, Antigen, Von Willebrand factor, hemic and lymphatic diseases, von Willebrand Disease, von Willebrand Factor, Von Willebrand disease, Epidemiology, Molecular, Medicine, Humans, In patient, Congenital Bleeding Disorder, Genotyping, Family Health, Molecular Epidemiology, biology, business.industry, Case-control study, Hematology, medicine.disease, Europe, von Willebrand Diseases, Multimer analysis, Mutation, Type 1, von Willebrand disease, von Willebrand factor, Case-Control Studies, Immunology, biology.protein, Biological Markers, business, Dimerization, Settore MED/15 - Malattie del Sangue, Biomarkers, circulatory and respiratory physiology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18c0143d4570adc6785b7038d9e83094Test
http://hdl.handle.net/2434/46213Test

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Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD

المصدر: Castaman, G, Lethagen, S, Federici, A B, Tosetto, A, Goodeve, A, Budde, U, Batlle, J, Meyer, D, Mazurier, C, Fressinaud, E, Goudemand, J, Eikenboom, J, Schneppenheim, R, Ingerslev, J, Vorlova, Z, Habart, D, Holmberg, L, Pasi, J, Hill, F, Peake, I & Rodeghiero, F 2008, ' Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD ', Blood, vol. 111, no. 7, pp. 3531-9 . https://doi.org/10.1182/blood-2007-08-109231Test

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Genotype, Immunology, medicine.disease_cause, Biochemistry, Hemostatics, Basal (phylogenetics), Genotype-phenotype distinction, Internal medicine, hemic and lymphatic diseases, von Willebrand Disease, Von Willebrand disease, Medicine, Humans, Deamino Arginine Vasopressin, Prospective Studies, Desmopressin, Prospective cohort study, Child, Aged, Mutation, Hematology, Factor VIII, business.industry, Cell Biology, Middle Aged, medicine.disease, Protein Structure, Tertiary, von Willebrand Diseases, Endocrinology, Ristocetin, Female, Blood Coagulation Tests, business, medicine.drug, Protein C

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a67a9b0f463beffe54279074bfa2bcb7Test
https://pure.au.dk/portal/da/publications/response-to-desmopressin-is-influenced-by-the-genotype-and-phenotype-in-type-1-von-willebrand-disease-vwd-results-from-the-european-study-mcmdm1vwdTest(1c177c90-0328-11de-a987-000ea68e967b).html

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