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المؤلفون: Jenny Goudemand, Ian R. Peake, John Pasi, Augusto B. Federici, Javier Batlle, Frank Hill, U. Budde, Claudine Mazurier, Jeroen Eikenboom, Reinhard Schneppenheim, David Habart, Anne Goodeve, K. Bertoncello, Zdena Vorlova, Dominique Meyer, F. Rodeghiero, Jørgen Ingerslev, Giancarlo Castaman, M. Bernardi, Stefan Lethagen, Alberto Tosetto, Lars Holmberg
المصدر: Journal of Thrombosis and Haemostasis. 5:715-721
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Adolescent, Ristocetin cofactor activity, Gastroenterology, Cohort Studies, Sex Factors, Von Willebrand factor, hemic and lymphatic diseases, ABO blood group system, Internal medicine, von Willebrand Factor, Von Willebrand disease, Humans, Medicine, Child, Aged, Aged, 80 and over, biology, business.industry, Age Factors, Infant, Hematology, Middle Aged, medicine.disease, Europe, von Willebrand Diseases, Child, Preschool, Immunology, cardiovascular system, biology.protein, Female, business, circulatory and respiratory physiology
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المؤلفون: Jenny Goudemand, Robert R. Montgomery, Anne Goodeve, John Pasi, David Habart, Claudine Mazurier, Sandra L. Haberichter, Javier Batlle, Giancarlo Castaman, Frank Hill, Francesco Rodeghiero, Lars Holmberg, Dominique Meyer, Zdena Vorlova, Jørgen Ingerslev, Ulrich Budde, Stefan Lethagen, Ian R. Peake, Augusto B. Federici, Jeroen Eikenboom, Reinhard Schneppenheim
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-2007-09-110940
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
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2da860dbc846a5d06939c1c9bc086dc2
https://europepmc.org/articles/PMC2384129/ -
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المؤلفون: U. Budde, Claudine Mazurier, Javier Batlle, Lars Holmberg, Giancarlo Castaman, A Perez, Jeroen Eikenboom, Jenny Goudemand, Zdena Vorlova, E. Drewke, K. Will, Reinhard Schneppenheim, Francesco Rodeghiero, Stefan Lethagen, Anne Goodeve, David Habart, Frank Hill, John Pasi, Ian R. Peake, Augusto B. Federici, Dominique Meyer, Jørgen Ingerslev
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.x
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
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18c0143d4570adc6785b7038d9e83094
http://hdl.handle.net/2434/46213 -
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المؤلفون: Francesco Rodeghiero, Javier Batlle, Frank Hill, Anne Goodeve, Zdena Vorlova, Jenny Goudemand, Ulrich Budde, Lars Holmberg, Stefan Lethagen, Ian R. Peake, Claudine Mazurier, Giancarlo Castaman, Augusto B. Federici, Edith Fressinaud, John Pasi, David Habart, Dominique Meyer, Reinhard Schneppenheim, Jørgen Ingerslev, Alberto Tosetto, Jeroen Eikenboom
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-2007-08-109231
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
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a67a9b0f463beffe54279074bfa2bcb7
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-mcmdm1vwd(1c177c90-0328-11de-a987-000ea68e967b).html -
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المؤلفون: Ian R. Peake, Augusto B. Federici, Andrea Guilliatt, Jenny Goudemand, Francesco Rodeghiero, Lars Holmberg, Ulrich Budde, Jeroen Eikenboom, Giancarlo Castaman, Anne Goodeve, Mohammad Hashemi Soteh, Dominique Meyer, John Pasi, Luciano Baronciani, Stefan Lethagen, Jørgen Ingerslev, David Habart, Will Lester, Frank Hill, Claudine Mazurier, Reinhard Schneppenheim, Javier Batlle, Zdena Vorlova, Christer Halldén
المصدر: Blood. 109(1)
مصطلحات موضوعية: Male, DNA Mutational Analysis, Gene mutation, Biochemistry, Gastroenterology, Severity of Illness Index, Cohort Studies, Biopolymers, Gene Frequency, hemic and lymphatic diseases, Surveys and Questionnaires, Genotype, Prevalence, Missense mutation, Family history, Promoter Regions, Genetic, Blood coagulation test, biology, Hematology, Europe, von Willebrand Diseases, Phenotype, Female, Blood Coagulation Tests, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Immunology, Mutation, Missense, Hemorrhage, ABO Blood-Group System, Von Willebrand factor, Internal medicine, von Willebrand Factor, medicine, Von Willebrand disease, Humans, Point Mutation, Allele frequency, Alleles, Family Health, Factor VIII, business.industry, Cell Biology, medicine.disease, Health Surveys, Amino Acid Substitution, biology.protein, RNA Splice Sites, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d572a443dc942881bf6bde9ebe2d1608
https://pubmed.ncbi.nlm.nih.gov/16985174 -
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المؤلفون: Javier Batlle, V. Van Marion, U. Budde, F Hill, Zdena Vorlova, John Pasi, Jenny Goudemand, Jeroen Eikenboom, Reinhard Schneppenheim, Ian R. Peake, Hein Putter, Augusto B. Federici, Giancarlo Castaman, Anne Goodeve, Francesco Rodeghiero, David Habart, Lars Holmberg, Claudine Mazurier, Dominique Meyer, Jørgen Ingerslev, Stefan Lethagen
المصدر: Journal of thrombosis and haemostasis : JTH. 4(4)
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Adolescent, Genetic Linkage, Locus (genetics), Von Willebrand factor, Genetic linkage, Risk Factors, hemic and lymphatic diseases, Internal medicine, von Willebrand Factor, Von Willebrand disease, medicine, Odds Ratio, Humans, Congenital Bleeding Disorder, Child, Blood Coagulation, Aged, Genes, Dominant, Genetics, Family Health, biology, business.industry, Haplotype, Infant, Hematology, Odds ratio, Plasma levels, Middle Aged, medicine.disease, Pedigree, Europe, von Willebrand Diseases, Child, Preschool, biology.protein, Female, business, circulatory and respiratory physiology
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المؤلفون: Zdena Vorlova, David Habart, Anne Goodeve, Francesco Rodeghiero, U. Budde, Javier Batlle, Alberto Tosetto, John Pasi, Jeroen Eikenboom, Claudine Mazurier, Frank Hill, Dominique Meyer, Ian R. Peake, Edith Fressinaud, Augusto B. Federici, Lars Holmberg, Jørgen Ingerslev, Reinhard Schneppenheim, Jenny Goudemand, Stefan Lethagen, Giancarlo Castaman
المصدر: Journal of thrombosis and haemostasis : JTH. 4(4)
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Adolescent, Mucocutaneous zone, Hemorrhage, Gastroenterology, ABO Blood-Group System, Cohort Studies, chemistry.chemical_compound, Von Willebrand factor, hemic and lymphatic diseases, Internal medicine, ABO blood group system, Surveys and Questionnaires, von Willebrand Factor, Von Willebrand disease, Medicine, Humans, Ristocetin, Child, Aged, Retrospective Studies, Aged, 80 and over, Family Health, Factor VIII, biology, business.industry, Infant, Retrospective cohort study, Hematology, Middle Aged, medicine.disease, Europe, von Willebrand Diseases, Phenotype, chemistry, Child, Preschool, Cohort, Immunology, biology.protein, Female, business, Cohort study
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المؤلفون: Zdena Vorlova, Petr Dulicek, Ivana Martinkova, J Ptak, Alena Buliková, Miloslava Matyskova, David Habart
المصدر: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis. 31(1)
مصطلحات موضوعية: Adult, Aged, 80 and over, medicine.medical_specialty, Intraoperative Care, business.industry, Hematology, Factor VIIa, Recombinant coagulation factor VIIa, Middle Aged, Gastroenterology, Recombinant Proteins, Von Willebrand disease type 2A, von Willebrand Diseases, Text mining, Internal medicine, medicine, Humans, In patient, Female, business, Aged
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المؤلفون: David Habart, Zdena Vorlova
المصدر: Acta Haematologica. 110:41-42
مصطلحات موضوعية: Von Willebrand Factor Gene, Genetic Linkage, DNA Mutational Analysis, Color, Electrophoresis, Capillary, Hematology, General Medicine, Biology, medicine.disease, Molecular biology, Fluorescence, Variable number tandem repeat, Capillary electrophoresis, Evaluation Studies as Topic, Tandem Repeat Sequences, von Willebrand Factor, Coagulopathy, medicine, Humans, Gene, Fluorescent Dyes
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b326a27a93a997dea23ef2732f16837
https://doi.org/10.1159/000072414