المؤلفون: John M. Cunningham, Yunyu Spence, Arnulfo Jaquilmac Pie, Susan Sleep, Savita Rangarajan, Andrew M. Davidoff, Keith Smith, Cecilia Rosales, Chris Harrington, David C. Linch, Catherine Y.C. Ng, Edward G. D. Tuddenham, Pratima Chowdary, Christopher L. Morton, Mark A. Kay, Etiena Basner-Tschakarjan, Jenny McIntosh, Bertil Glader, Amit C. Nathwani, John T. Gray, Junfang Zhou, Ulrike M. Reiss, John Pasi, James A. Allay, Pradip Rustagi, Federico Mingozzi, James O'Beirne, Arthur W. Nienhuis, John Coleman, Anne Riddell, Deokumar Srivastava, Katherine A. High

مصطلحات موضوعية: medicine.medical_specialty, business.industry, Transgene, Genetic enhancement, Genetic Vectors, General Medicine, Genetic Therapy, Dependovirus, Asymptomatic, Gastroenterology, Hemophilia B, Virus, Article, Viral vector, Alipogene tiparvovec, Factor IX, Internal medicine, Immunology, medicine, Humans, Vector (molecular biology), medicine.symptom, business, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39e983fb3d15006128dc0ba1780e55a7Test
https://europepmc.org/articles/PMC3265081Test/

المؤلفون: Jane Anderson, John V Anderson, Nicholas Harry Bunce, Andrew Kenneth Burroughs, A John Camm, Anthony W Clare, Michael L Clark, Charles Richard Astley Clarke, Juliet Compston, Annie Cushing, Andrew Davies, Len Doyal, Marinos Elia, Peter D Fairclough, Roger Finch, Anthony J Frew, Edwin AM Gale, Christopher J Gallagher, Alasdair MacIntosh Geddes, Meredydd Harries, Charles Hinds, Stephen T Holgate, Trevor A Howlett, Raymond Kruse Iles, William L Irving, Miriam J Johnson, Miles J Levy, T Andrew Lister, Christopher Niels Mallinson, Peter J Moss, Michael F Murphy, Donncha O’Gradaigh, David Paige, K John Pasi, Mark Peakman, Anisur Rahman, Sir Michael Rawlins, Michael Shipley, DBA Silk, Allister Vale, Francis Vaz, Seema Verma, James Stephen Wainscoat, David Watson, David Westaby, Peter D White, Muhammad Magdi Yaqoob

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::42b7509e30c0417d79f80681859131ddTest
https://doi.org/10.1016/b978-0-7020-2993-6.00003-1Test

المؤلفون: P. De Moerloose, Cédric Hermans, Pål Andre Holme, P Kotsi, John Pasi, M. von Depka, Jan Astermark, A Rocino, Christopher A. Ludlam, Claude Negrier, Jerzy Windyga, Robert Klamroth

المصدر: Haemophilia, Vol. 15, No 1 (2009) pp. 337-344

مصطلحات موضوعية: Curriculum, MEDLINE, Blood Coagulation Disorders, Inherited, Hemostatic Techniques/*standards, medicine, Humans, Genetics (clinical), ddc:616, Medical education, business.industry, Hemostatic Techniques, Thrombosis, General Medicine, Hematology, Hematology/*education/standards, Blood Coagulation Disorders, Inherited/therapy, medicine.disease, Thrombosis/*therapy, Europe, Education, Medical, Graduate/*methods, Education, Medical, Graduate, Clinical Competence, Clinical competence, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b3c5bfb85a968944b86902cdb2bc565Test
https://archive-ouverte.unige.ch/unige:19650Test

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-2007-09-110940Test

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/

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.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

المؤلفون: Barbara A. Konkle, Dorthe Viuff, John Pasi, Liselotte S. Ebbesen, Guy Young, Jørgen Ingerslev, Claude Negrier, Jorge Di Paola

المصدر: Young, G, Ebbesen, L S, Viuff, D, Di Paola, J, Konkle, B A, Negrier, C, Pasi, J & Ingerslev, J 2008, ' Evaluation of thromboelastography for monitoring recombinant activated factor VII ex vivo in haemophilia A and B patients with inhibitors: a multicentre trial ', Blood Coagulation and Fibrinolysis, vol. 19, no. 4, pp. 276-82 . https://doi.org/10.1097/MBC.0b013e3283001cdcTest

مصطلحات موضوعية: Adult, Male, Haemophilia A, Factor VIIa, Pharmacology, Haemophilia, Hemophilia A, Hemophilia B, law.invention, Tissue factor, law, Predictive Value of Tests, Medicine, Humans, Blood Coagulation, Whole blood, Aged, medicine.diagnostic_test, Dose-Response Relationship, Drug, business.industry, Hematology, General Medicine, Assay sensitivity, Middle Aged, medicine.disease, Thromboelastography, Blood Coagulation Factors, Recombinant Proteins, Thrombelastography, Immunology, Recombinant DNA, business, Ex vivo

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::299a4199c0d6f26502dfaeeff10dc69aTest
https://pure.au.dk/portal/da/publications/evaluation-of-thromboelastography-for-monitoring-recombinant-activated-factor-vii-ex-vivo-in-haemophilia-a-and-b-patients-with-inhibitors-a-multicentre-trialTest(cb8dee10-0310-11de-a987-000ea68e967b).html

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-2007-08-109231Test

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

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d572a443dc942881bf6bde9ebe2d1608Test
https://pubmed.ncbi.nlm.nih.gov/16985174Test

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1ebab7ae562f41dc95591ab4c9230a4Test
https://pubmed.ncbi.nlm.nih.gov/16634746Test

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

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd9b5ed5726c420fbbd7daf47392b2e6Test
https://pubmed.ncbi.nlm.nih.gov/16634745Test