المؤلفون: F. Bernardi, A. Dolce, M. Pinotti, A. D. Shapiro, E. Santagostino, A. Batorova, M. Lapecorella, J. F. Schved, J. Ingerslev, G. Mariani, International Factor VII Deficiency Study Group, F. Peyvandi

المساهمون: F. Bernardi, A. Dolce, M. Pinotti, A.D. Shapiro, E. Santagostino, F. Peyvandi, A. Batorova, M. Lapecorella, J.F. Schved, J. Ingerslev, G. Mariani, International Factor VII Deficiency Study Group

مصطلحات موضوعية: Settore MED/09 - Medicina Interna

Relation: info:eu-repo/semantics/altIdentifier/pmid/19245420; info:eu-repo/semantics/altIdentifier/wos/WOS:000265410300008; volume:7; issue:5; firstpage:774; lastpage:779; journal:JOURNAL OF THROMBOSIS AND HAEMOSTASIS; http://hdl.handle.net/2434/59087; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-65349161613

الاتاحة: http://hdl.handle.net/2434/59087
https://doi.org/10.1111/j.1538-7836.2009.03329.x

المؤلفون: Mariani, G, Herrmann, Fh, Schulman, S, Batorova, A, Wulff, K, Etro, Daniela, Dolce, A, Auerswald, G, Astermark, J, Schved, Jf, Ingerslev, J, Bernardi, Francesco, INTERNATIONAL FACTOR VII DEFICIENCY STUDY GROUP

المصدر: Journal of Thrombosis and Haemostasis. 1:2153-2158

مصطلحات موضوعية: Adult, Male, Heterozygote, medicine.medical_specialty, Pathology, Time Factors, Adolescent, Factor VII Deficiency, Gene mutation, Compound heterozygosity, Thrombophilia, Gastroenterology, Internal medicine, medicine, Humans, Aged, Venous Thrombosis, Disseminated intravascular coagulation, biology, business.industry, Homozygote, Factor V, Thrombosis, Hematology, Congenital FVII deficiency, Replacement therapy, Surgery, Disseminated Intravascular Coagulation, Middle Aged, medicine.disease, Zygosity, Venous thrombosis, Phenotype, Databases as Topic, Factor Xa, Mutation, biology.protein, Female, Prothrombin, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eccebf64b5f9bc3efb5b87b58af29a8
https://doi.org/10.1046/j.1538-7836.2003.00395.x

المؤلفون: G. Mariani, F. H. Herrmann, A. Dolce, A. Batorova, D. Etro, K. Wulff, J. F. Schved, G. Auerswald, J. Ingerslev, F. Bernardi, International factor VII Deficiency Study Group, F. Peyvandi

المساهمون: G. Mariani, F.H. Herrmann, A. Dolce, A. Batorova, D. Etro, F. Peyvandi, K. Wulff, J.F. Schved, G. Auerswald, J. Ingerslev, F. Bernardi, International factor VII Deficiency Study Group

مصطلحات موضوعية: Bleeding disorder, Bleeding symptom, FVII deficiency, Gene mutation, Polymorphisms, Settore MED/09 - Medicina Interna

Relation: info:eu-repo/semantics/altIdentifier/pmid/15735798; info:eu-repo/semantics/altIdentifier/wos/WOS:000227808200014; volume:93; issue:3; firstpage:481; lastpage:487; numberofpages:7; journal:THROMBOSIS AND HAEMOSTASIS; http://hdl.handle.net/2434/16888; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-20144382370

الاتاحة: http://hdl.handle.net/2434/16888
https://doi.org/10.1160/TH04-10-0650

المؤلفون: Mariani, G, Herrmann, Fh, Dolce, A, Batorova, A, Etro, Daniela, Peyvandi, F, Wulff, K, Schved, Jf, Auerswald, G, Ingerslev, J, Bernardi, Francesco, INTERNATIONAL FACTOR VII DEFICIENCY STUDY GROUP

المصدر: Mariani, G, Hermann, FH, Docle, A, Batorova, A, Etro, D, Peynandi, F, Wulff, K, Schved, JF, Auerswald, G, Ingerslev, J & Bernardi, F 2005, ' Clinical phenotypes and factor VII genotype in congenital factor VII deficiency ', Thromb. Haemost., vol. 93, pp. 481-487 .

مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pathology, Adolescent, Genotype, Factor VII Deficiency, Hemorrhage, Gene mutation, Gastroenterology, Asymptomatic, chemistry.chemical_compound, Sex Factors, Polymorphism (computer science), Interquartile range, Internal medicine, medicine, Coagulopathy, Humans, Expressivity (genetics), Child, factor VII deficiency, clinical phenotype, factor VII genotype, Aged, Aged, 80 and over, Factor VII, business.industry, Genetic Variation, Infant, Hematology, Middle Aged, medicine.disease, Phenotype, chemistry, Child, Preschool, Factor Xa, Mutation, Female, medicine.symptom, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c8dd1230dc586ecafa7e681568701f7
https://pubmed.ncbi.nlm.nih.gov/15735798