المؤلفون: Alzahrani FM, Al Faris AA, Bashawri LA, Hassan FM, El-Masry OS, Aldossary MA, Al Sultan O, Borgio JF, Alsahli MA, Goodeve A

المصدر: International Journal of General Medicine, Vol Volume 15, Pp 5385-5394 (2022)

مصطلحات موضوعية: vwf gene, von willebrand disease, saudi arabia, Medicine (General), R5-920

وصف الملف: electronic resource

Relation: https://www.dovepress.com/phenotypic-and-genotypic-signatures-of-vwf-exon-18-in-eastern-saudi-pa-peer-reviewed-fulltext-article-IJGM; https://doaj.org/toc/1178-7074

URL الوصول: https://doaj.org/article/ac15ad39291d48d98d8c3984f3175264

المؤلفون: Junjie Fan, Jing Ling, Huifeng Zhou, Jie He, Shaoyan Hu

المصدر: Turkish Journal of Hematology, Vol 37, Iss 4, Pp 296-298 (2020)

مصطلحات موضوعية: type 2b von willebrand disease, vwf gene, thrombocytopenia, Diseases of the blood and blood-forming organs, RC633-647.5

وصف الملف: electronic resource

Relation: https://jag.journalagent.com/z4/download_fulltext.asp?pdir=tjh&un=TJH-22058; https://doaj.org/toc/1308-5263

URL الوصول: https://doaj.org/article/6341eb58c48148e4b004e5c612e1c9a4

المؤلفون: Globokar, Barbara

المساهمون: Trebušak Podkrajšek, Katarina

مصطلحات موضوعية: Von Willebrandov faktor, Von Willebrandova bolezen, Von Willebrand disease, partial unprocessed pseudogene VWF, Von Willebrand factor, genetske spremembe VWF na eksonu 28, parcialni neobdelani psevdogen VWF, genetic variants of VWF gene on eksone 28

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3505::57a999a711d4a49b2316da37bb1160f4
https://repozitorij.uni-lj.si/IzpisGradiva.php?id=146456

المؤلفون: Pruthi, Rajiv K.^Aff2, Kluge, Michelle L.^{Aff3, Aff4}, Ashrani, Aneel A.^{Aff2, Aff3, Aff5}

المساهمون: Leonard, Debra G.B., editor^Aff1

المصدر: Molecular Pathology in Clinical Practice. :203-223

Degree: M.B.B.S.
M.S., C.G.C.
M.D., M.S.

المؤلفون: Jie He, Junjie Fan, Shaoyan Hu, Jing Ling, Huifeng Zhou

المصدر: Turkish Journal of Hematology, Vol 37, Iss 4, Pp 296-298 (2020)
Turkish Journal of Hematology

مصطلحات موضوعية: medicine.medical_specialty, lcsh:Internal medicine, Genotype, DNA Mutational Analysis, thrombocytopenia, von Willebrand Disease, Type 2, Gastroenterology, Diagnosis, Differential, Internal medicine, von Willebrand Factor, medicine, Von Willebrand disease, Humans, vwf gene, Letters to the Editor, Codon, lcsh:RC31-1245, Blood Coagulation, Alleles, business.industry, lcsh:RC633-647.5, Infant, Newborn, High-Throughput Nucleotide Sequencing, Hematology, lcsh:Diseases of the blood and blood-forming organs, medicine.disease, Severe thrombocytopenia, Amino Acid Substitution, Mutation (genetic algorithm), Mutation, type 2b von willebrand disease, Female, Blood Coagulation Tests, business

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dd8697d9d824a37253a5ae9a4320912
https://tjh.com.tr/jvi.aspx?pdir=tjh&plng=eng&un=TJH-22058

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المؤلفون: Cabrera, Noelia, Casaña, Pilar, Cid, Ana Rosa, Haya, Saturnino, Moret, Andrés, Aznar, Jose Antonio

المصدر: Annals of Hematology. March 2009 88(3):245-247

المؤلفون: Eva Galletta, Viviana Daidone, Alessandra Casonato, L. Sarolo

مصطلحات موضوعية: Male, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Population, von Willebrand Disease, Type 2, 030204 cardiovascular system & hematology, von Willebrand factor, Polymorphism, Single Nucleotide, Gastroenterology, Asymptomatic, VWF gene mutation, Diagnosis, Differential, 03 medical and health sciences, 0302 clinical medicine, Von Willebrand factor, hemic and lymphatic diseases, Internal medicine, Prevalence, Von Willebrand disease, Humans, Medicine, type 2N von Willebrand disease, education, Alleles, Genetics (clinical), education.field_of_study, Factor VIII, biology, business.industry, Heterozygote advantage, General Medicine, Hematology, medicine.disease, VWF FVIII binding, cardiovascular system, biology.protein, Female, Partial Thromboplastin Time, medicine.symptom, business, Protein Binding, circulatory and respiratory physiology, 030215 immunology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7797eb1bb56ccba406312cfd0aa0cb1
http://hdl.handle.net/11577/3269760

المؤلفون: Margherita Morpurgo, Alessandra Casonato, Giovanni Barbon, Maria Grazia Cattini, Giorgia Saga, Elena Pontara, Giuseppe Zanotti, Viviana Daidone

المصدر: British Journal of Haematology. 170:564-573

مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, ADAMTS13 Protein, VWF resistance to ADAMTS13 proteolysis, Hemorrhage, Plasma protein binding, VWF gene mutation, INDEL Mutation, Von Willebrand factor, hemic and lymphatic diseases, von Willebrand Factor, Von Willebrand disease, medicine, Disintegrin, Humans, Platelet, Thrombospondin, Metalloproteinase, biology, Chemistry, Medicine (all), Hematology, medicine.disease, ADAMTS13, Molecular biology, ADAM Proteins, Immunology, biology.protein, VWF-ADAMTS13 binding, Female, Collagen, Protein Binding, circulatory and respiratory physiology

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::419723bce8358681e0fffffb243bd058
https://doi.org/10.1111/bjh.13472

المؤلفون: Berber E., Ozbil M., Brown C., Baslar Z., Caglayan S.H., Lillicrap D.

المساهمون: İstanbul Arel Üniversitesi, Berber, E., Department of Molecular Biology and Genetics, Istanbul Arel University, Istanbul, Turkey, Moleküler Biyoloji Ve Genetik Bölümü, Istanbul Arel Üniversitesi, Tepekent Büyükçekmece, Istanbul, 34357, Turkey, Ozbil, M., Department of Molecular Biology and Genetics, Istanbul Arel University, Istanbul, Turkey, Brown, C., Department of Pathology and Molecular Medicine, Queen's University, Kingston, Canada, Baslar, Z., Department of Internal Medicine, Cerrahpasa Medical Faculty, Istanbul University, Istanbul, Turkey, Caglayan, S.H., Department of Molecular Biology and Genetics, Bo?aziçi University, Istanbul, Turkey, Lillicrap, D., Department of Pathology and Molecular Medicine, Queen's University, Kingston, Canada

مصطلحات موضوعية: ComputingMilieux_MANAGEMENTOFCOMPUTINGANDINFORMATIONSYSTEMS, ComputingMethodologies_PATTERNRECOGNITION, VWF gene, Type 1 VWD, Von Willebrand disease, ComputerSystemsOrganization_COMPUTER-COMMUNICATIONNETWORKS, VWF, Weibel-Palade bodies, InformationSystems_MISCELLANEOUS

URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3002::a7a35729512f05016fd11bc4c0f82ce6
https://hdl.handle.net/20.500.12294/1975