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المؤلفون: Mehmet Karaca, Sefayet Karaca, Tomris Cesuroglu, Mehmet Bozkurt, Renato Polimanti, Nujen Colak Bozkurt, Erdal Eskioglu
المساهمون: Sağlık Bilimleri Fakültesi, Polimanti, Renato -- 0000-0003-0745-6046, Bozkurt, Mehmet -- 0000-0002-8325-5249, Science Communication, Sociale Geneeskunde, RS: CAPHRI - R4 - Health Inequities and Societal Participation
المصدر: Pharmacogenomics, 16(10), 1109-18. Future Medicine Ltd.
Pharmacogenomics, 16(10), 1109-1118. Future Medicine Ltd.
Karaca, S, Bozkurt, N C, Cesuroglu, T, Karaca, M, Bozkurt, M, Eskioglu, E & Polimanti, R 2015, ' International warfarin genotype-guided dosing algorithms in the Turkish population and their preventive effects on major and life-threatening hemorrhagic events ', Pharmacogenomics, vol. 16, no. 10, pp. 1109-18 . https://doi.org/10.2217/pgs.15.58مصطلحات موضوعية: International Normalized Ratio/methods, Male, Drug Response, Turkish population, Genotype, Turkey, Turkish, Validation Study, Hemorrhagic Disorders, Thromboembolism/drug therapy, Warfarin/administration & dosage, Therapeutic index, SDG 3 - Good Health and Well-being, Thromboembolism, Ethnicity, Genetics, medicine, Humans, heterocyclic compounds, Drug Dosage Calculations, Hemorrhagic Disorders/genetics, International Normalized Ratio, cardiovascular diseases, Dosing, Pharmacogenetics/methods, Aged, Anticoagulants/administration & dosage, Pharmacology, business.industry, Warfarin dose, Warfarin, Anticoagulants, Middle Aged, language.human_language, Pharmacogenetics, Pharmacogenetic Algorithms, language, Molecular Medicine, Female, business, Algorithm, Algorithms, medicine.drug
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المؤلفون: Marguerite Neerman-Arbez, Philippe de Moerloose
المصدر: Seminars in Thrombosis and Hemostasis, Vol. 35, No 4 (2009) pp. 356-366
مصطلحات موضوعية: Risk, medicine.medical_specialty, Genotype, Fibrinogen, Hemorrhagic Disorders, Fibrinogen/ genetics/therapeutic use, Pregnancy, Prenatal Diagnosis, medicine, Coagulopathy, Humans, ddc:576.5, Dysfibrinogenemia, Intensive care medicine, Blood coagulation test, Afibrinogenemia, business.industry, Pregnancy Complications, Hematologic, Infant, Newborn, Thrombosis, Hematology, Hypofibrinogenemia, medicine.disease, Afibrinogenemia/congenital/diagnosis/ genetics, Hemorrhagic Disorders/ genetics, Surgery, Bleeding diathesis, Phenotype, Hemostasis, Pregnancy Complications, Hematologic/therapy, Female, Blood Coagulation Tests, Cardiology and Cardiovascular Medicine, business, Thrombosis/etiology, medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be22069c443b4642019e4da977a06761
https://pubmed.ncbi.nlm.nih.gov/19598064 -
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المؤلفون: Isabelle Bouchardy, Marguerite Neerman-Arbez, Michael A. Morris, Dung Vu, Bassam Abu-Libdeh
المصدر: Blood, Vol. 101, No 9 (2003) pp. 3492-3494
مصطلحات موضوعية: Male, DNA, Complementary, Immunology, Mutant, Nonsense mutation, Molecular Sequence Data, Genes, Recessive, Consanguinity, Hemorrhagic Disorders, medicine.disease_cause, Biochemistry, Afibrinogenemia/ diagnosis/embryology/genetics, medicine, Codon/genetics, Humans, Genetic Predisposition to Disease, Hemorrhagic Disorders/genetics, Amino Acid Sequence, Allele, Codon, Arabs/ genetics, Fibrinogen alpha chain, Genetics, ddc:616, Fibrinogen/chemistry/ genetics, Mutation, Afibrinogenemia, business.industry, Infant, Newborn, Fibrinogen, DNA, Complementary/genetics, Cell Biology, Hematology, medicine.disease, Arabs, Pedigree, Abortion, Spontaneous, Fetal Diseases/ diagnosis/genetics, Fetal Diseases, Congenital afibrinogenemia, Codon, Nonsense, Amniocentesis, Female, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d2bfe9ce6602551121137e2f9255a1f
https://archive-ouverte.unige.ch/unige:8937 -
4مورد إلكتروني
المصدر: Seminars in thrombosis and hemostasis, 31 (2
مصطلحات الفهرس: Sciences bio-médicales et agricoles, Adenosine Diphosphate -- physiology, Adenosine Triphosphate -- physiology, Animals, Cell Membrane Permeability -- physiology, Chlorides -- metabolism, Exocytosis, Extracellular Fluid -- metabolism, Hematopoiesis -- physiology, Hemorrhagic Disorders -- genetics, Humans, Mice, Mice, Knockout, Multigene Family, Muscle Contraction -- physiology, Muscle, Smooth -- physiology, Phenotype, Platelet Aggregation -- drug effects, Platelet Aggregation -- physiology, Receptors, G-Protein-Coupled -- chemistry, Receptors, G-Protein-Coupled -- classification, Receptors, G-Protein-Coupled -- drug effects, Receptors, G-Protein-Coupled -- genetics, Receptors, G-Protein-Coupled -- physiology, Receptors, Purinergic P2 -- chemistry, Receptors, Purinergic P2 -- classification, Receptors, Purinergic P2 -- drug effects, Receptors, Purinergic P2 -- genetics, Receptors, Purinergic P2 -- physiology, Signal Transduction -- drug effects, Signal Transduction -- physiology, ADP, Nucleotides, P2X receptors, P2Y receptors, Platelet aggregation, info:eu-repo/semantics/article, info:ulb-repo/semantics/articlePeerReview, info:ulb-repo/semantics/openurl/article
URL:
http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/50292 http://worldcat.org/search?q=on:EQY+http://difusion-oai.ulb.ac.be/oai/request+DCG_ENTIRE_REPOSITORY+CNTCOLL