المؤلفون: O.D. Shulga, E.A. Popko, A.S. Chabanova, O.G. Kotsiuba, Q. Hussain

المصدر: Medičnì Perspektivi, Vol 29, Iss 2, Pp 229-236 (2024)

مصطلحات موضوعية: funicular myelosis, b12 deficiency anemia, thrombophilia, folate cycle, homocysteine, methylenetetrahydrofolate reductase gene mutation, Medicine

وصف الملف: electronic resource

Relation: https://journals.uran.ua/index.php/2307-0404/article/view/307773; https://doaj.org/toc/2307-0404

URL الوصول: https://doaj.org/article/eea3702a376a410994bf377e7424556c

المؤلفون: Vraynko, Elif, Zafirovska, Biljana, Dimitrovska, Biljana, Bede, I., Tomeski, S., Kostova, Nela, Otljanska, Magdalena

المصدر: South East European Journal of Cardiology; Vol. 4 No. 1 (2023): SEE J Cardiol; 36-39 ; 1857-9361

مصطلحات موضوعية: Factor V Leiden mutation, Methylenetetrahydrofolate reductase gene mutation, Myocardial infarction, COVID-19 infection

وصف الملف: application/pdf

Relation: https://seejca.eu/index.php/seejca/article/view/6047/5532; https://seejca.eu/index.php/seejca/article/view/6047

الاتاحة: https://seejca.eu/index.php/seejca/article/view/6047
https://doi.org/10.3889/seejca.2023.6047

المؤلفون: Gülizar Demirok, Mehmet Fatih Kocamaz, Yasemin Topalak, Ahmet Sengün, Berati Hasanreisoglu

المصدر: Indian Journal of Ophthalmology, Vol 63, Iss 12, Pp 921-924 (2015)

مصطلحات موضوعية: A1298C mutation, central retinal artery occlusion, central retinal vein occlusion, methylenetetrahydrofolate reductase gene mutation, papillophlebitis, Ophthalmology, RE1-994

وصف الملف: electronic resource

Relation: http://www.ijo.in/article.asp?issn=0301-4738;year=2015;volume=63;issue=12;spage=921;epage=924;aulast=Demirok; https://doaj.org/toc/0301-4738; https://doaj.org/toc/1998-3689

URL الوصول: https://doaj.org/article/79ff349879a544518fba304707d35715

المؤلفون: Murat Albayrak, Simten Dagdas, Gülsüm Özet, Funda Ceran, Mesude Yilmaz, Osman Yokuş, Ozlem Sahin Balcik

المصدر: Volume: 1, Issue: 3 168-172
Journal of Clinical and Experimental Investigations
Journal of Clinical and Experimental Investigations, Vol 1, Iss 3, Pp 168-172 (2010)

مصطلحات موضوعية: medicine.medical_specialty, protein C deficiency, anticardiolipin antibody, Thrombophilia, Protein C deficiency, recurrent abortion, medicine, Recurrent abortion, actived protein-C resistance, prothrombin G20210A gene mutation, thrombophilia, clinical thrombophilia,recurrent abortion,factor V Leiden gene mutation,actived protein-C resistance,methylenetetrahydrofolate reductase gene mutation,prothrombin G20210A gene mutation,protein C deficiency,protein S deficiency, anti, Protein S deficiency, protein S deficiency, Gynecology, Lupus anticoagulant, trombofili, klinik trombofili,tekrarlayan abortus,factör V Leiden gene mutasyonu,aktive protein-C direnci,metilentetrahidrofolat redüktaz gen mutasyonu,protrombin G20210A gen mutasyonu,protein C eksikliği,protein S eksikliği,antikardiolipin a, business.industry, medicine.disease, methylenetetrahydrofolate reductase gene mutation, lupus anticoagulant, factor V Leiden gene mutation, clinical thrombophilia, Medicine, Anticardiolipin antibodies, business

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6996c52e63338eecbff7c0f204a9a26c
https://dergipark.org.tr/tr/pub/jcei/issue/9903/122571

المؤلفون: Yaliwal, Laxmi V., Desai, Rathnamala M.

مصطلحات موضوعية: neural tube defects, methylenetetrahydrofolate reductase gene mutation, Folate

Relation: http://www.bioline.org.br/abstract?id=hg12024; http://www.bioline.org.br/hg; http://www.ijhg.com/; http://hdl.handle.net/1807/50030

الاتاحة: http://hdl.handle.net/1807/50030
http://www.bioline.org.br/abstract?id=hg12024
http://www.bioline.org.br/hg
http://www.ijhg.com/

المؤلفون: Pinto, Raquel Borges

Thesis Advisors: Silveira, Themis Reverbel da

المصدر: Biblioteca Digital de Teses e Dissertações da UFRGSUniversidade Federal do Rio Grande do SulUFRGS.

مصطلحات موضوعية: Trombose da veia porta, Hipertensão portal, Protrombina, Transtornos da coagulação sangüínea, Criança, Adolescente, Portal vein thrombosis, Portal hypertension, Cirrhosis, Coagulation inhibitors proteins, Protein C, Protein S, Antithrombin, Factor V Leiden, G20210A prothrombin gene mutation, C677T methylenetetrahydrofolate reductase gene mutation

وصف الملف: application/pdf

الاتاحة: http://hdl.handle.net/10183/2538

المؤلفون: Laxmi V Yaliwal, Rathnamala M Desai

المصدر: Indian Journal of Human Genetics

مصطلحات موضوعية: Genetics, Folate, congenital, hereditary, and neonatal diseases and abnormalities, Mutation, Pregnancy, Transition (genetics), biology, business.industry, Neural tube, Case Report, Gene mutation, medicine.disease_cause, medicine.disease, digestive system diseases, methylenetetrahydrofolate reductase gene mutation, medicine.anatomical_structure, neural tube defects, Methylenetetrahydrofolate reductase, Anencephaly, biology.protein, medicine, Risk factor, business, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78e46b3b022d7e83cc58441f3f5eeb11
https://doi.org/10.4103/0971-6866.96680