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1دورية أكاديمية
المؤلفون: Odgerel Tsogbadrakh, Injinaash Ogoosambuu, Layala Jukhai, Munkhhbaatar Davaasumberel, Khatanbaatar Alexandr
المصدر: Central Asian Journal of Medical Sciences, Vol 6, Iss 1, Pp 379-383 (2020)
مصطلحات موضوعية: hereditary hemorrhagic telangiectasia, arteriovenous malformations, epistaxis, iron deficiency, acvrl1 gene mutation, Medicine, Medicine (General), R5-920
وصف الملف: electronic resource
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المؤلفون: Chen Zhang, Chunmei Piao, Xinyu Zhang, Hongsheng Zhang, Hong Gu, Qiangqiang Li
المصدر: Pulmonary Circulation
مصطلحات موضوعية: Pulmonary and Respiratory Medicine, medicine.medical_specialty, Poor prognosis, Lung, Vascular disease, business.industry, Incidence (epidemiology), ACVRL1, Gene mutation, medicine.disease, Pulmonary hypertension, Gastroenterology, ACVRL1 gene, medicine.anatomical_structure, Internal medicine, pulmonary hypertension, medicine, Original Research Article, gene mutation, business
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3دورية أكاديمية
المؤلفون: Du, Juan, Zhu, Yan, Zhang, Yu-Lin, Li, Sha, Huang, Jing, Luo, Xiao-Hua, Liu, Lin
المصدر: Journal of Thrombosis and Thrombolysis: A Journal for Translation, Application and Therapeutics in Thrombosis and Vascular Science. November 2015 40(4):515-519
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4دورية أكاديمية
لا يتم عرض هذه النتيجة على الضيوف.
تسجيل الدخول للوصول الكامل. -
5
المؤلفون: Ahmet Muzaffer Demir, Hakan Gurkan, Nihan Alkis, Mehmet Baysal
المصدر: Turkish Journal of Hematology.
مصطلحات موضوعية: medicine.medical_specialty, Cirrhosis, business.industry, Anemia, Internal medicine, medicine, Hematology, medicine.symptom, medicine.disease, business, Telangiectasia, Gastroenterology, ACVRL1 gene
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6
المؤلفون: O J Grøtta, C Hammarström, Eduard Baco, L F Qvigstad
المصدر: Scandinavian Journal of Urology. 54:449-451
مصطلحات موضوعية: medicine.medical_specialty, business.industry, Urology, 030232 urology & nephrology, Hemorrhage, Disease, 030204 cardiovascular system & hematology, Dermatology, ACVRL1 gene, Rendu-Osler-Weber disease, 03 medical and health sciences, 0302 clinical medicine, medicine.anatomical_structure, Nephrology, Mutation (genetic algorithm), otorhinolaryngologic diseases, medicine, Humans, Kidney Pelvis, Telangiectasia, Hereditary Hemorrhagic, Family history, Genetic diagnosis, business, Renal pelvis, Hereditary haemorrhagic telangiectasia
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7
المؤلفون: Caterina De Luca, Jacques Jani, Dominique A. Badr, Teresa Cos Sanchez, Valérie Segers, Kathelijn Keymolen, Elisa Bevilacqua, Mieke Cannie
المساهمون: Radiology, Supporting clinical sciences, Clinical sciences, Medical Genetics
مصطلحات موضوعية: medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, ACVRL1 gene, business.industry, Mucocutaneous zone, vein of Galen, Autosomal dominant trait, Arteriovenous malformation, Prenatal diagnosis, Telangiectases, Gene mutation, medicine.disease, Dermatology, hemic and lymphatic diseases, Prenatal Diagnosis, Genetics, medicine, otorhinolaryngologic diseases, hereditary hemorrhagic telangiectasia, Family history, medicine.symptom, Telangiectasia, business, Genetics (clinical)
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65ebd412f291f87f8ed80a99cd9a086a
https://doi.org/10.1002/ajmg.a.61535 -
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المؤلفون: Ana Protzel, Ada Chávez-Gil, María Luisa Guevara-Fujita, Luis Venegas-Tresierra, Milagros M. Dueñas-Roque, Alexis Murillo, Verónica Ángeles-Villalba, Alejandro Zevallos-Morales, Ricardo Fujita, Miguel Guevara-Cruz
المصدر: Repositorio Académico USMP
Universidad San Martín de Porres-USMP
USMP-Institucional
Universidad de San Martín de Porres
instacron:USMP
Genetics and Molecular Biology
Genetics and Molecular Biology, Volume: 43, Issue: 1, Article number: e20190126, Published: 27 FEB 2020
Genetics and Molecular Biology, Vol 43, Iss 1 (2020)مصطلحات موضوعية: 0106 biological sciences, 0301 basic medicine, Telangiectasia hemorrágica hereditaria, QH426-470, Biology, 01 natural sciences, 03 medical and health sciences, Exon, Perú, Genetics, medicine, Missense mutation, Normal protein, Telangiectasia, Molecular Biology, Gene, Hereditary Hemorrhagic Telangiectasia, Mutación, ACVRL1 gene, ENG, 030104 developmental biology, Human and Medical Genetics, Mutation (genetic algorithm), Familia, medicine.symptom, Osler-Weber-Rendu disease, Novel mutation, 010606 plant biology & botany
وصف الملف: text/html
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::244c4c541935423971b4c0a6a88ff719
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9
المؤلفون: Ahmet Muzaffer Demir, Mehmet Baysal, Ufuk Demirci, Selma Demir, Elif Gülsüm Ümit, Volkan Baş, Sedanur Karaman Gulsaran, Hakki Onur Kirkizlar, Hakan Gurkan
المصدر: Balkan Medical Journal.
مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, Bleeding episodes, Bevacizumab, business.industry, ACVRL1, General Medicine, Gastroenterology, ACVRL1 gene, Thalidomide, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, 030220 oncology & carcinogenesis, Internal medicine, Medicine, medicine.symptom, business, Telangiectasia, Genetic diagnosis, Gene, medicine.drug
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::9fd11b3f2297ea0e124ceadc2b3aa835
https://doi.org/10.4274/balkanmedj.galenos.2019.2019.7.2 -
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المؤلفون: Munenari Itoh, Akihiko Asahina, Daisuke Sawamura, Eijiro Akasaka, Hajime Nakano, Hidemi Nakagawa, Aya Yaginuma
المصدر: The Journal of Dermatology. 46:e22-e24
مصطلحات موضوعية: medicine.diagnostic_test, business.industry, Magnetic resonance imaging, Dermatology, General Medicine, Activin receptor, ACVRL1 gene, DNA Mutational Analysis, Mutation (genetic algorithm), Cancer research, medicine, medicine.symptom, Skin pathology, business, Telangiectasia, Novel mutation