المؤلفون: Tatiana A. Gaydina, Olga I. Patsap, Raisa T. Tairova

المصدر: Vestnik Dermatologii i Venerologii, Vol 98, Iss 4, Pp 85-94 (2022)

مصطلحات موضوعية: annular granuloma, annular elastolytic giant cell granuloma, ehlers–danlos syndrome, dermatoscopy, microangiopathy, col3a1 gene defect, hereditary connective tissue diseases, clinical case, Dermatology, RL1-803

وصف الملف: electronic resource

Relation: https://vestnikdv.ru/jour/article/viewFile/1338/pdf; https://doaj.org/toc/0042-4609; https://doaj.org/toc/2313-6294

URL الوصول: https://doaj.org/article/a4cbac7e98054587a5c76e2cd1b72392

المؤلفون: Tingting Wan, Jinyan Ye, Peiliang Wu, Mengshi Cheng, Baihong Jiang, Hailong Wang, Jianmin Li, Jun Ma, Liangxing Wang, Xiaoying Huang

المصدر: BMC Pulmonary Medicine, Vol 20, Iss 1, Pp 1-7 (2020)

مصطلحات موضوعية: Vascular Ehlers-Danlos syndrome, Pneumothorax, Intrapulmonary lesions, COL3A1 gene, Collagen type III, Diseases of the respiratory system, RC705-779

وصف الملف: electronic resource

Relation: http://link.springer.com/article/10.1186/s12890-020-1164-4; https://doaj.org/toc/1471-2466

URL الوصول: https://doaj.org/article/a798eea86be24c858aecb0a3857c6184

المؤلفون: Caroline Henrard, Hendrica Belge, Sophie Fastré, Silvia Di Monaco, Nicole Revencu, Frank Hammer, Agnès Pasquet, Alexandre Persu

المصدر: Blood Pressure, Vol 28, Iss 2, Pp 139-143 (2019)

مصطلحات موضوعية: cervical artery dissection, ehlers–danlos syndrome, fibromuscular dysplasia, carotid-cavernous fistula, col3a1 gene, Diseases of the circulatory (Cardiovascular) system, RC666-701

وصف الملف: electronic resource

Relation: https://doaj.org/toc/0803-7051; https://doaj.org/toc/1651-1999

URL الوصول: https://doaj.org/article/7379b015a6bd45b48a2c1dfbe0a43b36

المؤلفون: Wan, Tingting, Ye, Jinyan, Wu, Peiliang, Cheng, Mengshi, Jiang, Baihong, Wang, Hailong, Li, Jianmin, Ma, Jun, Wang, Liangxing^Aff1, Huang, Xiaoying^Aff1

المصدر: BMC Pulmonary Medicine. 20(1)

المؤلفون: Huljev Frković, Sanda, Slišković, Ana Marija, Toivonen, Mia, Crkvenac Gregorek, Andrea, Šutalo, Ana, Vrkić Kirhmajer, Majda

المصدر: Croatian Medical Journal. 63:394-398

مصطلحات موضوعية: Vascular Ehlers-Danlos Syndrome, celiprolol, COL3A1 gene, General Medicine

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67c52afffed016f236cd97b3066b78cc
https://doi.org/10.3325/cmj.2022.63.394

المؤلفون: Maria V. Gubanova, Larisa A. Dobrynina, Lyudmila A. Kalashnikova

المصدر: Анналы клинической и экспериментальной неврологии, Vol 10, Iss 4, Pp 45-51 (2017)

مصطلحات موضوعية: ehlers–danlos syndrome type iv, vascular type, col3a1 gene, mutation, dissection, aneurysm, Neurosciences. Biological psychiatry. Neuropsychiatry, RC321-571

وصف الملف: electronic resource

Relation: https://annaly-nevrologii.com/journal/pathID/article/viewFile/20/121; https://doaj.org/toc/2075-5473; https://doaj.org/toc/2409-2533

URL الوصول: https://doaj.org/article/a6cd5228fb4043d2a86c960c8fe79559

المؤلفون: Malfait, Fransiska^Aff3, De Paepe, Anne^Aff3

المساهمون: Lambris, John D., Series editor^Aff1, Halper, Jaroslava, editor^Aff2

المصدر: Progress in Heritable Soft Connective Tissue Diseases. 802:129-143

المؤلفون: А. N. Semyachkina, E. А. Nikolaeva, I. S. Dantsev, L. P. Melikyan, M. S. Pavlova

المصدر: Rossijskij Vestnik Perinatologii i Pediatrii, Vol 65, Iss 6, Pp 84-90 (2021)

مصطلحات موضوعية: Pathology, medicine.medical_specialty, genetic structures, Col3a1 gene, Disease, Pediatrics, behavioral disciplines and activities, Group A, col3a1 gene, RJ1-570, children, vascular type, medicine.artery, mutation p.gly798_pro815del, medicine, rupture of vessel walls, Renal artery, Aorta, ehlers–danlos syndrome, business.industry, Mortality rate, Hollow viscera, medicine.disease, nervous system, Ehlers–Danlos syndrome, diagnostic criteria, Pediatrics, Perinatology and Child Health, business, psychological phenomena and processes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2199c7a5ac1ee9cb636881bcc26d1e1
https://doi.org/10.21508/1027-4065-2020-65-6-84-90

المؤلفون: Debette, Stéphanie^{Aff1, Aff2}

المساهمون: Sharma, Pankaj, editor^AffID1, Meschia, James F, editor^AffID2

المصدر: Stroke Genetics. :207-221

Degree: M.D., Ph.D.

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