Auswahl der wissenschaftlichen Literatur zum Thema „IgA Vasculitis“
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Zeitschriftenartikel zum Thema "IgA Vasculitis"
Sugino, Hitomi, Yu Sawada und Motonobu Nakamura. „IgA Vasculitis: Etiology, Treatment, Biomarkers and Epigenetic Changes“. International Journal of Molecular Sciences 22, Nr. 14 (14.07.2021): 7538. http://dx.doi.org/10.3390/ijms22147538.
Der volle Inhalt der QuelleSotoodian, Bahman, Janet Robert, Muhammad N. Mahmood und Elaine Yacyshyn. „IgA Cutaneous Purpura Post–Renal Transplantation in a Patient With Long-Standing IgA Nephropathy“. Journal of Cutaneous Medicine and Surgery 19, Nr. 5 (15.04.2015): 498–503. http://dx.doi.org/10.1177/1203475415582135.
Der volle Inhalt der QuelleLevanon, S., V. Gotlieb, Y. Kraus, I. Novofastovski, S. Brikman, A. Fawaz, M. Aghbariyya et al. „POS0831 IgA VASCULITIS IN ADULTS, PEDIATRICS AND NON-VASCULITIC IgA NEPHROPATHY“. Annals of the Rheumatic Diseases 81, Suppl 1 (23.05.2022): 706.2–707. http://dx.doi.org/10.1136/annrheumdis-2022-eular.3368.
Der volle Inhalt der QuelleMarro, Julien, Andrew J. Chetwynd, Samuel Edwards, Rachael D. Wright und Louise Oni. „Increased Urinary IgA in Paediatric IgA Vasculitis Nephritis“. International Journal of Molecular Sciences 23, Nr. 23 (22.11.2022): 14548. http://dx.doi.org/10.3390/ijms232314548.
Der volle Inhalt der QuelleNüsken, Eva, und Lutz T. Weber. „IgA vasculitis nephritis“. Current Opinion in Pediatrics 34, Nr. 2 (07.02.2022): 209–16. http://dx.doi.org/10.1097/mop.0000000000001120.
Der volle Inhalt der QuelleOzen, Seza, und Erdal Sag. „Childhood vasculitis“. Rheumatology 59, Supplement_3 (29.04.2020): iii95—iii100. http://dx.doi.org/10.1093/rheumatology/kez599.
Der volle Inhalt der QuelleWinkler, Clay, Raymond Dobson und Michael Tranovich. „Low Back Pain and Swelling as an Atypical Presentation of IgA Vasculitis“. Clinical Practice and Cases in Emergency Medicine 4, Nr. 2 (14.04.2020): 241–43. http://dx.doi.org/10.5811/cpcem.2019.11.44574.
Der volle Inhalt der QuelleTang, Mengmeng, Xue Zhang, Xueqian Li, Lei Lei, Hejia Zhang, Chen Ling, Jie Ni, Jicheng Lv, Xiaorong Liu und Xiangmei Chen. „Serum levels of galactose-deficient IgA1 in Chinese children with IgA nephropathy, IgA vasculitis with nephritis, and IgA vasculitis“. Clinical and Experimental Nephrology 25, Nr. 1 (15.09.2020): 37–43. http://dx.doi.org/10.1007/s10157-020-01968-8.
Der volle Inhalt der QuelleHelander, S. D., F. R. De Castro und L. E. Gibson. „Henoch-Schönlein purpura: clinicopathologic correlation of cutaneous vascular IgA deposits and the relationship to leukocytoclastic vasculitis.“ Acta Dermato-Venereologica 75, Nr. 2 (01.03.1995): 125–29. http://dx.doi.org/10.2340/0001555575125129.
Der volle Inhalt der QuelleTakeuchi, Sora, Tamihiro Kawakami, Tatsuro Okano, Haruki Shida, Daigo Nakazawa, Utano Tomaru, Akihiro Ishizu und Takafumi Kadono. „Elevated Myeloperoxidase-DNA Complex Levels in Sera of Patients with IgA Vasculitis“. Pathobiology 89, Nr. 1 (23.11.2021): 23–28. http://dx.doi.org/10.1159/000519869.
Der volle Inhalt der QuelleDissertationen zum Thema "IgA Vasculitis"
Piram, Maryam. „Epidémiologie de la vascularite à IgA (purpura rhumatoïde) : incidence, étiologie“. Thesis, Université Paris-Saclay (ComUE), 2017. http://www.theses.fr/2017SACLS185.
Der volle Inhalt der QuelleHenoch-Schönlein purpura, recently renamed immunoglobulin A vasculitis (IgAV), is the most common systemic vasculitis in childhood in Western countries. The sites predominantly affected by this IgA-mediated, leukocytoclastic, small-vessel vasculitis are the skin, joints, gastrointestinal tract and kidneys. IgAV is often self-limiting, although chronic kidney disease can develop in some patients. Because the cause of IgAV is unknown, epidemiological studies are important to provide clues to understanding its etiology. The first part of this thesis, devoted to the epidemiology of IgAV, is a literature review summarizing the currently available knowledge on descriptive epidemiological aspects of IgAV and environmental and genetic risk determinants. The second part is a prospective survey describing the epidemiological characteristics of IgAV in Val de Marne, located in the southeast suburbs of Paris, France. With a 3-year study and 4-source capture–recapture analysis, we estimated the annual incidence of IgAV at 30/100,000 children (age ≤ 15 years). The few secular and geospatial variations in IgAV incidence and the observation of a seasonal pattern in IgAV incidence lend support to a role for a ubiquitous and communicable infectious trigger. The third part of the thesis addresses the concern suggested mainly by case reports of vaccination as a potential trigger of IgAV. In light of the lack of robust pharmacoepidemiological studies, we performed a case–crossover study, a variant of a traditional case–control study, to investigate the effect of vaccination on short-term risk of IgAV. The results indicated that vaccines commonly administered to children do not significantly increase the risk of IgAV in the 3 months after vaccine exposure. The results of this thesis enhance our knowledge of IgAV epidemiology and suggest that infections but not vaccines may play a role in the etiology of the disease. More epidemiological investigation is required, particularly in understudied areas and multiethnic populations, to gain insight in the burden of genetics in IgAV etiology
Pankhurst, Tanya. „Heterogeneity of injury in vasculitis : influence of anti neutrophil cytoplasm antibody IgG subclass and endothelial susceptibility“. Thesis, University of Birmingham, 2010. http://etheses.bham.ac.uk//id/eprint/718/.
Der volle Inhalt der QuelleBücher zum Thema "IgA Vasculitis"
Lai, Kar Neng, und Sydney C. W. Tang. Immunoglobulin A nephropathy. Herausgegeben von Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0066_update_001.
Der volle Inhalt der QuelleFabrizi, Fabrizio, und Patrice Cacoub. The patient with cryoglobulinaemia. Herausgegeben von Giuseppe Remuzzi. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0151.
Der volle Inhalt der QuelleLai, Kar Neng, und Sydney C. W. Tang. Immunoglobulin A nephropathy diagnosis. Herausgegeben von Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0067_update_001.
Der volle Inhalt der QuelleBuchteile zum Thema "IgA Vasculitis"
Watts, Richard A., David G. I. Scott und Chetan Mukhtyar. „IgA Vasculitis“. In Vasculitis in Clinical Practice, 127–37. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-14871-7_12.
Der volle Inhalt der QuelleFenoglio, Roberta, und Dario Roccatello. „IgA Vasculitis“. In Systemic Vasculitides: Current Status and Perspectives, 203–12. Cham: Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-40136-2_18.
Der volle Inhalt der QuelleSelvaskandan, Haresh, Chee Kay Cheung und Jonathan Barratt. „IgA Nephropathy and IgA Vasculitis“. In Primer on Nephrology, 451–65. Cham: Springer International Publishing, 2022. http://dx.doi.org/10.1007/978-3-030-76419-7_24.
Der volle Inhalt der QuelleKumar, Karunesh, Jutta Köglmeier und Keith J. Lindley. „Vasculitides Including IgA Vasculitis (Henoch–Schönlein Purpura)“. In Textbook of Pediatric Gastroenterology, Hepatology and Nutrition, 431–41. Cham: Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-80068-0_32.
Der volle Inhalt der QuelleGupta, Pallav, und Ramesh K. Gupta. „IgA Nephropathy and IgA Vasculitis (Henoch–Schonlein Purpura)“. In Pathology of Glomerular Diseases, 77–89. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-1430-0_8.
Der volle Inhalt der QuelleJennette, J. Charles. „IgA Nephropathy and IgA Vasculitis (Henoch-Schönlein Purpura)“. In Fundamentals of Renal Pathology, 69–78. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-39080-7_6.
Der volle Inhalt der QuelleShin, Jae Il. „IgA Vasculitis Nephritis (Henoch-Schönlein Purpura Nephritis)“. In Pediatric Kidney Disease, 765–82. Cham: Springer International Publishing, 2023. http://dx.doi.org/10.1007/978-3-031-11665-0_27.
Der volle Inhalt der QuelleShah, Firdosh, und Mitesh Kumar Dwivedi. „Microorganisms in Pathogenesis and Management of IgA Vasculitis and IgA Nephropathy“. In Role of Microorganisms in Pathogenesis and Management of Autoimmune Diseases, 111–25. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-19-4800-8_5.
Der volle Inhalt der QuelleWatts, Richard A. „Small vessel vasculitis“. In Oxford Textbook of Medicine, herausgegeben von Richard A. Watts, 4573–79. Oxford University Press, 2020. http://dx.doi.org/10.1093/med/9780198746690.003.0461.
Der volle Inhalt der QuelleEleftheriou, Despina, und Paul A. Brogan. „Paediatric vasculitis“. In Oxford Textbook of Rheumatology, 1141–52. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199642489.003.0136_update_001.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "IgA Vasculitis"
Thota, A., L. Ramirez, U. Naqvi, A. Mahgoub und A. Abdelrahman. „An Unusual Presentation of IgA Vasculitis“. In American Thoracic Society 2021 International Conference, May 14-19, 2021 - San Diego, CA. American Thoracic Society, 2021. http://dx.doi.org/10.1164/ajrccm-conference.2021.203.1_meetingabstracts.a2032.
Der volle Inhalt der QuelleHeld, M., A. Kozmar, M. Sestan, D. Turudic, N. Kifer, S. Srsen, A. Gagro, M. Frkovic und M. Jelusic. „POS0779 EXPLORING HMGB1, RAGE, Gd-IgA1 AND PCDH1 IN CHILDHOOD IgA VASCULITIS (IgAV)“. In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.3908.
Der volle Inhalt der QuelleKobrová, Kateřina, Lenka Minxová, Jakub Zieg, Sylva Skálová und Pavla Doležalová. „AB0998 SEVERE IGA VASCULITIS: CYCLOPHOSPHAMIDE IN QUESTION“. In Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.6731.
Der volle Inhalt der QuelleParolo Ribeiro, Mirian, Fabiana de Castro Machado, Andreas Nogueira Sales, Anna Leticia Sant' Anna Yanai, Pedro Henrique Moriguchi Cação, Caio Polimeno Guerzoni und Flavio Barboza. „JUVENILE SYSTEMIC LUPUS ERYTHEMATOSUS MIMICKING IGA VASCULITIS“. In SBR 2021 Congresso Brasileiro de Reumatologia. Sociedade Brasileira de Reumatologia, 2021. http://dx.doi.org/10.47660/cbr.2021.1982.
Der volle Inhalt der QuelleCamargo, Matheus Brunstein, Joana Mattioni Ourique, Sandra Helena Machado, Débora Kempf da Silva und Janine Margutti Lanzanova. „COMPLICATED IGA VASCULITIS IN CHILDREN CASE REPORT“. In XL Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2023. http://dx.doi.org/10.47660/cbr.2023.2450.
Der volle Inhalt der QuelleTeles, Ana Beatriz Queiroz, Julia Cruvinel Rabello, Júlia Andrade Ibiapina Parente, Thaís Fernanda Faria Moreira, Letícia Mello Matos, Beatriz Araújo Gonçalves Coelho, Larissa Dayrell Albuquerque et al. „ASSOCIATION BETWEEN PFAPA SYNDROME AND IGA VASCULITIS“. In XL Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2023. http://dx.doi.org/10.47660/cbr.2023.2368.
Der volle Inhalt der QuellePerim, Gabriela Camilotti, Carolina Tiemi Tonholo Ikedo, Rodrigo Lorenzetti Serrano, Edgard Torres dos Reis Neto, Alexandre Wagner Silva de Souza, Bruna Romagna Peterle, Lígia Magalhães Biló et al. „OVERLAP OF IGA-ASSOCIATED VASCULITIS AND PR3-ASSOCIATED ANCA VASCULITIS CASE REPORT“. In XL Congresso Brasileiro de Reumatologia. Sociedade Brasileiro de Reumatologia, 2023. http://dx.doi.org/10.47660/cbr.2023.2039.
Der volle Inhalt der QuelleGuliaev, Sergei, Leonid Strizhakov, Sergey Moiseev, Ivan Gmoshinskii und Vladimir Mazo. „SAT0229 INTESTINAL PERMEABILITY IN IGA-VASCULITIS IN ADULTS“. In Annual European Congress of Rheumatology, EULAR 2019, Madrid, 12–15 June 2019. BMJ Publishing Group Ltd and European League Against Rheumatism, 2019. http://dx.doi.org/10.1136/annrheumdis-2019-eular.3722.
Der volle Inhalt der QuelleNossent, J., W. Raymond, H. Keen, C. Inderjeeth und D. Preen. „OP0239 Pregnancy outcomes in patients with iga vasculitis“. In Annual European Congress of Rheumatology, EULAR 2018, Amsterdam, 13–16 June 2018. BMJ Publishing Group Ltd and European League Against Rheumatism, 2018. http://dx.doi.org/10.1136/annrheumdis-2018-eular.6150.
Der volle Inhalt der QuelleBatista-Liz, J. C., M. Sebastián Mora-Gil, L. Gabrie, R. Gálvez-Sánchez, M. T. Leonardo, A. Peñalba, B. Sevilla-Pérez et al. „AB1240 NLRP3 AND CASP1 GENES AS DISCRIMINATORY MARKERS BETWEEN IGA VASCULITIS AND IGA NEPHROPATHY?“ In EULAR 2024 European Congress of Rheumatology, 12-15 June. Vienna, Austria. BMJ Publishing Group Ltd and European League Against Rheumatism, 2024. http://dx.doi.org/10.1136/annrheumdis-2024-eular.4936.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "IgA Vasculitis"
Tota, Maciej, Vanessa Baron, Bouchra Derrough, Katie Musial, Andrzej Konieczny, Magdalena Krajewska, Kültigin Türkmen und Mariusz Kusztal. Secondary IgA Nephropathy without IgA vasculitis: a systematic review of case reports. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, Februar 2023. http://dx.doi.org/10.37766/inplasy2023.2.0022.
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