Репозиторий Университета

Год публикации: Все года 2018 2019 2020

Название	Дата публикации	Коллектив авторов	Журнал	DOI	Индекс цитирования	Ссылка на источник
From Schönlein-Henoch purpura to IgA-vasculitis: Pathogenetic aspects of the disease DefectiveIgAglycosylation Endotoxemia Hemorrhagicvasculitis IgA-nephropathy IgA-vasculitis Schönlein-Henochpurpura Shwartzmanreaction Systemicvasculitides	01.01.2018	Guliaev S. Strizhakov L. Moiseev S. Fomin V.	Terapevticheskii Arkhiv		0	Ссылка © 2018 Media Sphera Publishing Group.All Rights Reserved. Investigation's history and nomenclature's evolution of the IgA-vasculitis are presented in the article. Pathogenesis of the renal and skin damages is discussed in details, particularly abnormalities of the IgA-immunity and systemic endotoxemia. Relevant world's literature is cited. Читать тезис
CLIPPERS syndrome CLIPPERSsyndrome Glioma Lymphocyticinfiltration Lymphoma Magneticresonanceimaging Multiplesclerosis Ponsvarolii Vasculitides	01.01.2018	Schmidt T. Pronin I. Kazantsev K. Voskresenskaya O. Damulin I. Aleksandrov A. Yakhno N.	Nevrologiya, Neiropsikhiatriya, Psikhosomatika		0	Ссылка © 2018 Ima-Press Publishing House. All rights reservbed. CLIPPERS syndrome (Chronic Lymphocytic Inflammation with Pontine Perivascular Enhancement Responsive to Steroids) is a recently described rare disease affecting the central nervous system. It is characterized by subacute development of symptoms of lesions predominantly in the brain stem and cerebellum, by specific magnetic resonance imaging (MRI) changes, perivascular lymphocytic infiltration in the brain substance and a good response to glucocorticoid (GC) therapy. The paper describes CLIPPERS syndrome in a patient who has been followed up in a clinic for 10 years. During this period, different variants of clinical diagnosis have been considered. The final diagnosis was made only when comparing the clinical course and manifestations of the disease, MRI data, as well as the reaction to GC therapy and its discontinuation. Literature data and diagnostic criteria of this disease are presented. Читать тезис

Репозиторий Университета

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