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Titlebook: Auto-Inflammatory Syndromes; Pathophysiology, Dia Petros Efthimiou Book 2019 Springer Nature Switzerland AG 2019 auto-inflammatory syndrome

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樓主: 搖尾乞憐
11#
發(fā)表于 2025-3-23 11:26:54 | 只看該作者
Deficiency of the Interleukin-36 Receptor Antagonist (DITRA) and Generalized Pustular Psoriasistor antagonist . locus. The mutations encode for an unstable protein with poor interaction with its receptor allowing for an unopposed effect of IL-36 that results in enhanced production of pro-inflammatory cytokines and systemic inflammation.
12#
發(fā)表于 2025-3-23 14:41:14 | 只看該作者
Book 2019ease presentations, and clinical treatment guidelines. The book is divided into two sections, adult and pediatric, with chapters focusing on individuals diseases such as systemic arthritis, hyper-IgD, pap syndrome, idiopathic recurrent pericarditis, and familial Mediterranean fever. Chapters incorpo
13#
發(fā)表于 2025-3-23 18:51:19 | 只看該作者
gy of these diseases to inform clinical decision making.Cove.This book provides an overview of auto-inflammatory syndromes, covering the underlying immune mechanisms that lead to their development, specific disease presentations, and clinical treatment guidelines. The book is divided into two sectio
14#
發(fā)表于 2025-3-23 23:10:41 | 只看該作者
Background on Combinatorial Group Theoryancestry but has been described in almost all ethnic groups, including those living in Mediterranean countries and Asia. Fever is often prolonged and can be accompanied by serositis, arthritis, a skin rash with underlying fasciitis and periorbital oedema.
15#
發(fā)表于 2025-3-24 02:29:11 | 只看該作者
16#
發(fā)表于 2025-3-24 07:10:05 | 只看該作者
17#
發(fā)表于 2025-3-24 10:55:46 | 只看該作者
The TNF Receptor-Associated Autoinflammatory Syndrome (TRAPS)ancestry but has been described in almost all ethnic groups, including those living in Mediterranean countries and Asia. Fever is often prolonged and can be accompanied by serositis, arthritis, a skin rash with underlying fasciitis and periorbital oedema.
18#
發(fā)表于 2025-3-24 17:25:01 | 只看該作者
Blau Syndromeis characterized predominantly by granulomas in the affected areas. Management remains a challenge, as Blau syndrome is rare and evidence is lacking. Here, we describe in greater detail the clinical features, pathophysiology, diagnosis, management, and prognosis of Blau syndrome.
19#
發(fā)表于 2025-3-24 20:54:42 | 只看該作者
Cryopyrin-Associated Periodic Syndromes (CAPS)ral hearing loss, renal failure, hydrocephalus, and skeletal deformities. International efforts have advanced our understanding of the disease mechanisms. Through partnerships we dramatically increased our ability to rapidly diagnose CAPS, select optimal therapies, monitor disease activity, and prevent damage accrual.
20#
發(fā)表于 2025-3-25 03:12:04 | 只看該作者
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