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inflammatory arthropathies, inflammatory arthropathies, or
inflammatory arthropathies, inflammatory arthropathies, or

... Between 10-20% of persons with HLAB 27 have ankylosing spondylitis Less than 1% of persons without HLA B27 have ankyosing spondylitis HLA B27 pos monozygotic twins have 75% concordance for AS, and dizygotic twins only 25%, indicating that other genes are important as well. ...
psoriasis associated with chronic periodontitis: a rare
psoriasis associated with chronic periodontitis: a rare

... Chronic periodontitis is a consequence of a persistent bacterial infection and chronic inflammation of the supportive tissues surrounding the tooth, including the periodontal ligament, cementum and alveolar bone. Psoriasis is a chronic, remitting and relapsing inflammatory skin disorder with a stron ...
Anti-idiotypes and Immunity
Anti-idiotypes and Immunity

... may underline autoimmune diseases, such as rheumatoid arthritis, systemic lupus erythematosus and myasthenia gravis, which stem from an immunological attack on the body itself.  These interactions, known as idiotype-anti-idiotype reactions, can be exploited to manipulate the immune system. ...
Multiple Sclerosis Disease Report
Multiple Sclerosis Disease Report

... PAS provides two types of reports—disease and organization reports. Disease Reports discuss the burden, progression, and existing treatments for a given disease; highlight priority research areas; and provide an overview of relevant activities in the commercial and nonprofit research sectors. These ...
Two models of multiple sclerosis: Experimental allergic
Two models of multiple sclerosis: Experimental allergic

... appear and quickly worsen thereafter. By 3-4 weeks, lesions may already be coalescent to occupy the majority of the anterior and lateral columns (Fig. 2). One feature which is particularly evident in SJL/J mice is the presence of large numbers of macrophages which quickly populate the spinal cord co ...
Inflammation and autoimmunity in cerebral small vessel disease
Inflammation and autoimmunity in cerebral small vessel disease

... disease, is unknown. Hypotheses include atheroma, endothelial dysfunction, blood brain barrier dysfunction, or other as yet unknown process. Inflammation is thought to play a role. The imaging features of cerebral small vessel disease combined with symptoms such as dizziness or cognitive decline poi ...
(STEC) in Germany - ECDC
(STEC) in Germany - ECDC

... virulence characteristics of the bacteria. The patient’s age and the infecting dose also play an important role. Children under the age of 5 years are at higher risk of developing clinical disease when infected, and infants are at increased risk of death from dehydration and septicaemia. While the c ...
Supplement to Supplement to Rheumatology News
Supplement to Supplement to Rheumatology News

... he pathogenesis of rheumatoid arthritis (RA) is characterized by a continuous interaction of numerous cells, molecules, and processes. A striking pathological change is the transition of the synovial lining from 2 to 3 layers of fibroblast-like synoviocytes (FLS) into several layers of macrophage-li ...
Robert Friedland - ICAD-Me
Robert Friedland - ICAD-Me

... • We have more nucleotide sequences in our gut than in our own cells • We evolved with these organisms – they are not there “by accident” • Evolutionary conserved proteins are widespread and can lead to diseases via molecular mimicry through similarity of tertiary structures • Gut bacteria may be in ...
Lesson 64. Auto Immunity and auto immune diseases
Lesson 64. Auto Immunity and auto immune diseases

... defends the body against infections and certain other diseases by identifying, attacking, and destroying germs and other foreign substances. Sometimes the immune system makes a mistake and starts attacking the body’s own tissues or organs. This is called autoimmunity. There are many autoimmune disea ...
Treating Clostridium difficile Infection with Fecal Microbiota
Treating Clostridium difficile Infection with Fecal Microbiota

... b. At least 2 episodes of severe CDI resulting in hospitalization and associated with significant morbidity. 2. Moderate CDI not responding to standard therapy (vancomycin) for at least a week. 3. Severe (and perhaps even fulminant C difficile colitis) with no response to standard therapy after 48 h ...
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... might better be described as a syndrome rather than a single disease entity—a concept that has important implications with respect to the development of effective therapeutic strategies. The clinical heterogeneity of multiple sclerosis has been recognized for many years, but it is now apparent that ...
Clustering and commonalities among autoimmune diseases
Clustering and commonalities among autoimmune diseases

... 1.1.1. Nomenclature of diseases First, there is the haphazard nomenclature of disease, calling for a latter-day Linnaeus for a logical taxonomy in the clinical arena, applicable particularly to the autoimmune diseases. Nomenclature includes the ‘traditional’ (lupus, diabetes, rheumatoid), ‘eponymous ...
Primary Immunodeficiency and Autoimmunity: Lessons From Human
Primary Immunodeficiency and Autoimmunity: Lessons From Human

... All percentages in the table are rounded up to whole numbers. The focus is on monogenic PIDs, however Omenn syndrome, ALPS, CVID and IgAD are considered as polygenic. Sp. = sporadic (i.e. has been described in some references and may represent a weak association or simply case reports). For other ab ...
Therapies for Chronic Lyme Disease Kent Holtorf, MD
Therapies for Chronic Lyme Disease Kent Holtorf, MD

... Borrelia takes 12-24 hours (35-75 times longer--can be much longer when antibiotics are introduced) • The standard 10-14 days of antibiotics needed to reliably clear most “regular” infections would require the antibiotic to be present 24 hours per day for 1½ to 3 years for the same curative potentia ...
The Lung Immunology Group Department of Biological Sciences
The Lung Immunology Group Department of Biological Sciences

... • Associated with autoimmune disease such as the inflammatory bowel disease, ulcerative colitis • Neutrophils are markedly raised, as predicted from high local levels IL-8 • Associated with immune deficiency syndromes such as TAP deficiency syndrome ...
The spectrum of CMV disease in solid organ transplant recipients
The spectrum of CMV disease in solid organ transplant recipients

... (6). Symptoms of CMV disease can range from a viral syndrome to tissue-invasive disease and severe end-organ involvement (e.g., pancreatitis, pneumonitis, hepatitis, myocarditis, nephritis, or gastrointestinal disease) (1). In addition to directly attributable morbidity, CMV may also have an immunom ...
Granulomatous Reactivation during the Course of a Leprosy
Granulomatous Reactivation during the Course of a Leprosy

... during treatment. These reactions may be either attributed to an improvement in the immunological reactivity of the patient along with the treatment, or to relapse of the disease due to the proliferation of remaining bacilli. In certain patients these two conditions may be difficult to differentiate ...
ANA – Antinuclear Antibodies
ANA – Antinuclear Antibodies

...  Interpretation: No clinically significant antinuclear antibody is detected by IFA. A negative result suggests an absence of connective tissue disease. False negatives may occur, especially in scleroderma, polymyositis/dermatomyositis, or inactive systemic lupus erythematosus. False positive ANA EI ...
Mayo Clinic Series - Fibrosing Mediastinitis
Mayo Clinic Series - Fibrosing Mediastinitis

... exceedingly rare. Only 3 of 100,000 patients with histoplasmosis developed FM during an outbreak of this fungal infection in Indianapolis between 1978 and 1979.40 The precise pathogenetic mechanisms of FM remain unknown. The exuberant mediastinal fibrosis has been attributed to chronic inflammation ...
Embryogenesis of the Kidneys and Ureters
Embryogenesis of the Kidneys and Ureters

... characterized histologically by primitive ducts and cartilage. • Most hypodysplastic kidneys have ectopic ureteral orifices. • The more ectopic the orifice, the greater the degree of dysplasia ...
Personalised medicine in exacerbations of COPD: the beginnings EDITORIAL Sanjay Sethi
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... Can we better target systemic steroid use in exacerbations? Although a short course of systemic steroids is often regarded as benign, there is emerging evidence that this may not be the case in the setting of an exacerbation of COPD. The best described adverse effect is hyperglycaemia [6]. High-dose ...
Epstein-Barr Virus (EBV) Infections in Patients
Epstein-Barr Virus (EBV) Infections in Patients

... chronic-active infection and become undetectable weeks to months after onset. Elevated EBV-IgG antibodies suggest a past infection. In the patient population treated at The Center, elevated EBV antibody titer is a common finding. During a recent 33 day period, 32 patients seen at The Center had sero ...
Inflammation response in AD - UvA-DARE
Inflammation response in AD - UvA-DARE

... C3 convertase, which cleaves complement component C3 into C3b and C3a. C3a is a peptide mediator of local inflammation. C3b binds covalently to the pathogen membrane and opsonises it enabling phagocytes. C3b also activates another series of cleavage reactions resulting in more cytokines and a membra ...
How chronic inflammation can affect the brain and support the
How chronic inflammation can affect the brain and support the

... as for complement cascade proteins C1qB, C3 and C4, the IL1 receptor and receptor antagonist, and TGFβ have been observed in AD microglia (Walker et al., 1995; Shen et al., 1997; Strohmeyer et al., 2000). In peripheral monocytes a similar proinflammatory response has been demonstrated following stim ...
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Neuromyelitis optica

Neuromyelitis optica (NMO), also known as Devic's disease or Devic's syndrome, is a heterogeneous condition consisting of the simultaneous inflammation and demyelination of the optic nerve (optic neuritis) and the spinal cord (myelitis). It can be monophasic or recurrent.Currently at least two different causes are proposed based on the presence of autoantibodies against AQP4. AQP4+ NMO is currently considered an autoimmune disease (autoimmune astrocytopathy, or autoimmune astrocytic channelopathy) in which a person's own immune system attacks the astrocytes of the optic nerves and spinal cord. The cause of the AQP4- variants is unknown.Although inflammation may also affect the brain, the lesions are different from those observed in the related condition, multiple sclerosis. Spinal cord lesions lead to varying degrees of weakness or paralysis in the legs or arms, loss of sensation (including blindness), and/or bladder and bowel dysfunction.Devic's disease is now studied along a collection of similar diseases called ""Neuromyelitis optica spectrum diseases"". Some cases of this spectrum resemble multiple sclerosis (MS) in several ways, but require a different course of treatment for optimal results.In 2004, NMO-IgG (currently known as Anti-AQP IgG) was first described leading to the distinction between positive and negative cases.In Anti-AQP positive variants, CNS astrocytes, which are the basis for the glymphatic system are the target of the autoimmune attack. NMO-IgG-negative cases are less understood. It seems currently that astrocytes are spared in these IgG negative cases
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