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Idiopathic Thrombocytopenic Purpura
Idiopathic Thrombocytopenic Purpura

... IVIG and/or WinRho (the latter for Rh+ patients only, where it works by binding to RBC antigen and thereby busying the Fc receptors in the reticuloendothelial system so they can’t chomp up the platelets) Splenectomy: usually reserved for cases of severe thrombocytopenia that fail steroids; remission ...
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... • Avoid Colonoscopy, Barium enema • Symptoms Should Resolve <48 Hours • <25% Have Recurrent Attacks • 6% Recovered Patients Need Operation • Long-Term- High Fiber Diet ...
INFECTIVE ENDOCARDITIS
INFECTIVE ENDOCARDITIS

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... do not require hospitalization, and most who are hospitalized improve with supportive care and are discharged in fewer than 5 days. Characteristics that increase the risk of severe RSV disease are preterm birth, cyanotic or complicated congenital heart disease, chronic lung disease of prematurity an ...
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Optic Nerve: It is, Opathy, and Edema

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Tick article
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Noted Canadian Neurologist to Head Alzheimer`s Disease
Noted Canadian Neurologist to Head Alzheimer`s Disease

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Workshop  on Bronchoalveolar  lavage: in and  clinical  application
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Antibiotic treatment of Crohn`s Disease: Does it Work?

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Graves` Disease - American Thyroid Association
Graves` Disease - American Thyroid Association

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... confirmed, but it is an interesting observation as EBNA1 IgG levels, rather than VCA, are associated with an increased risk for MS 23–25. Overall, for all tested viral infections, there was a tendency towards higher IgG levels in people with BD than HC. Similarly, the titres of antimeasles IgG detec ...
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... Renal dysfunction, acute renal failure, osmotic nephrosis, and death may occur with immune globulin intravenous (IVIG) products in predisposed patients. Patients predisposed to renal dysfunction include those with any degree of preexisting renal insufficiency, diabetes mellitus, age greater than 65, ...
GAMUNEX-C Infusion Rate Chart
GAMUNEX-C Infusion Rate Chart

... Renal dysfunction, acute renal failure, osmotic nephrosis, and death may occur with immune globulin intravenous (IVIG) products in predisposed patients. Patients predisposed to renal dysfunction include those with any degree of preexisting renal insufficiency, diabetes mellitus, age greater than 65, ...
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... disease in cattle that causes degeneration in the brain and spinal cord. Although it is viewed as new disease, the father of modern medicine, Hippocrates wrote of a mad cow like disease in cattle and humans thousands of years ago. The disease may be most easily transmitted to human beings by eating ...
Rheumatoid arthritis: a review and dental care considerations
Rheumatoid arthritis: a review and dental care considerations

... The dentist should be conscious of the patient’s physical comfort level in the dental chair: altering the chair’s position, allowing the patient to shift positions, using pillows and other such aids, and scheduling shorter appointments all should be considered. Home oral hygiene procedures may prese ...
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... and treatment options. LRF’s T-Cell Lymphoma Transportation Assistance Fund grant program provides financial assistance to T-cell lymphoma patients who are uninsured or have adequate medical insurance but struggle to pay for transportation costs (e.g., mileage, parking, tolls, gas, train tickets, et ...
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Meniere`s disease
Meniere`s disease

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- University of East Anglia
- University of East Anglia

... The mechanisms underlying the effect of the ATG16L1 Thr300Ala genotype on NOD2 induced IL-1β responses were assessed at transcriptional and translational levels. Increased IL-1β mRNA and elevated intracellular pro-IL1β were observed 24 hours after MDP stimulation of PBMCs from individuals homozygous ...
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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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