The spleen is the largest unit of the mononuclear phagocyte system.

The mononuclear phagocyte system is part of both humoral and cell-mediated immunity.

Exoerythrocytic schizogony occurs in the mononuclear phagocyte system.

Microglia belong among cells of the mononuclear phagocyte system [ 75 ] .

As a part of the mononuclear phagocyte system, it metabolizes hemoglobin removed from senescent erythrocytes.

The mononuclear phagocyte system has an important role in defense against microorganisms, including mycobacteria, fungi, bacteria, protozoa, and viruses.

A histiocyte is an animal cell that is part of the mononuclear phagocyte system (also known as the reticuloendothelial system or lymphoreticular system).

Human and animal brucellosis share the persistence of the bacteria in tissues of the mononuclear phagocyte system, including the spleen, liver, lymph nodes, and bone marrow.

The mononuclear phagocyte system (MPS) is a part of the immune system that consists of the phagocytic cells located in reticular connective tissue.

Kupffer cells have a different embryological origin, coming from the myeloid line in the reticuloendohelial system (also called mononuclear phagocyte system) and are related to the immune system.

"Reticuloendothelial system" is an older term for the mononuclear phagocyte system, but it is used less commonly now, as it is understood that most endothelial cells are not macrophages.

The haemoglobin that is released after the mononuclear phagocyte system (located in the liver and spleen) withdraws old red blood cells from circulation is degraded into its components; iron, protoporphyrin and protein.

Hume, D.A., Robinson, A.P., MacPherson, G.G., Gordon, S."The mononuclear phagocyte system of the mouse defined by immunohistochemical localization of antigen F4/80.

Kupffer cells, also known as Browicz-Kupffer cells and stellate macrophages, are specialized macrophages located in the liver lining the walls of the sinusoids that form part of the reticuloendothelial system (RES) (also called mononuclear phagocyte system).

One of the main uses is in myocardial perfusion imaging.

Myocardial perfusion imaging can be abnormal in 30% of patients.

The best known example of a nuclear stress test is myocardial perfusion imaging.

Conclusion Following discussion it was agreed that myocardial perfusion imaging could be accepted in the evaluation of such cases.

Tc sestamibi is used for myocardial perfusion imaging, which shows how well the blood flows through the heart.

Nitrogen-13 is used to tag ammonia molecules for PET myocardial perfusion imaging.

Both adenosine and dipyridamole, which act on the A2A receptor, are used in myocardial perfusion imaging.

The large validated database supporting the use of myocardial perfusion imaging for this application is not available for these alternative techniques.

Myocardial perfusion imaging, a nuclear medicine procedure that illustrates the function of the heart muscle (myocardium)

Additionally echocardiography, myocardial perfusion imaging, and cardiac stress testing is not recommended in those at low risk who do not have symptoms.

In five patients myocardial perfusion imaging studies were performed; in each case there was evidence of infarction with minimal reversible ischaemia.

It produces hyperemia quickly and maintains it for a duration that is useful for radionuclide myocardial perfusion imaging.

"Myocardial perfusion imaging for risk stratification of patients on presentation with acute chest pain: cost-effectiveness of two service delivery models." (113Kb)

Along with CT, or computed tomography, researchers also looked at screening with echocardiography, ultrasound, and so-called myocardial perfusion imaging.

Radionuclide myocardial perfusion imaging (RMPI) is used to assess the effect of coronary artery disease on the heart.

After stress myocardial perfusion imaging (stress MPI), the patient's cardiologist may take some time to study the results of the scan before discussing the findings.

Recently, MCG was compared to myocardial perfusion imaging (MPI) scan or nuclear stress testing.

Myocardial perfusion imaging (MPI) is a form of functional cardiac imaging, used for the diagnosis of ischemic heart disease.

Myocardial perfusion imaging is a standard test to assess coronary artery disease (CAD) with more than 9 million Americans undergoing the test annually.

Using the latter approach, about 30% of initially asymptomatic patients had stress myocardial perfusion imaging in the standard-care arm of the DIAD study."

It is marketed under the brand name Cardiogen-82 (Bracco Diagnostics) in the use of Myocardial perfusion imaging (imaging of the heart).

Medical imaging techniques ranging from CT scans to myocardial perfusion imaging (or imaging of the heart), have become a regular part of medical diagnostics.

Other ligands include sestamibi for myocardial perfusion imaging and mercapto acetyl triglycine for MAG3 scan to measure renal function.

The Company is also advancing its late-stage drug candidate, Stedivaze, a pharmacologic stress agent in Phase III development for use during myocardial perfusion imaging.

Overall, 1,123 diabetic patients without symptomatic or previously diagnosed CAD were randomized to either screening with myocardial perfusion imaging or standard care without screening.

The severe form of this disorder can lead to Hurler syndrome.

Hurler syndrome is inherited, which means that your parents must pass the disease on to you.

Symptoms of Hurler syndrome most often appear between ages 3 and 8.

However, this medication is not a cure for Hurler syndrome.

Both parents need to pass down the faulty gene in order for you to develop Hurler syndrome.

Hurler syndrome is a disease with a poor outlook.

Laronidase may improve breathing and walking ability in people with Hurler syndrome.

Infants with severe Hurler syndrome appear normal at birth.

Experts recommend genetic counseling and testing for couples with a family history of Hurler syndrome who are considering having children.

Hurler syndrome was once known as "Gargoylism"

Laronidase is used to treat some of the symptoms of a genetic condition called Hurler syndrome.

Hurler syndrome is a metabolic disorder in which the body lacks the enzyme needed to break down certain sugars and proteins.

Persons with Hurler syndrome do not make a substance called lysosomal alpha-L-iduronidase.

The symptoms of I-cell disease are similar to but more severe than those of Hurler syndrome.

Hurler syndrome belongs to a group of diseases called mucopolysaccharidoses, or MPS.

Children with Hurler syndrome often die before age 10 from obstructive airway disease, respiratory infections, or cardiac complications.

A medical example is a heterokaryon composed of nuclei from Hurler syndrome and Hunter syndrome.

Children with Maroteaux-Lamy syndrome, usually have normal intellectual development but share many of the physical symptoms found in Hurler syndrome.

Hunter syndrome is X-linked while Hurler syndrome is autosomal recessive.

Hurler syndrome is often classified as a lysosomal storage disease, and is clinically related to Hunter Syndrome.

The purpose of this registry is to track the progression of this disorder and the effects that laronidase has on long-term treatment of Hurler syndrome.

She also wrote autobiographical works that addressed the death of Frank, her husband who died of cancer, and the story of their son suffering from Hurler syndrome.

Hurler syndrome is a rare, inherited disease of metabolism in which a person cannot break down long chains of sugar molecules called glycosaminoglycans (formerly called mucopolysaccharides).

ML II is a particularly severe form of ML that resembles one of the mucopolysaccharidoses called Hurler syndrome.

Because Hurler syndrome is an autosomal recessive disorder, affected persons have two non-working copies of the IDUA gene.

Hurler syndrome was once known as "Gargoylism"

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