Biogen Idec, Elan facing suits over MS drug side effects, The Boston Globe, September 10, 2013 NINDS
Progressive Multifocal Leukoencephalopathy Information Page, National Institute of Neurological Disorders and Stroke
Progressive Multifocal Leukoencephalopath This is a white matter of the brain disease caused by a virus infection.
Yout, 45, contends that taking Tysabri to regulate her multiple sclerosis caused her to develop
progressive multifocal leukoencephalopath (PML), which is a rare brain infection.
In a 2012 study, researchers reviewed the incidence of
progressive multifocal leukoencephalopathy (PML) in clients detected with autoimmune rheumatic conditions (ARD) such as RA, lupus, or Sjögren's syndrome.
However, understanding the importance of the T cell response could help researchers prevent the development of
progressive multifocal leukoencephalopathy in autoimmune patients.
These findings raise the possibility that viral shell mutations may influence the T cell response to John Cunningham polyomavirus in humans, and play a role in the development of
progressive multifocal leukoencephalopathy, the researchers wrote in the Journal of Virology.
Progressive multifocal leukoencephalopathy (PML) is a rare disease of the brain's white matter caused by the John Cunningham polyomavirus (JCV), a usually harmless virus that infects up to 80 percent of healthy adults.
Not exact matches
These include hip and elbow dysplasia, hypothyroidism, ear infections, diabetes, allergies, and a number of eye conditions such as
progressive retinal atrophy (PRA) and
multifocal retinal dysplasia (MRA).
Other eye diseases include, roughly in order of frequency, cataract, distichiasis,
progressive rod - cone degeneration (a form of PRA), CEA, iris coloboma, persistent pupilary membrane, cone degeneration, and canine
multifocal retinopathy.
The most common eye diseases in the breed are cataracts, distichiaisis, persistent pupilary membrane, and iris coloboma, with
Progressive Rod Cone Degeneration (PRCD), a form of progressive retinal atrophy (PRA), Collie Eye Anomaly (CEA), Canine Multifocal Retinopathy (CMR), and glaucoma have been seen bu
Progressive Rod Cone Degeneration (PRCD), a form of
progressive retinal atrophy (PRA), Collie Eye Anomaly (CEA), Canine Multifocal Retinopathy (CMR), and glaucoma have been seen bu
progressive retinal atrophy (PRA), Collie Eye Anomaly (CEA), Canine
Multifocal Retinopathy (CMR), and glaucoma have been seen but are rare.
Genes associated with the following forms of inherited canine retinal diseases were tested for association using fragment analysis in 11 PRA - affected and 11 unaffected Swedish vallhund dogs: canine
multifocal retinopathy (cmr; gene: BEST1)[8], [9], rod - cone dysplasia type 1 (rcd1; PDE6B) and type 3 (rcd3; PDE6A)[23]--[26],
progressive rod - cone degeneration (prcd; PRCD)[27], canine Leber congenital amaurosis (LCA; RPE65)[6], [7], cone - rod dystrophy (crdSWHD, NPHP4)[28], and achromatopsia / cone degeneration (ACHM / cd; CNGB3)[29], [30].