Results 181 to 190 of about 32,319 (241)

Progressive Multifocal Leukoencephalopathy

Seminars in Neurology, 1999
Before the AIDS epidemic, progressive multifocal leukoencephalopathy (PML) was a rare disorder occurring most often in association with leukemia and lymphoma. Current estimates indicate that PML ultimately develops in up to 5% of all patients with AIDS.
Eugene O Major
exaly   +3 more sources

Peroxisomal Leukoencephalopathy

Seminars in Neurology, 2012
Peroxisomal leukoencephalopathies include diseases belonging to the Zellweger spectrum and the rhizomelic chondrodysplasia punctata spectrum, as well as some single enzyme defects of peroxisomal β-oxidation. The authors present information on the clinical and diagnostic approach, and the characteristics of brain magnetic resonance imaging (MRI) in ...
Poll-The, Bwee Tien, Engelen, Marc
openaire   +3 more sources

Progressive Multifocal Leukoencephalopathy

CONTINUUM: Lifelong Learning in Neurology, 2008
Progressive multifocal leukoencephalopathy (PML) is an opportunistic viral infection of the human CNS that has gained new importance because of AIDS and newer immunosuppressive therapies. It destroys oligodendrocytes, leading to neurologic deficits associated with demyelination.PML most commonly occurs in patients who are HIV infected, but increasing ...
C, Arseni, F, Nerean tiu
  +8 more sources

Leukoencephalopathies in Adulthood

Seminars in Neurology, 2012
The understanding of the genetic basis of late-onset leukoencephalopathies has continued to increase in recent years. The most commonly presenting leukoencephalopathies in adulthood can be late-onset manifestations of metabolic pathways.
Jan-Mendelt, Tillema, Deborah L, Renaud
openaire   +2 more sources

Siblings With Leukoencephalopathy

Seminars in Pediatric Neurology, 2008
Two consanguineous siblings presented with developmental regression and emerging spasticity. Cranial magnetic resonance imaging in both showed diffuse leukoencephalopathy. Further investigation established the siblings as having complex 1 deficiency consequent to a novel homozygous mutation in NDUFV1, a nuclear-encoded subunit of complex 1.
Galen N, Breningstall   +2 more
openaire   +2 more sources

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