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Tocilizumab in Refractory Neuro Myelitis Optica Spectrum Disorder and Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease - Experience from a Tertiary Care Centre. [PDF]
Shaik RS +4 more
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Methotrexate-induced acute neurotoxicity in patients with osteosarcoma: a case report. [PDF]
Makos OL +5 more
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Neurological Infections in HIV: A Case-Based Review for Clinicians. [PDF]
Gupta N +8 more
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Peroxisomal Leukoencephalopathy
Seminars in Neurology, 2012Peroxisomal 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
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Progressive Multifocal Leukoencephalopathy
CONTINUUM: Lifelong Learning in Neurology, 2008Progressive 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 ...
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Psychiatric Clinics of North America, 2011
Leukoencephalopathy is a syndrome of neurologic deficits, including alteration of mental status, caused by pathologic changes in the cerebral white matter. The term, toxic leukoencephalopathy, encompasses a wide variety of exposures and clinical presentations.
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Leukoencephalopathy is a syndrome of neurologic deficits, including alteration of mental status, caused by pathologic changes in the cerebral white matter. The term, toxic leukoencephalopathy, encompasses a wide variety of exposures and clinical presentations.
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Neurology, 2015
Just 11 years ago, a new genetic white matter disease, leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL), was described in 7 children and 1 teenager.1 Clinical features were dominated by progressive motor deterioration without sphincter dysfunction; half of the patients had loss of position and vibratory ...
Don, Gilden, Raphael, Schiffmann
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Just 11 years ago, a new genetic white matter disease, leukoencephalopathy with brainstem and spinal cord involvement and elevated lactate (LBSL), was described in 7 children and 1 teenager.1 Clinical features were dominated by progressive motor deterioration without sphincter dysfunction; half of the patients had loss of position and vibratory ...
Don, Gilden, Raphael, Schiffmann
openaire +2 more sources

