Results 101 to 110 of about 133 (131)
Some of the next articles are maybe not open access.
Leigh’s Disease (Subacute Necrotizing Encephalomyelopathy)
1994Leigh’s disease is a rare neurodegenerative disease caused by disorders of pyruvate metabolism. Most cases occur sporadically but autosomal recessive inheritance has been reported. Respiratory failure is the most important manifestation in patients requiring neurocritical care.
Matthias Spranger, Michael N. Diringer
openaire +2 more sources
Leigh disease presenting as Guillain-Barré syndrome
Pediatric Neurology, 1993A 4-year-old male evidenced the criteria for the diagnosis of Guillain-Barré syndrome. Eventually a diagnosis of Leigh disease was made based on magnetic resonance imaging and mitochondrial enzyme deficiencies. Although chronic neuropathy has been reported with Leigh disease, this is the first reported patient with acute symmetric motor polyneuropathy.
openaire +3 more sources
Burden of Proof in the Postmortem Diagnosis of Mitochondrial Disease: Leigh Disease
Pediatric and Developmental Pathology, 2004CASE HISTORY This male infant weighed 6 lb 12 oz after a fullterm pregnancy. At age 2 to 3 months, he had been diagnosed with hypertrophic cardiomyopathy, hypotonia, lactic acidosis, and poor control of oral feeds. He had gastroesophageal reflux and subsequently required nasogastric tube feeds.
openaire +3 more sources
Onconephrology: The intersections between the kidney and cancer
Ca-A Cancer Journal for Clinicians, 2021Mitchell H Rosner +2 more
exaly
BIOCHEMICAL ABNORMALITIES IN LEIGH'S DISEASE
The Lancet, 1976S.D. Cederbaum, J.P. Blass, H.G. Dunn
openaire +2 more sources
Multidisciplinary standards of care and recent progress in pancreatic ductal adenocarcinoma
Ca-A Cancer Journal for Clinicians, 2020Aaron J Grossberg +2 more
exaly