نتایج جستجو برای: kearns sayre

تعداد نتایج: 927  

Journal: :British heart journal 1992
A M Remes I E Hassinen K Majamaa K J Peuhkurinen

Defects of mitochondrial DNA have been found at necropsy in the myocardium of patients with Kearns-Sayre syndrome. A patient with characteristics typical of Kearns-Sayre syndrome and a complete heart block is described. Southern blot analysis showed a deletion of 3.3 kb in the mitochondrial DNA in an endomyocardial biopsy specimen and in skeletal muscle. The deletion led to the disappearance of...

Journal: :Neuropediatrics 2007
V T Ramaekers J Weis J M Sequeira E V Quadros N Blau

Folate transport to the brain depends on ATP-driven folate receptor-mediated transport across choroid plexus epithelial cells. Failure of ATP production in Kearns-Sayre syndrome syndrome provides one explanation for the finding of low spinal fluid (CSF) 5-methyltetrahydrofolate (5MTHF) levels in this condition. Therefore, we suspect the presence of reduced folate transport across the blood-spin...

Journal: :Archives of neurology 2012
Nichola Z Lax Graham R Campbell Amy K Reeve Nobuhiko Ohno Jessica Zambonin Emma L Blakely Robert W Taylor Eduardo Bonilla Kurenai Tanji Salvatore DiMauro Evelyn Jaros Hans Lassmann Doug M Turnbull Don J Mahad

OBJECTIVE To explore myelin components and mitochondrial changes within the central nervous system in patients with well-characterized mitochondrial disorders due to nuclear DNA or mitochondrial DNA (mtDNA) mutations. DESIGN Immunohistochemical analysis, histochemical analysis, mtDNA sequencing, and real-time and long-range polymerase chain reaction were used to determine the pathogenicity of...

Journal: :AJNR. American journal of neuroradiology 1995
S H Wray J M Provenzale D R Johns K R Thulborn

PURPOSE To determine the spectrum of MR findings in patients with mitochondrial myopathy and correlate them with central nervous system symptoms and signs. METHODS We performed a prospective evaluation of the MR findings of eight patients with mitochondrial myopathy (three with Kearns-Sayre syndrome and five with chronic progressive external ophthalmoplegia), six of whom had central nervous s...

2013
Shun Katada Takayuki Mito Emi Ogasawara Jun-Ichi Hayashi Kazuto Nakada

Studies in patients have suggested that the clinical phenotypes of some mitochondrial diseases might transit from one disease to another (e.g., Pearson syndrome [PS] to Kearns-Sayre syndrome) in single individuals carrying mitochondrial (mt) DNA with a common deletion (ΔmtDNA), but there is no direct experimental evidence for this. To determine whether ΔmtDNA has the pathologic potential to ind...

Journal: :Nepalese Journal of Ophthalmology 1970

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