نتایج جستجو برای: leigh syndrome

تعداد نتایج: 623686  

Journal: :SN Comprehensive Clinical Medicine 2023

Abstract Leigh syndrome (LS) or subacute necrotizing encephalomyelopathy is a progressive, lethal, mitochondrial disease mostly presenting in childhood. We report 36-year-old African male to the Emergency Department with 6-month history of progressive dysarthria. Examination also showed oculomotor limitations for downgaze and convergence, mild right hemiparesis Babinski sign, absent lower limb ...

2017
Michele Ferrari Isha H. Jain Olga Goldberger Emanuele Rezoagli Robrecht Thoonen Kai-Hung Chen David E. Sosnovik Marielle Scherrer-Crosbie Vamsi K. Mootha Warren M. Zapol

MEDICAL SCIENCES Correction for “Hypoxia treatment reverses neurodegenerative disease in a mouse model of Leigh syndrome,” by Michele Ferrari, Isha H. Jain, Olga Goldberger, Emanuele Rezoagli, Robrecht Thoonen, Kai-Hung Chen, David E. Sosnovik, Marielle Scherrer-Crosbie, Vamsi K. Mootha, and Warren M. Zapol, which appeared in issue 21, May 23, 2017, of Proc Natl Acad Sci USA (114:E4241–E4250; f...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2017
Michele Ferrari Isha H. Jain Olga Goldberger Emanuele Rezoagli Robrecht Thoonen Kai-Hung Chen David E. Sosnovik Marielle Scherrer-Crosbie Vamsi K. Mootha Warren M. Zapol

MEDICAL SCIENCES Correction for “Hypoxia treatment reverses neurodegenerative disease in a mouse model of Leigh syndrome,” by Michele Ferrari, Isha H. Jain, Olga Goldberger, Emanuele Rezoagli, Robrecht Thoonen, Kai-Hung Chen, David E. Sosnovik, Marielle Scherrer-Crosbie, Vamsi K. Mootha, and Warren M. Zapol, which appeared in issue 21, May 23, 2017, of Proc Natl Acad Sci USA (114:E4241–E4250; f...

Journal: :The Turkish journal of pediatrics 2015
Özlem Ünal R Köksal Özgül Didem Yücel Dilek Yalnızoğlu Ayşegül Tokatlı H Serap Sivri Burcu Hişmi Turgay Coşkun Ali Dursun

Association of 3-methylglutaconic aciduria with impaired oxidative phosphorylation, deafness, encephalopathy, leigh-like lesions on brain imaging, progressive spasticity and dystonia defined as a distinct entity under the name of MEGDEL syndrome. It is an autosomal recessive disorder due to mutation in the serine active site-containing protein 1 (SERAC1). SERAC1 is localized at the interface be...

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