نتایج جستجو برای: neurometabolic

تعداد نتایج: 416  

Journal: :journal of cellular and molecular anesthesia 0
masoud nashibi anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran ardeshir tajbakhsh anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran farhad safari anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran kamran mottaghi anesthesiology research center, shahid beheshti university of medical sciences, tehran, iran

nieman-pick disease type c is a rare, autosomal recessive, neurometabolic disorder associated with the accumulation of unesterified cholesterol in lysosomes and late endosomes. because of multiple organ involvement and wide range of clinical manifestations, these patients will demand multiple diagnostic and therapeutic procedures requiring anesthesia. sincepathogenesis of this disease is still ...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran narjes jafari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran habibeh nejad biglari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran sayena jabbeh dari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran farzad ahmad abadi 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad-reza alaee 4. department of pediatric endocrinology, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, jafari n, nejad biglari h, jabbeh dari s, ahmad abadi f, alaee mr, nemati h, saket s, tonekaboni sh, taghdiri mm, ghofrani m. gm2-gangliosidosis (sandhoff and tay sachs disease): diagnosis and neuroimaging findings (an iranian pediatric case series) iran j child neurol. 2014 summer;8(3): 55-60.   abstract objective gm2-gangliosidosis disease is a rare aut...

Journal: :iranian journal of child neurology 0
parvaneh karimzadeh 1.pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran narjes jafari pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran farzad ahmadabadi pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran sayena jabbedari pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran mohammadmahdi taghdiri 1. pediatric neurologist, pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran hamid nemati pediatric neurology department, mofid children hospital, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, jafari n, jabbehdari s, taghdiri mm, nemati h, saket s, alaee mr, ghofrani m, tonakebni sh. methylmalonic acidemia: diagnosis and neuroimaging findings of this neurometabolic disorder (an iranian pediatric case series). iran j child neurol. 2013 summer; 7(3): 63-66.   objective methylmalonic acidemia is one of the inborn errors of metabolism resulting in ...

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