نتایج جستجو برای: neurometabolic

تعداد نتایج: 416  

2009
Christoph Arning Bernhard Thelen

EUROPSYCHOPHARMACOLOGY 1999 – VOL . 20 , NO . 6 © 1999 American College of Neuropsychopharmacology Published by Elsevier Science Inc. 0893-133X/99/$–see front matter 655 Avenue of the Americas, New York, NY 10010 PII S0893-133X(98)00089-X Neurometabolic Effects of Psilocybin, 3,4-Methylenedioxyethylamphetamine (MDE) and d-Methamphetamine in Healthy Volunteers A Double-Blind, Placebo-Controlled ...

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’s hospital, shahid beheshti university of medical sciences, tehran, iran farzad ahmadabadi 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 sayena jabbehdari pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad reza alaee 3. department of pediatric endocrinology, pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad ghofrani 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology department, mofid children’s hospital, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, ahmadabadi f, jafari n, jabbehdari s, alaee mr, ghofrani m, taghdiri mm, tonekaboni sh. biotinidase deficiency: a reversible neurometabolic disorder (an iranian pediatric case series). iran j child neurol. 2013 autumn; 7(4):47- 52.   objective biotinidase deficiency is one of the rare congenital metabolic disorders with autosomal recessive inheritance. if...

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 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 sayena jabbehdari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran mohammad-mahdi taghdiri 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 mohammad-reza alaee department of pediatric endocrinology, faculty of medicin, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, jafari n, ahmad abadi f, jabbehdari s, taghdiri mm, alaee mr, ghofrani m, tonekaboni sh, nejad biglari h. propionic acidemia: diagnosis and neuroimaging findings of this neurometabolic disorder. iran j child neurol. 2014 winter; 8(1):58-61.   objective propionic acidemia is one of the rare congenital neurometabolic disorders with autosomal recessive inher...

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 center of excellence, department of pediatric neurology, mofid children hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran narjes jafari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 2. pediatric neurology center of excellence, department of pediatric neurology, mofid children hospital, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran habibe nejad biglari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran sayena jabbehdari 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran 6. students’ research committee, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran mehdi alizadeh 3. pediatrician, mahneshan razi general hospital, zanjan medical university of medical sciences, zanjan, iran ghazal alizadeh 1. pediatric neurology research center, shahid beheshti university of medical sciences, tehran, iran

how to cite this article: karimzadeh p, jafari n, nejad biglari hb, jabbehdari s, alizadeh m, alizadeh gh, nejad biglari hm, sanii s. the clinical features and diagnosis of adrenoleukodystrophy: a case series of iranian family. iran j child neurol. winter 2016; 10(1):61-64. abstract objective adrenoleukodystrophy disorder is one of the x-linked genetic disorders caused by the myelin sheath brea...

Journal: :Molecular genetics and metabolism 2011
Sarah Mangold Nenad Blau Thomas Opladen Robert Steinfeld Britta Wessling Klaus Zerres Martin Häusler

BACKGROUND Cerebral folate deficiency (CFD) is increasingly recognized in various neurological conditions, raising the question of whether it might represent a clear-cut clinical syndrome. METHODS Retrospective analysis of patients with low cerebral spinal fluid (CSF) 5-methyltetrahydrofolate (5MTHF) values was performed. RESULTS 58 pediatric patients with low (-2nd to -3rd standard deviati...

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