List Of Volumes: 15 Volume(s) Year 2020 Year 2019 Year 2018 Year 2017 Year 2016 Year 2015 Year 2014 Year 2013 Volume 7, Number 4 (SUPPL.1) Volume 7, Number 4 Volume 7, Number 3 Volume 7, Number 2 Volume 7, Number 1 Year 2012 Year 2011 Year 2010 Year 2009 Year 2008 Year 2007 Year 2006
List Of Journal Paper(s): QUARTERLY IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN):2013, Volume 7, Number 4 (SUPPL.1) 16 Paper(s) 1 : MITOCHONDRIAL DISEASE Author(s): GHOFRANI MOHAMMAD* Page(s): From 1 To 2 Keyword(s): MITOCHONDRIAL DISEASE, CYTOPATHY, INHERITANCE, MUSCLE CELLS, METABOLIC Reference(s): (0) Citation(s): (0) FullText: 2 : MUSCLE BIOPSY FINDINGS IN MITOCHONDRIOPATHIES Author(s): NILIPOUR YALDA* Page(s): From 10 To 10 Keyword(s): MITOCHONDRIOPATHY, MITOCHONDRIAL MYOPATHY, MUSCLE BIOPSY, RAGGED-RED FIBER, COX-NEGATIVE FIBER Reference(s): (0) Citation(s): (0) FullText: 3 : MITOCHONDRIAL GENETICS, DISEASE AND INHERITANCE Author(s): HOUSHMAND MASSOUD* Page(s): From 11 To 11 Keyword(s): CHILDREN, MITOCHONDRIAL DISEASE, GENETIC STUDY, INHERITANCE Reference(s): (0) Citation(s): (0) FullText: 4 : PROTON MR SPECTROSCOPY IN THE DIAGNOSTIC EVALUATION OF SUSPECTED MITOCHONDRIAL DISEASE IN IRAN Author(s): RAHIMIAN ELHAM*,TAHSINI MAJID,TONEKABONI SEYED HASSAN,KARIMIZADEH PARVANEH Page(s): From 12 To 12 Keyword(s): PEDIATRICS, MITOCHONDRIAL DISEASE, NEUROIMAGING, PROTON MR SPECTROSCOPY Reference(s): (0) Citation(s): (0) FullText: 5 : ROLE OF TEAM WORK IN THE MANAGEMENT OF MITOCHONDRIAL DISEASE IN CHILDREN (CASE REPORT) Author(s): TONEKABONI SEYED HASSAN* Page(s): From 13 To 13 Keyword(s): MITOCHONDRIAL DISEASE, DIAGNOSIS, CHILDREN, CHRONIC EXTERNAL OPHTALMOPLEGIA, TEAM WORK Reference(s): (0) Citation(s): (0) FullText: 6 : CARNITINE TRANSPORTER DEFICIENCY Author(s): ALAEE MOHAMMAD REZA* Page(s): From 14 To 14 Keyword(s): CARNITINE TRANSPORTER DEFICIENCY, CARDIOMYOPATHY, NON KETOTIC HYPOGLYCEMIA Reference(s): (0) Citation(s): (0) FullText: 7 : NEUROLOGICAL FINDING OF MITOCHONDRIAL SYNDROMES (MERRF AND MELAS) Author(s): TAGHDIRI MOHAMMAD MAHDI* Page(s): From 15 To 15 Keyword(s): MELAS, MERRF, MITOCHONDRIAL SYNDROMES Reference(s): (0) Citation(s): (0) FullText: 8 : TREATMENT OF MITOCHONDRIAL CYTOPATHIES Author(s): SHAKIBA MARJAN* Page(s): From 16 To 17 Keyword(s): CHILDREN, MITOCHONDRIAL CYTOPATHIES, TREATMENT Reference(s): (0) Citation(s): (0) FullText: 9 : LEIGH DISEASE Author(s): SALEHPOUR SHADAB* Page(s): From 18 To 19 Keyword(s): LEIGH DISEASE, MITOCHONDROPATHY, NEUROMETABOLIC, NEURODEGENERATIVE Reference(s): (0) Citation(s): (0) FullText: 10 : PEARSON SYNDROME AND NEUROPATHY, ATAXIA AND RETINITIS PIGMENTOSA (NARP) Author(s): MAHVELATI SHAMSABADI FARHAD* Page(s): From 20 To 21 Keyword(s): MITOCHONDRIA, DNA, DISORDERS, PEARSON SYNDROME, NARP Reference(s): (0) Citation(s): (0) FullText: 11 : KEARNS-SAYRE SYNDROME Author(s): JAVADZADEH MOHSEN* Page(s): From 22 To 23 Keyword(s): KEARNS-SAYRE, MITOCHONDRIAL, ATAXIA, RETINOPATHY Reference(s): (0) Citation(s): (0) FullText: 12 : LEBER HEREDITARY OPTIC NEUROPATHY Author(s): SHALBAFAN BITA* Page(s): From 24 To 24 Keyword(s): LEBER HEREDITOMY OPTIC NEUROPHATY, MITOCHONDRIAL DISEASE, CHILDREN Reference(s): (0) Citation(s): (0) FullText: 13 : ROLE AND FUNCTION OF MITOCHONDRIA Author(s): ZAMANI GHOLAMREZA* Page(s): From 3 To 4 Keyword(s): MITOCHONDRIA, STRUCTURE, FUNCTION, GENETIC Reference(s): (0) Citation(s): (0) FullText: 14 : MITOCHONDRIAL DISORDERS: CLINICAL, PATHOLOGIC AND GENETIC CLASSIFICATION Author(s): ASHRAFI MAHMOUD REZA,TAVASOLI ALIREZA* Page(s): From 5 To 7 Keyword(s): MITOCHONDRIA, MITOCHONDRIAL ENCEPHALOMYOPATHY, NDNA, MDNA Reference(s): (0) Citation(s): (0) FullText: 15 : DIAGNOSTIC CRITERIA FOR PEDIATRIC MITOCHONDRIAL DISORDERS Author(s): KARIMZADEH PARVANEH* Page(s): From 8 To 8 Keyword(s): DIAGNOSTIC CRITERIA, MITOCHONDRIAL DISORDERS, MITOCHONDRIAL ENCEPHLOMYOPATHIES Reference(s): (0) Citation(s): (0) FullText: 16 : CLINCAL NEUROPHYSIOLOGY IN MITOCHONDRIAL DISORDERS Author(s): MOHAMMADI MAHMOUD* Page(s): From 9 To 9 Keyword(s): PEDIATRIC, CLINICAL NEUROPHYSIOLOGY, MITOCHONDRIAL DISORDER Reference(s): (0) Citation(s): (0) FullText:
