Keywords: Optic nerve; Second cranial nerve; Optic neuropathy; mtDNA; Oxidative phosphorylation; Mitochondrial; Respiratory chain; ADOA; Autosomal dominant optic atrophy; AION; Anterior ischemic optic neuropathy; AROA; Autosomal recessive optic atrophy; ATP; Adenos
مقالات ISI (ترجمه نشده)
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: ASS; atypical apraxia of speech; ALS; amyotrophic lateral sclerosis; ATG; autophagy-related; BD; Behçet disease; BPAN; Ã-propeller protein associated neurodegeneration; CMT2B; Charcot-Marie-Tooth neuropathy 2B; DMRV; distal myopathies with rimmed vacuol
Keywords: Atypical PKAN; Dysmorphia syndrome; Dystonia; Eye of the tiger sign; Irritability; PKAN; pantothenate kinase-associated neurodegeneration; NBIA; neurodegeneration with brain iron accumulation; MRI; magnetic resonance imaging;
Keywords: Fe3Â +; Â Ferric ion; Fe+Â 2; ferrous ion; GI; gastrointestinal tract; LIP; Labile Iron Pool (LIP); NBIA; neurodegeneration with brain iron accumulation; NTBI; Non-Transferrin Bound Iron; PCD; programmed cell death; RBC; red blood cell; RCD; Regulated cel
Keywords: Human brain; Whole-transcriptome analysis; WGCNA; NBIA; Iron metabolism;
Keywords: Iron chelation; NBIA; Superficial siderosis; Parkinson's disease; Multiple sclerosis; Friedreich's ataxia;
Keywords: DCF; dichlorofluorescein; DFO; deferoxamine; DHR-123; dihydrorhodamine 123; FAC; ferric ammonium citrate; iNs; induced neurons; IRP1; iron regulatory protein 1; LIP; labile iron pool; NBIA; neurodegeneration with brain iron accumulation; PKAN; pantothenat
Keywords: BBB; blood-brain barrier; DAB; 3,3â²-diaminobenzidine tetrahydrochloride; iNOS; inducible nitric oxide synthetase; KPBS; potassium phosphate-buffered saline; NBIA; neurodegeneration with brain iron accumulation; NO; nitric oxide; NTBI; non-transferrin
Keywords: Wilson disease; NBIA; Neurodegeneration with brain iron accumulation; Manganism; Primary familial brain calcification; Chelating therapy;
Keywords: Fucosidosis; Dystonia; MRI; Angiokeratoma; NBIA; Neurodegeneration with brain iron accumulation
Keywords: NBIA; PKAN; PLA26G; Eye of the tiger sign
Keywords: LB; Lewy body; PD; Parkinson's disease; SN; substantia nigra; ROS; reactive oxygen species; IRE/IRP; iron responsive element/iron responsive protein; NBIA; neurodegeneration with brain iron accumulation; KRS; Kufor-Rakeb syndrome; LRRK2; leucine rich re
Keywords: Dystonia; Gabapentin; Cerebral palsy; NBIA; WHO International Classification of function; Dystonia severity Assement Plan; ChildrenGMFCS, Gross Motor Function Classification System; DSAP, Dystonia Severity Assessment Plan; ICF-CY, WHO International Classi
A de novo C19orf12 heterozygous mutation in a patient with MPAN
Keywords: NBIA; MPAN; C19orf12; Heterozygous mutation; De novo mutation;
Aceruloplasminemia and putaminal cavitation
Keywords: Aceruloplasminemia; Chorea; Dystonia; NBIA; Putaminal cavitation;
Novel founder intronic variant in SLC39A14 in two families causing Manganism and potential treatment strategies
Keywords: Congenital manganism; SLC39A14; Manganese toxicity; BID; twice daily; CaNa2EDTA; edetate calcium disodium; CBC; complete blood count; cDNA; complementary DNA; dCT; delta cycle threshold; ddCT; double delta cycle threshold; DMSA; dimercaptosuccinic acid; M
Non-cell-autonomous actions of α-synuclein: Implications in glial synucleinopathies
Keywords: Astrocyte; Microglia; Neurodegeneration; Neuroinflammation; Parkinson disease; Protein aggregation; Multiple system atrophy; AD; Alzheimer disease; CJD; Creutzfeldt-Jakob disease; CNP; 3â²-cyclic nucleotide 3â²-phosphodiesterase; CSF; cerebrospinal fl
Mutations in DDHD1, encoding a phospholipase A1, is a novel cause of retinopathy and neurodegeneration with brain iron accumulation
Keywords: DDHD1; Hereditary spastic paraplegia; Retinopathy; Phospholipids; NBIA;
Changes in Red Blood Cell membrane lipid composition: A new perspective into the pathogenesis of PKAN
Keywords: PKAN; Pantothenate Kinase-Associated Neurodegeneration; PKAN; NBIA; Phospholipids; Membrane; Erythrocytes; Oxidized lipids; Mitochondria; Neurodegenerative diseases; Biomarkers;
A 30-year history of MPAN case from Russia
Keywords: Spastic ataxia; C19orf12; TruSight panels; NBIA;
Parkinsonian-Pyramidal syndromes: A systematic review
Keywords: Parkinsonism; Pyramidal signs; NBIA; Juvenile parkinsonism; Spasticity;
WDR45 mutations in Rett (-like) syndrome and developmental delay: Case report and an appraisal of the literature
Keywords: WDR45; NBIA; BPAN; Rett syndrome; Intellectual disability;
Identification of mutation in GTPBP2 in patients of a family with neurodegeneration accompanied by iron deposition in the brain
Keywords: GTPBP2; Neurodegenerative disease; Ataxia; NBIA; Cognitive dysfunction; Exome sequencing;
Knock-down of pantothenate kinase 2 severely affects the development of the nervous and vascular system in zebrafish, providing new insights into PKAN disease
Keywords: Pank2; NBIA; Neurodegeneration; Coenzyme A; Pantethine; Morpholino; Zebrafish;
C19orf12 gene mutations in patients with neurodegeneration with brain iron accumulation
Keywords: C19orf12; NBIA; MPAN; Iron accumulation;
Analysis of the C19orf12 and WDR45 genes in patients with neurodegeneration with brain iron accumulation
Keywords: NBIA; neurodegeneration with brain iron accumulation; MPAN; mitochondrial membrane protein-associated neurodegeneration; BPAN; beta-propeller protein-associated neurodegeneration; PKAN; panthothenate kinase-associated neurodegeneration; PLAN; Phospholipas
Neuroimaging studies and whole exome sequencing of PLA2G6-associated neurodegeneration in a family with intrafamilial phenotypic heterogeneity
Keywords: NBIA; Intrafamilial phenotypic variability; PLAN; PLA2G6; Whole exome sequencing;
Exome sequencing reveals a novel WDR45 frameshift mutation and inherited POLR3A heterozygous variants in a female with a complex phenotype and mixed brain MRI findings
Keywords: NBIA; 4H syndrome; Demyelinating disease; Leukodystrophy; WDR45; POLR3A; Whole exome sequencing
Novel homozygous PANK2 mutation causing atypical pantothenate kinase-associated neurodegeneration (PKAN) in a Cypriot family
Keywords: Pantothenate kinase-associated neurodegeneration; PKAN; Neurodegeneration with brain iron accumulation; NBIA; Pantothenate kinase 2; PANK2;
Efficacy and safety of deferiprone for the treatment of pantothenate kinase-associated neurodegeneration (PKAN) and neurodegeneration with brain iron accumulation (NBIA): Results from a four years follow-up
Keywords: PKAN; NBIA; Iron; Deferiprone; Magnetic resonance imaging;
Beta-propeller protein-associated neurodegeneration (BPAN), a rare form of NBIA: Novel mutations and neuropsychiatric phenotype in three adult patients
Keywords: BPAN; NBIA; Neuropsychiatry; Parkinsonism; Dystonia; Intellectual disability;
PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease
Keywords: Neurodegeneration with brain iron accumulation; NBIA; PLA2G6; INAD; PLAN;
A novel FTL mutation responsible for neuroferritinopathy with asymmetric clinical features and brain anomalies
Keywords: Neurodegeneration with brain iron accumulation; NBIA; Neuroferritinopathy; Ferritinopathy; FTL; Dystonia;
Lead-induced iron overload and attenuated effects of ferroportin 1 overexpression in PC12 cells
Keywords: AD; Alzheimer's disease; DFO; desferrioxamine mesylate; DMT1; divalent metal transporter 1; Fe; iron; FP1; ferroportin 1; NBIA; neurodegeneration with brain iron accumulation; Pb; lead; Lead; Iron; Ferroportin 1; Overexpression; PC12 cells; Neurotoxic
Transcranial ultrasound in neurodegeneration with brain iron accumulation (NBIA)
Keywords: NBIA; TCS; Sonography; Hallervorden-Spatz-Syndrome
Differential participation of phospholipase A2 isoforms during iron-induced retinal toxicity. Implications for age-related macular degeneration
Keywords: [14C]DPPC; 1-[14C]palmitoyl-2-[14C]palmitoyl-sn-glycero-3-phosphocholine; [14C]PAPC; 1-palmitoyl-2-[14C]arachidonoyl-sn-glycero-3-phosphocholine; 4-HNE; 4-hydroxynonenal; AA; arachidonic acid; AMD; age-related macular degeneration; ATK; arachidonoyl trifl
Hereditary spastic paraplegias with autosomal dominant, recessive, X-linked, or maternal trait of inheritance
Keywords: ACP33; Maspardin gene; AD; Autosomal dominant; ALS; Amyotrophic lateral sclerosis; AP; Adaptor Protein complex; AR; Autosomal recessive; ATL1; Atlastin-1 gene; BMP; Bone morphogenic protein; BSCL2; Berardinelli-Seip congenital lipodystrophy gene; CYP7B1;
Brain, blood, and iron: Perspectives on the roles of erythrocytes and iron in neurodegeneration
Keywords: Neuroacanthocytosis; Neurodegeneration; Iron; NBIA
Deep Brain Stimulation: Current and Future Clinical Applications
Keywords: AD; Alzheimer disease; AN; anterior nucleus; CM; centromedian; DBS; deep brain stimulation; ET; essential tremor; GPi; globus pallidus internus; GTS; Gilles de la Tourette syndrome; IPG; implantable pulse generator; MCS; minimally conscious state; NAc; nu
Expression of PLA2G6 in human fetal development: Implications for infantile neuroaxonal dystrophy
Keywords: INAD; infantile neuroaxonal dystrophy; NBIA; neurodegeneration with brain iron accumulation; PCW; post-conception weeks; PKAN; pantothenate-kinase associated neurodegeneration; SVZ; subventricular zone; VZ; ventricular zone; PLA2G6; INAD; Neurodegeneratio
Low-frequency rTMS of the premotor cortex reduces complex movement patterns in a patient with pantothenate kinase-associated neurodegenerative disease (PKAN)
Keywords: PKAN; NBIA; Dystonia; Repetitive transcranial magnetic stimulation; rTMSPKAN; NBIA; Dystonie; Stimulation magnétique transcrânienne répétitive
PANK2 gene analysis confirms genetic heterogeneity in neurodegeneration with brain iron accumulation (NBIA) but mutations are rare in other types of adult neurodegenerative disease
Keywords: PANK2; Neurodegeneration; PKAN; NBIA; Mutation;