Keywords: کمبود فولات مغزی; Folate; Folate receptor; Autoimmunity; Cerebral folate deficiency; Autism spectrum disorder; Schizophrenia; Depression;
مقالات ISI کمبود فولات مغزی (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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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: کمبود فولات مغزی; Mitochondrial disease; Epilepsy; Seizure; Neuronal energy depletion; Oxidative stress; Coenzyme Q10; Cerebral folate deficiency; l-arginine; Immune dysfunction; Calcium homeostasis and signaling;
Keywords: کمبود فولات مغزی; Autism; Epilepsy; Mitochondrial dysfunction; Mitochondrial disease; Cerebral folate deficiency; Metabolic disorders; Comorbidities;
Keywords: کمبود فولات مغزی; Autoimmunity; Folate receptor; Treatment; Schizophrenia; Cerebral folate deficiency
Keywords: کمبود فولات مغزی; Cerebral folate deficiency; Neurological regression; Treatable disorder; Hypomyelination; Inborn error of metabolism5MTHF, 5-methyltetrahydrofolate; CSF, cerebrospinal fluid; FR, folate receptor
Case ReportSevere leukoencephalopathy with cortical involvement and peripheral neuropathy due to FOLR1 deficiency
Keywords: کمبود فولات مغزی; Cerebral folate deficiency; FOLR1; Leukoencephalopathy; Peripheral neuropathy; Cortical insult; Folinic acid therapy;
The proton-coupled folate transporter (PCFT-SLC46A1) and the syndrome of systemic and cerebral folate deficiency of infancy: Hereditary folate malabsorption
Keywords: کمبود فولات مغزی; Proton-coupled folate transporter; PCFT; SLC46A1; Reduced folate carrier; RFC; SLC19A1; Folate receptors; FRα; Folates; Folic acid; Methotrexate; Pemetrexed; Hereditary folate malabsorption; HFM; Cerebral folate deficiency; CFD; 5-Formyltetrahydrofolate
The first Chinese case report of hereditary folate malabsorption with a novel mutation on SLC46A1
Keywords: کمبود فولات مغزی; Hereditary folate malabsorption; Cerebral folate deficiency; Megaloblastic anemia; Intracranial calcification; Proton-coupled folate transporter; SLC46A1 gene
Electroencephalographic and seizure manifestations in two patients with folate receptor autoimmune antibody-mediated primary cerebral folate deficiency
Keywords: کمبود فولات مغزی; Cerebral folate deficiency; Seizures; Folate; Autoantibody; FOLR-1; Folate receptor;
Cerebral folate deficiency: A neurometabolic syndrome?
Keywords: کمبود فولات مغزی; Cerebral folate deficiency; Antiepileptics; Mental retardation; Epilepsy; Ataxia;
Pyridoxal phosphate-responsive seizures in a patient with cerebral folate deficiency (CFD) and congenital deafness with labyrinthine aplasia, microtia and microdontia (LAMM)
Keywords: کمبود فولات مغزی; 5HIAA; 5-hydroxyindoleacetic acid; 5MTHF; 5-methyltetrahydrofolic acid; FRα; folate receptor alpha; FOLR1; folate receptor α gene; HVA; homovanillic acid; 3OMD; 3-O-methyl-dopa; LAMM; labyrinth aplasia, microtia and microdontia; FGF3; fibroblast growth
Analysis of 5-methyltetrahydrofolate in serum of healthy children
Keywords: کمبود فولات مغزی; 5-Methyltetrahydrofolate; 5MTHF; Cerebral folate deficiency; HPLC; Electrochemical detection; Serum; Children; Folates