Keywords: مید; AL amyloidosis; Renal failure; End-stage renal disease; Autologous stem cell transplantation; Melphalan; MIDD;
مقالات ISI مید (ترجمه نشده)
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Keywords: مید; MDs; mitochondrial diseases; PEO; progressive external ophthalmoplegia; MELAS; mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes; MERRF; myoclonic epilepsy with ragged-red fibres; MIDD; maternally inherited diabetes and deafness;
Keywords: مید; CNS; central nervous system; NARP; Neuropathy Ataxia Retinitis Pigmentosa; KSS; Kearns-Sayre Syndrome; MILS; Maternally Inherited Leigh Syndrome; AMD; Age-related Macular Degeneration; MIDD; Mitochondrial Syndrome of Maternally Inherited Diabetes and Deaf
Keywords: مید; AD; autosomal dominant; ADNIV; autosomal dominant neovascular inflammatory vitreoretinopathy; AR; autosomal recessive; AR-1; autosomal recessive-1 allele identified; ARMS; amplification refractory mutation system; AZOOR; acute zonal occult outer retinopat
Keywords: مید; monogenic diabetes; young type 2 diabetes; personalised medicine; CRP; C-reactive protein; HNF1A; hepatocyte nuclear factor 1 alpha; HNF4A; hepatocyte nuclear factor 4 alpha; HNF1B; hepatocyte nuclear factor 1 beta; GCK; glucokinase; IPSAD; International
Keywords: مید; AHS; Alpers-Huttenlocher Syndrome; EPC; epilepsia-partialis-continua; KSS; Kearns-Sayre Syndrome; MELAS; Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-like episodes; MIDD; Maternally Inherited Diabetes and Deafness; mtDNA; Mitochondrial DNA;
Keywords: مید; OM; otitis media; MEM; middle ear mucosa; WGA; wheat germ agglutinin; STA; Solanumtuberosum lectin; UEA-I; Ulexeuropaeus isoagglutinin I; LCA; Lensculinaris agglutinin; GNA; Galanthusnivalis agglutinin; MFI; mean fluorescence intensity; Otitis media; Midd
Keywords: مید; BM; bone marrow; CKD; chronic kidney disease; CLL; chronic lymphocytic leukemia; eGFR; estimated glomerular filtration rate; GN; glomerulonephritis; MGRS; monoclonal gammopathy of renal significance; MGUS; monoclonal gammopathy of undetermined significanc
Keywords: مید; Kidney; Multiple myeloma; Amyloidosis; MIDD; Cast nephropathy;
Keywords: مید; ADP; adenosine diphosphate; ALT; alanine aminotransferase; ATP; adenine triphosphate; CoA; coenzyme A; FAD; flavin adenine dinucleotide; FADH2; reduced flavin adenine dinucleotide; GPT; glutamate pyruvate transaminase; HIV; human immunodeficiency virus; L
Keywords: مید; AED; antiepileptic drug; AHS; Alpers-Huttenlocher-syndrome; CNS; central nervous system; COX; Cytochrome-c-oxidase; CPEO; mitochondrial or nuclear chronic progressive external ophthalmoplegia; CSF; cerebro-spinal fluid; EMP; enecephalomyopathy; EP; ence
Anatomic & metabolic brain markers of the m.3243A>G mutation: A multi-parametric 7T MRI study
Keywords: مید; 15-WLT; 15-Words Learning Task; ADL; Activities daily life; ASL; Arterial spin labeling; CBF; Cerebral blood flow; cGM; Cortical gray matter; CSF; Cerebral spinal fluid; CN; Caudate nucleus; CNR; Contrast-to-noise ratio; DN; Dentate nucleus; EPI; Echo pla
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A>G and the ND1 m.3308T>C mutations associated with multiple mitochondrial deletions
Keywords: مید; MIDD; m.1555A>G; m.3308T>C; Mitochondrial deletions
Demander un diagnostic génétique en diabétologie
Keywords: مید; Diabète monogénique; MODY; MIDD; diagnostic génétique; Monogenic diabetes; MODY; MIDD; genetic testing;
Diagnostic clinique et biologique du diabète mitochondrial et particularités de sa prise en charge
Keywords: مید; MIDD; Diabète mitochondrial; Mutation 3243A > G de l’ADNmtMIDD; Mitochondrial diabetes; 3243A > G mtDNA mutation
Atteinte rétinienne et myopathies génétiques
Keywords: مید; Rétinite pigmentaire; Dystrophie maculaire réticulaire; Maladie de Coats; Syndrome de Kearn et Sayre; MELAS; MIDD; Dystrophie musculaire facio-scapulo-humérale; Retinitis pigmentosa; Pattern retinal dystrophy; Coats disease; Kearn Sayre Syndrome; MELAS
Quand et pourquoi rechercher un diabète monogénique ?
Keywords: مید; Diabète monogénique; MODY; MIDD; diabète néonatal; diagnostic moléculaire; corrélation phénotype/génotype; Monogenic diabetes; MODY; MIDD; neonatal diabetes; genetic testing; phenotype/genotype correlation;
Research ReportIschemic tolerance following low dose NMDA involves modulation of cellular stress proteins
Keywords: مید; CPP; (±)-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid; ER; endoplasmic reticulum; GABA; gamma-aminobutyric acid; GRP; glucose-regulated protein; HSP; heat shock protein; ip; intraperitoneal; iv; intravenous; MCA; middle cerebral artery; MCAO; midd
Mitochondrial DNA A3243G mutation involved in familial diabetes, chronic intestinal pseudo-obstruction and recurrent pancreatitis
Keywords: مید; Mitochondria; MELAS; MIDD; Pancreatitis; CIPO; Chronic intestinal pseudo obstructionMitochondrie; MELAS; MIDD; POIC; Pancréatite; Pseudo obstruction intestinale chronique
Mutational analysis of the mitochondrial tRNALeu(UUR) gene in Tunisian patients with mitochondrial diseases
Keywords: مید; A3243G mutation; tRNALeu(UUR) gene; Mitochondrial ND1 gene; Diabetes; Hearing loss; MIDD; T3396C
Influence of tissue fixation on the microextraction and identification of amyloid proteins
Keywords: مید; AA amyloid; amyloid A protein-derived amyloid; AL amyloid; immunoglobulin light-chain-derived amyloid; anti-AL1 antibody; antibody directed against λ-light-chain-derived amyloid proteins; anti-λ-light chain(DAKO) antibody; comercially available antibody
Diabètes mitochondriaux
Keywords: مید; Diabète sucré; Génétique du diabète; Diabète mitochondrial; ADN mitochondrial; Mutations; Délétions; MIDD; Rétinopathie; Néphropathie; Myopathie; Dystrophie maculaire réticulée; MELAS; Diabetes mellitus; Genetics; Mitochondrial diabetes; Mitoc
Distinct nuclear gene expression profiles in cells with mtDNA depletion and homoplasmic A3243G mutation
Keywords: مید; ES; enrichment score; GO; gene ontology; GSEA; gene set enrichment analysis; MIDD; maternally inherited diabetes and deafness; mtDNA; mitochondrial DNA; OXPHOS; oxidative phosporylation; PLA; probe level analysis; Mitochondria; mtDNA; Expression; Diabetes