Keywords: سندرم هورلر; Pediatric carpal tunnel; carpal tunnel syndrome; Hurler syndrome; mucopolysaccharidosis; enzyme replacement therapy;
مقالات ISI سندرم هورلر (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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.
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: سندرم هورلر; Mucopolysaccharidoses; Lysosomal storage diseases; Behavior; Child behavior disorders; Mental disorders; CNS; central nervous system; GAG; glycosaminoglycan; MPS; mucopolysaccharidosis; MPS IH; Hurler syndrome; T-DSM-IV-S; Turgay Diagnostic and Statistica
Keywords: سندرم هورلر; AEq; age-equivalent; BASC; Behavior Assessment System for Children; ASQ; Ages and Stages Questionnaire; BSID; Bayley Scales of Infant and Toddler Development; CBCL; Child Behavior Checklist; CNS; central nervous system; DAS; Differential Ability Scales; G
Keywords: سندرم هورلر; HS; Hurler syndrome; WT; wild type; BMP; bis(monoacylglycero)phosphate; PG; phosphatidylglycerol; LA; linoleic acid; DHA/EPA; docosahexaenoic/eicosapentaenoic acid; HF; high fat; Lysosomal disease; Hurler syndrome; Mucopolysaccharidosis 1; Phospholipid; N
Keywords: سندرم هورلر; Hematopoietic cell transplantation; Mucopolysaccharidosis; Hurler syndrome
Keywords: سندرم هورلر; Fabry disease; Williams syndrome; Hurler syndrome; Hunter syndrome; Heerfordt syndrome; Sjögren syndrome;
Keywords: سندرم هورلر; Mucopolysaccharidosis I; Hurler syndrome; Cornea; Myofibroblasts; Corneal clouding; CollagenMPS1-H, mucopolysaccharidosis I-Hurler; GAG, glycosaminoglycans; BCVA, best corrected visual acuity; PB, phosphate buffer; PBS, phosphate buffered saline
Metabolic Syndrome and Cardiovascular Risk Factors after Hematopoietic Cell Transplantation in Severe Mucopolysaccharidosis Type I (Hurler Syndrome)
Keywords: سندرم هورلر; Metabolic syndrome; Hematopoietic cell transplantation; Mucopolysaccharidosis; Hurler syndrome; Dyslipidemia;
CRISPR-Cas9-mediated gene editing in human MPS I fibroblasts
Keywords: سندرم هورلر; Hurler syndrome; Mucopolysaccharidosis; Gene editing; CRISPR-Cas9;
Immune tolerance induction for laronidase treatment in mucopolysaccharidosis I
Keywords: سندرم هورلر; Mucopolysaccharidosis type I; Enzyme replacement therapy; Immune tolerance; Laronidase; Hurler syndrome; Anti-drug antibodies;
Elements of lentiviral vector design toward gene therapy for treating mucopolysaccharidosis I
Keywords: سندرم هورلر; Lysosomal disease; Hurler syndrome; Mucopolysaccharidosis; Lentivirus; Gene therapy
Obstructive sleep apnea syndrome after hematopoietic stem cell transplantation in children with mucopolysaccharidosis type I
Keywords: سندرم هورلر; OSAS; obstructive sleep apnea syndrome; MPS I; mucopolysaccharidosis I; HSCT; hematopoietic stem cell transplantation; PSG; polysomnography; AHI; apnea-hypopnea index; GAG; glycosaminoglycan; IDUA; a-L-iduronidase; MPS I-H; Hurler syndrome; MPS I-S; Sch
Residual α-l-iduronidase activity in fibroblasts of mild to severe Mucopolysaccharidosis type I patients
Keywords: سندرم هورلر; 4MU; 4-methylumbelliferone; ERT; enzyme-replacement therapy; HSCT; hematopoietic stem cell transplantation; IDUA; α-l-iduronidase; MPS; mucopolysaccharidosis; MPS IH; Hurler syndrome; MPS IH/S; Hurler-Scheie syndrome; MPS IS; Scheie syndrome; Mucopolys
The mucopolysaccaridoses
Keywords: سندرم هورلر; Hunter syndrome; Hurler syndrome; Morquio syndrome; mucopolysaccaridoses; mucopolysaccaridosis; Sanfilippo syndrome
Hallazgos neurorradiológicos en una serie de pacientes con mucopolisacaridosis
Keywords: سندرم هورلر; Espacios perivasculares de Virchow-Robin; Manifestaciones neurológicas; Mucopolisacaridosis; Neuroimagen; SÃndrome de Hurler; SÃndrome de Hunter; Hurler syndrome; Hunter syndrome; Neuroimaging findings; Neurological signs and symptoms; Mucopolysacchari
Neuroimaging findings in patient series with mucopolysaccharidosis
Keywords: سندرم هورلر; Hurler syndrome; Hunter syndrome; Neuroimaging findings; Neurological signs and symptoms; Mucopolysaccharidoses; Virchow–Robin perivascular spacesEspacios perivasculares de Virchow–Robin; Manifestaciones neurológicas; Mucopolisacaridosis; Neuroimagen; Sín
Intraperitoneal implant of recombinant encapsulated cells overexpressing alpha-l-iduronidase partially corrects visceral pathology in mucopolysaccharidosis type I mice
Keywords: سندرم هورلر; alginate microcapsules; cell encapsulation; cell therapy; gene therapy; Hurler syndrome; mucopolysaccharidosis type I
The designer aminoglycoside NB84 significantly reduces glycosaminoglycan accumulation associated with MPS I-H in the Idua-W392X mouse
Keywords: سندرم هورلر; Suppression; Readthrough; Aminoglycosides; MPS I-H; Nonsense mutations; Hurler syndrome;
Direct gene transfer to the CNS prevents emergence of neurologic disease in a murine model of mucopolysaccharidosis type I
Keywords: سندرم هورلر; Mucopolysaccharidosis; Hurler syndrome; Lysosomal storage disease; Iduronidase; AAV; Gene transfer; Intracerebroventricular; Water maze;
Dried Blood Spot Analysis: An Easy and Reliable Tool to Monitor the Biochemical Effect of Hematopoietic Stem Cell Transplantation in Hurler Syndrome Patients
Keywords: سندرم هورلر; Mucopolysaccharidosis I; Hurler syndrome; Hematopoietic stem cell transplantation; Iduronidase; Clinical enzyme tests; Dried blood spot
Prenatal diagnosis of the Hurler syndrome by microsatellite markers analysis
Keywords: سندرم هورلر; Hurler syndrome; Mucopolysaccharidosis type IH; Alpha-l-iduronidase; Prenatal diagnosis (DPN); Mutation; Trophoblast biopsy; Microsatellites markers; Syndrome de Hurler; Mucopolysaccharidose type IH; Alpha-l-iduronidase; Diagnostic prénatal (DPN); Mutati
Evaluation of heparin cofactor II-thrombin complex as a biomarker on blood spots from mucopolysaccharidosis I, IIIA and IIIB mice
Keywords: سندرم هورلر; Biomarker; Mucopolysaccharide disease; Newborn screening; Heparin cofactor II-thrombin; Serpin-protease complex; Blood spots; Serum; Dermatan sulphate; Heparan sulphate; Hurler syndrome; Sanfilippo syndrome;
Characterization of an MPS I-H knock-in mouse that carries a nonsense mutation analogous to the human IDUA-W402X mutation
Keywords: سندرم هورلر; MPS I; Hurler syndrome; Mouse; W402X mutation; α-l-iduronidase
Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II
Keywords: سندرم هورلر; Mucopolysaccharidosis; Hurler syndrome; Hunter syndrome; Enzyme replacement therapy; Stem cell transplant; Magnetic resonance imaging; Central nervous system; Outcomes
Risk Factor Analysis of Outcomes after Unrelated Cord Blood Transplantation in Patients with Hurler Syndrome
Keywords: سندرم هورلر; Hurler syndrome; (Umbilical) cord blood; Stem cell transplantation
Upregulation of elastase proteins results in aortic dilatation in mucopolysaccharidosis I mice
Keywords: سندرم هورلر; Hurler syndrome; Lysosomal storage disease; Elastin; Aorta; Gene therapy
Musculoskeletal complications encountered in the lysosomal storage disorders
Keywords: سندرم هورلر; enzyme replacement therapy; Gaucher disease; hematopoietic stem cell transplantation; Hurler syndrome; lysosomal storage disorder; mucopolysaccharidosis
Progression of multiple behavioral deficits with various ages of onset in a murine model of Hurler syndrome
Keywords: سندرم هورلر; Animal model; Lysosomal storage disease; Hurler syndrome; Behavior profile; Spatial learning; Open-field; Locomotion
The Clinical Outcome of Hurler Syndrome after Stem Cell Transplantation
Keywords: سندرم هورلر; Hurler Syndrome; Mucopolysaccharidosis I; Stem cell transplantation; Clinical outcome; Long-term outcome