Keywords: سندرم شکارچی; Hunter syndrome; Mucopolysaccharidoses; Hunter Outcome Survey (HOS); Glycosaminoglycans (GAG); Adults; Adolescents; Children; Enzyme replacement treatment (ERT); Idursulfase; Splenomegaly; Carpal tunnel syndrome; Airway obstructionSíndrome de Hunter; Muco
مقالات ISI سندرم شکارچی (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: سندرم شکارچی; Hunter syndrome; Mucopolysaccharidoses; Hunter Outcome Survey (HOS); Glycosaminoglycans (GAG); Adults; Adolescents; Children; Enzyme replacement treatment (ERT); Idursulfase; Splenomegaly; Carpal tunnel syndrome; Airway obstructionSíndrome de Hunter; Muco
Keywords: سندرم شکارچی; Fabry disease; Williams syndrome; Hurler syndrome; Hunter syndrome; Heerfordt syndrome; Sjögren syndrome;
Keywords: سندرم شکارچی; cost-effectiveness; Hunter syndrome; iduronate-2-sulfatase; mucopolysaccharidosis
Hematopoietic Stem Cell Transplantation for Patients with Mucopolysaccharidosis II
Keywords: سندرم شکارچی; Mucopolysaccharidosis II; Hunter syndrome; Hematopoietic stem cell transplantation; Enzyme replacement therapy; Iduronate-2-sulfatase;
The levels of urinary glycosaminoglycans of patients with attenuated and severe type of mucopolysaccharidosis II determined by liquid chromatography-tandem mass spectrometry
Keywords: سندرم شکارچی; Mucopolysaccharidosis; Glycosaminoglycans; LC-MS/MS; Hunter syndrome
Molecular diagnosis of 65 families with mucopolysaccharidosis type II (Hunter syndrome) characterized by 16 novel mutations in the IDS gene: Genetic, pathological, and structural studies on iduronate-2-sulfatase
Keywords: سندرم شکارچی; MPS type II; Iduronate-2-sulfatase; Hunter syndrome; Genotypephenotype correlation; Homology modeling;
Identification of 17 novel mutations in 40 Argentinean unrelated families with mucopolysaccharidosis type II (Hunter syndrome)
Keywords: سندرم شکارچی; Genetic testing; Genotype–phenotype correlation; Hunter syndrome; Lysosomal storage disorder; Mucopolysaccharidosis type II
Genetic Analysis of 17 Children with Hunter Syndrome: Identification and Functional Characterization of Four Novel Mutations in the Iduronate-2-Sulfatase Gene
Keywords: سندرم شکارچی; Hunter syndrome; Mucopolysaccharidosis type II; Iduronate-2-sulfatase; Mutations; Glycosaminoglycans
Extension of the molecular analysis to the promoter region of the iduronate 2-sulfatase gene reveals genomic alterations in mucopolysaccharidosis type II patients with normal coding sequence
Keywords: سندرم شکارچی; μg/ml; micrograms per milliliters; μl; microliters; bp; base pairs; cDNA; DNA complementary to RNA; cm; centimeters; dbSNPs; Single Nucleotide Polymorphism Database; del; deletion; DMEM; Dulbecco's modified Eagle medium; GAGs; glycosaminoglycans; h; hou
Mucopolysaccharidosis type II in a female carrying a heterozygous stop mutation of the iduronate-2-sulfatase gene and showing a skewed X chromosome inactivation
Keywords: سندرم شکارچی; Hunter syndrome; Iduronate-2-sulfatase; Elaprase®; Mexico; MPSII; X-linked disease
The mucopolysaccaridoses
Keywords: سندرم شکارچی; Hunter syndrome; Hurler syndrome; Morquio syndrome; mucopolysaccaridoses; mucopolysaccaridosis; Sanfilippo syndrome
Effect of rapid cessation of enzyme replacement therapy: A report of 5 cases and a review of the literature
Keywords: سندرم شکارچی; Mucopolysaccharidosis type II; Hunter syndrome; Enzyme replacement therapy;
Hallazgos neurorradiológicos en una serie de pacientes con mucopolisacaridosis
Keywords: سندرم شکارچی; 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 شکارچی; Hurler syndrome; Hunter syndrome; Neuroimaging findings; Neurological signs and symptoms; Mucopolysaccharidoses; Virchow–Robin perivascular spacesEspacios perivasculares de Virchow–Robin; Manifestaciones neurológicas; Mucopolisacaridosis; Neuroimagen; Sín
First experience of enzyme replacement therapy with idursulfase in Spanish patients with Hunter syndrome under 5 years of age: Case observations from the Hunter Outcome Survey (HOS)
Keywords: سندرم شکارچی; Case series; Children; Hunter Outcome Survey; Hunter syndrome; Idursulfase; Mucopolysaccharidosis type II
Home treatment with intravenous enzyme replacement therapy with idursulfase for mucopolysaccharidosis type II - data from the Hunter Outcome Survey
Keywords: سندرم شکارچی; BiPAP; bi-level positive airway pressure; CPAP; continuous positive airway pressure; ERT; enzyme replacement therapy; GAG; glycosaminoglycan; HOS; Hunter Outcome Survey; I2S; iduronate-2-sulfatase; IRR; infusion-related reaction; MPS II; mucopolysaccharid
Japan Elaprase® Treatment (JET) study: Idursulfase enzyme replacement therapy in adult patients with attenuated Hunter syndrome (Mucopolysaccharidosis II, MPS II)
Keywords: سندرم شکارچی; Mucopolysaccharidosis II; Hunter syndrome; Clinical trial; Enzyme replacement therapy; Idursulfase; Elaprase
Treatment reduces or stabilizes brain imaging abnormalities in patients with MPS I and II
Keywords: سندرم شکارچی; Mucopolysaccharidosis; Hurler syndrome; Hunter syndrome; Enzyme replacement therapy; Stem cell transplant; Magnetic resonance imaging; Central nervous system; Outcomes
Early response to idursulfase treatment in a 3 year-old boy affected of Hunter syndrome
Keywords: سندرم شکارچی; Idursulfatase; Early treatment; Hunter syndrome;
Gene therapy of Hunter syndrome: Evaluation of the efficiency of muscle electro gene transfer for the production and release of recombinant iduronate-2-sulfatase (IDS)
Keywords: سندرم شکارچی; Hunter syndrome; Iduronate-2-sulfatase; Electro gene transfer; Hyaluronidase; Muscle; Gene therapy
Preclinical dose ranging studies for enzyme replacement therapy with idursulfase in a knock-out mouse model of MPS II
Keywords: سندرم شکارچی; Idursulfase; Hunter syndrome; Mucopolysaccharidosis II; Mouse model; Dose; Enzyme replacement therapy
A phase I/II clinical trial of enzyme replacement therapy in mucopolysaccharidosis II (Hunter syndrome)
Keywords: سندرم شکارچی; Mucopolysaccharidosis II; MPS II; Hunter syndrome; Iduronate-2-sulfatase; Glycosaminoglycans; Enzyme replacement therapy; Idursulfase; Lysosomal storage disorder
Complications of tracheotomy in patients with mucopolysaccharidoses type II (Hunter syndrome)
Keywords: سندرم شکارچی; Mucopolysaccharidoses; Hunter syndrome; Tracheotomy; Complications; Tracheal stenosis