Newborn screening of mucopolysaccharidoses: past, present, and future-Reference-Cited by-同舟云学术

Newborn screening of mucopolysaccharidoses: past, present, and future

Published:2020-04-10 Issue:7 Volume:65 Page:557-567
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Arunkumar Nivethitha,Langan Thomas J.,Stapleton Molly,Kubaski Francyne,Mason Robert W.,Singh Rajendra,Kobayashi Hironori,Yamaguchi Seiji,Suzuki Yasuyuki,Orii Kenji,Orii Tadao,Fukao Toshiyuki,Tomatsu Shunji

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/s10038-020-0744-8.pdf

Reference76 articles.

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2. Furujo M, Kubo T, Kosuga M, Okuyama T. Enzyme replacement therapy attenuates disease progression in two Japanese siblings with mucopolysaccharidosis type VI. Mol Genet Metab. 2011;104:597–602.

3. McGill JJ, Inwood AC, Coman DJ, Lipke ML, De Lore D, Swiedler SJ, et al. Enzyme replacement therapy for mucopolysaccharidosis VI from 8 weeks of age–a sibling control study. Clin Genet. 2010;77:492–8.

4. Kubaski F, Yabe H, Suzuki Y, Seto T, Hamazaki T, Mason RW, et al. Hematopoietic stem cell transplantation for patients with mucopolysaccharidosis II. Biol Blood Marrow Transplant. 2017;23:1795–803.

5. Patel P, Suzuki Y, Tanaka A, Yabe H, Kato S, Shimada T, et al. Impact of enzyme replacement therapy and hematopoietic stem cell therapy on growth in patients with Hunter syndrome. Mol Genet Metab Rep. 2014;1:184–96.

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