Literature DB >> 21708141

Rapid, single-step assay for Hunter syndrome in dried blood spots using digital microfluidics.

Ramakrishna Sista, Allen E Eckhardt, Tong Wang, Márcia Séllos-Moura, Vamsee K Pamula.   

Abstract

Entities:  

Mesh：

Year:  2011        PMID： 21708141     DOI： 10.1016/j.cca.2011.06.015

Source DB:  PubMed          Journal:  Clin Chim Acta        ISSN： 0009-8981            Impact factor:   3.786


× No keyword cloud information.
  10 in total

1.  Detection by Urinary GAG Testing of Mucopolysaccharidosis Type II in an At-Risk Spanish Population.

Authors:  Laura López-Marín; Luis G Gutiérrez-Solana; Luis Aldamiz-Echevarria Azuara; Rogelio Simón de Las Heras; Anna Duat Rodríguez; Verónica Cantarín Extremera
Journal:  JIMD Rep       Date:  2013-02-02

Review 2.  Newborn Screening for Lysosomal Storage Disorders.

Authors:  Roy W A Peake; Olaf A Bodamer
Journal:  J Pediatr Genet       Date:  2016-12-02

Review 3.  Newborn screening for lysosomal storage diseases.

Authors:  Michael H Gelb; C Ronald Scott; Frantisek Turecek
Journal:  Clin Chem       Date:  2014-12-04       Impact factor: 8.327

4.  High-throughput assay of 9 lysosomal enzymes for newborn screening.

Authors:  Zdenek Spacil; Haribabu Tatipaka; Mariana Barcenas; C Ronald Scott; Frantisek Turecek; Michael H Gelb
Journal:  Clin Chem       Date:  2013-01-11       Impact factor: 8.327

5.  Multiplex newborn screening for Pompe, Fabry, Hunter, Gaucher, and Hurler diseases using a digital microfluidic platform.

Authors:  Ramakrishna S Sista; Tong Wang; Ning Wu; Carrie Graham; Allen Eckhardt; Theodore Winger; Vijay Srinivasan; Deeksha Bali; David S Millington; Vamsee K Pamula
Journal:  Clin Chim Acta       Date:  2013-05-07       Impact factor: 3.786

6.  Rapid assays for Gaucher and Hurler diseases in dried blood spots using digital microfluidics.

Authors:  Ramakrishna S Sista; Tong Wang; Ning Wu; Carrie Graham; Allen Eckhardt; Deeksha Bali; David S Millington; Vamsee K Pamula
Journal:  Mol Genet Metab       Date:  2013-03-24       Impact factor: 4.797

7.  Newborn screening for hunter disease: a small-scale feasibility study.

Authors:  G J G Ruijter; D A Goudriaan; A M Boer; J Van den Bosch; A T Van der Ploeg; L H Elvers; S S Weinreich; A J Reuser
Journal:  JIMD Rep       Date:  2013-11-23

Review 8.  Emerging Approaches for Fluorescence-Based Newborn Screening of Mucopolysaccharidoses.

Authors:  Rajendra Singh; Shaileja Chopra; Carrie Graham; Melissa Langer; Rainer Ng; Anirudh J Ullal; Vamsee K Pamula
Journal:  Diagnostics (Basel)       Date:  2020-05-11

9.  A click-flipped enzyme substrate boosts the performance of the diagnostic screening for Hunter syndrome.

Authors:  Markus Schwarz; Philipp Skrinjar; Michael J Fink; Stefan Kronister; Thomas Mechtler; Panagiotis I Koukos; Alexandre M J J Bonvin; David C Kasper; Hannes Mikula
Journal:  Chem Sci       Date:  2020-10-23       Impact factor: 9.825

10.  Presentation and Treatments for Mucopolysaccharidosis Type II (MPS II; Hunter Syndrome).

Authors:  Molly Stapleton; Francyne Kubaski; Robert W Mason; Hiromasa Yabe; Yasuyuki Suzuki; Kenji E Orii; Tadao Orii; Shunji Tomatsu
Journal:  Expert Opin Orphan Drugs       Date:  2017-03-08       Impact factor: 0.694
  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.