A modified liquid chromatography/tandem mass spectrometry method for predominant disaccharide units of urinary glycosaminoglycans in patients with mucopolysaccharidoses

Author:

Chuang Chih-Kuang,Lin Hsiang-Yu,Wang Tuen-Jen,Tsai Chia-Chen,Liu Hsuan-Liang,Lin Shuan-Pei

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Reference33 articles.

1. Neufeld EF, Muenzer J: The mucopolysaccharidoses. The Metabolic and Molecular Bases of Inherited Disease. Edited by: Scriver CR, Beaudet AL, Valle D. 2001, McGraw-Hill Book Company, New York, 3421-3452. 8

2. Clarke LA: Clinical diagnosis of lysosomal storage diseases. Organelle Diseases. Clinical Features, Diagnosis, Pathogenesis and Management. Edited by: Applegarth DA, Dimmick JE, Hall JG. 1997, Chapman and Hall Medical, London, 45-97.

3. Besley GTN, Wraith JE: Lysosomal disorders. Curr Paediatri. 1997, 7: 128-134. 10.1016/S0957-5839(97)80195-9.

4. Wraith JE: Mucopolysaccharidoses. Curr Paediatri. 1996, 6: 74-79. 10.1016/S0957-5839(96)80065-0.

5. Lin HY, Shih SC, Chuang CK, Lee K, Chen M, Lin HC, Chiu PC, Niu DM, Lin SP: Assessment of hearing loss by pure-tone audiometry in patients with mucopolysaccharidoses. Mol Genet Metab. 2014, 111: 533-538. 10.1016/j.ymgme.2014.02.003.

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