6.
Chuang C, Lin H, Wang T, Huang Y, Chan M, Liao H
. Status of newborn screening and follow up investigations for Mucopolysaccharidoses I and II in Taiwan. Orphanet J Rare Dis. 2018; 13(1):84.
PMC: 5970538.
DOI: 10.1186/s13023-018-0816-4.
View
7.
Lin H, Lee C, Lo Y, Tu R, Chang Y, Chang C
. An At-Risk Population Screening Program for Mucopolysaccharidoses by Measuring Urinary Glycosaminoglycans in Taiwan. Diagnostics (Basel). 2019; 9(4).
PMC: 6963841.
DOI: 10.3390/diagnostics9040140.
View
8.
Bodamer O, Giugliani R, Wood T
. The laboratory diagnosis of mucopolysaccharidosis III (Sanfilippo syndrome): A changing landscape. Mol Genet Metab. 2014; 113(1-2):34-41.
DOI: 10.1016/j.ymgme.2014.07.013.
View
9.
He Q, Trim P, Lau A, King B, Hopwood J, Hemsley K
. Synthetic Disaccharide Standards Enable Quantitative Analysis of Stored Heparan Sulfate in MPS IIIA Murine Brain Regions. ACS Chem Neurosci. 2019; 10(8):3847-3858.
DOI: 10.1021/acschemneuro.9b00328.
View
10.
Tomatsu S, Fujii T, Fukushi M, Oguma T, Shimada T, Maeda M
. Newborn screening and diagnosis of mucopolysaccharidoses. Mol Genet Metab. 2013; 110(1-2):42-53.
PMC: 4047214.
DOI: 10.1016/j.ymgme.2013.06.007.
View
11.
Wang D, Eadala B, Sadilek M, Chamoles N, Turecek F, Scott C
. Tandem mass spectrometric analysis of dried blood spots for screening of mucopolysaccharidosis I in newborns. Clin Chem. 2005; 51(5):898-900.
DOI: 10.1373/clinchem.2004.047167.
View
12.
Taylor J, Clinard K, Powell C, Rehder C, Young S, Bali D
. The North Carolina Experience with Mucopolysaccharidosis Type I Newborn Screening. J Pediatr. 2019; 211:193-200.e2.
DOI: 10.1016/j.jpeds.2019.04.027.
View
13.
DAvanzo F, Rigon L, Zanetti A, Tomanin R
. Mucopolysaccharidosis Type II: One Hundred Years of Research, Diagnosis, and Treatment. Int J Mol Sci. 2020; 21(4).
PMC: 7072947.
DOI: 10.3390/ijms21041258.
View
14.
Fachel F, Francio L, Poletto E, Schuh R, Teixeira H, Giugliani R
. Gene editing strategies to treat lysosomal disorders: The example of mucopolysaccharidoses. Adv Drug Deliv Rev. 2022; 191:114616.
DOI: 10.1016/j.addr.2022.114616.
View
15.
Heon-Roberts R, Nguyen A, Pshezhetsky A
. Molecular Bases of Neurodegeneration and Cognitive Decline, the Major Burden of Sanfilippo Disease. J Clin Med. 2020; 9(2).
PMC: 7074161.
DOI: 10.3390/jcm9020344.
View
16.
Zhou J, Lin J, Leung W, Wang L
. A basic understanding of mucopolysaccharidosis: Incidence, clinical features, diagnosis, and management. Intractable Rare Dis Res. 2020; 9(1):1-9.
PMC: 7062595.
DOI: 10.5582/irdr.2020.01011.
View
17.
Beneto N, Vilageliu L, Grinberg D, Canals I
. Sanfilippo Syndrome: Molecular Basis, Disease Models and Therapeutic Approaches. Int J Mol Sci. 2020; 21(21).
PMC: 7659972.
DOI: 10.3390/ijms21217819.
View
18.
Zhang H, Dickson P, Stiles A, Chen A, Le S, McCaw P
. Comparison of dermatan sulfate and heparan sulfate concentrations in serum, cerebrospinal fluid and urine in patients with mucopolysaccharidosis type I receiving intravenous and intrathecal enzyme replacement therapy. Clin Chim Acta. 2020; 508:179-184.
DOI: 10.1016/j.cca.2020.05.035.
View
19.
Kumar A, Masi S, Ghomashchi F, Chennamaneni N, Ito M, Scott C
. Tandem Mass Spectrometry Has a Larger Analytical Range than Fluorescence Assays of Lysosomal Enzymes: Application to Newborn Screening and Diagnosis of Mucopolysaccharidoses Types II, IVA, and VI. Clin Chem. 2015; 61(11):1363-71.
PMC: 4737431.
DOI: 10.1373/clinchem.2015.242560.
View
20.
Chuang C, Tu Y, Lee C, Lo Y, Chang Y, Liu M
. Updated Confirmatory Diagnosis for Mucopolysaccharidoses in Taiwanese Infants and the Application of Gene Variants. Int J Mol Sci. 2022; 23(17).
PMC: 9456254.
DOI: 10.3390/ijms23179979.
View