Author:
Bianchi Pier Marco,Gaini Renato,Vitale Silvano
Publisher
Springer Science and Business Media LLC
Reference61 articles.
1. Gonuldas B¸, Yılmaz T, Sivri SH, Gucer KS, Kılınc K, Genc GA, et al. Mucopolysaccharidosis: otolaryngologic findings, obstructive sleep apnea and accumulation of glucosaminoglycans in lymphatic tissue of the upper airway. Int J Pediatr Otorhinolaryngol. 2014;78:944–9.
2. Mesolella M, Cimmino M, Cantone E, Marino A, Cozzolino M, Della Casa R, et al. Management of otolaryngological manifestations in mucopolysaccharidoses: our experience. Acta Otorhinolaryngol Ital. 2013;33:267–72.
3. Kiely BT, Kohler JL, Coletti HY, Poe MD, Escolar ML. Early disease progression of hurler syndrome. Orphanet J Rare Dis. 2017;12:32.
4. Guffon B, Heron B, Chabrol B, Feillet F, Montauban V, Valayannopoulos V. Diagnosis, quality of life, and treatment of patients with hunter syndrome in the French healthcare system: a retrospective observational study. Orphanet J Rare Dis. 2015;10:43.
5. Keilmann A, Iain TN, Bruce A, Molte D, Malm G. Hearing loss in patients with mucopolysaccharidosis II: data from HOS—the hunter outcome survey. J Inherit Metab Dis. 2012;35:343–53.
Cited by
19 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献