The humanistic burden of Pompe disease: are there still unmet needs? A systematic review
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s12883-017-0983-2.pdf
Reference68 articles.
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2. Ebbink BJ, Aarsen FK, van Gelder CM, van den Hout JMP, Weisglas-Kuperus N, Jaeken J, et al. Cognitive outcome of classic infantile Pompe patients receiving enzyme therapy. BMC Musculoskelet Disord. 2013;14(Suppl 2):14.
3. van Gelder CM, van Capelle CI, Ebbink BJ, Moor-van Nugteren I, van den Hout JM, Hakkesteegt MM, et al. Facial-muscle weakness, speech disorders and dysphagia are common in patients with classic infantile Pompe disease treated with enzyme therapy. J Inherit Metab Dis. 2012;35:505–11.
4. Bhengu L, Davidson A, du Toit P, Els C, Gerntholzt T, Govendrageloo K, et al. Diagnosis and management of Pompe disease. S Afr Med. 2014;104:273–4.
5. Chien Y-H, Hwu W-L, Lee N-C. Pompe disease: early diagnosis and early treatment make a difference. Pediatr Neonatol. 2013;54:219–27.
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