Late-onset pompe disease: Case report of a patient with an uncommon mutation and observational clinical trial as to response to enzyme replacemant therapy (ERT) with alglucosidase alfa over a 12-month-period

Autor:	N Strigl-Pill
Rok vydání:	2010
Předmět:	Pediatrics medicine.medical_specialty business.industry Late onset Disease Surgery Clinical trial Physiology (medical) medicine Observational study Neurology (clinical) business Alglucosidase alfa medicine.drug
Zdroj:	Klinische Neurophysiologie. 41
ISSN:	1439-4081 1434-0275
DOI:	10.1055/s-0030-1250913
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::c9e225f1a884d33a3bf823eed3564aee https://doi.org/10.1055/s-0030-1250913 Zobrazit plný text záznamu