Source:http://linkedlifedata.com/resource/pubmed/id/17041744
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2006-11-19
|
pubmed:abstractText |
A patient with atypical infantile Pompe disease suffered acute respiratory insufficiency at the age of 8 years which resulted in complete immobilization and dependence on assisted ventilation. Shortly after initiation of enzyme replacement therapy, she regained her mobility and, after 20 months of treatment, she now leads an almost normal life with limited restrictions.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
1573-2665
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
29
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
763
|
pubmed:dateRevised |
2007-3-21
|
pubmed:meshHeading |
pubmed-meshheading:17041744-Child,
pubmed-meshheading:17041744-Female,
pubmed-meshheading:17041744-Glycogen Storage Disease Type II,
pubmed-meshheading:17041744-Humans,
pubmed-meshheading:17041744-Respiratory Insufficiency,
pubmed-meshheading:17041744-Time Factors,
pubmed-meshheading:17041744-Treatment Outcome,
pubmed-meshheading:17041744-alpha-Glucosidases
|
pubmed:year |
2006
|
pubmed:articleTitle |
Sudden deterioration in nonclassical infantile-onset Pompe disease responding to alglucosidase alfa infusion therapy: a case report.
|
pubmed:affiliation |
Department of Paediatric Neurology, University Hospital La Paz, Paseo Castellana, 261, 28046, Madrid, Spain. ipascualp.hulp@salud.madrid.org
|
pubmed:publicationType |
Journal Article,
Case Reports
|