Ten years' experience of enzyme infusion therapy of Norrbottnian (type 3) Gaucher disease.

Ten years' experience of enzyme infusion therapy of Norrbottnian (type 3) Gaucher disease.

Item
http://www.wikidata.org/entity/Q40348519
GBA2 Mutations Cause a Marinesco-Sjögren-Like Syndrome: Genetic and Biochemical StudiesRandomized, controlled trial of miglustat in Gaucher's disease type 3.Biomarkers for lysosomal storage disorders: identification and application as exemplified by chitotriosidase in Gaucher disease.Gaucher disease: clinical profile and therapeutic developments.Impact of imiglucerase supply shortage on clinical and laboratory parameters in Norrbottnian patients with Gaucher disease type 3Biomarkers in the diagnosis of lysosomal storage disorders: proteins, lipids, and inhibodies.Elevated plasma glucosylsphingosine in Gaucher disease: relation to phenotype, storage cell markers, and therapeutic responseUpdate on pharmacological treatment of Progressive Myoclonus Epilepsies.Norrbottnian clinical variant of Gaucher disease in Southern Italy.Enzyme replacement in neuronal storage disorders in the pediatric population.
P2860

Ten years' experience of enzyme infusion therapy of Norrbottnian (type 3) Gaucher disease.

Item
http://www.wikidata.org/entity/Q40348519
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年論文
@yue
2006年論文
@zh-hant
2006年論文
@zh-hk
2006年論文
@zh-mo
2006年論文
@zh-tw
2006年论文
@wuu
2006年论文
@zh
2006年论文
@zh-cn
name
Ten years' experience of enzym ...... nian (type 3) Gaucher disease.
@en
type
label
Ten years' experience of enzym ...... nian (type 3) Gaucher disease.
@en
prefLabel
Ten years' experience of enzym ...... nian (type 3) Gaucher disease.
@en
P1433
P1476
P2093
P304
P31
P356
P407
P433
P478
P577
P698
P356
P1433
P1476
Ten years' experience of enzym ...... nian (type 3) Gaucher disease.
@en
P2093
P304
P31
P356
P407
P433
P478
P577
P698