Pages that link to "Q34464137"
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The following pages link to Congenital disorders of glycosylation and the pediatric liver. (Q34464137):
Displaying 9 items.
- Identification and characterization of a cDNA encoding a dolichyl pyrophosphate phosphatase located in the endoplasmic reticulum of mammalian cells (Q28588980) (← links)
- Cryptogenic liver disease in four children: a novel congenital disorder of glycosylation (Q33232586) (← links)
- New disorders in carbohydrate metabolism: congenital disorders of glycosylation and their impact on the endocrine system (Q34181480) (← links)
- Prenatal diagnosis of liver and biliary tract disease (Q35682614) (← links)
- Clinical observation of salvianolic acid B in treatment of liver fibrosis in chronic hepatitis B. (Q36308206) (← links)
- A zebrafish model of congenital disorders of glycosylation with phosphomannose isomerase deficiency reveals an early opportunity for corrective mannose supplementation (Q36486017) (← links)
- Posttranscriptional regulation of uridine diphosphate glucuronosyltransferases (Q38386709) (← links)
- rhIGF-1 Therapy for Growth Failure and IGF-1 Deficiency in Congenital Disorder of Glycosylation Ia (PMM2 Deficiency). (Q40479090) (← links)
- Congenital disorder of glycosylation type Ia: a non-progressive encephalopathy associated with multisystemic involvement (Q48911608) (← links)