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Congenital disorder of glycosylation type 1B

Also Known As:
Carbohydrate-deficient glycoprotein syndrome type 1B; Mannosephosphate isomerase deficiency; Protein-losing enteropathy-hepatic fibrosis syndrome; Saguenay-Lac Saint-Jean syndrome
Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

Bio-Agent Context: Research Results

Experts

1. Hadzic, Nedim: 1 article (10/2015)
2. Hegarty, Robert: 1 article (10/2015)
3. Dhawan, Anil: 1 article (10/2015)
4. Gissen, Paul: 1 article (10/2015)
5. Le Bizec, C: 1 article (11/2002)
6. Saudubray, J M: 1 article (11/2002)
7. Mitchell, G: 1 article (11/2002)
8. Durand, G: 1 article (11/2002)
9. Seta, N: 1 article (11/2002)
10. Pelletier, V: 1 article (11/2002)

Related Diseases

1. Type C Niemann-Pick Disease (Niemann Pick Disease, Type C)
2. Ornithine Carbamoyltransferase Deficiency Disease
3. Congenital, Hereditary, and Neonatal Diseases and Abnormalities (Congenital Disorders)
4. Galactosemias (Galactosemia)

Related Drugs and Biologics

1. Ornithine Carbamoyltransferase (Ornithine Transcarbamylase)
2. Tyrosinemia type 1