The liver in congenital disorders of glycosylation: Ultrastructural features

Keyphrases

• Bile Canaliculi 25%
• Cardiomyopathy 25%
• Cellularity 25%
• Congenital Disorders of Glycosylation 100%
• Diagnostic Element 25%
• Electron Microscopy 25%
• Failure to Thrive 25%
• Genetic Disease 25%
• Glycoprotein Biosynthesis 25%
• Hepatocytes 25%
• Heterogenic 25%
• Hypertransaminasemia 50%
• Kupffer Cells 25%
• Large Droplets 25%
• Lining Cells 25%
• Liver 100%
• Liver Biopsy 25%
• Liver Involvement 25%
• Lysosomal Disease 25%
• Mild Fibrosis 25%
• Myelinosomes 50%
• Steatosis 50%
• Transferrin Isoelectric Focusing 25%
• Ultrastructural Features 100%
• Ultrastructural Findings 25%

Medicine and Dentistry

• Bile Canaliculus 33%
• Cardiomyopathy 33%
• Congenital Disorder of Glycosylation 100%
• Congenital Disorder of Glycosylation Type 1x 33%
• Diagnosis 33%
• Disease 33%
• Electron Microscopy 33%
• Elevated Transaminases 66%
• Failure to Thrive 33%
• Fibrosis 33%
• Genetic Disorder 33%
• Glycoprotein 33%
• Hepatocyte 33%
• Isoelectric Focusing 33%
• Kupffer Cell 33%
• Liver Biopsy 33%
• Patient with Congenital Disorder 33%
• Steatosis 66%
• Transferrin 33%

Biochemistry, Genetics and Molecular Biology

• Anabolism 25%
• Congenital Disorder of Glycosylation 100%
• Electron Microscopy 25%
• Elevated Transaminases 50%
• Genetic Disorder 25%
• Glycoprotein 25%
• Hepatocyte 25%
• Isoelectric Focusing 25%
• Kupffer Cell 25%
• Transferrin 25%