The liver in congenital disorders of glycosylation: Ultrastructural features

Ultrastructural Pathology

Volumn 31, Issue 3, 2007, Pages 189-197

  Iancu, Theodore C ^a   Mahajnah, Muhammad ^a   Manov, Irena ^a   Cherurg, Sigal ^b   Knopf, Carlos ^a   Mandel, Hanna ^a  

^a TECHNION ISRAEL INSTITUTE OF TECHNOLOGY   (Israel)

^b Kupat Cholim Meuchedet ^*  (Israel)

Author keywords

Cardiomyopathy; Congenital disorders of glycosylation; Electron microscopy; Failure to thrive; Hypertransaminasemia; Lysosomal storage disease; Lysosomes; Myelinosomes

Indexed keywords

CAPTOPRIL;

ARTICLE; CARDIOMYOPATHY; CASE REPORT; CONGENITAL DISORDER OF GLYCOSYLATION; ELECTRON MICROSCOPY; FAILURE TO THRIVE; FATTY LIVER; HUMAN; HUMAN CELL; HUMAN TISSUE; HYPERTRANSAMINASEMIA; KUPFFER CELL; LIVER; LIVER BIOPSY; LIVER CELL; LIVER FIBROSIS; MALE; METABOLIC DISORDER; PRIORITY JOURNAL; SIBLING; ULTRASTRUCTURE;

CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME; CARDIOMYOPATHIES; CHILD, PRESCHOOL; CONSANGUINITY; GENES, RECESSIVE; GLYCOSYLATION; HEPATOCYTES; HUMANS; INFANT; ISOELECTRIC FOCUSING; LIVER; MALE; MICROSCOPY, ELECTRON, TRANSMISSION; SIBLINGS; TRANSFERRIN;

EID: 34447130291     PISSN: 01913123     EISSN: 15210758     Source Type: Journal    
DOI: 10.1080/01913120701348286     Document Type: Article

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