Aggressive therapy improves cirrhosis in glycogen storage disease type IX

Molecular Genetics and Metabolism

Volumn 109, Issue 2, 2013, Pages 179-182

  Tsilianidis, Laurie A ^a   Fiske, Laurie M ^b   Siegel, Sara ^b   Lumpkin, Chris ^b   Hoyt, Kate ^b   Wasserstein, Melissa ^c   Weinstein, David A ^b  

^a LERNER RESEARCH INSTITUTE   (United States)

^b UNIVERSITY OF FLORIDA COLLEGE OF MEDICINE   (United States)

^c MOUNT SINAI SCHOOL OF MEDICINE   (United States)

Author keywords

Cirrhosis; Glycogen storage disease type IX; GSD; PhK; Treatment; XLG

Indexed keywords

ALANINE AMINOTRANSFERASE; ASPARTATE AMINOTRANSFERASE; GLYCOGEN; LACTIC ACID; PROTEIN; STARCH; TRIACYLGLYCEROL;

ABDOMINAL DISTENSION; ARTICLE; CASE REPORT; ECHOGRAPHY; GENE; GLYCOGEN STORAGE DISEASE; GLYCOGEN STORAGE DISEASE TYPE 9; GROWTH RATE; HEPATOMEGALY; HUMAN; HUMAN TISSUE; HYPOGLYCEMIA; KETOACIDOSIS; LIVER BIOPSY; LIVER CIRRHOSIS; LIVER FIBROSIS; LIVER TRANSPLANTATION; MALE; MUTATIONAL ANALYSIS; NAUSEA AND VOMITING; PHKA2 GENE; PRIORITY JOURNAL; PROTEIN INTAKE;

ADMINISTRATION, ORAL; CHILD; DIETARY PROTEINS; GLYCOGEN STORAGE DISEASE; HUMANS; MALE; STARCH; TREATMENT OUTCOME;

EID: 84878519131     PISSN: 10967192     EISSN: 10967206     Source Type: Journal    
DOI: 10.1016/j.ymgme.2013.03.009     Document Type: Article

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