Intermittent and recurrent hepatomegaly due to glycogen storage in a patient with type 1 diabetes: Genetic analysis of the liver glycogen phosphorylase gene (PYGL)

Diabetes Research and Clinical Practice

Volumn 65, Issue 2, 2004, Pages 175-182

  Tomihira, Masako ^a   Kawasaki, Eiji ^b   Nakajima, Hiromu ^c   Imamura, Yutaka ^a   Sato, Yuichi ^a   Sata, Michio ^d   Kage, Masayoshi ^d   Sugie, Hideo ^e   Nunoi, Kiyohide ^a  

^a ST MARY S HOSPITAL   (Japan)

^b NAGASAKI UNIVERSITY   (Japan)

^c OSAKA MEDICAL CENTER FOR CANCER AND CARDIOVASCULAR DISEASES   (Japan)

^d KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^e Hamamatsu City Med Ctr Devmtl M   (Japan)

Author keywords

Liver glycogen storage; Mauriac syndrome; Polymorphisms; PYGL; Type 1 diabetes

Indexed keywords

GLYCOGEN PHOSPHORYLASE;

ACIDEMIA; ADULT; AMINO ACID SEQUENCE; AMINOTRANSFERASE BLOOD LEVEL; ARTICLE; CASE REPORT; CLINICAL FEATURE; CONSCIOUSNESS; DIABETIC KETOACIDOSIS; ELECTRON MICROSCOPY; FEMALE; GENETIC ANALYSIS; GENOTYPE; GLYCOGEN LIVER LEVEL; GLYCOGEN STORAGE DISEASE; GROWTH RETARDATION; HEPATOMEGALY; HOSPITAL ADMISSION; HUMAN; HUMAN TISSUE; HYPERGLYCEMIA; HYPOGLYCEMIA; INSULIN DEPENDENT DIABETES MELLITUS; LIVER BIOPSY; MEDICAL EXAMINATION; MICROSCOPY; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; RECURRENT DISEASE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADULT; DIABETES MELLITUS, TYPE 1; FEMALE; GLYCOGEN PHOSPHORYLASE; HEPATOMEGALY; HUMANS; LIVER; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 3042520992     PISSN: 01688227     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.diabres.2003.12.004     Document Type: Article

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