Gastric dysmotility associated with accumulation of mitochondrial A3243G mutation in the stomach

Internal Medicine

Volumn 43, Issue 12, 2004, Pages 1126-1130

  Fujii, Akihiro ^c   Yoneda, Makoto ^c   Ohtani, Masahiro ^c   Nakagawa, Hiroto ^c   Kumano, Takanori ^c   Hayashi, Koji ^c   Muramatsu, Atsushi ^c   Takabatake, Satoru ^a   Ibi, Tohru ^b   Sahashi, Ko ^b   Azuma, Takeshi ^c   Kuriyama, Masaru ^c  

^a Fukui General Hospital   (Japan)

^b AICHI MEDICAL UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^c UNIVERSITY OF FUKUI   (Japan)

Author keywords

Gastric dysmotility; Gastric emptying; Gastric myoelectrical activity; Mitochondrial DNA mutation

Indexed keywords

ALANINE; GLYCINE; MITOCHONDRIAL DNA; PARACETAMOL;

ADULT; AMINO ACID SUBSTITUTION; ARTICLE; CASE REPORT; CHILD; DNA DETERMINATION; DRUG BLOOD LEVEL; EPIGASTRIC PAIN; FEMALE; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; LEUKOCYTE; MALE; MOUTH MUCOSA; MYOELECTRICITY; NAUSEA AND VOMITING; POSTPRANDIAL STATE; RISK FACTOR; SKELETAL MUSCLE; STOMACH ANTRUM; STOMACH DISEASE; STOMACH EMPTYING; STOMACH MOTILITY; STOMACH MUCOSA; SYMPTOMATOLOGY;

ADULT; CHILD; DNA, MITOCHONDRIAL; FEMALE; GASTRIC EMPTYING; GASTROINTESTINAL MOTILITY; HUMANS; MALE; MIDDLE AGED; MYOELECTRIC COMPLEX, MIGRATING; POINT MUTATION; STOMACH; STOMACH DISEASES;

EID: 19944427650     PISSN: 09182918     EISSN: None     Source Type: Journal    
DOI: 10.2169/internalmedicine.43.1126     Document Type: Article

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