A Novel Von Hippel-Lindau case with germline mutation at codon 167 (CGG to TGG) having endocrine microadenomatosis of the pancreas

Digestive Diseases and Sciences

Volumn 52, Issue 11, 2007, Pages 3145-3148

  Akatsu, Tomotaka ^a   Aiura, Koichi ^a   Ito, Yasuhiro ^a   Ueda, Masakazu ^a   Kameyama, Kaori ^a   Kitajima, Masaki ^a  

^a KEIO UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

Clear cell; Endocrine tumor; Germline mutation; Microadenomatosis; Pancreas; Von Hippel Lindau

Indexed keywords

ABDOMINAL ANGIOGRAPHY; ADENOMATOSIS; ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; CODON; DISEASE ASSOCIATION; FEMALE; GENE MUTATION; GERM LINE; HISTOLOGY; HUMAN; HUMAN TISSUE; LABORATORY TEST; METASTASIS; MICROSCOPY; NEPHRECTOMY; PANCREAS DISEASE; PANCREATICODUODENECTOMY; PRIORITY JOURNAL; VON HIPPEL LINDAU DISEASE;

ADENOMA, ISLET CELL; ADULT; CODON; DIAGNOSIS, DIFFERENTIAL; FEMALE; GERM-LINE MUTATION; HIPPEL-LINDAU DISEASE; HUMANS; MULTIPLE ENDOCRINE NEOPLASIA TYPE 1; PANCREATIC NEOPLASMS; TOMOGRAPHY, X-RAY COMPUTED;

EID: 34848897545     PISSN: 01632116     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10620-007-9780-x     Document Type: Article

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