Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors

Journal of Clinical Endocrinology and Metabolism

Volumn 94, Issue 10, 2009, Pages 3640-3646

  Newey, Paul J ^a   Jeyabalan, Jeshmi ^a   Walls, Gerard V ^a   Christie, Paul T ^a   Gleeson, Fergus V ^b   Gould, Steve ^c   Johnson, Paul R V ^c   Phillips, Rachel R ^b   Ryan, Fiona J ^c   Shine, Brian ^a   Bowl, Michael R ^a   Thakker, Rajesh V ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b CHURCHILL HOSPITAL   (United Kingdom)

^c JOHN RADCLIFFE HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOGRANIN A; GASTRIN; GASTROINTESTINAL HORMONE; INSULIN; SYNAPTOPHYSIN;

ADOLESCENT; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CONFERENCE PAPER; EUROPE; FEMALE; GENE; GENE MUTATION; HUMAN; HUMAN TISSUE; HYPOPHYSIS ADENOMA; IMMUNOHISTOCHEMISTRY; MEN1 GENE; MULTIPLE ENDOCRINE NEOPLASIA; NEUROENDOCRINE TUMOR; PANCREAS TUMOR; PENETRANCE; PRIMARY HYPERPARATHYROIDISM; PRIORITY JOURNAL; PROLACTINOMA; SCHOOL CHILD; TUMOR VOLUME;

EID: 70349932651     PISSN: 0021972X     EISSN: 0021972X     Source Type: Journal    
DOI: 10.1210/jc.2009-0564     Document Type: Conference Paper

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