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

scientific article published on 21 July 2009

Asymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1210/JC.2009-0564
P698PubMed publication ID19622622
P5875ResearchGate publication ID26686212

P50authorRajesh ThakkerQ17502119
Michael R BowlQ59582965
Jeshmi JeyabalanQ125320206
P2093author name stringPaul R V Johnson
Fergus V Gleeson
Paul J Newey
Paul T Christie
Gerard V Walls
Brian Shine
Fiona J Ryan
Steve Gould
Rachel R Phillips
P433issue10
P407language of work or nameEnglishQ1860
P921main subjectmultiple endocrine neoplasiaQ1553018
multiple endocrine neoplasia type 1Q3347154
P304page(s)3640-3646
P577publication date2009-07-21
P1433published inThe Journal of Clinical Endocrinology and MetabolismQ3186902
P1476titleAsymptomatic children with multiple endocrine neoplasia type 1 mutations may harbor nonfunctioning pancreatic neuroendocrine tumors
P478volume94

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cites work (P2860)
Q37056120Causes of death and prognostic factors in multiple endocrine neoplasia type 1: a prospective study: comparison of 106 MEN1/Zollinger-Ellison syndrome patients with 1613 literature MEN1 patients with or without pancreatic endocrine tumors
Q38545523Challenges and controversies in management of pancreatic neuroendocrine tumours in patients with MEN1.
Q49957735Current and emerging therapies for PNETs in patients with or without MEN1.
Q94464331Editorial: Early Genetic and Clinical Diagnosis in MEN1
Q37785239Endocrine Cancer Predisposition Syndromes: Hereditary Paraganglioma, Multiple Endocrine Neoplasia Type 1, Multiple Endocrine Neoplasia Type 2, and Hereditary Thyroid Cancer
Q34167625Genetic screening for multiple endocrine neoplasia syndrome type 1 (MEN-1): when and how
Q47165101Hypercalcemic Disorders in Children.
Q43066318Imaging in multiple endocrine neoplasia type 1: recent studies show enhanced sensitivities but increased controversies
Q51336795Is Routine Screening of Young Asymptomatic MEN1 Patients Necessary?
Q90669649La néoplasie endocrinienne multiple de type 1 : mise au point après le congrès de l’ENETS 2019: Multiple Endocrine Neoplasia Type 1: Development after the ENETS 2019 Congress
Q33922666Late onset asymptomatic pancreatic neuroendocrine tumor - A case report on the phenotypic expansion for MEN1.
Q36377417MEN1 in children and adolescents: Data from patients of a regional referral center for hereditary endocrine tumors
Q38951675Multiple Endocrine Neoplasia: A Genetically Diverse Group of Familial Tumor Syndromes
Q38411934Multiple endocrine neoplasia syndromes 1 and 2: manifestations and management in childhood and adolescence
Q86555949Multiple endocrine neoplasia type 1
Q28296266Multiple endocrine neoplasia type 1 (MEN1) and type 4 (MEN4)
Q36911589Pasireotide Therapy of Multiple Endocrine Neoplasia Type 1-Associated Neuroendocrine Tumors in Female Mice Deleted for an Men1 Allele Improves Survival and Reduces Tumor Progression
Q35661980Proliferation rates of multiple endocrine neoplasia type 1 (MEN1)-associated tumors
Q92354342Proposition of adjustments to the ACMG-AMP framework for the interpretation of MEN1 missense variants
Q90675538Questions and Controversies About Parathyroid Pathophysiology in Children With Multiple Endocrine Neoplasia Type 1
Q57032522Results of Duodenopancreatic Reoperations in Multiple Endocrine Neoplasia Type 1
Q50009808Synchronous Solid Pseudopapillary Tumor and Insulinoma in an Adolescent MEN1 Patient Presenting with Diagnostic Dilemmas
Q97887355Unusual Combination of MEN-1 and the Contiguous Gene Deletion Syndrome of CAH and Ehlers-Danlos Syndrome (CAH-X)
Q38852179Utility of chromogranin A, pancreatic polypeptide, glucagon and gastrin in the diagnosis and follow-up of pancreatic neuroendocrine tumours in multiple endocrine neoplasia type 1 patients