Research
Print page Print page
Switch language
The Capital Region of Denmark - a part of Copenhagen University Hospital
Published

Juvenile polyposis of the stomach--a novel cause of hypergastrinemia

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

APA

CBE

MLA

Vancouver

Author

Papay, Karen D ; Falck, Vincent G ; Poulsen, Steen Seier ; Panaccione, Remo ; Rehfeld, Jens F. ; Storr, Martin A. / Juvenile polyposis of the stomach--a novel cause of hypergastrinemia. In: Nature reviews. Gastroenterology & hepatology. 2010 ; Vol. 7, No. 10. pp. 583-8.

Bibtex

@article{4895a0b41fd646c182fb104e4c4ef2a9,
title = "Juvenile polyposis of the stomach--a novel cause of hypergastrinemia",
abstract = "A 38-year-old female presented with a 3-year history of postprandial abdominal pain, refractory nausea, vomiting and hematemesis. She appeared malnourished and her symptoms were refractory to previous treatment with acid-suppressive drugs, prokinetics and antiemetics. Her medical history was significant for a diagnosis of juvenile polyposis syndrome at the age of 14 resulting in a transverse colectomy, and a diagnosis of Crohn's disease in her residual colon at the age of 35 resulting in a total colectomy.",
author = "Papay, {Karen D} and Falck, {Vincent G} and Poulsen, {Steen Seier} and Remo Panaccione and Rehfeld, {Jens F.} and Storr, {Martin A}",
year = "2010",
month = "10",
day = "1",
doi = "10.1038/nrgastro.2010.138",
language = "English",
volume = "7",
pages = "583--8",
journal = "Nature Reviews Gastroenterology and Hepatology",
issn = "1759-5045",
publisher = "Nature Publishing Group",
number = "10",

}

RIS

TY - JOUR

T1 - Juvenile polyposis of the stomach--a novel cause of hypergastrinemia

AU - Papay, Karen D

AU - Falck, Vincent G

AU - Poulsen, Steen Seier

AU - Panaccione, Remo

AU - Rehfeld, Jens F.

AU - Storr, Martin A

PY - 2010/10/1

Y1 - 2010/10/1

N2 - A 38-year-old female presented with a 3-year history of postprandial abdominal pain, refractory nausea, vomiting and hematemesis. She appeared malnourished and her symptoms were refractory to previous treatment with acid-suppressive drugs, prokinetics and antiemetics. Her medical history was significant for a diagnosis of juvenile polyposis syndrome at the age of 14 resulting in a transverse colectomy, and a diagnosis of Crohn's disease in her residual colon at the age of 35 resulting in a total colectomy.

AB - A 38-year-old female presented with a 3-year history of postprandial abdominal pain, refractory nausea, vomiting and hematemesis. She appeared malnourished and her symptoms were refractory to previous treatment with acid-suppressive drugs, prokinetics and antiemetics. Her medical history was significant for a diagnosis of juvenile polyposis syndrome at the age of 14 resulting in a transverse colectomy, and a diagnosis of Crohn's disease in her residual colon at the age of 35 resulting in a total colectomy.

U2 - 10.1038/nrgastro.2010.138

DO - 10.1038/nrgastro.2010.138

M3 - Journal article

VL - 7

SP - 583

EP - 588

JO - Nature Reviews Gastroenterology and Hepatology

JF - Nature Reviews Gastroenterology and Hepatology

SN - 1759-5045

IS - 10

ER -

ID: 31046514