Results 91 to 100 of about 5,629 (238)
Clinical and genetic characteristics of Multiple Endocrine Neoplasia type 1 (MEN 1) syndrome in a small cohort of Swiss patients [PDF]
, 2015 Multiple endocrine neoplasia type 1 (MEN1) syndrome is a polyglandular autosomal dominant transmitted disease characterized by the combined occurrence of several endocrine gland tumors.
ROSSIER, S.
core
Gastrins and gastrinomas [PDF]
Postgraduate Medical Journal, 1984 Summary The past 20 years have seen gastrin attain true hormonal status. Its structure has been characterized, it has been synthesized, radioimmunoassays for its measurement in blood and tissues have been developed and its physiology and metabolism elucidated.
openaire +2 more sources
Síndrome de Zollinger-Ellison: revisión del conocimiento actual
Revista Colombiana de Cirugía, 2016 El síndrome de Zollinger-Ellison se caracteriza por la presencia de úlceras pépticas resistentes al tratamiento que se deben a la hipersecreción ectópica de gastrina por un tumor neuroendocrino, que es el gastrinoma y que resulta en la hipersecreción de ...
Marcelo A. Beltrán
doaj
Neuroendocrine Tumors (NETs) : A population-based study of incidence and survival in Girona province, 1994-2004 [PDF]
, 2012 Els tumors neuroendocrins (TNEs) són un grup de neoplàsies poc freqüents i heterogènies i amb un ampli espectre d'agressivitat. Hi ha molt poca informació epidemiològica a nivell mundial, l'objectiu d'aquest estudi ha estat el de reportar-ne les dades a ...
Alsina Maqueda, Maria +3 more
core
Malignant pancreatic gastrinoma in a maned wolf (Chrysocyon brachyurus): case report
Arquivo Brasileiro de Medicina Veterinária e ZootecniaA captive 12-year-old female maned wolf (Chrysocyon brachyurus), previously diagnosed with visceral leishmaniasis, developed severe myiasis in the right ear, followed by prostration and death.
T.F. Carvalho +5 more
doaj +1 more source
Metastasized pancreatic neuroendocrine tumor in a teenage girl: a case report [PDF]
, 2015 Introduction: Metastasized pancreatic neuroendocrine tumors are extremely rare malignancies, especially in children. Therefore, therapeutic options are limited, and few standardized therapy regimens exist.
Günther, Patrick +2 more
core +1 more source
The Relationship of Gastrinoma in MEN 1 to Helicobacter pylori infection [PDF]
, 2020 Ryan Endall +3 more
openalex +1 more source
Zollinger-Ellison syndrome associated with neurofibromatosis type 1: a case report
BMC Cancer, 2005 Background Neurofibromatosis type 1 is an autosomal dominant neurocutaneous disorder with characteristic features of skin and central nervous system involvement. Gastrointestinal involvement is rare, but the risk of malignancy development is considerable.
Choi Sung-Kyu +9 more
doaj +1 more source
Case Reports in Medicine, 2011 Introduction. Gastrinoma should be suspected when the peptic ulcer(s) is postbulbar, multiple, refractory, or recurrent, or ulcer is associated with nephrolithiasis, hypocalcaemia, or erosive esophagitis. The majority of gastrinomas are malignant.
Seyed Saeid Sarkeshikian +1 more
doaj +1 more source
Evolution of clinical ideas about Zollinger-Ellison syndrome
Терапевтический архив, 2014 The paper gives the current views of the diagnosis and treatment of Zollinger-Ellison syndrome (ZES). It underlines the importance of including ZES in differential diagnosis in patient with frequently recurrent and standard-dose proton pump inhibitor ...
I V Maev +3 more
doaj