نتایج جستجو برای: endocrine imaging

تعداد نتایج: 500609  

Journal: :iranian journal of radiation research 0
s. rabie mahdavi department of medical physics, babol university of medical sciences, babol, iran a. shirazi department of biophysics, faculty of medicine, tehran university of medical sciences, tehran, iran d. sardari department of biophysics, faculty of medicine, tehran university of medical sciences, tehran, iran l. sadri azad research and science university, tehran, iran

abstractbackground: delivering the radiation dose to the target volume and minimizing the dose to normal tissues are the main objectives in radiotherapy. the aim of our study is to enhance the contrast of the portal image to increase the accuracy of delineation of the organs in the irradiation field.   methods: the software was written based on local enhancement of the pixel values in image mat...

2016
Zhen Huo Tao Lu Zhiyong Liang Fan Ping Jie Shen Jingjing Lu Wenbing Ma Dachun Zhao Dingrong Zhong

BACKGROUND Isolated hypothalamic-pituitary Langerhans cell histiocytosis (HPLCH) is very rare. We investigated the clinicopathological characteristics, endocrine function changes, BRAFV600E mutations and treatments of isolated HPLCH. METHODS We identified seven patients with isolated HPLCH by reviewing the clinical and pathological files in our hospital from 2007 to 2015. The clinical charact...

Journal: :Endocrine journal 2010
Yuji Tani Toru Sugiyama Shinichi Hirooka Hajime Izumiyama Yukio Hirata

A 75-year-old woman was admitted to our hospital because of a poor glycemic control. She was found to have Cushingoid feature and dynamic endocrine tests showed elevated plasma ACTH and cortisol levels, lack of their circadian rhythm, non-suppressibility to high-dose dexamethasone, responsiveness to CRH, but not to DDAVP, and suppression to octreotide. Pituitary MRI showed an equivocal small le...

Journal: :Arquivos brasileiros de cirurgia digestiva : ABCD = Brazilian archives of digestive surgery 2012
Flávia Thaiana Bonato Júlio Cezar Uili Coelho Andrea Petruzzielo Jorge Eduardo Fouto Matias Gustavo Arantes Ferreira

BACKGROUND Insulinoma is a pancreatic neuroendocrine tumor originated from pancreatic islet beta cells. Although rare, is the most common pancreatic endocrine tumor, with about four cases per million people. The preferential treatment of insulinoma is surgical. AIM To analyze the epidemiological, pathological, clinical and surgical patients treated in the last decade in two surgical services....

Journal: :Mechanisms of Development 2009
Emilie Pacary Julian Heng Diogo Castro François Guillemot

During development, the pancreatic endocrine cells are specified within the epithelium. They will subsequently delaminate and migrate out of the epithelium in order to form the islets. Neurogenin3 (Ngn3) is a bHLH transcription factor that is responsible for differentiation of all endocrine cell types, but whether or not it has a role in their migration is still an open question. By using the c...

Journal: :Mechanisms of Development 2009
Timm Haack Bernd Schwendele Andrew Renault

During development, the pancreatic endocrine cells are specified within the epithelium. They will subsequently delaminate and migrate out of the epithelium in order to form the islets. Neurogenin3 (Ngn3) is a bHLH transcription factor that is responsible for differentiation of all endocrine cell types, but whether or not it has a role in their migration is still an open question. By using the c...

Journal: :Mechanisms of Development 2009
Richard L. Mort Ian J. Jackson

During development, the pancreatic endocrine cells are specified within the epithelium. They will subsequently delaminate and migrate out of the epithelium in order to form the islets. Neurogenin3 (Ngn3) is a bHLH transcription factor that is responsible for differentiation of all endocrine cell types, but whether or not it has a role in their migration is still an open question. By using the c...

Journal: :The Yale Journal of Biology and Medicine 1996
M. Mignon G. Cadiot J. P. Marmuse M. J. Lewin

Zollinger-Ellison syndrome (ZES) is a rare disease. Its management concerns symptoms related to the gastric acid overproduction that characterizes the syndrome and to the gastrin-producing tumor(s) usually located in the duodenal wall and/or the endocrine pancreas. Acid hypersecretion is now controlled by the use of powerful antisecretory agents. Management of the malignant process(es) has beco...

Journal: :Mechanisms of Development 2009
Mathieu Gouzi Kerstin Johansson Nancy Thompson Josselin Soyer Gérard Gradwohl Anne Grapin-Botton

During development, the pancreatic endocrine cells are specified within the epithelium. They will subsequently delaminate and migrate out of the epithelium in order to form the islets. Neurogenin3 (Ngn3) is a bHLH transcription factor that is responsible for differentiation of all endocrine cell types, but whether or not it has a role in their migration is still an open question. By using the c...

Journal: :Archives of disease in childhood 1998
A Cade M Walters J W Puntis R J Arthur M D Stringer

AIM To evaluate long term detailed pancreatic endocrine and exocrine function in children with persistent hyperinsulinaemic hypoglycaemia of infancy (PHHI) after 85-95% pancreatectomy. METHODS Six children with PHHI between 0.9 and 12.7 years after pancreatic resection underwent clinical and investigative follow up at 1.0 to 14.9 years of age. One child with PHHI who had not had pancreatectom...

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