نتایج جستجو برای: fap

تعداد نتایج: 1830  

Journal: :Journal of pediatric psychology 2007
Edward D Huntley John V Campo Ronald E Dahl Daniel S Lewin

OBJECTIVE To describe sleep problems among youth with and without functional abdominal pain (FAP). METHODS Participants were 8-15 years of age diagnosed with FAP (n = 67) or healthy pain-free comparisons (n = 80). Parents and participants completed instruments assessing sleep, psychiatric status, and FAP symptoms. Parent and child reports of sleep problems were compared across groups and the ...

Background and Objectives: Familial adenomatous polyposis (FAP) is an inherited disorder and a rare form of colorectal cancer. This disease appears equally in both sexes and its occurrence is more in the second or third decade of life. Mutations and alterations of the mitochondrial genome, especially the D-loop region, have been reported in various human tumors. But the exact role of these muta...

Journal: :Archives of neurology 2005
Yukio Ando Masaaki Nakamura Shukuro Araki

Transthyretin-related familial amyloidotic polyneuropathy (FAP) is a fatal hereditary amyloidosis. Until 20 years ago, FAP was thought to be restricted to endemic occurrence in certain areas. However, owing to progress in biochemical and molecular genetic analyses, FAP is now believed to occur worldwide. As of today, reports of about 100 different points of single or double mutations, or a dele...

Journal: :گوارش 0
narimantas evaldassamalavicius

introduction: due to the whole network of polyposis registers worldwide and early prophylactic treatment, survival of familial adenomatosis (fap) patients is improved. extracolonic manifestations are remarkable feature of fap. two extracolonic manifestations (duodenal adenomatosis, leading duodenal cancer and desmoid tumours) play a very important role in the reasons of death in polyposis popul...

2017
Dan Wang Shengyun Liang Zhao Zhang Guoru Zhao Yuan Hu Shengran Liang Xipeng Zhang Santasree Banerjee

Familial adenomatous polyposis (FAP) is an autosomal dominant precancerous condition, clinically characterized by the presence of multiple colorectal adenomas or polyps. Patients with FAP has a high risk of developing colorectal cancer (CRC) from these colorectal adenomatous polyps by the mean age of diagnosis at 40 years. Germline mutations of the APC gene cause familial adenomatous polyposis ...

Journal: :Inflammatory bowel diseases 2011
Garrett C Zella Elizabeth J Hait Tiffany Glavan Dirk Gevers Doyle V Ward Christopher L Kitts Joshua R Korzenik

BACKGROUND Pouchitis occurs in up to 50% of patients with ulcerative colitis (UC) undergoing ileal pouch anal anastomosis (IPAA). Pouchitis rarely occurs in patients with familial adenomatous polyposis (FAP) who undergo IPAA. Our aim was to compare mucosal and luminal flora in patients with UC-associated pouchitis (UCP), healthy UC pouches (HUC), and healthy FAP pouches (FAP). METHODS Ninetee...

2013
Morten S Dueholm Mads T Søndergaard Martin Nilsson Gunna Christiansen Allan Stensballe Michael T Overgaard Michael Givskov Tim Tolker-Nielsen Daniel E Otzen Per H Nielsen

The fap operon, encoding functional amyloids in Pseudomonas (Fap), is present in most pseudomonads, but so far the expression and importance for biofilm formation has only been investigated for P. fluorescens strain UK4. In this study, we demonstrate the capacity of P. aeruginosa PAO1, P. fluorescens Pf-5, and P. putida F1 to express Fap fibrils, and investigated the effect of Fap expression on...

Journal: :Pediatrics 2013
Grace D Shelby Kezia C Shirkey Amanda L Sherman Joy E Beck Kirsten Haman Angela R Shears Sara N Horst Craig A Smith Judy Garber Lynn S Walker

BACKGROUND Cross-sectional studies link functional abdominal pain (FAP) to anxiety and depression in childhood, but no prospective study has evaluated psychiatric status in adulthood or its relation to pain persistence. METHODS Pediatric patients with FAP (n = 332) and control subjects (n = 147) were tracked prospectively and evaluated for psychiatric disorders and functional gastrointestinal...

2011
David F. Schaeffer Eric M. Yoshida David A. Owen Kenneth W. Berean

It has been well established in the literature that the cribriform-morular variant of papillary thyroid carcinoma (CMVPTC) has been observed with higher frequency in familial adenomatous polyposis (FAP) patients. In the usual setting, patients with FAP are identified based on their germline mutations and the diagnosis of thyroid neoplasm is made after the FAP diagnosis. We herein report a case ...

Journal: :Journal of cell science 2001
H Ungefroren M L Kruse A Trauzold S Roeschmann C Roeder A Arlt D Henne-Bruns H Kalthoff

In this study we investigated the functional role of FAP-1 as a potential inhibitor of CD95 (Fas, APO-1)-mediated apoptosis in pancreatic cancer cells. Stable transfection of the CD95-sensitive, FAP-1-negative cell line Capan-1 with an FAP-1 cDNA resulted in a strongly decreased sensitivity to CD95-induced apoptosis, as measured by DNA fragmentation and caspase-3 activity. Inhibition of cellula...

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