نتایج جستجو برای: polyposis

تعداد نتایج: 11192  

2006
Eileen Friedman Scott Gillin Martin Lipkin

We have developed a method for the routine primary culture of human colonie epithelial cells. Cultured cells exhibited char acteristic epithelial structures, including a brush border and junctional complexes. Flask-like goblet cells containing mucus were also seen within the epithelial monolayer. [3H]Thymidine labeling indices were used to distinguish between cultured cells from familial polypo...

Journal: :Gut 1991
F M Giardiello G J Offerhaus E I Traboulsi J C Graybeal I H Maumenee A J Krush L S Levin S V Booker S R Hamilton

Familial adenomatous polyposis is an autosomal dominant disease characterised by the development of hundreds of colorectal adenomas in young adults. Occult radio-opaque jaw lesions and pigmented ocular fundus lesions (formerly called congenital hypertrophy of the retinal pigment epithelium) are extraintestinal phenotypic markers for this disorder. We evaluated the usefulness of the combination ...

Journal: :Human molecular genetics 2014
Laura Valle Eva Hernández-Illán Fernando Bellido Gemma Aiza Adela Castillejo María-Isabel Castillejo Matilde Navarro Nuria Seguí Gardenia Vargas Carla Guarinos Miriam Juarez Xavier Sanjuán Silvia Iglesias Cristina Alenda Cecilia Egoavil Ángel Segura María-José Juan María Rodriguez-Soler Joan Brunet Sara González Rodrigo Jover Conxi Lázaro Gabriel Capellá Marta Pineda José Luís Soto Ignacio Blanco

Germline mutations in DNA polymerase ɛ (POLE) and δ (POLD1) have been recently identified in families with multiple colorectal adenomas and colorectal cancer (CRC). All reported cases carried POLE c.1270C>G (p.Leu424Val) or POLD1 c.1433G>A (p.Ser478Asn) mutations. Due to the scarcity of cases reported so far, an accurate clinical phenotype has not been defined. We aimed to assess the prevalence...

2014
M. GELARDI L. IANNUZZI S. TAFURI G. PASSALACQUA N. QUARANTA

Rhinitis and rhinosinusitis (with/without polyposis), either allergic or non-allergic, represent a major medical problem. Their associated comorbidities and relationship with family history have so far been poorly investigated. We assessed these aspects in a large population of patients suffering from rhinosinusal diseases. Clinical history, nasal cytology, allergy testing and direct nasal exam...

Journal: :WMJ : official publication of the State Medical Society of Wisconsin 2008
David Rabago Emily Guerard Don Bukstein

BACKGROUND Rhinosinusitis is a common, expensive disorder with a significant impact on patients' quality of life. Chronic sinus symptoms are associated with allergic rhinitis, asthma, and nasal polyposis. Saline nasal irrigation is an adjunctive therapy for rhinosinusitis and sinus symptoms. Prior studies suggest that hypertonic saline nasal irrigation (HSNI) may be effective for symptoms assoc...

2016
Amy L. Masson Bente A. Talseth-Palmer Tiffany-Jane Evans Patrick McElduff Allan D. Spigelman Garry N. Hannan Rodney J. Scott

Familial Adenomatous Polyposis (FAP) is the second most common inherited predisposition to colorectal cancer (CRC) associated with the development of hundreds to thousands of adenomas in the colon and rectum. Mutations in APC are found in ~ 80% polyposis patients with FAP. In the remaining 20% no genetic diagnosis can be provided suggesting other genes or mechanisms that render APC inactive may...

Journal: :Gut 1998
M P Buisine J F Colombel M Lecomte-Houcke P Gower J P Aubert N Porchet A Janin

BACKGROUND Cap polyposis is a rare disease characterised by mucoid and bloody diarrhoea, with polyps covered by a cap of mucoid and fibrinopurulent exudate. The pathogenesis is not known. AIMS To pour some light on cap polyposis pathogenesis, by examining the mucus of patients and analysing the expression of five mucin genes, MUC2, MUC3, MUC4, MUC5AC, and MUC5B. PATIENT AND METHODS The stud...

Journal: :The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology 2005
Cüneyt Kayaalp Sevil Işik Soner Akbaba Gürel Neşşar Erkan Oymaci Canbek Seven

The aim of this study was to assess whether restorative proctocolectomy was suitable as an initial procedure for selected familial adenomatous polyposis patients with coexisting colorectal cancer. Six malignancy patients who underwent restorative proctocolectomy for familial adenomatous polyposis were reviewed. At the time of restorative proctocolectomy, cancer was not suspected in four patient...

Journal: :Journal of medical genetics 2004
M Roupret J Catto F Coulet A-R Azzouzi N Amira T Karmouni G Fromont M Sibony G Vallancien B Gattegno M Meuth F C Hamdy O Cussenot

U pper urinary tract transitional cell carcinoma (UUTTCC) accounts for 5% of all urothelial carcinomas. Hereditary non-polyposis colorectal cancer (HNPCC) is an autosomal dominant syndrome predisposing to colorectal cancer that accounts for about 5% of all colorectal cancers. It is revealed by colorectal cancer (63%) or extracolonic cancers, most often of the endometrium (9%) or ovary, but some...

Introduction: To evaluate the most sensitive symptom to predict early recurrence of nasal polyposis. Prospective longitudinal cohort study. Tertiary university referral center with accredited otorhinolaryngology residency programs.  Materials and Methods: In this prospective study, we evaluated 62 patients with diffuse nasal polyposis. All patients underwent functional endoscopic sinus surgery...

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