Results 91 to 100 of about 10,344 (216)

Copy-Number Variants in Patients with a Strong Family History of Pancreatic Cancer [PDF]

, 2007
Copy-number variants such as germ-line deletions and amplifications are associated with inherited genetic disorders including familial cancer. The gene or genes responsible for the majority of familial clustering of pancreatic cancer have not been ...
Brune, K., Goggins, M., Hruban, R. H., Klein, A. P., Krasnitz, A., Lakshmi, B., Lucito, R., Maitra, A., Palmisano, E., Pandey, A., Sebat, J., Suresh, S., Walter, K., Wigler, M. H.   +13 more
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Seguridad y eficacia de la polipectomía en intestino delgado utilizando enteroscopio asistido por balones en pacientes pediátricos con síndrome de Peutz-Jeghers

Revista de Gastroenterología de México, 2018
Resumen: Introducción y objetivos: El síndrome de Peutz-Jeghers (SPJ) es una enfermedad hereditaria, autosómica dominante caracterizada por la presencia de pólipos hamartomatosos en el tubo digestivo de predominio en el intestino delgado y que se ...
G. Blanco-Velasco, O.V. Hernández-Mondragón, J.M. Blancas-Valencia, V. Paz-Flores, D. Fuentes-Hernández, P. Rodríguez-González, B. González-Ortíz   +6 more
doaj   +1 more source

A kettős-ballonos endoszkópia szerepe a vékonybél betegségeinek diagnózisában és kezelésében összehasonlítva a kapszulás endoszkópiával [PDF]

, 2009
A legutóbbi évekig csak a vékonybél kezdeti szakasza volt megközelíthetô a diagnosztikus vagy terápiás endoszkópos beavatkozások számára. Egy új, kettôs ballonos (DBE) endoszkópos eljárás, amely nagy felbontású képet szolgáltat, mindkettôre ...
Fuszek, Péter, Gemela, Orsolya, Horváth, Henrik Csaba, Lakatos, Péter László, Nagypál, Anna, Nemeth, Artúr, Papp, János Mihály, Pák, Gábor, Rácz, István, Zubek, László   +9 more
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Laugier-Hunziker Syndrome: A Case Report [PDF]

, 2011
Laugier-Hunziker syndrome (LHS) is a rare, acquired mucocutaneous hyperpigmentation often associated with longitudinal melanonychia. It is important to differentiate this condition from the pigmentary disorders of the oral mucosa.
Demet Kartal, Levent Kartal, Murat Borlu
core   +1 more source

Hereditary colorectal cancer syndromes: Epidemiological studies on Peutz-Jeghers syndrome & Lynch syndrome [PDF]

, 2011
Colorectal cancer (CRC) is the second most common malignancy among women after breast cancer, and the third most common malignancy among men after lung and prostate cancer in the European Union. In the Netherlands, approximately 10000 cases are diagnosed
Lier, M.G.F. (Margot) van
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Post-translational regulation contributes to the loss of LKB1 expression through SIRT1 deacetylase in osteosarcomas [PDF]

, 2017
background: The most prevalent form of bone cancer is osteosarcoma (OS), which is associated with poor prognosis in case of metastases formation. Mice harbouring liver kinase B1 (LKB1+/−) develop osteoblastoma-like tumours.
A Alexander, A Calles, A Longhi, A Ylikorkala, Adrienne M Flanagan, AF Baas, B Bai, BY Shorning, CS Lim, CX Deng, D Lee, D Zhong, DG Hardie, F Lan, F Wang, F Yeung, FM Giardiello, G Lao, G Ottaviani, H Gaude, H Ji, HJ Bae, Hongtao Ye, J Ban, J Boudeau, J Godlewski, J Li, J Robinson, J van Loosdregt, JC Strum, JI Partanen, JM Lizcano, JR Knight, K Li, K Patel, L Ottaviano, L Shi, L Zhang, LA Boardman, Laure Alice Duhamel, LR Saunders, M Fernanda Amary, M Kovac, M Momcilovic, M Sanchez-Cespedes, M Sanchez-Cespedes, M Yamakuchi, M Yamakuchi, Malihe Eskandarpour, ME Ritchie, MF Amary, Nadège Presneau, RC Gentleman, Roberto Tirabosco, S Lain, S Lorenz, S Takeda, S Takeda, SA Hawley, SB Sobottka, SN Wingo, T Bouras, X Chen, Y Shi, Y Sun, Y Yin, Y Zu, YS Hori, Z Zheng, ZY Wu   +69 more
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[Peutz-Jeghers syndrome].

Anales de pediatria (Barcelona, Spain : 2003), 2008
Peutz-Jeghers syndrome is an inherited disorder which usually debuts during childhood. It is characterized by mucocutaneous pigmentation and hamartomatous polyps in the gastrointestinal tract. Numerous reports indicate a high incidence of gastrointestinal and extraintestinal cancer in these patients, their appearance at a young age, as well as its ...
M J, Pérez Rodríguez, F M, Anaya Barea, E, Galiano Fernández, D, de Diego Sierra, I, Condado Sánchez-Rojas   +4 more
openaire   +1 more source

Síndrome de Peutz - Jeghers: Seguimiento de una familia Syndrome of Peutz - Jeghers: Follow to family

Revista Colombiana de Cirugía, 2007
El síndrome Peutz - Jeghers es una enfermedad con pólipos del colon con un patrón autosómico dominante, su tipo histológico es hamartomatoso y aunque es muy rara la transformación maligna, se ha postulado una secuencia hamartoma - carcinoma.
María Helena Gaitán Buitrago, Alejandro Vélez Hoyos, Luis G Carvajal-Carmona, José Ignacio Restrepo R, Hernán Restrepo, Mario Hernán Ruiz Vélez, Fabián Juliao Baños, Rodrigo Castaño Llano   +7 more
doaj  

LKB1 tumor suppression in Peutz-Jeghers Syndrome [PDF]

, 2008
Kasvainten, ajatellaan syntyvän yksittäisen solun perimän mutaatioista, jonka seurauksena tuon solun kasvu häiriintyy. Ruoansulatuskanavan polyyppien syntyä käytetään usein mallina siitä, miten nämä epiteelisoluun kerääntyvät mutaatiot aiheuttavat ...
Katajisto, Pekka
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Osseous metaplasia in an ulcerating tubular adenoma of the colon: a case report [PDF]

, 2008
Introduction Heterotopic bone is rarely found in the gastrointestinal tract. Here we report a rare case of metaplastic ossification within a benign ulcerating adenoma and review the literature concerning the aetiology.
Victoria White, Aidan G Shaw, Gillian M Tierney, Jonathan N Lund, David Semeraro, HT Van Patter, WE Delaney, CW Hall, MR Schevach, GY Lauwers, MC Papadopoulos, WI Al-Daraji, GM Groisman, MH Sperling, S Haque, T Narita, A Cavazza, AB Shafritz, NS Apostolidis, P Godbole   +19 more
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