Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Demian A Fullerton"'
Autor:
Ximena Cid, Pablo Florenzano, Nicole Lustig, Luis Manuel Sanhueza, Demian A Fullerton, Germán Ramos, Natalie Thone
Publikováno v:
Revista médica de Chile v.142 n.8 2014
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Constrictive Pericarditis (CP) is an unusual disease. Its most common causes are idiopathic or secondary to cardiac surgery. Less frequently it is caused by connective tissue diseases. We report a 30 years old woman hospitalized due to progressive dy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::71070d07a0768e33a43e816937e1c2ab
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872014000800015
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872014000800015
Autor:
Nicole, Lustig, Pablo, Florenzano, Luis Manuel, Sanhueza, Ximena, Cid, Germán, Ramos, Natalie, Thone, Demian A, Fullerton
Publikováno v:
Revista medica de Chile. 142(8)
Constrictive Pericarditis (CP) is an unusual disease. Its most common causes are idiopathic or secondary to cardiac surgery. Less frequently it is caused by connective tissue diseases. We report a 30 years old woman hospitalized due to progressive dy
Autor:
Felipe, Bellolio R, Karin, Alvarez V, Marjorie, De la Fuente L, Francisca, León G, Demian A, Fullerton M, Gonzalo, Soto D, Pilar, Carvallo de S Q, Francisco, López-Köstner
Publikováno v:
Revista medica de Chile. 134(7)
Among colorectal cancer hereditary variants, two syndromes show a predisposition to the disease based on germline mutations: Familial Adenomatous Polyposis (FAP) and Hereditary Nonpolyposis Colorectal Cancer (HNPCC).To screen mutations in FAP and HNP
Autor:
Francisco, López-Köstner, Demian A, Fullerton, Udo, Kronberg, Gonzalo, Soto, Alvaro, Zúñiga, Johanna, Argandoña, Vanesa, Miranda, Eliana, Pinto
Publikováno v:
Revista medica de Chile. 134(8)
First degree relatives of patients with colorectal carcinoma are at a higher risk of having the disease than the general population. Therefore, they should be subjected to screening colonoscopy.To assess the effectiveness of colonoscopy among first d
Autor:
Demian A Fullerton, Eliana Pinto T, Gonzalo Soto D, Francisco López-Köstner, Johanna Argandoña, Udo Kronberg, Vanesa Miranda B, Álvaro Zúñiga D
Publikováno v:
Revista médica de Chile v.134 n.8 2006
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
Background: First degree relatives of patients with colorectal carcinoma are at a higher risk of having the disease than the general population. Therefore, they should be subjected to screening colonoscopy. Aim: To assess the effectiveness of colonos
Autor:
Demian A, Fullerton, Francisco, López, Rodolfo, Avendaño, Rodrigo, Aparicio, Ignacio, Wistuba
Publikováno v:
Revista medica de Chile. 132(8)
We report a 67 years old male with a history of pulmonary tuberculosis at the age of 15, that consults for malaise, weight loss and productive cough. Chest X ray examination showed a left pleural effusion. A pleural tap obtained a sterile exudate. A
Autor:
Ignacio I Wistuba O, Rodolfo Avendaño H, Francisco López K, Demian A Fullerton, Rodrigo Aparicio R
Publikováno v:
Revista médica de Chile v.132 n.8 2004
SciELO Chile
CONICYT Chile
instacron:CONICYT
SciELO Chile
CONICYT Chile
instacron:CONICYT
We report a 67 years old male with a history of pulmonary tuberculosis at the age of 15, that consults for malaise, weight loss and productive cough. Chest X ray examination showed a left pleural effusion. A pleural tap obtained a sterile exudate. A
Publikováno v:
Revista medica de Chile. 132(5)
Hereditary nonpolyposis colorectal cancer (HNPCC) accounts for 3 to 5% of all colorectal cancer (CC). It is an autosomal dominant syndrome with 80% of penetrance for this disease.To analyze the pedigree and surgical treatment of HNPCC.We retrospectiv
Publikováno v:
Revista médica de Chile. 132
Background: Hereditary nonpolyposis colorectal cancer (HNPCC) accounts for 3 to 5% of all colorectal cancer (CC). It is an autosomal dominant syndrome with 80% of penetrance for this disease. Aim: To analyze the pedigree and surgical treatment of HNP