نتایج جستجو برای: amsterdam ii criteria

تعداد نتایج: 832174  

2016
Miguel G. Echevarria Ignazio Scimemi Alexey Vladimirov

Miguel G. Echevarria, Ignazio Scimemi, and Alexey Vladimirov Nikhef Theory Group, Science Park 105, 1098XG Amsterdam, The Netherlands Department of Physics and Astronomy, VU University Amsterdam, De Boelelaan 1081, NL-1081 HV Amsterdam, The Netherlands Departamento de Física Teórica II, Facultad de Ciencias Físicas, Universidad Complutense de Madrid, 28040 Madrid, Spain Institut für Theoretisch...

Journal: :Clinical cancer research : an official journal of the American Association for Cancer Research 2005
Xavier Llor Elisenda Pons Rosa M Xicola Antoni Castells Cristina Alenda Virgínia Piñol Montserrat Andreu Sergi Castellví-Bel Artemio Payá Rodrigo Jover Xavier Bessa Anna Girós Anna Roca Miquel A Gassull

PURPOSE Hereditary nonpolyposis colorectal cancer (HNPCC) is the commonest form of inherited colorectal cancer. Whereas it has been known that mismatch repair gene mutations are the underlying cause of HNPCC, an undetermined number of patients do not have these alterations. The main objectives of this study were to assess the relevance of clinically defined HNPCC patients without characteristic...

Journal: :Journal of medical genetics 2000
M Montera N Resta C Simone G Guanti C Marchese S Civitelli A Mancini S Pozzi L De Salvo D Bruzzone A Donadini L Romio C Mareni

EDITOR—Hereditary non-polyposis colorectal cancer (HNPCC) is a heterogeneous autosomal dominant disease with incomplete penetrance. The frequency is estimated at 1:200/1:1000. HNPCC results from constitutional mutation in one of the five human mismatch repair genes (MMR) that have so far been implicated: hMSH2, hMLH1, hPMS1, hPMS2, and hMSH6. 2 hMSH2 and hMLH1 account for the majority of mutati...

2000

EDITOR—Hereditary non-polyposis colorectal cancer (HNPCC) is a heterogeneous autosomal dominant disease with incomplete penetrance. The frequency is estimated at 1:200/1:1000. HNPCC results from constitutional mutation in one of the five human mismatch repair genes (MMR) that have so far been implicated: hMSH2, hMLH1, hPMS1, hPMS2, and hMSH6. 2 hMSH2 and hMLH1 account for the majority of mutati...

Journal: :iranian red crescent medical journal 0
koorosh ahmadi department of emergency medicine, alborz university of medical sciences, karaj, ir iran morteza talebi doluee department of emergency medicine , imam reza hospital, mashhad university of medical sciences, mashhad , ir iran seyyed mohsen pouryaghobi department of anesthesiology, alborz university of medical sciences, karaj, ir iran fermoozan nikpasand faculty of medicine, islamic azad university, tehran, ir iran morteza hariri emergency medicine resident, school of medicine, mashhad university of medical sciences, mashhad, ir iran elham pishbin department of emergency medicine , imam reza hospital, mashhad university of medical sciences, mashhad , ir iran; department of emergency medicine, imam reza hospital, mashhad university of medical sciences, mashhad, ir iran. tel: +98-9153176347

conclusions the results of this study indicated that patients with sepsis had lower serum vitamin d levels than healthy controls. also, patients with more severe disease had lower serum vitamin d levels, but to evaluate causation and determine whether vitamin d supplementation could be effective in reducing the risk or severity of sepsis, randomized controlled trials should be conducted. result...

2000

EDITOR—Hereditary non-polyposis colorectal cancer (HNPCC) is a heterogeneous autosomal dominant disease with incomplete penetrance. The frequency is estimated at 1:200/1:1000. HNPCC results from constitutional mutation in one of the five human mismatch repair genes (MMR) that have so far been implicated: hMSH2, hMLH1, hPMS1, hPMS2, and hMSH6. 2 hMSH2 and hMLH1 account for the majority of mutati...

2000

EDITOR—Hereditary non-polyposis colorectal cancer (HNPCC) is a heterogeneous autosomal dominant disease with incomplete penetrance. The frequency is estimated at 1:200/1:1000. HNPCC results from constitutional mutation in one of the five human mismatch repair genes (MMR) that have so far been implicated: hMSH2, hMLH1, hPMS1, hPMS2, and hMSH6. 2 hMSH2 and hMLH1 account for the majority of mutati...

2005
B. LEONARD HOLMAN H. GREEN JOHN E. MARKIS DAVID A. PHILLIPS

Correlation of postmortem anatomic findings with electrocardiographic changes in patients with myocardial infarction. Circulation 55: 279, 1977 23. Starr JW, Wagner GS, Draffin RM, Reed JB, Behar VS: Vectorcardiographic criteria for the diagnosis of anterior myocardial infarction, Circulation 53: 229, 1976 24. Fenoglio JJ, Sylva FG, Freidman PL, Wit AL: Survival of subendocardial Purkinje fiber...

2005
H. GREEN JOHN E. MARKIS DAVID A. PHILLIPS

Correlation of postmortem anatomic findings with electrocardiographic changes in patients with myocardial infarction. Circulation 55: 279, 1977 23. Starr JW, Wagner GS, Draffin RM, Reed JB, Behar VS: Vectorcardiographic criteria for the diagnosis of anterior myocardial infarction, Circulation 53: 229, 1976 24. Fenoglio JJ, Sylva FG, Freidman PL, Wit AL: Survival of subendocardial Purkinje fiber...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید