نتایج جستجو برای: fujimoto

تعداد نتایج: 674  

2017
Taeko Matsuura Kenichiro Maeda Kenneth Sutherland Taisuke Takayanagi Shinichi Shimizu Seishin Takao Naoki Miyamoto Hideaki Nihongi Chie Toramatsu Yoshihiko Nagamine Rintaro Fujimoto Ryusuke Suzuki Masayori Ishikawa Kikuo Umegaki Hiroki Shirato

Title Biological effect of dose distortion by fiducial markers in spot-scanning proton therapy with a limited number of fields: A simulation study Author(s) Matsuura, Taeko; Maeda, Kenichiro; Sutherland, Kenneth; Takayanagi, Taisuke; Shimizu, Shinichi; Takao, Seishin; Miyamoto, Naoki; Nihongi, Hideaki; Toramatsu, Chie; Nagamine, Yoshihiko; Fujimoto, Rintaro; Suzuki, Ryusuke; Ishikawa, Masayori;...

2016
Victoria Bîrluţiu Rareş Mircea Bîrluţiu Ioan Sorin Zaharie

Kikuchi-Fujimoto disease is an idiopathic histiocytic necrotizing lymphadenitis with an autoimmune component triggered by the involvement of CD8 cytotoxic T lymphocyte due to a genetic predisposition. Cases are diagnosed more frequently in female patients, especially in young adults, in all races, more commonly in East Asia, and only isolated in Europe and America. We present the case of a 51-y...

Journal: :Journal of the Korean Ophthalmological Society 2018

Journal: :Revista Brasileira de Reumatologia 2017

Journal: :American Journal of Ophthalmology Case Reports 2016

Journal: :Cukurova Medical Journal 2022

Kikuchi Fujimoto disease (KFD) is a rare, generally benign and self limited condition with an unknown etiology. There isn’t guideline for treatment of KFD, recommendations are based on clinical experience management typically supportive. However, sometimes more ominous course the may be experienced. Thus, patients severe disease, refractory symptoms recurrences, definite efficient options requi...

2015
Majid Reza Erfanian Taghvaei Maryam Mirzaie Ali Parsa Taghi Ghiasi Moghadam

INTRODUCTION Kikuchi-Fujimoto Disease (KFD) is a benign, self-limited, inflammatory disorder, first reported in Japan. This condition is more prevalent among women and typically occurs in the third decade of life. It normally manifests as persistent, isolated cervical adenopathy with a recurrence rate of 3%. The identification of this condition is of high significance, given the risk of misdiag...

Journal: :Journal of Microbiology and Infectious Diseases 2012

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