WordNet
- enduring trying circumstances with even temper or characterized by such endurance; "a patient smile"; "was patient with the children"; "an exact and patient scientist"; "please be patient"
- a person who requires medical care; "the number of emergency patients has grown rapidly"
- of or relating to or resembling a cyst
- of or relating to a normal cyst (as the gallbladder or urinary bladder)
- development of excess fibrous connective tissue in an organ
- a closed sac that develops abnormally in some body structure
PrepTutorEJDIC
- (人が)『忍耐強い』,しんぼう強い,がまん強い / (行動が)根気のよい,忍耐を示す / 〈C〉『患者』,医者にかかっている人
- 胞嚢(ほうのう)性の
- 線維症(線維性結合線維が増殖し過ぎる症状)
- 胞嚢(ほうのう)
UpToDate Contents
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- 1. 嚢胞性線維症：肝胆道系疾患 cystic fibrosis hepatobiliary disease
- 2. 嚢胞性線維症：消化器疾患の概要 cystic fibrosis overview of gastrointestinal disease
- 3. 嚢胞性線維症：肺疾患治療の概要 cystic fibrosis overview of the treatment of lung disease
- 4. 嚢胞性線維症：栄養上の問題 cystic fibrosis nutritional issues
- 5. 嚢胞性線維症に関連する糖尿病 cystic fibrosis related diabetes mellitus
English Journal
- Simultaneous detection of celiac disease-specific IgA antibodies and total IgA.
- Grossmann K1, Röber N2, Hiemann R3, Rödiger S3, Schierack P3, Reinhold D4, Laass MW5, Conrad K2, Roggenbuck D6,7.
- Auto- immunity highlights.Auto Immun Highlights.2016 Dec;7(1):2. doi: 10.1007/s13317-016-0073-2. Epub 2016 Jan 30.
- PURPOSE: Celiac disease (CD) serology requires analysis of tissue transglutaminase type-2 (TG2autoAbs), deamidated gliadin (DGAbs), and as reference endomysial autoantibodies (EmA). Total IgA assessment helps to determine IgA-deficient CD patients. The novel multiplex indirect immunofluorescence (II
- PMID 26831868
- Manipulating proteostasis to repair the F508del-CFTR defect in cystic fibrosis.
- Esposito S1, Tosco A2, Villella VR1, Raia V3, Kroemer G4,5,6,7,8,9,10, Maiuri L11,12.
- Molecular and cellular pediatrics.Mol Cell Pediatr.2016 Dec;3(1):13. doi: 10.1186/s40348-016-0040-z. Epub 2016 Mar 14.
- Cystic fibrosis (CF) is a lethal monogenic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene that entails the (diagnostic) increase in sweat electrolyte concentrations, progressive lung disease with chronic inflammation and recurrent bacterial infecti
- PMID 26976279
- Update on host-pathogen interactions in cystic fibrosis lung disease.
- Hector A1, Frey N1, Hartl D2.
- Molecular and cellular pediatrics.Mol Cell Pediatr.2016 Dec;3(1):12. doi: 10.1186/s40348-016-0039-5. Epub 2016 Feb 23.
- Bacterial and fungal infections are hallmarks of cystic fibrosis (CF) lung disease. In the era of long-term inhaled antibiotics and increasing CF patient survival, new "emerging" pathogens are detected in CF airways, yet their pathophysiological disease relevance remains largely controversial and in
- PMID 26905568
Japanese Journal
- Report of Two Cases of Mycobacterium europaeum from Iran
- Pourahmad Fazel,Shojaei Hasan,Heidarieh Parvin [他],Khosravi Azardokht,Hashemi Abodolrazagh
- Japanese Journal of Infectious Diseases 65(6), 539-541, 2012
- … Herein, we report repeated isolation of Mycobacterium europaeum from the sputum samples of an Iranian human immunodeficiency virus-infected patient and a cystic fibrosis patient with chronic pulmonary disease. …
- NAID 130002588764
- Distal intestinal obstruction syndromeを認めた嚢胞性線維症の1例
- 向井 基,松藤 凡,加治 建 [他],池江 隆正,川野 孝文,松久保 眞,右田 美里
- 日本小児外科学会雑誌 47(5), 848-851, 2011-08-20
- … 回,気管支喘息重積発作のため入院したが,9病日より腹部膨満が出現した.16病日に腸閉塞の診断で開腹手術を行った.回腸遠位部に食物残渣の貯留を認めた.汗中塩素濃度が207mEq/lと異常高値であり,cystic fibrosis transmembrane conductance regulator(CFTR)遺伝子のdeletion解析で,エクソン16,17a,17bにまたがる完全欠失のホモ接合が判明し,嚢胞性線維症の診断が確定した.イレウス症状は嚢胞性線維症の一症状であるdistal …
- NAID 110008711758
- A Rare Mutation in Cystic Fibrosis Transmembrane Conductance Regulator Gene in a Recurrent Pancreatitis Patient Without Respiratory Symptoms
- 古谷野伸,Hirano Yoshiki,Nagamori Tsunehisa,Tanno Satoshi,Murono Koichi,Fujieda Kenji
- Pancreas 39(5), 686-688, 2010-07-00
- http://journals.lww.com/pancreasjournal/pages/default.aspx
- NAID 120004418819
Related Links
- Cystic fibrosis is a serious inherited disease which mainly affects the lungs and pancreas, but can involve other organs. Symptoms usually begin in early... Skip to content Patient - Trusted medical information and support Skip to ...
- Pathogenesis The abnormality in the cystic fibrosis transmembrane conductance regulator (CFTR) explains the pathology of cystic fibrosis. Read more More on pathogenesis The CFTR acts as a cAMP-activated gated ion channel ...
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★リンクテーブル★
| リンク元 | 「嚢胞性線維症患者」 |
| 関連記事 | 「cystic」 |
「嚢胞性線維症患者」
「cystic」
- adj.
- 嚢胞性の