Cystic fibrosis in the 21st century
著者
書誌事項
Cystic fibrosis in the 21st century
(Progress in respiratory research, v. 34)
Karger, 2006
- タイトル別名
-
Cystic fibrosis in the twenty-first century
大学図書館所蔵 全3件
  青森
  岩手
  宮城
  秋田
  山形
  福島
  茨城
  栃木
  群馬
  埼玉
  千葉
  東京
  神奈川
  新潟
  富山
  石川
  福井
  山梨
  長野
  岐阜
  静岡
  愛知
  三重
  滋賀
  京都
  大阪
  兵庫
  奈良
  和歌山
  鳥取
  島根
  岡山
  広島
  山口
  徳島
  香川
  愛媛
  高知
  福岡
  佐賀
  長崎
  熊本
  大分
  宮崎
  鹿児島
  沖縄
  韓国
  中国
  タイ
  イギリス
  ドイツ
  スイス
  フランス
  ベルギー
  オランダ
  スウェーデン
  ノルウェー
  アメリカ
注記
Includes bibliographical references and indexes
内容説明・目次
内容説明
Cystic fibrosis used to be thought of as a respiratory and digestive disease, with a uniformly and rapidly fatal outcome. The spectrum of the disease has broadened into the mild atypical case, presenting in middle age, with the potential for complications in virtually every system of the body. In the past few years there has been an explosion of knowledge of the basic science of the defect. The editors have therefore invited the leading scientists and clinicians in the field of cystic fibrosis to describe the recent advances in this disease. Although there are many 'Recent Advances' texts, previous books have been selective in their choice of topics. This book is the first to cover the entire field of this complex disease, and encompasses the rapidly moving topics of the basic molecular and cellular biology as well as the recent multi-system, multi-disciplinary advances in the clinical care of patients. The authors have been charged with writing only about new developments and not to rehash old literature. The bulk of the references is therefore less than five years old. This book addresses all professionals who treat cystic fibrosis and want to have an update of new findings in the field, particularly of those outside their immediate specialisation. It will also be useful for basic researchers interested in related scientific areas and the clinical context of their work.
目次
- Part One: The Basics
- The CFTR Gene: Structure, Mutations and Specific Therapeutic Approaches: Nissim-Rafinia, M.
- Linde, L.
- Kerem, B.
- Exquisite and Multi-Level Regulation of CFTR Expression: Trezise, A.E.O.
- Intracellular Processing of CFTR: Barriere, H.
- Lukacs, G.L.
- Structure of the Cystic Fibrosis Transmembrane Conductance Regulator: Stratford, F.L.L.
- Bear, C.E.
- Function of CFTR Protein: Ion Transport: Chen, J-H
- Cai, Z.
- Li, H.
- Sheppard, D.N.
- Cystic Fibrosis. Function of CFTR Protein: Regulatory Functions: Coakley, R.D.
- Stutts, M.J.
- Function of CFTR Protein: Developmental Role: Gill, D.
- Larson, J.E.
- Genotype-Phenotype Correlations in Cystic Fibrosis: Dorfmann, R.
- Zielenski, J.
- Diagnosis of Cystic Fibrosis, CFTR-Related Disease and Screening: Karczeski, B.A.
- Cutting, G.R.
- CF Modifier Genes: Griesenbach, U.
- Alton, E.W.F.W.
- Davies J.C.
- Animal Models: Dorin, J.R.
- In vitro/ex vivo Fluorescence Assays of CFTR Chloride Channel Function: Verkman, A.S.
- Galietta, L.J.V.
- In vivo Measurement of Airway Potential Difference to Assess CFTR Function in Man: Middleton, P.
- Alton, E.W.F.W.
- Arrays and Proteomics: Ogilvie, V.
- MacGregor, G. Part Two: The Airway
- Pathogenesis of Pulmonary Disease in Cystic Fibrosis: Mall, M.
- Boucher, R.C.
- Infection vs Inflammation: Ziady, A.G.
- Davis, P.B.
- Pseudomonas aeruginosa: Clinical Research: Armstrong, D.
- Pseudomonas aeruginosa: Basic Research: Scott, F.W.
- Pitt, T.L.
- Other Gram-Negative Organisms - Burkholderia cepacia Complex and Stenotrophomonas maltophilia: Govan, J.R.W.
- Staphylococcus aureus and MRSA: Conway, S.
- Denton, M.
- Nontuberculous Mycobacterial Lung Disease in Patients with Cystic Fibrosis: Griffith, D.E.
- Respiratory Fungal Infections and Allergic Bronchopulmonary Aspergillosis: Que, C.
- Geddes, D.
- Advanced Disease Management and Advances in Transplant Medicine: Carby, M.R.
- Hodson, M.E.
- Current and Novel Antimicrobial Approaches: Davies, J.C.
- Anti-Inflammatory Agents - A Clinical Perspective: Hilliard, T.N.
- Balfour-Lynn, I.M.
- Recent Advances in Infant and Pre-School Lung Function: Ranganathan, S.
- Recent Advances in Imaging: Oikonomou, A.
- Hansell, D.M.
- New Pharmacological Approaches for Treatment of Cystic Fibrosis: Rubenstein, R.C.
- Gene and Stem Cell Therapy: Boyd, A.C.
- Part Three: Digestive Tract
- Gut Disease: Clinical Manifestations, Pathophysiology, Current and New Treatments: Taylor, C.J.
- Hardcastle, J.
- Pancreatic Involvement: Clinical Manifestations, Pathophysiology and New Treatments: Lindley, K.J.
- Cystic Fibrosis: Liver Disease: Westaby, D.
- Part Four: Other Organs
- Fertility, Contraception, Incontinence and Pregnancy: Thorpe-Beeston, J.G.
- Arthritis, Vasculitits and Bone Disease: Elkin, S.
- Diabetes in Cystic Fibrosis: Bridges, N., Spowart, K.
- Part Five: Multidisciplinary Care
- Challenges for Nurses: Madge, S.
- Dietetics: Wolfe, S.
- Morton, A.
- Physiotherapy: Pryor, J.A.
- Main, E.
- Agent, P.
- Bradley, J.M.
- Psychological Interventions: Bryon, M.
- Part Six: The Future
- The Future: Bush, A.
- Griesenbach, U.
- Davies, J.C.
- Alton, E.W.F.W.
- Jaffe, A.
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