Nova Publishers
My Account Nova Publishers Shopping Cart
HomeBooksSeriesJournalsReference CollectionseBooksInformationSalesImprintsFor Authors
  Top » Catalog » Books » Medicine » Genetic Disorders » My Account  |  Cart Contents  |  Checkout   
Quick Find
Use keywords to find the product you are looking for.
Advanced Search
What's New? more
Advances in Materials Science Research. Volume 32
Shopping Cart more
0 items
Shipping & Returns
Privacy Notice
Conditions of Use
Contact Us
01.ADHD and Fetal Alcohol Spectrum Disorders (FASD)
02.Prader-Willi Syndrome
03.Life Span Development in Genetic Disorders: Behavioral and Neurobiological Aspects
04.Genotoxicity: Evaluation, Testing and Prediction
05.Birth Defects: New Research
06.ADHD and Fetal Alcohol Spectrum Disorders (FASD)
07.Cystic Fibrosis: Etiology, Diagnosis and Treatments
08.Signal Transduction Research Trends
09.From Traditional to Ecological: Understanding Attention Deficit Disorders through Quantitative and Qualitative Research
10.Asperger Syndrome - A Gift or a Curse?
Notifications more
NotificationsNotify me of updates to Cystic Fibrosis: Etiology, Diagnosis and Treatments
Tell A Friend
Tell someone you know about this product.
Cystic Fibrosis: Etiology, Diagnosis and Treatments
Retail Price: $220.00
10% Online Discount
You Pay:

Editors: Paul N. Leatte
Book Description:
Cystic Fibrosis (also known as CF, mucovoidosis, or mucoviscidosis) is a hereditary disease affecting the exocrine (mucus) glands of the lungs, liver, pancreas, and intestines, causing progressive disability due to multisystem failure. Abnormally thick mucus results in frequent lung infections. Diminished secretion of pancreatic enzymes is the main cause of poor growth, greasy stools, and deficiency in fat-soluble vitamins. Males can be infertile due to the condition congenital bilateral absence of the vas deferens. Often, symptoms of CF appear in infancy and childhood. Meconium ileus is a typical finding in newborn babies with CF.Individuals with CF can be diagnosed prior to birth by genetic testing. Newborn screening tests are increasingly common and effective(although false positives may occur, and children need to be brought in for a sweat test to distinguish disease vs carrier status). The diagnosis of CF may be confirmed if high levels of salt are found during a sweat test, although some false positives may occur.There is no known cure for CF. This new book presents important research in the field.

Table of Contents:

Chapter 1. Newborn screening for cystic fibrosis, pp.1-28
(Anne Deucher and Iris Schrijver, Departments of Pathology, Stanford University School of Medicine, Stanford, CA, and others)

Chapter 2. Cystic fibrosis and respiratory viral infections, pp.29-64
(Dennis Wat, Adult Cystic Fibrosis Unit, Papworth Hospital, Cambridge, United Kingdom)

Chapter 3. Cystic fibrosis, pseudomonas aeruginosa infection, and relevance of innate immune response: challenge for hematopoietic stem cell transplantation , pp.65-86
(Massimo Conese, Department of Biomedical Sciences, University of Foggia, Italy)

Chapter 4. Neutrophil elastase-mediated modulation of pathophysiology in cystic fibrosis lung disease, pp.87-112
(Xin Xu, German Luy, Janelle Chiasera, Amit Gaggar and Karen Bernard, University of Alabama at Birmingham, Birmingham, Alabama, and others)

Chapter 5. Genotypic hetereogeneity of the molecular basis of cystic fibrosis: the paradigm of lithuanian population genetic testing, pp.113-128
(Sergio Giannattasio, Antonella Bobba, Paolo Lattanzio, Nicoletta Guaragnella, Vaidutis Kučinskas, Ersilia Marra, CNR Istituto di Biomembrane e Bioenergetica, Italy, and others)

Chapter 6. Serum transferrin microheterogeneity in cystic fibrosis, pp.129-136
(E. Marklová, Z. Albahri, H. Vaníček1, V. Vávrová, Dept of Paediatrics, University Hospital, Hradec Králové, and others)

Chapter 7. Effects of the lack of transport of thiocyanate in cystic fibrosis lung disease, pp.137-142
(Melanie Childers, Alan Himmel, Jim Caldwell, Share International Foundation Sequim, WA)

Chapter 8. Treatments for cystic fibrosis: the role of adherence, importance and burden, pp.143-156
(Lynn B. Myers, Department of Psychology, School of Social Sciences, Brunel University, UK)

Chapter 9. Cystic Fibrosis – update on diagnosis and treatment, pp.157-166
(Melinda Solomon and Hartmut Grasemann, Division of Respiratory Medicine, Department of Paediatrics, The Hospital for Sick Children, University of Toronto and others)

Chapter 10. How effective are nutritional interventions in children and adults with cystic fibrosis? , pp.167-186
(Helen McCabe, Newcastle Upon Tyne Hospitals, UK and Helen White, Dept Nutrition and Dietetics, Leeds Metropolitan University, Leeds, UK)

Chapter 11. Sweat test: recommendations for good practice and analytical criteria of the methods used, pp.187-206
(Rota Michčle, Borgard Jean-Pierre, Sitruk-Khalfon Dominique, Marchand Martine Feldmann Delphine, Vassault Anne, Nguyen-Khoa Thao, Biochemistry Laboratory, France, and others)

Chapter 12. New trends in the inhibition of Pseudomonas aeruginosa quorum sensing activity, pp.207-216
(Mario Zucca, Sabrina Crivellaro, and Dianella Savoia, Department of Clinical and Biological Sciences, University of Torino, Italy)

Chapter 13. Ocular surface changes in patients with cystic fibrosis, pp.217-230
(Malgorzata Mrugacz, Department of Pediatric Ophthalmology Medical University of Bialystok, Poland)

Chapter 14. Pseudo-Bartter Syndrome in cystic fibrosis, pp.231-236
(Mehmet Kose, Nural Kiper, Department of Pediatrics, Erciyes University, and others)

Chapter 15. Management of cystic fibrosis-related arthritis, pp.237-248
(Judith Thornton, Satyapal Rangaraj and Daniel Hawley, Greater Manchester, Lancashire & South Cumbria Medicines for Children Research Network, Manchester, UK and others)

Index, pp.249-275

      Genetics - Research and Issues
   Binding: Hardcover
   Pub. Date: 2009
   Pages: pp.275
   ISBN: 978-1-60741-833-7
   Status: AV
Status Code Description
AN Announcing
FM Formatting
PP Page Proofs
FP Final Production
EP Editorial Production
PR At Prepress
AP At Press
AV Available
Customers who bought this product also purchased
Cell, Gene, and Molecular Therapy: New Concepts
Cell, Gene, and Molecular Therapy: New Concepts
Advances in Disease Epidemiology
Advances in Disease Epidemiology
Infectious Pregnancy Complications
Infectious Pregnancy Complications
Comorbidity of Depression and Alcohol Use Disorders
Comorbidity of Depression and Alcohol Use Disorders
Alcohol-Related Cognitive Disorders: Research and Clinical Perspectives
Alcohol-Related Cognitive Disorders: Research and Clinical Perspectives
Nutritional Factors and Osteoporosis Prevention
Nutritional Factors and Osteoporosis Prevention
Special Focus Titles
01.Multicultural and Citizenship Awareness through Language: Cross Thematic Practices in Language Pedagogy
02.The Brainstem and Behavior
03.Sustainable Development: The Context of Use of Indigenous Plants for Local Economic Growth
04.Cancer versus Nutraceuticals
05.Fundamentals of Fuel Injection and Emission in Two-Stroke Engines
06.Free to Love: Schema Therapy for Christians
07.Textiles: Advances in Research and Applications
08.Cheese Production, Consumption and Health Benefits
09.Education in Lesotho: Prospects and Challenges
10.Work-Life Balance in the 21st Century: Perspectives, Practices, and Challenges
11.Electrical Measurements: Introduction, Concepts and Applications
12.Potassium Channels in Health and Disease

Nova Science Publishers
© Copyright 2004 - 2018

Cystic Fibrosis: Etiology, Diagnosis and Treatments