To see the other types of publications on this topic, follow the link: Cystic fibrosis; Genetic diseases.

Books on the topic 'Cystic fibrosis; Genetic diseases'

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 books for your research on the topic 'Cystic fibrosis; Genetic diseases.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse books on a wide variety of disciplines and organise your bibliography correctly.

1

Cunningham, James C. An introduction to cystic fibrosis for patients and families. 5th ed. Bethesda, MD: Cystic Fibrosis Foundation, 2003.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
2

Cunningham, James C. An introduction to cystic fibrosis for patients and families. 4th ed. Bethesda, MD: Cystic Fibrosis Foundation, 1999.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
3

Wackym, Phillip A. Molecular temporal bone pathology, parts III and IV. Philadelphia, PA: Lippincott-Raven, 1998.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
4

Copyright Paperback Collection (Library of Congress), ed. The changeling plague. New York: Roc, 2003.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
5

Gregory, Pemberton Stephen, ed. The troubled dream of genetic medicine: Disease and ethnicity in Tay-Sachs, cystic fibrosis, and sickle cell disease. Baltimore: Johns Hopkins University Press, 2006.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
6

Wailoo, Keith. The troubled dream of genetic medicine: Ethnicity and innovation in Tay-Sachs, cystic fibrosis, and sickle cell disease. Baltimore: Johns Hopkins University Press, 2006.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
7

Genetic Disorders Sourcebook: Basic Consumer Health Information About Hereditary Diseases and Disorders, Including Cystic Fibrosis, Down Syndrome, Hemophilia, ... Disease (Health Reference Series). 2nd ed. Detroit, Mich.: Omnigraphics, 2000.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
8

Byrnes, Isabel Stenzel. The power of two: A twin triumph over cystic fibrosis. Columbia: University of Missouri Press, 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
9

Giddings, Sharon. Cystic fibrosis. New York: Chelsea House, 2009.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
10

The birth of a genetics policy: Social issues of newborn screening. Farnham, Surrey: Ashgate, 2013.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
11

Gold, Susan Dudley. Cystic fibrosis. New York: Crestwood House, 2000.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
12

Silverstein, Alvin. Cystic fibrosis. New York: F. Watts, 1994.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
13

Naissance d'une politique de la génétique: Dépistage, biomédecine, enjeux sociaux. Paris: Presses universitaires de France, 2011.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
14

Apel, Melanie Ann. Cystic fibrosis: The ultimate teen guide. Lanham, Md: Scarecrow Press, 2006.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
15

Azuma, Arata, and Michael S. Schechter, eds. Treatment of Cystic Fibrosis and Other Rare Lung Diseases. Basel: Springer Basel, 2017. http://dx.doi.org/10.1007/978-3-0348-0977-1.

Full text
APA, Harvard, Vancouver, ISO, and other styles
16

1932-, Elston Robert C., ed. Multipoint mapping and linkage based upon affected pedigree members: Genetic Analysis Workshop 6, proceedings of a workshop held at Gulf Park, Long Beach, Mississippi, October 10-12, 1988. New York: Liss, 1988.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
17

Cystic Fibrosis Association of Ireland, ed. A walk in my shoes. Dublin: Original Writing, 2010.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
18

Love, Cynthia B. Genetic testing for cystic fibrosis: January 1989 through February 1997 : 1224 citations. Bethesda, Md. (8600 Rockville Pike, Bethesda 20894): U.S. Dept. of Health and Human Services, Public Health Service, National Institutes of Health, National Library of Medicine, Reference Section, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
19

NIH Consensus Development Conference on Genetic Testing for Cystic Fibrosis (1997 National Institutes of Health). NIH Consensus Development Conference on Genetic Testing for Cystic Fibrosis: [program and abstracts]. Bethesda, Md: National Institutes of Health, Continuing Medical Education, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
20

United States. Congress. Senate. Committee on Small Business. Research on childhood diseases by entrepreneurs: Hearing before the Committee on Small Business, United States Senate, One Hundred Third Congress, second session ... Thursday, May 26, 1994. Washington: U.S. G.P.O., 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
21

United States. Congress. Senate. Committee on Small Business. Research on childhood diseases by entrepreneurs: Hearing before the Committee on Small Business, United States Senate, One Hundred Third Congress, second session ... Thursday, May 26, 1994. Washington: U.S. G.P.O., 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
22

Macfarlane, Dawn J. The purification of neutrophil collagenase and gelatinase B from CF sputum &: The modulation of collagen production in human lung fibroblasts by inflammatory cytokines. Dublin: University College Dublin, 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
23

Tirkos, Sam. Investigation of S100A8 and S100A9 as potential genetic modifiers of the pulmonary phenotype in cystic fibrosis mice. Ottawa: National Library of Canada, 2003.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
24

30 days of hope for strength in chronic illness. Birmingham, AL: New Hope Publishers, 2016.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
25

NIH Consensus Development Conference on Genetic Testing for Cystic Fibrosis (1997 National Institutes of Health). NIH Consensus Development Conference on Genetic Testing for Cystic Fibrosis: April 14-16, 1997, Natcher Conference Center, National Institutes of Health, Bethesda, Md. Bethesda, Md: National Institutes of Health, Continuing Medical Education, 1997.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
26

Ala-Kokko, Leena. Collagen gene expression in fibrotic human skin diseases and in rats with experimental liver fibrosis: Effects of cortisol and malotilate. Oulu: University of Oulu, 1987.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
27

William, Skach, ed. Cystic fibrosis methods and protocols. Totowa, N.J: Humana Press, 2002.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
28

Kriemler, Susi. Exercise, physical activity, and cystic fibrosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199232482.003.0033.

Full text
Abstract:
Cystic fibrosis (CF) is the most common genetic autosomal recessive disease of the Caucasian race, generally leading to death in early adulthood.1 The frequency of the gene carrier (heterozygote) is 1:20–25 in Caucasian populations, 1:2000 in African-Americans, and practically non-existent in Asian populations. The disease occurs in about 1 in every 2500 life births of the white population. Mean survival has risen from 8.4 years in 1969 to 32 years in 2000 due to improvements in treatment. The genetic defect causes a pathological electrolyte transport through the cell membranes by a defective chloride channel membrane transport protein [cystic fibrosis transmembrane conductance regulator (CFTR)]. With respect to the function, this affects mainly the exocrine glands of secretory cells, sinuses, lungs, pancreas, liver, and the reproductive tract of the human body leading to a highly viscous, water-depleted secretion. The secretion cannot leave the glands and in consequence causes local inflammation and destruction of various organs. The main symptoms include chronic inflammatory pulmonary disease with a progressive loss of lung function, exocrine and sometimes endocrine pancreas insufficiency, and an excessive salt loss through the sweat glands.1 A summary of the signs and symptoms of CF will be given with a special emphasis on the effect of exercise performance and capacity.
APA, Harvard, Vancouver, ISO, and other styles
29

Kriemler, Susi, Thomas Radtke, and Helge Hebestreit. Exercise, physical activity, and cystic fibrosis. Edited by Neil Armstrong and Willem van Mechelen. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198757672.003.0027.

Full text
Abstract:
Cystic fibrosis (CF) is a genetic disease resulting in an impaired mucociliary clearance, chronic bacterial airway infection, and inflammation. The progressive destruction of the lungs is the main cause of morbidity and premature death. Diverse other organ systems such as heart, muscles, bones, gastro-intestinal tract, and sweat glands are often also affected and interfere with exercise capacity. Hence, exercise capacity is reduced as the disease progresses mainly due to reduced functioning of the muscles, heart, and/or lungs. Although there is still growing evidence of positive effects of exercise training in CF on exercise capacity, decline of pulmonary function, and health-related quality of life, the observed effects are encouraging and exercise should be implemented in all patient care. More research is needed to understand pathophysiological mechanisms of exercise limitations and to find optimal exercise modalities to slow down disease progression, predict long-term adherence, and improve health-related quality of life.
APA, Harvard, Vancouver, ISO, and other styles
30

Preconception and Prenatal Carrier Screening for Cystic Fibrosis: Clinical and Laboratory Guidelines. Amer College of Obstetricians &, 2001.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
31

Kathy, Massimini, ed. Genetic disorders sourcebook: Basic consumer health information about hereditary diseases and disorders, including cystic fibrosis, Down syndrome ... 2nd ed. Detroit, MI: Omnigraphics, 2000.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
32

Skach, William R. Cystic Fibrosis: Methods and Protocols (Methods in Molecular Medicine). Humana Press, 2002.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
33

The Power of Two: A Twin Triumph over Cystic Fibrosis. University of Missouri Press, 2007.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
34

Michels, Virginia V. Genetics. Oxford University Press, 2012. http://dx.doi.org/10.1093/med/9780199755691.003.0276.

Full text
Abstract:
Genetic factors play a role in the development of many types of human disease. Genetic determinants may be chromosome abnormalities (Down syndrome, Kleinfelter syndrome, Turner syndrome), single gene defects (dilated and hypertrophic cardiomyopathies, Ehlers-Danlos syndrome, Marfan syndrome, neurofibromatosis, tuberous sclerosis, Gaucher disease, cystic fibrosis, sickle cell disease), mitochondrial mutations (MELAS, MERRF, Kearns-Sayre syndrome), or epigenetic or multifactorial factors. Genetics testing methods are also reviewed.
APA, Harvard, Vancouver, ISO, and other styles
35

The Power of Two: A Twin Triumph over Cystic Fibrosis, Updated and Expanded Edition. University of Missouri, 2014.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
36

Sayer, John A., and Roslyn J. Simms. Nephronophthisis. Edited by Neil Turner. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199592548.003.0317_update_001.

Full text
Abstract:
Nephronophthisis (NPHP) is a clinically heterogeneous autosomal recessive cystic kidney disease and the leading genetic cause of end-stage renal failure in children and young adults. Whilst enlarged dysplastic cystic kidneys are associated with infantile NPHP, more typically renal ultrasound reveals normal kidney size and corticomedullary cysts in a child with polyuria and secondary enuresis. Extrarenal manifestations occur in 10–15% including retinal degeneration, cerebellar vermis hypoplasia and liver fibrosis, requiring referral to other specialists. Mutations in 18 genes have been identified to cause NPHP, but a genetic diagnosis still cannot be found in many patients. NPHP is classified as a ciliopathy because of the localization of the protein products of the associated genes. Currently there is no specific therapy for NPHP.
APA, Harvard, Vancouver, ISO, and other styles
37

Multipoint Mapping & Linkage Based Upon Affect Pedigree Mem. John Wiley & Sons, 1990.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
38

Cystic Fibrosis: Current Topics (Cystic Fibrosis--Current Topics). John Wiley & Sons, 1996.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
39

Korneluk. Cystic Fibrosis And You. 2nd ed. Carleton Univ Pr, 1996.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
40

A, Dodge J., Brock D. J. H, and Widdicombe J. W, eds. Cystic fibrosis-- current topics. Chichester: J. Wiley, 1993.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
41

Gold, Susan Dudley, Gilbert R. Grimes, and Lucille A. Lester. Cystic Fibrosis (Health Watch). Enslow Publishers, 2000.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
42

Jasper's Story: Living with Cystic Fibrosis. Hachette Children's Group, 2017.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
43

Slack, Jonathan. 3. Mutations and gene variants. Oxford University Press, 2014. http://dx.doi.org/10.1093/actrade/9780199676507.003.0003.

Full text
Abstract:
All gene variants originate as mutations. Most variants in the genome of any given individual are not new mutations but have been inherited from previous generations. ‘Mutations and gene variants’ shows that mutations can occur in any cell of the body, but in order to be inherited they must occur in the DNA of the reproductive cells. There are numerous genetic diseases caused by a single mutation in one gene, and the examples considered here are cystic fibrosis, haemophilia, achondroplasia, and Holt-Oram Syndrome. In such cases, the inheritance of the abnormal gene variant follows simple Mendelian rules. The origin of cancer is explained as a combination of mutations occurring in a single cell of the body. Inherited gene variants predisposing to cancer do so because they reduce the number of new mutations required.
APA, Harvard, Vancouver, ISO, and other styles
44

Abramovitz, Melissa. Diseases and Disorders - Cystic Fibrosis (Diseases and Disorders). Lucent Books, 2003.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
45

Dodge, J. A., J. H. Widdicombe, and D. J. H. Brock. Volume 2, Cystic Fibrosis--Current Topics. John Wiley & Sons, 1995.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
46

D. J. H. Brock (Editor), J. A. Dodge (Editor), and J. H. Widdicombe (Editor), eds. Volume 1, Cystic Fibrosis--Current Topics. John Wiley & Sons, 1993.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
47

Bush, Andrew, 1954 Apr. 24-, ed. Cystic fibrosis in the 21st century. Basel: Karger, 2006.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
48

United States. Congress. Office of Technology Assessment., ed. Genetic counseling and cystic fibrosis carrier screening: Results of a survey. Washington, DC: Congress of the U.S., Office of Technology Assessment, 1992.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
49

US GOVERNMENT. Genetic Counseling and Cystic Fibrosis Carrier Screening: Results of a Survey (Background Paper). Office of Technology Assessment, 1992.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
50

Yarden, Jennifer S. Genetic Modulators of Pulmonary Function in Cystic Fibrosis & Genetic Susceptibility Factors of Emphysema. Leuven University Press, 2005.

Find full text
APA, Harvard, Vancouver, ISO, and other styles
We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!

To the bibliography