Bibliografías temáticas / Fibrosis / Libros
Siga este enlace para ver otros tipos de publicaciones sobre el tema: Fibrosis.

Libros sobre el tema "Fibrosis"

Autor: Grafiati
Publicado: 4 de junio de 2021
Última modificación: 25 de julio de 2025

Crea una cita precisa en los estilos APA, MLA, Chicago, Harvard y otros

Elija tipo de fuente:

Consulte los 50 mejores mejores libros para su investigación sobre el tema "Fibrosis".

Junto a cada fuente en la lista de referencias hay un botón "Agregar a la bibliografía". Pulsa este botón, y generaremos automáticamente la referencia bibliográfica para la obra elegida en el estilo de cita que necesites: APA, MLA, Harvard, Vancouver, Chicago, etc.

También puede descargar el texto completo de la publicación académica en formato pdf y leer en línea su resumen siempre que esté disponible en los metadatos.

Explore libros sobre una amplia variedad de disciplinas y organice su bibliografía correctamente.

1

Rittié, Laure, ed. Fibrosis. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7113-8.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
2

David, Evered, Whelan Julie, Ciba Foundation, and Symposium on Fibrosis (1984 : Ciba Foundation), eds. Fibrosis. Pitman, 1985.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
3

Symposium on Fibrosis (1984 : London), ed. Fibrosis. Pitman, 1985.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
4

Symposium, Ciba Foundation. Fibrosis. Pitman, 1985.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
5

Varga, John, David A. Brenner, and Sem H. Phan, eds. Fibrosis Research. Humana Press, 2005. http://dx.doi.org/10.1385/1592599400.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
6

Silverstein, Alvin. Cystic fibrosis. F. Watts, 1994.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
7

Davis, Stephanie Duggins, Margaret Rosenfeld, and James Chmiel, eds. Cystic Fibrosis. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-42382-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
8

Moss, Richard B., ed. Cystic Fibrosis. Humana Press, 1990. http://dx.doi.org/10.1007/978-1-4612-0475-6.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
9

Amaral, Margarida D., and Karl Kunzelmann, eds. Cystic Fibrosis. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-117-8.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
10

Amaral, Margarida D., and Karl Kunzelmann, eds. Cystic Fibrosis. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-120-8.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
11

Gold, Susan Dudley. Cystic fibrosis. Crestwood House, 2000.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
12

B, Davis Pamela, ed. Cystic fibrosis. M. Dekker, 1993.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
13

1951-, Goodfellow P., ed. Cystic fibrosis. Oxford University Press, 1989.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
14

B, Fiel Stanley, ed. Cystic fibrosis. Saunders, 1998.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
15

E, Hodson Margaret, Geddes Duncan M, and Bush, Andrew, 1954 Apr. 24-, eds. Cystic fibrosis. 3rd ed. Hodder Arnold, 2007.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
16

Jacqueline, Langwith, ed. Cystic fibrosis. Greenhaven Press, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
17

Giddings, Sharon. Cystic fibrosis. Chelsea House, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
18

Bjorklund, Ruth. Cystic fibrosis. Marshall Cavendish Benchmark, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
19

S, Valiathan M., Somers Krishna, Kartha C. Chandrasekharan, and Symposium on Endomyocardial Fibrosis (1991 : Trivandrum, India), eds. Endomyocardial fibrosis. Oxford University Press, 1993.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
20

Mandolfo, Anna. Cystic fibrosis. Dulphar Laboratories, 1991.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
21

O, Warner J., ed. Cystic fibrosis. Churchill Livingstone, 1992.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
22

M, Geddes Duncan, and Hodson Margaret E, eds. Cystic fibrosis. Chapman & Hall Medical, 1995.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
23

Posadas, A. Salcedo, and Rosa María Girón Moreno. Fibrosis quística. Ergón, 2005.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
24

Rosaler, Maxine. Cystic fibrosis. The Rosen Pub. Group, 2007.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
25

J, David T., Goeting Nicola L. M, and Duphar Medical Relations, eds. Cystic fibrosis. Duphar Medical Relations, 1991.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
26

Capewell, Gillian. Cystic fibrosis. Office of Health Economics, 1986.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
27

Gillian, Capewell, and Association of the British Pharmaceutical Industry. Office of Health Economics., eds. Cystic fibrosis. Office of Health Economics, 1986.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
28

Dennis, Shale, ed. Cystic fibrosis. BMJ Publishing Group, 1996.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
29

Lewis, Allen Julian, Rubenstein Ronald, and Panitch Howard B, eds. Cystic fibrosis. Informa Healthcare USA, 2010.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
30

1949-, Phan Sem Hin, and Thrall Roger S. 1947-, eds. Pulmonary fibrosis. Marcel Dekker, 1995.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
31

Meyer, Keith C., and Steven D. Nathan, eds. Idiopathic Pulmonary Fibrosis. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-99975-3.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
32

Meyer, Keith C., and Steven D. Nathan, eds. Idiopathic Pulmonary Fibrosis. Humana Press, 2014. http://dx.doi.org/10.1007/978-1-62703-682-5.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
33

Willis, Monte S., Cecelia C. Yates, and Jonathan C. Schisler, eds. Fibrosis in Disease. Springer International Publishing, 2019. http://dx.doi.org/10.1007/978-3-319-98143-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
34

Nakamura, Hiroyuki, and Kazutetsu Aoshiba, eds. Idiopathic Pulmonary Fibrosis. Springer Japan, 2016. http://dx.doi.org/10.1007/978-4-431-55582-7.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
35

Hodson, Margaret, Duncan Geddes, and Andrew Bush. Cystic Fibrosis. 3rd ed. A Hodder Arnold Publication, 2007.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
36

Hodson, Margaret, Duncan Geddes, and Andrew Bush. Cystic Fibrosis. Taylor & Francis Group, 2007.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
37

Evered, David, and Julie Whelan. Fibrosis. Wiley & Sons, Incorporated, John, 2009.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
38

Staff, CIBA Foundation Symposium. Fibrosis. Wiley & Sons, Limited, John, 2008.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
39

Korn, Joseph. Fibrosis. John Wiley and Sons Ltd, 2007.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
40

Webb, A. K. Cystic Fibrosis. European Respiratory Society, 2006.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
41

Spilsbury, Richard. Cystic Fibrosis. Rosen Publishing Group, 2018.

Buscar texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
42

Beattie, R. Mark, Anil Dhawan, and John W.L. Puntis. Cystic fibrosis. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780198569862.003.0021.

Texto completo
Resumen
Gastrointestinal manifestations 156Management of gastrointestinal symptoms in children with CF 158Nutrition in CF 158Nutritional management 159Vitamins 160The incidence of cystic fibrosis (CF) is around 1 in 2500. Cases are diagnosed as a consequence of population screening or high-risk screening, or following presentation with clinical symptoms typical of the disorder. The basic defect is in the CFTR (cystic fibrosis transmembrane conductance regulator) protein which codes for a cyclic adenosine monophosphate-regulated chloride transporter in epithelial cells of exocrine organs. This is invol
Los estilos APA, Harvard, Vancouver, ISO, etc.
43

Yaqoob, Muhammad M., Katherine Bennett-Richards, and Islam Junaid. Retroperitoneal fibrosis. Edited by Adrian Woolf. Oxford University Press, 2015. http://dx.doi.org/10.1093/med/9780199592548.003.0357.

Texto completo
Resumen
Retroperitoneal fibrosis (RPF) is a rare but multifaceted disease which encompasses a range of conditions characterized by the presence of a fibro-inflammatory tissue, which usually surrounds the abdominal aorta, iliac arteries, and extends into the retroperitoneum to entrap ureters with resultant unilateral or bilateral obstruction, usually at the junction between the middle and lower thirds of the ureter. The condition is progressive: initially, the fibrous tissue is fairly cellular, later becoming relatively acellular. The mechanism by which obstruction occurs is probably due to loss of per
Los estilos APA, Harvard, Vancouver, ISO, etc.
44

Webb, A. K., and F. A. Ratjen, eds. Cystic Fibrosis. European Respiratory Society Journals Ltd, 2006. http://dx.doi.org/10.1183/1025448x.erm3506.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
45

Mall, Marcus A., and J. Stuart Elborn, eds. Cystic Fibrosis. European Respiratory Society, 2014. http://dx.doi.org/10.1183/1025448x.erm6414.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
46

Razzaque, M. S., and T. Taguchi, eds. Renal Fibrosis. S. Karger AG, 2003. http://dx.doi.org/10.1159/isbn.978-3-318-00964-4.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
47

Bright-Thomas, Rowland J., and Andrew M. Jones. Cystic fibrosis. Edited by Patrick Davey and David Sprigings. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780199568741.003.0132.

Texto completo
Resumen
Cystic fibrosis is the most common lethal autosomal recessive disorder in Caucasians. There is no known survival advantage of the heterozygote carrier state. Chronic progressive pulmonary infection and bronchiectasis are the major causes of morbidity and mortality. The disease affects all ductal systems where the basic defect is manifest, including the pancreas, gastrointestinal tract, sinuses, hepatobiliary system, and male reproductive system, and has significant effects on nutrition and growth.
Los estilos APA, Harvard, Vancouver, ISO, etc.
48

Horsley, Alex, Steve Cunningham, and Alistair Innes, eds. Cystic Fibrosis. Oxford University Press, 2010. http://dx.doi.org/10.1093/med/9780199582709.001.0001.

Texto completo
Los estilos APA, Harvard, Vancouver, ISO, etc.
49

Martin, David, and Junzheng Wu. Cystic Fibrosis. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199764495.003.0021.

Texto completo
Resumen
Cystic fibrosis (CF) is an inherited chronic disease that affects about 30,000 children and adults in the United States and 70,000 worldwide. CF is the most common fatal inherited disorder affecting Caucasians in the United States. While its presentation can vary in severity, the most common clinical manifestations are progressive lung damage and chronic digestive problems due to exocrine gland dysfunction and the production of thick viscous mucus. Careful perioperative management is important to avoid respiratory complications.
Los estilos APA, Harvard, Vancouver, ISO, etc.
50

Tinch, Brian, David Martin, and Junzheng Wu. Cystic Fibrosis. Edited by Erin S. Williams, Olutoyin A. Olutoye, Catherine P. Seipel, and Titilopemi A. O. Aina. Oxford University Press, 2018. http://dx.doi.org/10.1093/med/9780190678333.003.0018.

Texto completo
Resumen
Cystic fibrosis is an inherited disorder. The diagnosis should be suspected in an infant who has meconium ileus or infants presenting to the operating room with volvulus. Cystic fibrosis is characterized by frequent mucous plugging in the respiratory tract which may manifest as wheezing and frequent intermittent flare-ups of respiratory decompensation. Optimization of the affected child’s respiratory status prior to elective surgery is mandatory to prevent difficulty with intraoperative ventilation. While the laryngeal mask airway may be used for short procedures, the use of an endotracheal tu
Los estilos APA, Harvard, Vancouver, ISO, etc.
También puede estar interesado en las bibliografías sobre el tema "Fibrosis" para otros tipos de fuentes:
Artículos de revistas Tesis
Ofrecemos descuentos en todos los planes premium para autores cuyas obras están incluidas en selecciones literarias temáticas. ¡Contáctenos para obtener un código promocional único!

Pasar a la bibliografía