Accedi

Bibliografie tematiche / Fibrosis / Libri

Segui questo link per vedere altri tipi di pubblicazioni sul tema: Fibrosis.

Libri sul tema "Fibrosis"

Autore: Grafiati

Pubblicato: 4 giugno 2021

Ultima modifica: 25 luglio 2025

Cita una fonte nei formati APA, MLA, Chicago, Harvard e in molti altri stili

Scegli il tipo di fonte:

Vedi i top-50 libri per l'attività di ricerca sul tema "Fibrosis".

Accanto a ogni fonte nell'elenco di riferimenti c'è un pulsante "Aggiungi alla bibliografia". Premilo e genereremo automaticamente la citazione bibliografica dell'opera scelta nello stile citazionale di cui hai bisogno: APA, MLA, Harvard, Chicago, Vancouver ecc.

Puoi anche scaricare il testo completo della pubblicazione scientifica nel formato .pdf e leggere online l'abstract (il sommario) dell'opera se è presente nei metadati.

Vedi i libri di molte aree scientifiche e compila una bibliografia corretta.

1

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

2

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

3

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

4

Symposium, Ciba Foundation. Fibrosis. Pitman, 1985.

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

5

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

6

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

8

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

9

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

10

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

11

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

12

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

13

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

14

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

15

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

16

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

17

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

18

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

19

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

20

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

21

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

22

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

23

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

24

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

25

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

26

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

27

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

28

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

29

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

30

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

34

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

35

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

36

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

37

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

38

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

39

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

40

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

41

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

Cerca il testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Abstract (sommario):

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

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Abstract (sommario):

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

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

45

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

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Abstract (sommario):

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.

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Gli stili APA, Harvard, Vancouver, ISO e altri

49

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

Testo completo

Abstract (sommario):

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.

Gli stili APA, Harvard, Vancouver, ISO e altri

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.

Testo completo

Abstract (sommario):

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

Gli stili APA, Harvard, Vancouver, ISO e altri

Offriamo sconti su tutti i piani premium per gli autori le cui opere sono incluse in raccolte letterarie tematiche. Contattaci per ottenere un codice promozionale unico!