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Showing 25 to 36 of 44 entries
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Bibliography. Current world literature. Cystic fibrosis.

Current opinion in pulmonary medicine

[No authors listed]
PMID: 16444841
Curr Opin Pulm Med. 2005 Nov;11(6):555-62.

No abstract available.

Cite
Bibliography. Current world literature. Cystic fibrosis. Curr Opin Pulm Med. 2005;11(6):555-62
(2005). Bibliography. Current world literature. Cystic fibrosis. Current opinion in pulmonary medicine, 11(6), 555-62.
"Bibliography. Current world literature. Cystic fibrosis." Current opinion in pulmonary medicine vol. 11,6 (2005): 555-62.
Bibliography. Current world literature. Cystic fibrosis. Curr Opin Pulm Med. 2005 Nov;11(6):555-62. PMID: 16444841.
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Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis.

Scientific reports

Nielsen S, Needham B, Leach ST, Day AS, Jaffe A, Thomas T, Ooi CY.
PMID: 27143104
Sci Rep. 2016 May 04;6:24857. doi: 10.1038/srep24857.

Cystic fibrosis (CF) is a genetic disorder that leads to formation of thick epithelial secretions in affected organs. Chronic microbial infections associated with thick mucus secretions are the hallmarks of lung disease in CF. Despite similar conditions existing in...

Cite
Nielsen S, Needham B, Leach ST, et al. Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis. Sci Rep. 2016;6:24857doi: 10.1038/srep24857.
Nielsen, S., Needham, B., Leach, S. T., Day, A. S., Jaffe, A., Thomas, T., & Ooi, C. Y. (2016). Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis. Scientific reports, 624857. https://doi.org/10.1038/srep24857
Nielsen, Shaun, et al. "Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis." Scientific reports vol. 6 (2016): 24857. doi: https://doi.org/10.1038/srep24857
Nielsen S, Needham B, Leach ST, Day AS, Jaffe A, Thomas T, Ooi CY. Disrupted progression of the intestinal microbiota with age in children with cystic fibrosis. Sci Rep. 2016 May 04;6:24857. doi: 10.1038/srep24857. PMID: 27143104; PMCID: PMC4855157.
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Systematic Review of the Prevalence of Kidney Stones in Cystic Fibrosis.

Journal of endourology

Moryousef J, Kwong J, Kishibe T, Ordon M.
PMID: 33906435
J Endourol. 2021 Nov;35(11):1693-1700. doi: 10.1089/end.2021.0151. Epub 2021 Sep 17.

No abstract available.

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Moryousef J, Kwong J, Kishibe T, et al. Systematic Review of the Prevalence of Kidney Stones in Cystic Fibrosis. J Endourol. 2021;35(11):1693-1700doi: 10.1089/end.2021.0151.
Moryousef, J., Kwong, J., Kishibe, T., & Ordon, M. (2021). Systematic Review of the Prevalence of Kidney Stones in Cystic Fibrosis. Journal of endourology, 35(11), 1693-1700. https://doi.org/10.1089/end.2021.0151
Moryousef, Joseph, et al. "Systematic Review of the Prevalence of Kidney Stones in Cystic Fibrosis." Journal of endourology vol. 35,11 (2021): 1693-1700. doi: https://doi.org/10.1089/end.2021.0151
Moryousef J, Kwong J, Kishibe T, Ordon M. Systematic Review of the Prevalence of Kidney Stones in Cystic Fibrosis. J Endourol. 2021 Nov;35(11):1693-1700. doi: 10.1089/end.2021.0151. Epub 2021 Sep 17. PMID: 33906435.
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Sensitive markers to detect progression of lung disease in children with cystic fibrosis.

The European respiratory journal

Stahl M.
PMID: 34244301
Eur Respir J. 2021 Jul 08;58(1). doi: 10.1183/13993003.00236-2021. Print 2021 Jul.

No abstract available.

Cite
Stahl M. Sensitive markers to detect progression of lung disease in children with cystic fibrosis. Eur Respir J. 2021;58(1)doi: 10.1183/13993003.00236-2021.
Stahl, M. (2021). Sensitive markers to detect progression of lung disease in children with cystic fibrosis. The European respiratory journal, 58(1), . https://doi.org/10.1183/13993003.00236-2021
Stahl, Mirjam. "Sensitive markers to detect progression of lung disease in children with cystic fibrosis." The European respiratory journal vol. 58,1 (2021). doi: https://doi.org/10.1183/13993003.00236-2021
Stahl M. Sensitive markers to detect progression of lung disease in children with cystic fibrosis. Eur Respir J. 2021 Jul 08;58(1). doi: 10.1183/13993003.00236-2021. Print 2021 Jul. PMID: 34244301.
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[Radiologic pattern of the lungs in cases of mucoviscidosis in infants].

Polski przeglad radiologii i medycyny nuklearnej

Kozlowski K.
PMID: 5864936
Pol Przegl Radiol Med Nukl. 1965 Nov-Dec;29(6):625-33.

No abstract available.

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Kozlowski K. Obraz radiologiczny płuc w torbielowatym zwyrodnieniu trzustki (mucoviscidosis) u niemowlat. [Radiologic pattern of the lungs in cases of mucoviscidosis in infants]. Pol Przegl Radiol Med Nukl. 1965;29(6):625-33
Kozlowski, K. (1965). Obraz radiologiczny płuc w torbielowatym zwyrodnieniu trzustki (mucoviscidosis) u niemowlat. [Radiologic pattern of the lungs in cases of mucoviscidosis in infants]. Polski przeglad radiologii i medycyny nuklearnej, 29(6), 625-33.
Kozlowski, K. "Obraz radiologiczny płuc w torbielowatym zwyrodnieniu trzustki (mucoviscidosis) u niemowlat." [Radiologic pattern of the lungs in cases of mucoviscidosis in infants]. Polski przeglad radiologii i medycyny nuklearnej vol. 29,6 (1965): 625-33.
Kozlowski K. Obraz radiologiczny płuc w torbielowatym zwyrodnieniu trzustki (mucoviscidosis) u niemowlat. [Radiologic pattern of the lungs in cases of mucoviscidosis in infants]. Pol Przegl Radiol Med Nukl. 1965 Nov-Dec;29(6):625-33. Polish. PMID: 5864936.
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Cystic fibrosis. Pathogenesis of the pulmonary lesion.

Minnesota medicine

Gibbs GE.
PMID: 5824149
Minn Med. 1969 Sep;52(9):1433-4.

No abstract available.

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Gibbs GE. Cystic fibrosis. Pathogenesis of the pulmonary lesion. Minn Med. 1969;52(9):1433-4
Gibbs, G. E. (1969). Cystic fibrosis. Pathogenesis of the pulmonary lesion. Minnesota medicine, 52(9), 1433-4.
Gibbs, G E. "Cystic fibrosis. Pathogenesis of the pulmonary lesion." Minnesota medicine vol. 52,9 (1969): 1433-4.
Gibbs GE. Cystic fibrosis. Pathogenesis of the pulmonary lesion. Minn Med. 1969 Sep;52(9):1433-4. PMID: 5824149.
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[Mental and emotional aspects of pancreatic cystic fibrosis (mucoviscidosis)].

L'union medicale du Canada

Belmonte MM.
PMID: 5362147
Union Med Can. 1969 Nov;98(11):1943-5.

No abstract available.

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Belmonte MM. Aspects psychiques et émotifs dans la fibrose kystique du pancréas (mucoviscidose) [Mental and emotional aspects of pancreatic cystic fibrosis (mucoviscidosis)]. Union Med Can. 1969;98(11):1943-5
Belmonte, M. M. (1969). Aspects psychiques et émotifs dans la fibrose kystique du pancréas (mucoviscidose) [Mental and emotional aspects of pancreatic cystic fibrosis (mucoviscidosis)]. L'union medicale du Canada, 98(11), 1943-5.
Belmonte, M M. "Aspects psychiques et émotifs dans la fibrose kystique du pancréas (mucoviscidose)" [Mental and emotional aspects of pancreatic cystic fibrosis (mucoviscidosis)]. L'union medicale du Canada vol. 98,11 (1969): 1943-5.
Belmonte MM. Aspects psychiques et émotifs dans la fibrose kystique du pancréas (mucoviscidose) [Mental and emotional aspects of pancreatic cystic fibrosis (mucoviscidosis)]. Union Med Can. 1969 Nov;98(11):1943-5. French. PMID: 5362147.
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Cystic fibrosis: nature and prognosis.

Minnesota medicine

Warwick WJ.
PMID: 6046244
Minn Med. 1967 Jul;50(7):1049-53.

No abstract available.

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Warwick WJ. Cystic fibrosis: nature and prognosis. Minn Med. 1967;50(7):1049-53
Warwick, W. J. (1967). Cystic fibrosis: nature and prognosis. Minnesota medicine, 50(7), 1049-53.
Warwick, W J. "Cystic fibrosis: nature and prognosis." Minnesota medicine vol. 50,7 (1967): 1049-53.
Warwick WJ. Cystic fibrosis: nature and prognosis. Minn Med. 1967 Jul;50(7):1049-53. PMID: 6046244.
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Glucose intolerance in cystic fibrosis.

Archives of disease in childhood

Taylor CJ, Baxter PS, Hardcastle J, Hardcastle PT, Goldhill J.
PMID: 2730134
Arch Dis Child. 1989 May;64(5):759. doi: 10.1136/adc.64.5.759.
Free PMC Article

No abstract available.

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Taylor CJ, Baxter PS, Hardcastle J, et al. Glucose intolerance in cystic fibrosis. Arch Dis Child. 1989;64(5):759doi: 10.1136/adc.64.5.759.
Taylor, C. J., Baxter, P. S., Hardcastle, J., Hardcastle, P. T., & Goldhill, J. (1989). Glucose intolerance in cystic fibrosis. Archives of disease in childhood, 64(5), 759. https://doi.org/10.1136/adc.64.5.759
Taylor, C J, et al. "Glucose intolerance in cystic fibrosis." Archives of disease in childhood vol. 64,5 (1989): 759. doi: https://doi.org/10.1136/adc.64.5.759
Taylor CJ, Baxter PS, Hardcastle J, Hardcastle PT, Goldhill J. Glucose intolerance in cystic fibrosis. Arch Dis Child. 1989 May;64(5):759. doi: 10.1136/adc.64.5.759. PMID: 2730134; PMCID: PMC1792014.
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I won't let cystic fibrosis stop me from living my best life.

The Lancet. Respiratory medicine

Baxter L.
PMID: 33773122
Lancet Respir Med. 2021 Aug;9(8):823-824. doi: 10.1016/S2213-2600(21)00162-4. Epub 2021 Mar 24.

No abstract available.

Cite
Baxter L. I won't let cystic fibrosis stop me from living my best life. Lancet Respir Med. 2021;9(8):823-824doi: 10.1016/S2213-2600(21)00162-4.
Baxter, L. (2021). I won't let cystic fibrosis stop me from living my best life. The Lancet. Respiratory medicine, 9(8), 823-824. https://doi.org/10.1016/S2213-2600(21)00162-4
Baxter, Lucy. "I won't let cystic fibrosis stop me from living my best life." The Lancet. Respiratory medicine vol. 9,8 (2021): 823-824. doi: https://doi.org/10.1016/S2213-2600(21)00162-4
Baxter L. I won't let cystic fibrosis stop me from living my best life. Lancet Respir Med. 2021 Aug;9(8):823-824. doi: 10.1016/S2213-2600(21)00162-4. Epub 2021 Mar 24. PMID: 33773122.
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Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?.

American journal of respiratory and critical care medicine

Ranganathan SC, Hall GL, Sly PD, Stick SM, Douglas TA.
PMID: 27911585
Am J Respir Crit Care Med. 2017 Jun 15;195(12):1567-1575. doi: 10.1164/rccm.201606-1107CI.

The past decade has seen significant advances in understanding of the pathogenesis and progression of lung disease in cystic fibrosis (CF). Pulmonary inflammation, infection, and structural lung damage manifest very early in life and are prevalent among preschool children...

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Ranganathan SC, Hall GL, Sly PD, et al. Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?. Am J Respir Crit Care Med. 2017;195(12):1567-1575doi: 10.1164/rccm.201606-1107CI.
Ranganathan, S. C., Hall, G. L., Sly, P. D., Stick, S. M., Douglas, T. A. (2017). Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?. American journal of respiratory and critical care medicine, 195(12), 1567-1575. https://doi.org/10.1164/rccm.201606-1107CI
Ranganathan, Sarath C, et al. "Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?." American journal of respiratory and critical care medicine vol. 195,12 (2017): 1567-1575. doi: https://doi.org/10.1164/rccm.201606-1107CI
Ranganathan SC, Hall GL, Sly PD, Stick SM, Douglas TA. Early Lung Disease in Infants and Preschool Children with Cystic Fibrosis. What Have We Learned and What Should We Do about It?. Am J Respir Crit Care Med. 2017 Jun 15;195(12):1567-1575. doi: 10.1164/rccm.201606-1107CI. PMID: 27911585; PMCID: PMC6850725.
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Bibliography. Current world literature. Cystic fibrosis.

Current opinion in pulmonary medicine

[No authors listed]
PMID: 12398101
Curr Opin Pulm Med. 2002 Nov;8(6):561-6.

No abstract available.

Cite
Bibliography. Current world literature. Cystic fibrosis. Curr Opin Pulm Med. 2002;8(6):561-6
(2002). Bibliography. Current world literature. Cystic fibrosis. Current opinion in pulmonary medicine, 8(6), 561-6.
"Bibliography. Current world literature. Cystic fibrosis." Current opinion in pulmonary medicine vol. 8,6 (2002): 561-6.
Bibliography. Current world literature. Cystic fibrosis. Curr Opin Pulm Med. 2002 Nov;8(6):561-6. PMID: 12398101.
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Showing 25 to 36 of 44 entries