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[Cystic fibrosis in the past, present and future].

Ceskoslovenska pediatrie

Houstĕk J, Vávrová V.
PMID: 3427676
Cesk Pediatr. 1987 Nov;42(11):645-9.

No abstract available.

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Houstĕk J, Vávrová V. Cystická fibróza v minulosti, prítomnosti a budoucnosti. [Cystic fibrosis in the past, present and future]. Cesk Pediatr. 1987;42(11):645-9
Houstĕk, J., & Vávrová, V. (1987). Cystická fibróza v minulosti, prítomnosti a budoucnosti. [Cystic fibrosis in the past, present and future]. Ceskoslovenska pediatrie, 42(11), 645-9.
Houstĕk, J, and Vávrová, V. "Cystická fibróza v minulosti, prítomnosti a budoucnosti." [Cystic fibrosis in the past, present and future]. Ceskoslovenska pediatrie vol. 42,11 (1987): 645-9.
Houstĕk J, Vávrová V. Cystická fibróza v minulosti, prítomnosti a budoucnosti. [Cystic fibrosis in the past, present and future]. Cesk Pediatr. 1987 Nov;42(11):645-9. Czech. PMID: 3427676.
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Cystic fibrosis in Europe: patients live longer but are we ready?.

The European respiratory journal

Schwarz C, Hartl D.
PMID: 26130774
Eur Respir J. 2015 Jul;46(1):11-2. doi: 10.1183/09031936.00026615.

No abstract available.

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Schwarz C, Hartl D. Cystic fibrosis in Europe: patients live longer but are we ready?. Eur Respir J. 2015;46(1):11-2doi: 10.1183/09031936.00026615.
Schwarz, C., & Hartl, D. (2015). Cystic fibrosis in Europe: patients live longer but are we ready?. The European respiratory journal, 46(1), 11-2. https://doi.org/10.1183/09031936.00026615
Schwarz, Carsten, and Hartl, Dominik. "Cystic fibrosis in Europe: patients live longer but are we ready?." The European respiratory journal vol. 46,1 (2015): 11-2. doi: https://doi.org/10.1183/09031936.00026615
Schwarz C, Hartl D. Cystic fibrosis in Europe: patients live longer but are we ready?. Eur Respir J. 2015 Jul;46(1):11-2. doi: 10.1183/09031936.00026615. PMID: 26130774.
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Research in progress-electronic patient records: a new era.

Thorax

Peckham D, Whitaker P, White H.
PMID: 25504824
Thorax. 2015 May;70(5):473-5. doi: 10.1136/thoraxjnl-2014-206573. Epub 2014 Dec 10.

Clinical information systems and electronic records are starting to appear in secondary care and herald new potentials for improving health provision and capturing high quality data. In 2006, we set up a program to develop electronic patient records (EPR)...

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Peckham D, Whitaker P, White H. Research in progress-electronic patient records: a new era. Thorax. 2014;70(5):473-5doi: 10.1136/thoraxjnl-2014-206573.
Peckham, D., Whitaker, P., & White, H. (2015). Research in progress-electronic patient records: a new era. Thorax, 70(5), 473-5. https://doi.org/10.1136/thoraxjnl-2014-206573
Peckham, D, et al. "Research in progress-electronic patient records: a new era." Thorax vol. 70,5 (2015): 473-5. doi: https://doi.org/10.1136/thoraxjnl-2014-206573
Peckham D, Whitaker P, White H. Research in progress-electronic patient records: a new era. Thorax. 2015 May;70(5):473-5. doi: 10.1136/thoraxjnl-2014-206573. Epub 2014 Dec 10. PMID: 25504824.
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Impact of COVID-19 on mental health: Effects on screening, care delivery, and people with cystic fibrosis (Commentary).

Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society

Havermans T.
PMID: 34930541
J Cyst Fibros. 2021 Dec;20:39-40. doi: 10.1016/j.jcf.2021.08.006.

No abstract available.

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Havermans T. Impact of COVID-19 on mental health: Effects on screening, care delivery, and people with cystic fibrosis (Commentary). J Cyst Fibros. 2021;20:39-40doi: 10.1016/j.jcf.2021.08.006.
Havermans, T. (2021). Impact of COVID-19 on mental health: Effects on screening, care delivery, and people with cystic fibrosis (Commentary). Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2039-40. https://doi.org/10.1016/j.jcf.2021.08.006
Havermans, Trudy. "Impact of COVID-19 on mental health: Effects on screening, care delivery, and people with cystic fibrosis (Commentary)." Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society vol. 20 (2021): 39-40. doi: https://doi.org/10.1016/j.jcf.2021.08.006
Havermans T. Impact of COVID-19 on mental health: Effects on screening, care delivery, and people with cystic fibrosis (Commentary). J Cyst Fibros. 2021 Dec;20:39-40. doi: 10.1016/j.jcf.2021.08.006. PMID: 34930541; PMCID: PMC8683123.
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Protecting clinical trials in cystic fibrosis during the SARS-CoV-2 pandemic: risks and mitigation measures.

Trials

van Koningsbruggen-Rietschel S, Dunlevy F, Bulteel V, Hayes K, Verbrugge A, Janssens HM, Dufeu N, Simmonds NJ, Dupont LJ, Downey DG.
PMID: 34454570
Trials. 2021 Aug 28;22(1):578. doi: 10.1186/s13063-021-05457-5.

The SARS-CoV-2 pandemic has disrupted clinical trials worldwide. The European Cystic Fibrosis Society-Clinical Trials Network (ECFS-CTN) has tracked clinical trial disruption by surveying its 58 trial sites across 17 European countries and collated information on measures to mitigate the...

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van Koningsbruggen-Rietschel S, Dunlevy F, Bulteel V, et al. Protecting clinical trials in cystic fibrosis during the SARS-CoV-2 pandemic: risks and mitigation measures. Trials. 2021;22(1):578doi: 10.1186/s13063-021-05457-5.
van Koningsbruggen-Rietschel, S., Dunlevy, F., Bulteel, V., Hayes, K., Verbrugge, A., Janssens, H. M., Dufeu, N., Simmonds, N. J., Dupont, L. J., & Downey, D. G. (2021). Protecting clinical trials in cystic fibrosis during the SARS-CoV-2 pandemic: risks and mitigation measures. Trials, 22(1), 578. https://doi.org/10.1186/s13063-021-05457-5
van Koningsbruggen-Rietschel, Silke, et al. "Protecting clinical trials in cystic fibrosis during the SARS-CoV-2 pandemic: risks and mitigation measures." Trials vol. 22,1 (2021): 578. doi: https://doi.org/10.1186/s13063-021-05457-5
van Koningsbruggen-Rietschel S, Dunlevy F, Bulteel V, Hayes K, Verbrugge A, Janssens HM, Dufeu N, Simmonds NJ, Dupont LJ, Downey DG. Protecting clinical trials in cystic fibrosis during the SARS-CoV-2 pandemic: risks and mitigation measures. Trials. 2021 Aug 28;22(1):578. doi: 10.1186/s13063-021-05457-5. PMID: 34454570; PMCID: PMC8402966.
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[Incidence and diagnosis of cystic fibrosis (mucoviscidosis). Experiences with night sweat collection].

Kinderarztliche Praxis

Thal W, Abu-Amna M, Klaer U.
PMID: 5499541
Kinderarztl Prax. 1970 Nov;38(11):514-9.

No abstract available.

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Thal W, Abu-Amna M, Klaer U. Zur Häufigkeit und Diagnose der zystischen Fibrose (Mucoviszidose). Erfahrungen mit der Nachtschweiss-Gewinnung. [Incidence and diagnosis of cystic fibrosis (mucoviscidosis). Experiences with night sweat collection]. Kinderarztl Prax. 1970;38(11):514-9
Thal, W., Abu-Amna, M., & Klaer, U. (1970). Zur Häufigkeit und Diagnose der zystischen Fibrose (Mucoviszidose). Erfahrungen mit der Nachtschweiss-Gewinnung. [Incidence and diagnosis of cystic fibrosis (mucoviscidosis). Experiences with night sweat collection]. Kinderarztliche Praxis, 38(11), 514-9.
Thal, W, et al. "Zur Häufigkeit und Diagnose der zystischen Fibrose (Mucoviszidose). Erfahrungen mit der Nachtschweiss-Gewinnung." [Incidence and diagnosis of cystic fibrosis (mucoviscidosis). Experiences with night sweat collection]. Kinderarztliche Praxis vol. 38,11 (1970): 514-9.
Thal W, Abu-Amna M, Klaer U. Zur Häufigkeit und Diagnose der zystischen Fibrose (Mucoviszidose). Erfahrungen mit der Nachtschweiss-Gewinnung. [Incidence and diagnosis of cystic fibrosis (mucoviscidosis). Experiences with night sweat collection]. Kinderarztl Prax. 1970 Nov;38(11):514-9. German. PMID: 5499541.
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[Cystic fibrosis at present: current state and new perspectives].

Minerva pediatrica

Balsamo V, Pardo F.
PMID: 7799880
Minerva Pediatr. 1994 Sep;46(9):XIII-XIV.

No abstract available.

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Balsamo V, Pardo F. La fibrosi cistica oggi: realtà e nuove prospettive. [Cystic fibrosis at present: current state and new perspectives]. Minerva Pediatr. 1994;46(9):XIII-XIV
Balsamo, V., & Pardo, F. (1994). La fibrosi cistica oggi: realtà e nuove prospettive. [Cystic fibrosis at present: current state and new perspectives]. Minerva pediatrica, 46(9), XIII-XIV.
Balsamo, V, and Pardo, F. "La fibrosi cistica oggi: realtà e nuove prospettive." [Cystic fibrosis at present: current state and new perspectives]. Minerva pediatrica vol. 46,9 (1994): XIII-XIV.
Balsamo V, Pardo F. La fibrosi cistica oggi: realtà e nuove prospettive. [Cystic fibrosis at present: current state and new perspectives]. Minerva Pediatr. 1994 Sep;46(9):XIII-XIV. Italian. PMID: 7799880.
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Cystic fibrosis-related diabetes in children--gaps in the evidence?.

Nature reviews. Endocrinology

Rana M, Munns CF, Selvadurai H, Donaghue KC, Craig ME.
PMID: 20498678
Nat Rev Endocrinol. 2010 Jul;6(7):371-8. doi: 10.1038/nrendo.2010.85. Epub 2010 May 25.

As the life span of patients with cystic fibrosis has increased, so has the prevalence of cystic fibrosis-related diabetes mellitus. However, screening practices for cystic fibrosis-related diabetes mellitus vary widely, which affects accurate estimates of the health burden of...

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Rana M, Munns CF, Selvadurai H, et al. Cystic fibrosis-related diabetes in children--gaps in the evidence?. Nat Rev Endocrinol. 2010;6(7):371-8doi: 10.1038/nrendo.2010.85.
Rana, M., Munns, C. F., Selvadurai, H., Donaghue, K. C., & Craig, M. E. (2010). Cystic fibrosis-related diabetes in children--gaps in the evidence?. Nature reviews. Endocrinology, 6(7), 371-8. https://doi.org/10.1038/nrendo.2010.85
Rana, Malay, et al. "Cystic fibrosis-related diabetes in children--gaps in the evidence?." Nature reviews. Endocrinology vol. 6,7 (2010): 371-8. doi: https://doi.org/10.1038/nrendo.2010.85
Rana M, Munns CF, Selvadurai H, Donaghue KC, Craig ME. Cystic fibrosis-related diabetes in children--gaps in the evidence?. Nat Rev Endocrinol. 2010 Jul;6(7):371-8. doi: 10.1038/nrendo.2010.85. Epub 2010 May 25. PMID: 20498678.
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Adult cystic fibrosis.

JAMA

Boyle MP.
PMID: 17940235
JAMA. 2007 Oct 17;298(15):1787-93. doi: 10.1001/jama.298.15.1787.

Cystic fibrosis is a multisystem disease characterized primarily by chronic pulmonary infection and bronchiectasis, pancreatic exocrine impairment, and elevated sweat chloride. In the last 4 decades, new treatment strategies and aggressive nutritional management have resulted in a significant increase...

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Boyle MP. Adult cystic fibrosis. JAMA. 2007;298(15):1787-93doi: 10.1001/jama.298.15.1787.
Boyle, M. P. (2007). Adult cystic fibrosis. JAMA, 298(15), 1787-93. https://doi.org/10.1001/jama.298.15.1787
Boyle, Michael P. "Adult cystic fibrosis." JAMA vol. 298,15 (2007): 1787-93. doi: https://doi.org/10.1001/jama.298.15.1787
Boyle MP. Adult cystic fibrosis. JAMA. 2007 Oct 17;298(15):1787-93. doi: 10.1001/jama.298.15.1787. PMID: 17940235.
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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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[Neonatal screening of mucoviscidosis].

Archives francaises de pediatrie

Gilly R, Barbier Y, Garcia I.
PMID: 3329501
Arch Fr Pediatr. 1987;44:731-4.

No abstract available.

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Gilly R, Barbier Y, Garcia I. Le dépistage néonatal de la mucoviscidose. [Neonatal screening of mucoviscidosis]. Arch Fr Pediatr. 1987;44:731-4
Gilly, R., Barbier, Y., & Garcia, I. (1987). Le dépistage néonatal de la mucoviscidose. [Neonatal screening of mucoviscidosis]. Archives francaises de pediatrie, 44731-4.
Gilly, R, et al. "Le dépistage néonatal de la mucoviscidose." [Neonatal screening of mucoviscidosis]. Archives francaises de pediatrie vol. 44 (1987): 731-4.
Gilly R, Barbier Y, Garcia I. Le dépistage néonatal de la mucoviscidose. [Neonatal screening of mucoviscidosis]. Arch Fr Pediatr. 1987;44:731-4. French. PMID: 3329501.
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[Japanese clinical statistical data of patients with cystic fibrosis].

Nihon rinsho. Japanese journal of clinical medicine

Matsuno S, Sunamura M, Takeda K, Kobari M.
PMID: 1344413
Nihon Rinsho. 1992 Nov;50:727-32.

No abstract available.

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Matsuno S, Sunamura M, Takeda K, et al. [Japanese clinical statistical data of patients with cystic fibrosis]. Nihon Rinsho. 1992;50:727-32
Matsuno, S., Sunamura, M., Takeda, K., & Kobari, M. (1992). [Japanese clinical statistical data of patients with cystic fibrosis]. Nihon rinsho. Japanese journal of clinical medicine, 50727-32.
Matsuno, S, et al. "[Japanese clinical statistical data of patients with cystic fibrosis]." Nihon rinsho. Japanese journal of clinical medicine vol. 50 (1992): 727-32.
Matsuno S, Sunamura M, Takeda K, Kobari M. [Japanese clinical statistical data of patients with cystic fibrosis]. Nihon Rinsho. 1992 Nov;50:727-32. Japanese. PMID: 1344413.
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Showing 1 to 12 of 15 entries