囊腫性纖維化 (Chinese Wikipedia)

Analysis of information sources in references of the Wikipedia article "囊腫性纖維化" in Chinese language version.

refsWebsite

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32nih.gov

4^th place

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17doi.org

2^nd place

23^rd place

10web.archive.org

1^st place

3cysticfibrosis.ca

low place

3cff.org

low place

3archive.org

6^th place

4^th place

3semanticscholar.org

11^th place

332^nd place

2google.ca

838^th place

259^th place

2worldcat.org

5^th place

12^th place

1chestpubs.org

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1books.google.com

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1imj.ie

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1biomedcentral.com

2,747^th place

1,988^th place

1harvard.edu

18^th place

57^th place

archive.org

Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. The Journal of Pediatrics. April 1998, 132 (4): 589–95. PMID 9580754. doi:10.1016/S0022-3476(98)70344-0.
Hamosh A, FitzSimmons SC, Macek M, Knowles MR, Rosenstein BJ, Cutting GR. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. The Journal of Pediatrics. February 1998, 132 (2): 255–9. PMID 9506637. doi:10.1016/S0022-3476(98)70441-X .
Yu H, Nasr SZ, Deretic V. Innate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosis. Infection and Immunity. April 2000, 68 (4): 2142–7. PMC 97396 . PMID 10722612. doi:10.1128/IAI.68.4.2142-2147.2000.

biomedcentral.com

ojrd.biomedcentral.com

Xiaobei Guo; et al. Clinical and genetic characteristics of cystic fibrosis in CHINESE patients: a systemic review of reported cases. Orphanet Journal of Rare Diseases. 2018, (13). doi:10.1186/s13023-018-0968-2.

books.google.com

Tobias E. Essential Medical Genetics. John Wiley & Sons. 2011: 312. ISBN 978-1-118-29370-6. （原始内容存档于2016-04-17）.

cff.org

Genetic Carrier Testing. Cystic Fibrosis Foundation. 2007. （原始内容存档于2010-03-23）.
Annual Data Report 2016 Cystic Fibrosis Foundation Patient Registry (PDF): 4. [19 June 2018]. （原始内容 (PDF)存档于19 June 2018）.
Cystic Fibrosis Foundation. CFTR Modulator Therapies. [2023-12-23]. （原始内容存档于2024-07-03）.

chestpubs.org

chestjournal.chestpubs.org

Yankaskas JR, Marshall BC, Sufian B, Simon RH, Rodman D. Cystic fibrosis adult care consensus conference report. Chest. 2004, 125 (90010): 1–39. PMID 14734689. doi:10.1378/chest.125.1_suppl.1S. ^{[失效連結]}

cysticfibrosis.ca

The Canadian Facts & Figures on Cystic Fibrosis. cysticfibrosis.ca. （原始内容存档于2013-06-16）.
Canadian Cystic Fibrosis Patient Data Registry Report (PDF). Canadian Cystic Fibrosis Foundation. 2007 [2010-03-14]. （原始内容 (PDF)存档于2010-07-15）.
Medications. Cystic Fibrosis Canada. 2011. No. 10684-5100 RR0001. （原始内容存档于2011-09-04）.

doi.org

O'Sullivan, BP; Freedman, SD. Cystic fibrosis.. Lancet. 30 May 2009, 373 (9678): 1891–904. PMID 19403164. doi:10.1016/s0140-6736(09)60327-5.
Andersen DH. Cystic fibrosis of the pancreas and its relation to celiac disease: a clinical and pathological study. Am J Dis Child. 1938, 56: 344–399. doi:10.1001/archpedi.1938.01980140114013.
Massie, J; Delatycki, MB. Cystic fibrosis carrier screening.. Paediatric respiratory reviews. December 2013, 14 (4): 270–5. PMID 23466339. doi:10.1016/j.prrv.2012.12.002.
Yankaskas JR, Marshall BC, Sufian B, Simon RH, Rodman D. Cystic fibrosis adult care consensus conference report. Chest. 2004, 125 (90010): 1–39. PMID 14734689. doi:10.1378/chest.125.1_suppl.1S. ^{[失效連結]}
Ong, T; Ramsey, BW. Update in Cystic Fibrosis 2014.. American Journal of Respiratory and Critical Care Medicine. 15 September 2015, 192 (6): 669–75. PMID 26371812. doi:10.1164/rccm.201504-0656UP.
Nazareth, D; Walshaw, M. Coming of age in cystic fibrosis - transition from paediatric to adult care.. Clinical medicine (London, England). October 2013, 13 (5): 482–6. PMID 24115706. doi:10.7861/clinmedicine.13-5-482.
Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. The Journal of Pediatrics. April 1998, 132 (4): 589–95. PMID 9580754. doi:10.1016/S0022-3476(98)70344-0.
Hamosh A, FitzSimmons SC, Macek M, Knowles MR, Rosenstein BJ, Cutting GR. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. The Journal of Pediatrics. February 1998, 132 (2): 255–9. PMID 9506637. doi:10.1016/S0022-3476(98)70441-X .
Xiaobei Guo; et al. Clinical and genetic characteristics of cystic fibrosis in CHINESE patients: a systemic review of reported cases. Orphanet Journal of Rare Diseases. 2018, (13). doi:10.1186/s13023-018-0968-2.
Davis PB. Cystic fibrosis since 1938. American Journal of Respiratory and Critical Care Medicine. March 2006, 173 (5): 475–82. PMID 16126935. S2CID 1770759. doi:10.1164/rccm.200505-840OE.
MacKenzie T, Gifford AH, Sabadosa KA, Quinton HB, Knapp EA, Goss CH, Marshall BC. Longevity of patients with cystic fibrosis in 2000 to 2010 and beyond: survival analysis of the Cystic Fibrosis Foundation patient registry. Annals of Internal Medicine. August 2014, 161 (4): 233–41. PMC 4687404 . PMID 25133359. doi:10.7326/m13-0636.
Habib, Al-Rahim R.; Kajbafzadeh, Majid; Desai, Sameer; Yang, Connie L.; Skolnik, Kate; Quon, Bradley S. A Systematic Review of the Clinical Efficacy and Safety of CFTR Modulators in Cystic Fibrosis. Scientific Reports. 2019-05-10, 9 (1): 7234. Bibcode:2019NatSR...9.7234H. ISSN 2045-2322. PMC 6510767 . PMID 31076617. doi:10.1038/s41598-019-43652-2.
Lopes-Pacheco, Miquéias. CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine. Frontiers in Pharmacology. 2020, 10: 1662. ISSN 1663-9812. PMC 7046560 . PMID 32153386. doi:10.3389/fphar.2019.01662 .
Yu H, Nasr SZ, Deretic V. Innate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosis. Infection and Immunity. April 2000, 68 (4): 2142–7. PMC 97396 . PMID 10722612. doi:10.1128/IAI.68.4.2142-2147.2000.
Ratjen F, Döring G. Cystic fibrosis. Lancet. February 2003, 361 (9358): 681–9. PMID 12606185. S2CID 24879334. doi:10.1016/S0140-6736(03)12567-6.
Rosenstein BJ, Zeitlin PL. Cystic fibrosis. Lancet. January 1998, 351 (9098): 277–82. PMID 9457113. S2CID 44627706. doi:10.1016/S0140-6736(97)09174-5 .
Moorcroft AJ, Dodd ME, Webb AK. Exercise limitations and training for patients with cystic fibrosis. Disability and Rehabilitation. 1998, 20 (6–7): 247–53. PMID 9637933. doi:10.3109/09638289809166735.

google.ca

books.google.ca

Hodson, Margaret; Geddes, Duncan; Bush, Andrew (编). Cystic fibrosis 3rd. London: Hodder Arnold. 2012: 3 [2016-04-02]. ISBN 978-1-4441-1369-3. （原始内容存档于2016-03-05）.
Buckingham, Lela. Molecular diagnostics fundamentals, methods, and clinical applications 2nd. Philadelphia: F.A. Davis Co. 2012: 351 [2016-04-02]. ISBN 978-0-8036-2975-2. （原始内容存档于2016-03-04）.

harvard.edu

ui.adsabs.harvard.edu

Habib, Al-Rahim R.; Kajbafzadeh, Majid; Desai, Sameer; Yang, Connie L.; Skolnik, Kate; Quon, Bradley S. A Systematic Review of the Clinical Efficacy and Safety of CFTR Modulators in Cystic Fibrosis. Scientific Reports. 2019-05-10, 9 (1): 7234. Bibcode:2019NatSR...9.7234H. ISSN 2045-2322. PMC 6510767 . PMID 31076617. doi:10.1038/s41598-019-43652-2.

imj.ie

Farrell P, Joffe S, Foley L, Canny GJ, Mayne P, Rosenberg M. Diagnosis of cystic fibrosis in the Republic of Ireland: epidemiology and costs. Irish Medical Journal. September 2007, 100 (8): 557–60. PMID 17955689. （原始内容存档于2013-12-03）.

nih.gov

ncbi.nlm.nih.gov

O'Sullivan, BP; Freedman, SD. Cystic fibrosis.. Lancet. 30 May 2009, 373 (9678): 1891–904. PMID 19403164. doi:10.1016/s0140-6736(09)60327-5.
Massie, J; Delatycki, MB. Cystic fibrosis carrier screening.. Paediatric respiratory reviews. December 2013, 14 (4): 270–5. PMID 23466339. doi:10.1016/j.prrv.2012.12.002.
Yankaskas JR, Marshall BC, Sufian B, Simon RH, Rodman D. Cystic fibrosis adult care consensus conference report. Chest. 2004, 125 (90010): 1–39. PMID 14734689. doi:10.1378/chest.125.1_suppl.1S. ^{[失效連結]}
Ong, T; Ramsey, BW. Update in Cystic Fibrosis 2014.. American Journal of Respiratory and Critical Care Medicine. 15 September 2015, 192 (6): 669–75. PMID 26371812. doi:10.1164/rccm.201504-0656UP.
Nazareth, D; Walshaw, M. Coming of age in cystic fibrosis - transition from paediatric to adult care.. Clinical medicine (London, England). October 2013, 13 (5): 482–6. PMID 24115706. doi:10.7861/clinmedicine.13-5-482.
Rowe SM, Miller S, Sorscher EJ. Cystic fibrosis. N Engl J Med. 2005 May 12;352(19):1992-2001. PMID 15888700
Maldonado M, Martinez A, Alobid I, Mullol J. The antrochoanal polyp. Rhinology. 2004 Dec;42(4):178-82. Review. PMID 15626248
Ramsey B, Richardson MA. Impact of sinusitis in cystic fibrosis. Allergy Clin Immunol. 1992 Sep;90(3 Pt 2):547-52. PMID 1527348
Eggermont E, De Boeck K. Small-intestinal abnormalities in cystic fibrosis patients. Eur J Pediatr. 1991 Oct;150(12):824-8. Review. PMID 1743211
Kulczycki LL, Shwachman H. Studies in cystic fibrosis of the pancreas; occurrence of rectal prolapse. N Engl J Med. 1958 Aug 28;259(9):409-12. PMID 13578072
Cohn JA, Friedman KJ, Noone PG, Knowles MR, Silverman LM, Jowell PS. Relation between mutations of the cystic fibrosis gene and idiopathic pancreatitis. N Engl J Med. 1998 Sep 3;339(10):653-8. PMID 9725922
Malfroot A, Dab I. New insights on gastro-oesophageal reflux in cystic fibrosis by longitudinal follow up. Arch Dis Child. 1991 Nov;66(11):1339-45. PMID 175564
Khoshoo V, Udall JN Jr. Meconium ileus equivalent in children and adults. Am J Gastroenterol. 1994 Feb;89(2):153-7. PMID 8304294
Williams SG, Westaby D, Tanner MS, Mowat AP. Liver and biliary problems in cystic fibrosis. Br Med Bull. 1992 Oct;48(4):877-92. PMID 1458306
Moran A, Pyzdrowski KL, Weinreb J, Kahn BB, Smith SA, Adams KS, Seaquist ER.Insulin sensitivity in cystic fibrosis. Diabetes. 1994 Aug;43(8):1020-6. PMID 8039595
Haworth CS, Selby PL, Webb AK, Dodd ME, Musson H, McL Niven R, Economou G, Horrocks AW, Freemont AJ, Mawer EB, Adams JE. Low bone mineral density in adults with cystic fibrosis. Thorax. 1999 Nov;54(11):961-7. PMID 10525552
McCallum TJ, Milunsky JM, Cunningham DL, Harris DH, Maher TA, Oates RD. Fertility in men with cystic fibrosis: an update on current surgical practices and outcomes. Chest. 2000 Oct;118(4):1059-62. PMID 11035677
Dodge JA. Male fertility in cystic fibrosis. Lancet. 1995 Sep 2;346(8975):587-8. PMID 7650999
Augarten A, Yahav Y, Kerem B, Halle D, Laufer J, Szeinberg A, Dor J, Mashiach S, Gazit E, Madgar I. Congenital bilateral absence of vas deferens in the absence of cystic fibrosis. Lancet 344: 1473-1474, 1994. PMID 7968122
Gilljam M, Antoniou M, Shin J, Dupuis A, Corey M, Tullis DE. Pregnancy in cystic fibrosis. Fetal and maternal outcome. Chest. 2000 Jul;118(1):85-91. PMID 10893364
Rosenstein BJ, Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. The Journal of Pediatrics. April 1998, 132 (4): 589–95. PMID 9580754. doi:10.1016/S0022-3476(98)70344-0.
Hamosh A, FitzSimmons SC, Macek M, Knowles MR, Rosenstein BJ, Cutting GR. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. The Journal of Pediatrics. February 1998, 132 (2): 255–9. PMID 9506637. doi:10.1016/S0022-3476(98)70441-X .
Farrell P, Joffe S, Foley L, Canny GJ, Mayne P, Rosenberg M. Diagnosis of cystic fibrosis in the Republic of Ireland: epidemiology and costs. Irish Medical Journal. September 2007, 100 (8): 557–60. PMID 17955689. （原始内容存档于2013-12-03）.
Stern, RC. The diagnosis of cystic fibrosis. N Engl J Med 1997; 336:487. PMID 9017943
Davis PB. Cystic fibrosis since 1938. American Journal of Respiratory and Critical Care Medicine. March 2006, 173 (5): 475–82. PMID 16126935. S2CID 1770759. doi:10.1164/rccm.200505-840OE.
MacKenzie T, Gifford AH, Sabadosa KA, Quinton HB, Knapp EA, Goss CH, Marshall BC. Longevity of patients with cystic fibrosis in 2000 to 2010 and beyond: survival analysis of the Cystic Fibrosis Foundation patient registry. Annals of Internal Medicine. August 2014, 161 (4): 233–41. PMC 4687404 . PMID 25133359. doi:10.7326/m13-0636.
Habib, Al-Rahim R.; Kajbafzadeh, Majid; Desai, Sameer; Yang, Connie L.; Skolnik, Kate; Quon, Bradley S. A Systematic Review of the Clinical Efficacy and Safety of CFTR Modulators in Cystic Fibrosis. Scientific Reports. 2019-05-10, 9 (1): 7234. Bibcode:2019NatSR...9.7234H. ISSN 2045-2322. PMC 6510767 . PMID 31076617. doi:10.1038/s41598-019-43652-2.
Lopes-Pacheco, Miquéias. CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine. Frontiers in Pharmacology. 2020, 10: 1662. ISSN 1663-9812. PMC 7046560 . PMID 32153386. doi:10.3389/fphar.2019.01662 .
Yu H, Nasr SZ, Deretic V. Innate lung defenses and compromised Pseudomonas aeruginosa clearance in the malnourished mouse model of respiratory infections in cystic fibrosis. Infection and Immunity. April 2000, 68 (4): 2142–7. PMC 97396 . PMID 10722612. doi:10.1128/IAI.68.4.2142-2147.2000.
Ratjen F, Döring G. Cystic fibrosis. Lancet. February 2003, 361 (9358): 681–9. PMID 12606185. S2CID 24879334. doi:10.1016/S0140-6736(03)12567-6.
Rosenstein BJ, Zeitlin PL. Cystic fibrosis. Lancet. January 1998, 351 (9098): 277–82. PMID 9457113. S2CID 44627706. doi:10.1016/S0140-6736(97)09174-5 .
Moorcroft AJ, Dodd ME, Webb AK. Exercise limitations and training for patients with cystic fibrosis. Disability and Rehabilitation. 1998, 20 (6–7): 247–53. PMID 9637933. doi:10.3109/09638289809166735.

semanticscholar.org

api.semanticscholar.org

Davis PB. Cystic fibrosis since 1938. American Journal of Respiratory and Critical Care Medicine. March 2006, 173 (5): 475–82. PMID 16126935. S2CID 1770759. doi:10.1164/rccm.200505-840OE.
Ratjen F, Döring G. Cystic fibrosis. Lancet. February 2003, 361 (9358): 681–9. PMID 12606185. S2CID 24879334. doi:10.1016/S0140-6736(03)12567-6.
Rosenstein BJ, Zeitlin PL. Cystic fibrosis. Lancet. January 1998, 351 (9098): 277–82. PMID 9457113. S2CID 44627706. doi:10.1016/S0140-6736(97)09174-5 .

web.archive.org

Hodson, Margaret; Geddes, Duncan; Bush, Andrew (编). Cystic fibrosis 3rd. London: Hodder Arnold. 2012: 3 [2016-04-02]. ISBN 978-1-4441-1369-3. （原始内容存档于2016-03-05）.
Buckingham, Lela. Molecular diagnostics fundamentals, methods, and clinical applications 2nd. Philadelphia: F.A. Davis Co. 2012: 351 [2016-04-02]. ISBN 978-0-8036-2975-2. （原始内容存档于2016-03-04）.
Tobias E. Essential Medical Genetics. John Wiley & Sons. 2011: 312. ISBN 978-1-118-29370-6. （原始内容存档于2016-04-17）.
The Canadian Facts & Figures on Cystic Fibrosis. cysticfibrosis.ca. （原始内容存档于2013-06-16）.
Genetic Carrier Testing. Cystic Fibrosis Foundation. 2007. （原始内容存档于2010-03-23）.
Farrell P, Joffe S, Foley L, Canny GJ, Mayne P, Rosenberg M. Diagnosis of cystic fibrosis in the Republic of Ireland: epidemiology and costs. Irish Medical Journal. September 2007, 100 (8): 557–60. PMID 17955689. （原始内容存档于2013-12-03）.
Canadian Cystic Fibrosis Patient Data Registry Report (PDF). Canadian Cystic Fibrosis Foundation. 2007 [2010-03-14]. （原始内容 (PDF)存档于2010-07-15）.
Annual Data Report 2016 Cystic Fibrosis Foundation Patient Registry (PDF): 4. [19 June 2018]. （原始内容 (PDF)存档于19 June 2018）.
Medications. Cystic Fibrosis Canada. 2011. No. 10684-5100 RR0001. （原始内容存档于2011-09-04）.
Cystic Fibrosis Foundation. CFTR Modulator Therapies. [2023-12-23]. （原始内容存档于2024-07-03）.

worldcat.org

Habib, Al-Rahim R.; Kajbafzadeh, Majid; Desai, Sameer; Yang, Connie L.; Skolnik, Kate; Quon, Bradley S. A Systematic Review of the Clinical Efficacy and Safety of CFTR Modulators in Cystic Fibrosis. Scientific Reports. 2019-05-10, 9 (1): 7234. Bibcode:2019NatSR...9.7234H. ISSN 2045-2322. PMC 6510767 . PMID 31076617. doi:10.1038/s41598-019-43652-2.
Lopes-Pacheco, Miquéias. CFTR Modulators: The Changing Face of Cystic Fibrosis in the Era of Precision Medicine. Frontiers in Pharmacology. 2020, 10: 1662. ISSN 1663-9812. PMC 7046560 . PMID 32153386. doi:10.3389/fphar.2019.01662 .