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تليف كيسي (Arabic Wikipedia)

Analysis of information sources in references of the Wikipedia article "تليف كيسي" in Arabic language version.

refsWebsite
Global rank Arabic rank
48nih.gov
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25web.archive.org
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1st place
5cff.org
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3sickkids.on.ca
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2alghad.com
6,954th place
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2vrtx.com
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2chestnet.org
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8,295th place
1kaahe.org
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2,207th place
1worldcat.org
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1webteb.com
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1al-health.net
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1altibbi.com
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1wikipedia.org
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1almrsal.com
7,632nd place
198th place
1aemps.gob.es
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1europa.eu
68th place
91st place
1redaccionmedica.com
low place
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1shareholder.com
6,233rd place
9,271st place
1smu.org.uy
low place
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aemps.gob.es

al-health.net

alghad.com

almrsal.com

altibbi.com

cff.org

chestnet.org

journal.publications.chestnet.org

journal.chestnet.org

europa.eu

ema.europa.eu

kaahe.org

nih.gov

ncbi.nlm.nih.gov

  • Yankaskas JR, Marshall BC, Sufian B, Simon RH, Rodman D. (2004). «Cystic Fibrosis adult care consensus conference report»[وصلة مكسورة]. Chest 125: 1-39. doi:10.1378/chest.125.1_suppl.1S. PMID 14734689. نسخة محفوظة 25 أبريل 2015 على موقع واي باك مشين. [وصلة مكسورة]
  • Rowe SM, Miller S, Sorscher EJ. «Cystic Fibrosis.» N Engl J Med. 2005 may 12;352(19):1992-2001. PMID 158887000.
  • Maldonado M, Martínez A, Alobid I, Mullol J. «The antrochoanal polyp.» Rhinology. 2004 dic;42(4):178-82. Rev. 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. Rev. PMID 1743211
  • Sun L, Rommens JM, Corvol H, Li W, Li X, Chiang TA, Lin F, Dorfman R, Busson PF, Parekh RV, Zelenika D, Blackman SM, Corey M, Doshi VK, Henderson L, Naughton KM, O'Neal WK, Pace RG, Stonebraker JR, Wood SD, Wright FA, Zielenski J, Clement A, Drumm ML, Boëlle PY, Cutting GR, Knowles MR, Durie PR, Strug LJ. «Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis.» Nat Genet. 2012 Apr 1. PMID 22466613.
  • Kulczycki LL, Shwachman H. "Studies in cystic fibrosis of the pancreas; occurrence of rectal prolapse." N Engl J Med. 1958 ag 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. Agosto 1994;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
  • Gibson LE, Cooke RE. "A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilising pilocarpine by iontophoresis." Pediatrics mar;23(3):545-9. PMID 13633369
  • Stern, RC. "The diagnosis of cystic fibrosis." N Engl J Med 1997; 336:487. PMID 9017943
  • Saiman L. Microbiology of early CF lung disease. Paediatr Respir Rev. 2004;5 Supl A:S367-9. PMID 14980298
  • Tummler B, Koopmann U, Grothues D, Weissbrodt H, Steinkamp G, von der Hardt H. Nosocomial acquisition of Pseudomonas aeruginosa by cystic fibrosis patients. J Clin Microbiol. 1991 jun;29(6):1265-7. PMID 1907611
  • Centers for Disease Control and Prevention (CDC). Pseudomonas cepacia at summer camps for persons with cystic fibrosis. MMWR Morb Mortal Wkly Rep. 1993 jun 18;42(23):456-9. PMID 7684813
  • Pegues DA, Carson LA, Tablan OC, FitzSimmons SC, Roman SB, Miller JM, Jarvis WR.Acquisition of Pseudomonas cepacia at summer camps for patients with cystic fibrosis. Summer Camp Study Group. J Pediatr. 1994 may;124(5 Pt 1):694-702. PMID 7513755
  • Pankhurst CL, Philpott-Howard J. The environmental risk factors associated with medical and dental equipment in the transmission of Burkholderia (Pseudomonas) cepacia in cystic fibrosis patients. J Hosp Infect. 1996 Apr;32(4):249-55. PMID 8744509
  • Jones AM, Govan JR, Doherty CJ, Dodd ME, Isalska BJ, Stanbridge TN, Webb AK. Identification of airborne dissemination of epidemic multiresistant strains of Pseudomonas aeruginosa at a CF centre during a cross infection outbreak. Thorax. 2003 jun;58(6):525-7. PMID 12775867
  • Hoiby N. Isolation and treatment of cystic fibrosis patients with lung infections caused by Pseudomonas (Burkholderia) cepacia and multiresistant Pseudomonas aeruginosa. Neth J Med. 1995 jun;46(6):280-7. PMID 7643943
  • Elias, S, Annas, GJ, Simpson, JL. Carrier screening for cystic fibrosis: Implications for obstetric and gynecologic practice. Am J Obstet Gynecol 1991; 164:1077. PMID 2014829
  • Tabor A, Philip J, Madsen M, Bang J, Obel EB, Norgaard-Pedersen B. Randomised controlled trial of genetic amniocentesis in 4606 low-risk women. Lancet. 1986 jun 7;1(8493):1287-93. PMID 2423826
  • Pai VB, Nahata MC. Efficacy and safety of aerosolized tobramycin in cystic fibrosis. Pediatr Pulmonol. 2001 oct;32(4):314-27. Rev. PMID 11568993
  • Westerman EM, Le Brun PP, Touw DJ, Frijlink HW, Heijerman HG. Effect of nebulized colistin sulphate and colistin sulphomethate on lung function in patients with cystic fibrosis: a pilot study. J Cyst Fibros. 2004 mar;3(1):23-8. PMID 15463883
  • Hansen CR, Pressler T, Koch C, Hoiby N.Long-term azithromycin treatment of cystic fibrosis patients with chronic Pseudomonas aeruginosa infection; an observational cohort study. J Cyst Fibros. 2005 mar;4(1):35-40. PMID 15752679
  • Kuver R, Lee SP. Hypertonic saline for cystic fibrosis. N Engl J Med. 2006 abr 27;354(17):1848-51; respuesta del autor 1848-51. PMID 16642591
  • Lieberman J. "Dornase aerosol effect on sputum viscosity in cases of cystic fibrosis." JAMA. 1968 jul 29;205(5):312-3. PMID 5694947
  • Moran F, Bradley J. Non-invasive ventilation for cystic fibrosis. Cochrane Database Syst Rev. 2003;(2):CD002769. Rev. PMID 12804435
  • Onady GM, Stolfi A. Insulin and oral agents for managing cystic fibrosis-related diabetes. Cochrane Database Syst Rev. 2005 jul 20;(3):CD004730. Rev. PMID 16034943
  • Conway SP, Oldroyd B, Morton A, Truscott JG, Peckham DG. Effect of oral bisphosphonates on bone mineral density and body composition in adult patients with cystic fibrosis: a pilot study. Thorax. 2004 ag;59(8):699-703. PMID 15282392
  • Hardin DS, Rice J, Ahn C, Ferkol T, Howenstine M, Spears S, Prestidge C, Seilheimer DK, Shepherd R. Growth hormone treatment enhances nutrition and growth in children with cystic fibrosis receiving enteral nutrition.J Pediatr. 2005 mar;146(3):324-8. PMID 15756212
  • Marks SC, Kissner DG. Management of sinusitis in adult cystic fibrosis. Am J Rhinol. 1997 en-feb;11(1):11-4. PMID 9065342
  • Phillipson GT, Petrucco OM, Matthews CD. Congenital bilateral absence of the vas deferens, cystic fibrosis mutation analysis and intracytoplasmic sperm injection. Hum Reprod. 2000 feb;15(2):431-5. PMID 10655317
  • Simultaneous liver and pancreas transplantation in patients with cystic fibrosis. Transplant Proc. 2005 oct;37(8):3567-9. PMID 16298663
  • Belkin RA, Henig NR, Singer LG, Chaparro C, Rubenstein RC, Xie SX, Yee JY, Kotloff RM, Lipson DA, Bunin GR. Risk factors for death of patients with cystic fibrosis awaiting lung transplantation. Am J Respir Crit Care Med. 2006 mar 15;173(6):659-66. Epub 2005 dic 30. PMID 16387803
  • Tate S, Elborn S. Progress towards gene therapy for cystic fibrosis.Expert Opin Drug Deliv. 2005 mar;2(2):269-80. Rev. PMID 16296753
  • Rosenstein BJ and Cutting GR. The diagnosis of cystic fibrosis: a consensus statement. Cystic Fibrosis Foundation Consensus Panel. J Pediatr. 1998 abr;132(4):589-95. Rev. PMID 9580754
  • Hamosh A, Fitz-Simmons SC, Macek M Jr, Knowles MR, Rosenstein BJ, Cutting GR. Comparison of the clinical manifestations of cystic fibrosis in black and white patients. J Pediatr. 1998 feb;132(2):255-9. PMID 9506637
  • Kerem B, Chiba-Falek O, Kerem E. Cystic fibrosis in Jews: frequency and mutation distribution. Genet Test. 1997;1(1):35-9. Rev. PMID 10464623
  • Wiuf C. Do delta F508 heterozygotes have a selective advantage? Genet Res. 2001 ag;78(1):41-7. PMID 11556136
  • Gabriel SE, Brigman KN, Koller BH, Boucher RC, Stutts MJ. Cystic fibrosis heterozygote resistance to cholera toxin in the cystic fibrosis mouse model. Science. 1994 oct 7;266(5182):107-9. PMID 7524148
  • Cuthbert AW, Halstead J, Ratcliff R, Colledge WH, Evans MJ. The genetic advantage hypothesis in cystic fibrosis heterozygotes: a murine study. J Physiol. 1995 enero 15;482 (Pt 2):449-54. PMID 7714835
  • Hogenauer C, Santa Ana CA, Porter JL, Millard M, Gelfand A, Rosenblatt RL, Prestidge CB, Fordtran JS. Active intestinal chloride secretion in human carriers of cystic fibrosis mutations: an evaluation of the hypothesis that heterozygotes have subnormal active intestinal chloride secretion. Am J Hum Genet. 2000 dic;67(6):1422-7. Epub 2000 oct 30. PMID 11055897
  • Pier GB, Grout M, Zaidi T, Meluleni G, Mueschenborn SS, Banting G, Ratcliff R, Evans MJ, Colledge WH. Salmonella typhi uses CFTR to enter intestinal epithelial cells. Nature. 1998 may 7;393(6680):79-82. PMID 9590693
  • Busch R. "On the history of cystic fibrosis." Acta Univ Carol [Med] (Praga). 1990;36(1-4):13-5. PMID 2130674
  • Rommens JM, Iannuzzi MC, Kerem B, Drumm ML, Melmer G, Dean M, Rozmahel R, Cole JL, Kennedy D, Hidaka N, et al. Identification of the cystic fibrosis gene: chromosome walking and jumping. Science. 1989 sep 8;245(4922):1059-65. PMID 2772657

redaccionmedica.com

shareholder.com

files.shareholder.com

sickkids.on.ca

genet.sickkids.on.ca

  • «Cystic Fibrosis Mutation Database: Statistics». Genet.sickkids.on.ca. 25 de abril de 2011. Consultado el 17 de diciembre de 2011. نسخة محفوظة 01 أغسطس 2017 على موقع واي باك مشين.
  • Short DB, Trotter KW, Reczek D, Kreda SM, Bretscher A, Boucher RC, Stutts MJ, Milgram SL. An apical PDZ protein anchors the cystic fibrosis transmembrane conductance regulator to the cytoskeleton. J Biol Chem. 1998 jul 31;273(31):19797-801. PMID 9677412 نسخة محفوظة 07 نوفمبر 2017 على موقع واي باك مشين.
  • "Cystic Fibrosis Mutation Database: Statistics". مؤرشف من الأصل في 2018-07-30. {{استشهاد ويب}}: الوسيط غير المعروف |editorial= تم تجاهله يقترح استخدام |publisher= (مساعدة)، الوسيط غير المعروف |fecha= تم تجاهله يقترح استخدام |date= (مساعدة)، والوسيط غير المعروف |fechaacceso= تم تجاهله يقترح استخدام |access-date= (مساعدة)

smu.org.uy

vrtx.com

investors.vrtx.com

web.archive.org

webteb.com

wikipedia.org

es.wikipedia.org

  • Lieberman J. "Dornase aerosol effect on sputum viscosity in cases of cystic fibrosis." JAMA. 1968 jul 29;205(5):312-3. PMID 5694947

worldcat.org