Mucoviscidose (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Mucoviscidose" in French language version.

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aappublications.org

pediatrics.aappublications.org

  • (en) Andersen DH. Therapy and prognosis of fibrocystic disease of the pancreas. Pediatrics 1949; 3: 406-417. Résumé, Texte complet
  • (en) Kessler, W. R. and D. H. Andersen. Heat prostration in fibrocystic disease of the pancreas and other conditions. Pediatrics 1951; 8:648-55. Résumé
  • (en) Di Sant' Agnese PA, Darling RC, Perera GA, et al. Abnormal electrolyte composition of sweat in cystic fibrosis of the pancreas: clinical implications and relationship to the disease. Pediatrics 1953; 12:549–563. PMID 13111855, Abstract
  • (en) Gibson LE, Cooke RE. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas utilising pilocarpine electrophoresis. Pediatrics 1959; 23:545-549. abstract
  • (en) Shwachman H, Kulczycki LL. « Long-term study of 105 cystic fibrosis patients » Am J Dis Child 1958; 96:6-15. Texte intégral
  • (en) Matthews LW, Doershuk CF, Spector S. « Mist tent therapy of obstructive pulmonary lesion of cystic fibrosis » Pediatrics 1967; 39:176-185. PMID 6017955, Texte intégral
  • (en) Bau SK, Aspin N, Wood DE, Levison H. « The measurement of fluid deposition in humans following mist tent therapy » Pediatrics 1971; 48:605-612. PMID 5114748, Texte intégral

ac.edu

accessmylibrary.com

  • Quinton P. M., « Physiological basis of cystic fibrosis: a historical perspective », Physiological reviews, vol. 79, no 1,‎ , p. 3-22 (ISSN 0031-9333, résumé, lire en ligne)

ajcn.org

  • (en) Sawka MN, Montain SJ. Fluid and electrolyte supplementation for exercise heat stress. Am J Clin Nutr. 2000 Aug;72(2 Suppl):564S-72S. PMID 10919961 ajcn.org

ameli.fr

ap-hop-paris.fr

bioch.ap-hop-paris.fr

archive.is

atlasgeneticsoncology.org

atsjournals.org

ajrccm.atsjournals.org

  • Mowska, Patryk, Daniel Lorentzen, Katherine Excoffon, Joseph Zabner, Paul B. McCray, William M. Nauseef, Corinne Dupuy, and Botond Bánfi. A novel host defense system of airways is defective in cystic fibrosis. American Journal of Respiratory and Critical Care Medicine, 1 Nov. 2006. Web. 26 Nov. 2009. http://ajrccm.atsjournals.org/cgi/reprint/175/2/174.pdf
  • Mowska, Patryk, Daniel Lorentzen, Katherine Excoffon, Joseph Zabner, Paul B. McCray, William M. Nauseef, Corinne Dupuy, and Botond Bánfi. A novel host defense system of airways is defective in cystic fibrosis. American Journal of Respiratory and Critical Care Medicine, 1 Nov. 2006. Web. 26 Nov. 2009. http://ajrccm.atsjournals.org/cgi/reprint/175/2/174.pdf.
  • (en) Stewart B, Zabner J, Shuber AP, Welsh MJ, McCray PB. « Normal sweat chloride values do not exclude the diagnosis of cystic fibrosis » Am J Respir Crit Care Med. 1995; 151: 899-903. Résumé
  • (en) Hoffmann T, Böhmer O, Hüls G, Terbrack HG, Bittner P, Klingmüller V, Heerd E, Lindemann H : Conventionnal and modified nasal potential-difference. Measurement in cystic fibrosis. Am J Respir Crit Care Med 1997 ; 155 : 1908-13. PMID 9196094, Abstract Am.J.Respir.Crit.Care Med.
  • (en) Kelvin H.-V. Tan, Michael Mulheran, Alan J. Knox and Alan R. Smyth, « Aminoglycoside Prescribing and Surveillance in Cystic Fibrosis », American Journal of Respiratory and Critical Care Medicine, vol. 167, no 6,‎ , p. 819-823 (PMID 12623858, lire en ligne)

ajrcmb.atsjournals.org

bioalaxia.eu

biomedcentral.com

bmcgenomics.biomedcentral.com

blackwell-synergy.com

  • (en) Conway SP, Miller MG, Ramsden C, Littlewood JM. Intensive treatment of pseudomonas chest infection in cystic fibrosis: a comparison of tobramycin and ticarcillin and netilmicin and ticarcillin. Acta Paediatr Scand 1985; 74:107-113. Acta Paediatrica

bmj.com

thorax.bmj.com

books.google.com

  • « The child will soon die whose brows tastes salty when kissed. » Ernst Ludwig Rochholz, Almanac of Children’s Songs and Games from Switzerland. Publié en 1857 par J. J. Weber. Titre original : Alemannisches Kinderlied und Kinderspiel aus der SchweizGesammelt (Leipzig 1857). Consulter le livre.

ccne-ethique.fr

cff.org

cftrust.org.uk

chestjournal.org

  • (en) Desmarquest P, Feldmann D, Tamalat A et al. « Genetype analysis and phenotypic manifestations of children with intermediate sweat chloride test results » Chest 2000; 118: 1591- 1597. PMID 11115444, Résumé, Texte complet
  • (en) Andrew Fogarty, Richard Hubbard, John Britton. International Comparison of Median Age at Death From Cystic Fibrosis. Chest. 2000;117:1656-1660. « The international median age at death increased from 8 years in 1974 to 21 years in 1994 ».
  • (en) James R. Yankaskas MD, George B. Mallory Jr. MD and Consensus Committee, « Lung Transplantation in Cystic Fibrosis : Consensus Conference Statement », Chest, no 113,‎ , p. 217-226 (résumé, lire en ligne)
  • (en) Gilljam M, Antoniou M, Shin J, Dupuis A, Corey M, Tullis DE., « Pregnancy in Cystic Fibrosis : Fetal and Maternal Outcome », Chest, vol. 118, no 1,‎ , p. 85-91 (résumé, lire en ligne)
  • (en) Goss, CH, Rubenfeld, GD, Otto, K, et al, « The Effect of Pregnancy on Survival in Women With Cystic Fibrosis », Chest, vol. 124,‎ , p. 1460-1468 (résumé, lire en ligne)

cmaj.ca

  • (en) Kent, NE, Farquaharson, DF, « Cystic fibrosis in pregnancy », Canadian Medical Association Journal, vol. 149, no 6,‎ , p. 809-813 (résumé)

cochrane.org

cricinfo.com

content-aus.cricinfo.com

ctsnetjournals.org

ats.ctsnetjournals.org

  • (en) Pasque MK, Cooper JD, Kaiser LR, et al. Improved technique for bilateral lung transplantation: rationale and initial clinical experience. Ann Thorac Surg 1990; 49:785-791. PMID 2339934,The Annals of Thoracic Surgery

jtcs.ctsnetjournals.org

  • (en) Starnes VA, Barr M, Cohen R et al. « Living donor lobar lung transplantation experience: intermediate results » J Thorac Cardiovasc Surg. 1996; 112:1284-1291. PMID 8911325,J Thorac Cardiovasc Surg

cysticfibrosis.ca

cysticfibrosisjournal.com

  • (en) Stephanie Trend, Angela M. Fonceca, William G. Ditcham et Anthony Kicic, « The potential of phage therapy in cystic fibrosis: Essential human-bacterial-phage interactions and delivery considerations for use in Pseudomonas aeruginosa -infected airways », Journal of Cystic Fibrosis, vol. 16, no 6,‎ , p. 663–670 (ISSN 1569-1993, DOI 10.1016/j.jcf.2017.06.012, lire en ligne, consulté le )
  • (en) S. Aslam, R. T. Schooley, P. C. Grint et I. P. Bilinsky, « P084 Bacteriophage treatment of multidrug-resistant Pseudomonas aeruginosa pneumonia in a cystic fibrosis patient », Journal of Cystic Fibrosis, vol. 17,‎ , S83 (ISSN 1569-1993 et 1873-5010, DOI 10.1016/S1569-1993(18)30381-3, lire en ligne, consulté le )

cysticfibrosismedicine.com

doi.org

dx.doi.org

dovepress.com

  • (en) Jean-Marc Rolain, Sami Hraiech et Fabienne Bregeon, « Bacteriophage-based therapy in cystic fibrosis-associated Pseudomonas aeruginosa infections: rationale and current status », Drug Design, Development and Therapy, vol. 9,‎ , p. 3653 (ISSN 1177-8881, DOI 10.2147/DDDT.S53123, lire en ligne, consulté le )

ecfsoc.org

elsevier.com

em-consulte.com

  • (fr) Un modèle murin mimant les manifestations pulmonaires de la mucoviscidose vient d’être mis au point. Revue des Maladies Respiratoires. Vol 22, n° spécial - juin 2005. p. 11-19. Doi : RMR-06-2005-22-6-0761-8425-101019-200505321. Texte intégral

emedicine.com

  • (en) Girish D Sharma, « Cystic Fibrosis », sur emedicine.com, (consulté le ).

ersjournals.com

erj.ersjournals.com

  • (en) Rodgers HC, Knox AJ. Pharmacological treatment of the biochemical defect in cystic fibrosis airways. Eur Resp J 2001; 17:1314-1321. PMID 11491179, Texte complet

fibrosekystique.ca

  • (fr) Fondation canadienne de la fibrose kystique, Rapport du Registre canadien de données sur les patients, Toronto, Ontario, (lire en ligne)

findarticles.com

  • (en) Catherine M. Wallace, « Naked Before God: The Return of a Broken Disciple », Anglican Theological Review,‎ (lire en ligne, consulté le )

google.fr

books.google.fr

googleusercontent.com

webcache.googleusercontent.com

has-sante.fr

inist.fr

cat.inist.fr

  • (fr) Labbé A, Bellon G, Héraud MC, Arbre P, Goddon G, Alton E : Détermination des différences de potentiel transépithélial (DDPTE) nasal dans la mucoviscidose. Arch Fr Pediatr 1991 ; 48 : 617-20. INIST.
  • (fr) Grosskofpf C, Farriaux JP, Vidailhet M, Briard ML, Navarro J, Turck D, Travert G, Belot V, Bloch J, Roussel P. «Le programme national de dépistage néonatal de la mucoviscidose: mise en place et organisation». Archives de Pédiatrie 2003; 10(Suppl 2): S364-369. Inist
  • (fr) Christiane Knoop (Hôpital Erasme - Institut de Mucoviscidose de l'ULB), « Transplantation pulmonaire pour mucoviscidose », Kinéréa, Société de kinésithérapie de réanimation, Paris, France, no 37,‎ , p. 58-63 (ISSN 0999-9183, résumé, lire en ligne)
  • (fr) Albert-Gérard Logeais. Mucoviscidose : quelle est la place des associations de malades dans la nouvelle organisation des soins ? La Revue du Praticien 2003,53:121-122. INIST.

inserm.fr

ipbs.fr

isiknowledge.com

cel.isiknowledge.com

  • « Wehe dem Kind, das beim Kuß auf die Stirn salzig schmekt, es ist verhext und muss bald sterben », en anglais « Woe to the child kissed on the brow who tastes salty, for he is cursed and soon must die. » Welsh MJ and Smith AE. Cystic fibrosis. Sci Am 273: 52–59, dec 1995. PMID 8525348, ISI.

issn.org

portal.issn.org

  • Quinton P. M., « Physiological basis of cystic fibrosis: a historical perspective », Physiological reviews, vol. 79, no 1,‎ , p. 3-22 (ISSN 0031-9333, résumé, lire en ligne)
  • (fr) Christiane Knoop (Hôpital Erasme - Institut de Mucoviscidose de l'ULB), « Transplantation pulmonaire pour mucoviscidose », Kinéréa, Société de kinésithérapie de réanimation, Paris, France, no 37,‎ , p. 58-63 (ISSN 0999-9183, résumé, lire en ligne)
  • Martina Rossitto, Ersilia V. Fiscarelli et Paola Rosati, « Challenges and Promises for Planning Future Clinical Research Into Bacteriophage Therapy Against Pseudomonas aeruginosa in Cystic Fibrosis. An Argumentative Review », Frontiers in Microbiology, vol. 9,‎ (ISSN 1664-302X, PMID 29780361, PMCID PMC5945972, DOI 10.3389/fmicb.2018.00775, lire en ligne, consulté le )
  • (en) Jean-Marc Rolain, Sami Hraiech et Fabienne Bregeon, « Bacteriophage-based therapy in cystic fibrosis-associated Pseudomonas aeruginosa infections: rationale and current status », Drug Design, Development and Therapy, vol. 9,‎ , p. 3653 (ISSN 1177-8881, DOI 10.2147/DDDT.S53123, lire en ligne, consulté le )
  • (en) Stephanie Trend, Angela M. Fonceca, William G. Ditcham et Anthony Kicic, « The potential of phage therapy in cystic fibrosis: Essential human-bacterial-phage interactions and delivery considerations for use in Pseudomonas aeruginosa -infected airways », Journal of Cystic Fibrosis, vol. 16, no 6,‎ , p. 663–670 (ISSN 1569-1993, DOI 10.1016/j.jcf.2017.06.012, lire en ligne, consulté le )
  • (en) Elaine M. Waters, Daniel R. Neill, Basak Kaman et Jaspreet S. Sahota, « Phage therapy is highly effective against chronic lung infections with Pseudomonas aeruginosa », Thorax, vol. 72, no 7,‎ , p. 666–667 (ISSN 0040-6376 et 1468-3296, PMID 28265031, DOI 10.1136/thoraxjnl-2016-209265, lire en ligne, consulté le )
  • (en) S. Aslam, R. T. Schooley, P. C. Grint et I. P. Bilinsky, « P084 Bacteriophage treatment of multidrug-resistant Pseudomonas aeruginosa pneumonia in a cystic fibrosis patient », Journal of Cystic Fibrosis, vol. 17,‎ , S83 (ISSN 1569-1993 et 1873-5010, DOI 10.1016/S1569-1993(18)30381-3, lire en ligne, consulté le )
  • Diana D. Semler, Karlene H. Lynch et Jonathan J. Dennis, « The Promise of Bacteriophage Therapy for Burkholderia cepacia Complex Respiratory Infections », Frontiers in Cellular and Infection Microbiology, vol. 1,‎ (ISSN 2235-2988, PMID 22919592, PMCID PMC3417384, DOI 10.3389/fcimb.2011.00027, lire en ligne, consulté le )
  • (en) Karlene H Lynch, Paul Stothard et Jonathan J Dennis, « Genomic analysis and relatedness of P2-like phages of the Burkholderia cepacia complex », BMC Genomics, vol. 11, no 1,‎ , p. 599 (ISSN 1471-2164, PMID 20973964, PMCID PMC3091744, DOI 10.1186/1471-2164-11-599, lire en ligne, consulté le )
  • (en) Helen Spencer, Graham F. Hatfull, Robert T. Schooley et Deborah Jacobs-Sera, « Engineered bacteriophages for treatment of a patient with a disseminated drug-resistant Mycobacterium abscessus », Nature Medicine, vol. 25, no 5,‎ , p. 730–733 (ISSN 1546-170X, DOI 10.1038/s41591-019-0437-z, lire en ligne, consulté le )

jimmunol.org

jle.com

  • Emmanuelle Girodon-Boulandet, Catherine Costa, « Génétique de la mucoviscidose », Médecine thérapeutique / Pédiatrie, vol. 8, no 3,‎ , p. 126-34 (lire en ligne)
  • Données épidémiologiques d’après Monaghan et Feldman, Prenat Diagn 1999; 19:604-9. Cité par Girodon-Boulandet dans Génétique de la mucoviscidose, Médecine thérapeutique / Pédiatrie 2005;8(3):126-34.
  • (fr) Jean-Jacques Robert, « Diabète de la mucoviscidose », Médecine thérapeutique / Pédiatrie, vol. 8, no 3,‎ , p. 217-24 (lire en ligne)
  • M. Marchand, C. Jarreau, M. Chauffert, I. Garcia, D. Asselin, J.-P. Thouvenot, A.-F. Genest., « The sweat test », Annales de biologie clinique, vol. 56, no 2,‎ , p. 215-21 (lire en ligne)

just-gregory.net

legifrance.gouv.fr

lesjta.com

liberation.fr

liebertonline.com

  • (en) F. Charles Hiller. Cystic Fibrosis Masquerading as Asthma and Bronchitis in Young Adults. Pediatric Asthma, Allergy & Immunology. December 1, 2003, 16(4): 319-324. doi:10.1089/088318703322751363. En ligne

lungusa.org

masson.fr

  • (fr) R. Matran, T. Perez, V. Neve, S. Robin, R. Neviere. Actualités sur les explorations diagnostiques de la mucoviscidose. Revue des maladies respiratoires. ISSN 0761-8425. Congrès La mucoviscidose de l'enfant à l'adulte. Congrès No4, Lille, FRANCE (27/03/2003) 2003, vol. 20, no2, CAHIER1, pp. S21-S25. En ligne

metapress.com

versita.metapress.com

muco-cftr.fr

multijoueur.ca

nature.com

nejm.org

content.nejm.org

  • (en) Knowles MR, Gatzy JT, Boucher RC. Increased bioelectric potential difference across respiratory epithelia in cystic fibrosis. N Eng J Med 1981; 305:1489-95. Résumé
  • (en) Highsmith WE, Burch LH, Zhou Z et al., « A novel mutation in the CF gene in patients with pulmonary diseases but normal sweat chloride concentration », N Engl J Med, vol. 331, no 15,‎ , p. 974-80. (résumé)
  • (en) Strong TV, Smit LS, Turpin SV, Cole JL, Tom Hon C, Markiewicz D, Petty TL, Craig MW, Rosenow EC, Tsui L-C, Lannuzzi MC, Knowles MR and Collins FS. Cystic fibrosis gene mutation in two sisters with mild disease and normal sweat electrolyte levels. N Engl J Med, 1991; 325; 1630-34. Lien
  • (en) Nixon PA, Orenstein DM, Kelsey SF, Doershuk CF. The prognostic value of exercise testing in patients with cystic fibrosis. N Engl J Med 1992 ; 327 : 1785-8. Résumé

nejm.org

nih.gov

ncbi.nlm.nih.gov

  • (en) Scotet V, Duguépéroux I, Saliou P, Rault G, Roussey M, Audrézet MP, Férec C. « Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, France » Orphanet J Rare Dis. 2012;7:14. PMID 22380742 DOI 10.1186/1750-1172-7-14
  • (en) Childers M, Eckel G, Himmel A, Caldwell J. « A new model of cystic fibrosis pathology: lack of transport of glutathion and its thiocyanate conjugates » Med Hypotheses. 2007;68(1):101-12. PMID 16934416
  • « Wehe dem Kind, das beim Kuß auf die Stirn salzig schmekt, es ist verhext und muss bald sterben », en anglais « Woe to the child kissed on the brow who tastes salty, for he is cursed and soon must die. » Welsh MJ and Smith AE. Cystic fibrosis. Sci Am 273: 52–59, dec 1995. PMID 8525348, ISI.
  • (en) Busch R. On the history of cystic fibrosis. Acta Univ. Carol. 36: 13-15, 1990. PMID 2130674
  • (en) Busch R. On the history of cystic fibrosis. Acta Univ Carol [Med] (Praha). 1990;36(1-4):13-5. PMID 2130674
  • (en) Andersen, Dorothy H. The Present Diagnosis and Therapy of Cystic Fibrosis of the Pancreas. Proc R Soc Med. 1949 Jan;42(1):25–32. PMID 18123627
  • (en) Darling RC, diSant'Agnese PA, Perera GA, Andersen DH. Electrolyte abnormalities of the sweat in fibrocystic disease of the pancreas. A J Med Sci 1953; 225:67-70. PMID 13007698.
  • (en) Di Sant' Agnese PA, Darling RC, Perera GA, et al. Abnormal electrolyte composition of sweat in cystic fibrosis of the pancreas: clinical implications and relationship to the disease. Pediatrics 1953; 12:549–563. PMID 13111855, Abstract
  • (en) Shwachman H, Mahmoodian A. Pilocarpine iontophoresis sweat testing : Results of seven years'experience. Fourth International Conference on Cystic Fibrosis of the Pancreas (Mucoviscidosis). Berne/Grindewald 1966, part I Mod Probl Paediatr 1967 ; 10 : 158. PMID 6054626
  • (en) Legrys VA. Sweat testing for the diagnosis of cystic fibrosis : practical considerations. Pediatrics 1996 ; 129:892-7. PMID 8969732
  • (en) Quinton, P. M. Suggestion of an abnormal anion exchange mechanism in sweat glands of cystic fibrosis patients. Pediatr Res 1982; 16:533-537, PMID 7110773
  • (en) Quinton PM. Chloride impermeability in cystic fibrosis. Nature 1983; 301:421-2. PMID 6823316
  • (en) Eiberg H, Mohr J, Schmiegelow K, Nielsen LS, Williamson R. Linkage relationships of paraoxonasse (PON) with other genetic markers: indication of cystic fibrosis synteny. Clin Genet 1985; 28:265-71. PMID 2998653
  • (en) B. S. Kerem, J. M. Rommens, J. A. Buchanan, D. Markiewicz, T. K. Cox, A. Chakravarti, M. Buchwald et L. C. Tsui, Identification of the Cystic Fibrosis Gene : Genetic Analysis, dans Science, vol. 245, 1989, p. 1073-1080. Résumé. PMID 2570460.
  • (en) J. R. Riordan, J. M. Rommens, B.-S. Kerem, N. Alon, R. Rozmahel, Z. Grzelczak, J. Zelenski, S. Lok, N. Plavsic, J. L. Chou, M. L. Drumm, M. C. Iannuzzi, F. S. Collins et T. C. Tsui, « Identification of the Cystic Fibrosis Gene : Cloning and Characterization of the Complementary DNA », dans Science, vol. 245, 1989, p. 1066-1073. Erratum dans Science, vol. 245, no 4925, septembre 1989, p. 1437. Résumé. PMID 2475911.
  • (en) J. M. Rommens, M. C. Iannuzzi, B.-S. Kerem, M. L. Drumm, G. Melmer, M. Dean, R. Rozmahel, J. L. Cole, D. Keneddy, N. Hidaka, M. Zsiga, M. Buchwald, J. R. Riordan, L. C. Tsui et F. S. Collins, « Identification of the Cystic Fibrosis Gene : Chromosome Waalking and Jumping », dans Science, vol 245, 1989, p. 1059-1065. Résumé. PMID 2772657.
  • (en) Bear CE, Li CH, Kartner N, Bridges RJ, Jensen TJ, Ramjeesingh M, Riordan JR. Purification and functional reconsititution of the cystic fibrosis transmembrane conductance regulator (CFTR). Cell 1992; 68:809-18. PMID 1371239
  • (en) Gandevia B, Anderson CM. « The effect of bronchodilator aerosol on ventilatory capacity in fibrocystic disease of the pancreas » Arch Dis Child 1959; 34:511-515. PMID 13826268, Texte intégral
  • (en) Stoppelman MRH, Shwachman H. « Effect of antibiotic therapy on mucoviscidosis: bacteriologic study » New Eng J Med. 1954;251:759-763. PMID 13214325
  • (en) Shwachman H, Silverman BK, Patterson, Zheutlin LJ. « Antibiotics in treatment of pancreatic fibrosis with emphasis on terramycin » JAMA 1952; 149:1101-1108. PMID 14938116
  • (en) Bishop HC, Koop CE. « Management of meconium ileus, resection, Roux-en-Y anastomosis and ileostomy irrigation with pancreatic enzymes » Ann Surg 1957; 50:835-836. PMID 13403593, Texte intégral
  • (en) Matthews LW, Spector S. « Breakthrough in cystic fibrosis » Pediatrics 1961; 27:351. PMID 13768289
  • (en) Matthews LW, Doershuk CF, Spector S. « Mist tent therapy of obstructive pulmonary lesion of cystic fibrosis » Pediatrics 1967; 39:176-185. PMID 6017955, Texte intégral
  • (en) Bau SK, Aspin N, Wood DE, Levison H. « The measurement of fluid deposition in humans following mist tent therapy » Pediatrics 1971; 48:605-612. PMID 5114748, Texte intégral
  • (en) Chang N, Levison H, Cunningham et al. « An evaluation of nightly mist therapy for patients with cystic fibrosis » Am Rev Resp Dis 1973; 107:672-675. PMID 4697676
  • (en) Alderson PO, Secker-Walker RH, Strominger DB, Markham J, Hill RL. « Pulmonary deposition of aerosols in children with cystic fibrosis » J Pediatr. 1974; 84:479-484. PMID 4599607
  • (en) Lawson D. « Cystic fibrosis-Assessing the effects of treatment » Arch Dis Child. 1972; 47:1-4. PMID 5018653, Texte intégral
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