These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

172 related articles for article (PubMed ID: 29040601)

  • 21. The European cystic fibrosis patient registry: the power of sharing data.
    Sheppard DN
    J Cyst Fibros; 2010 Dec; 9 Suppl 2():S1-2. PubMed ID: 20980207
    [No Abstract]   [Full Text] [Related]  

  • 22. Fibrosing colonopathy in cystic fibrosis: results of a case-control study.
    Smyth RL; Ashby D; O'Hea U; Burrows E; Lewis P; van Velzen D; Dodge JA
    Lancet; 1995 Nov; 346(8985):1247-51. PubMed ID: 7475715
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Highlights from the 30th North American Cystic Fibrosis Conference, Orlando 2016.
    Shawcross A; Barry PJ
    Paediatr Respir Rev; 2018 Mar; 26():1-3. PubMed ID: 28400241
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Agreement between the Danish Cancer Registry and the Danish Lung Cancer Registry.
    Christensen J; Kejs AMT; Schmidt LKH; Søgaard J; Rasted MC; Andersen O; Jakobsen E
    Dan Med J; 2020 Aug; 67(8):. PubMed ID: 32741437
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Cystic fibrosis related diabetes is not independently associated with increased Stenotrophomonas maltophilia infection: Longitudinal data from the UK CF Registry.
    Frost F; Nazareth D; Shaw M; Walshaw MJ
    J Cyst Fibros; 2019 Mar; 18(2):294-298. PubMed ID: 30741162
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Cystic fibrosis mortality trends in France.
    Bellis G; Cazes MH; Parant A; Gaimard M; Travers C; Le Roux E; Ravilly S; Rault G
    J Cyst Fibros; 2007 May; 6(3):179-86. PubMed ID: 16916626
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Survival patterns in cyctic fibrosis.
    Warwick WJ; Pogue RE; Gerber HU; Nesbitt CJ
    J Chronic Dis; 1975 Dec; 28(11-12):609-22. PubMed ID: 1239460
    [No Abstract]   [Full Text] [Related]  

  • 28. Epidemiology of CF: How registries can be used to advance our understanding of the CF population.
    Jackson AD; Goss CH
    J Cyst Fibros; 2018 May; 17(3):297-305. PubMed ID: 29275954
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The UK National Barrett's Oesophagus Registry: a study between two centres.
    Caygill CP; Reed PI; McIntyre A; Hill MJ
    Eur J Cancer Prev; 1998 Apr; 7(2):161-4. PubMed ID: 9818779
    [No Abstract]   [Full Text] [Related]  

  • 30. Comparative demographics of the European cystic fibrosis population: a cross-sectional database analysis.
    McCormick J; Mehta G; Olesen HV; Viviani L; Macek M; Mehta A;
    Lancet; 2010 Mar; 375(9719):1007-13. PubMed ID: 20304245
    [TBL] [Abstract][Full Text] [Related]  

  • 31. The European Cystic Fibrosis Society Patient Registry: valuable lessons learned on how to sustain a disease registry.
    Viviani L; Zolin A; Mehta A; Olesen HV
    Orphanet J Rare Dis; 2014 Jun; 9():81. PubMed ID: 24908055
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Completeness and Accuracy of Death Registry Data in Golestan, Iran.
    Hasanpour-Heidari S; Jafari-Delouei N; Shokoohifar N; Sedaghat SM; Moghaddami A; Hosseinpour R; Poorabbasi M; Gholami M; Semnani S; Naeimi-Tabiei M; Honarvar MR; Fazel A; Etemadi A; Bray F; Roshandel G
    Arch Iran Med; 2019 Jan; 22(1):1-6. PubMed ID: 30821154
    [TBL] [Abstract][Full Text] [Related]  

  • 33. The changing epidemiology of cystic fibrosis.
    FitzSimmons SC
    Curr Probl Pediatr; 1994; 24(5):171-9. PubMed ID: 8070278
    [No Abstract]   [Full Text] [Related]  

  • 34. Cystic fibrosis patient registries: A valuable source for clinical research.
    Dasenbrook EC; Sawicki GS
    J Cyst Fibros; 2018 Jul; 17(4):433-440. PubMed ID: 29555479
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [The presentation of the project for realizing a national registry for cystic fibrosis].
    Barletta L; Bossi A; Bettinelli ME; Giunta A
    Epidemiol Prev; 1991; 13(48-49):192-3. PubMed ID: 1843313
    [No Abstract]   [Full Text] [Related]  

  • 36. Does newborn screening influence the young cystic fibrosis cohort included in national registries?
    De Boeck K; Munck A; de Monestrol I; Gulmans V; Lemonnier L; Middleton PG; Wanyama S; Thomas M
    Eur Respir J; 2017 Jan; 49(1):. PubMed ID: 28077474
    [No Abstract]   [Full Text] [Related]  

  • 37. Cystic fibrosis in adults. Recommendations for care of patients in the UK. Summary of a report of The Royal College of Physicians.
    J R Coll Physicians Lond; 1991 Jan; 25(1):12-5. PubMed ID: 2023147
    [No Abstract]   [Full Text] [Related]  

  • 38. [Swiss registry for patients with cystic fibrosis: design, programming, implementation and first examples of use].
    Schöni-Affolter F; Oswald P; Wandt-Baumann C; Kriemler S; Schöni MH
    Schweiz Med Wochenschr; 2000 Sep; 130(39):1373-81. PubMed ID: 11059028
    [TBL] [Abstract][Full Text] [Related]  

  • 39. UK Cancer Registry statistics--can the partially sighted lead the blind?
    Skidmore FD
    Eur J Surg Oncol; 1996 Oct; 22(5):467-8. PubMed ID: 8903486
    [No Abstract]   [Full Text] [Related]  

  • 40. Psychosocial impact of cystic fibrosis in adolescence.
    Harrop M
    Paediatr Nurs; 2007 Dec; 19(10):41-5. PubMed ID: 18196861
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.