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Progeria (Finnish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Progeria" in Finnish language version.

refsWebsite
Global rank Finnish rank
4web.archive.org
1st place
1st place
4nih.gov
4th place
12th place
3doi.org
2nd place
10th place
2worldcat.org
5th place
9th place
1rarediseases.org
5,181st place
low place
1uta.edu
low place
low place
1news-medical.net
8,069th place
3,714th place
1fda.gov
447th place
676th place
1hayleyspage.com
low place
low place
1bbc.co.uk
8th place
14th place
1nature.com
234th place
201st place
1iltasanomat.fi
3,405th place
13th place

bbc.co.uk (Global: 8th place; Finnish: 14th place)

news.bbc.co.uk

doi.org (Global: 2nd place; Finnish: 10th place)

dx.doi.org

  • Paola Scaffidi, Tom Misteli: Lamin A-Dependent Nuclear Defects in Human Aging. Science (New York, N.Y.), 27.4.2006, 312. vsk, nro 5776. doi:10.1126/ Artikkelin verkkoversio. (englanniksi)
  • Debora R. Bertola, Henian Cao, Lilian M. J. Albano, Daniela P. Oliveira, Fernando Kok, Maria Joaquina Marques-Dias, Chong A. Kim, Robert A. Hegele: Cockayne syndrome type A: novel mutations in eight typical patients. Journal of Human Genetics, 2006-08, 51. vsk, nro 8, s. 701–705. doi:10.1007/s10038-006-0011-7 ISSN 1435-232X Artikkelin verkkoversio. (englanniksi)
  • Leslie B. Gordon, Heather Shappell, Joe Massaro, Ralph B. D’Agostino, Joan Brazier, Susan E. Campbell, Monica E. Kleinman, Mark W. Kieran: Association of Lonafarnib Treatment vs No Treatment With Mortality Rate in Patients With Hutchinson-Gilford Progeria Syndrome. JAMA, 24.4.2018, 319. vsk, nro 16, s. 1687. doi:10.1001/jama.2018.3264 ISSN 0098-7484 Artikkelin verkkoversio. (englanniksi)

fda.gov (Global: 447th place; Finnish: 676th place)

hayleyspage.com (Global: low place; Finnish: low place)

iltasanomat.fi (Global: 3,405th place; Finnish: 13th place)

nature.com (Global: 234th place; Finnish: 201st place)

  • Debora R. Bertola, Henian Cao, Lilian M. J. Albano, Daniela P. Oliveira, Fernando Kok, Maria Joaquina Marques-Dias, Chong A. Kim, Robert A. Hegele: Cockayne syndrome type A: novel mutations in eight typical patients. Journal of Human Genetics, 2006-08, 51. vsk, nro 8, s. 701–705. doi:10.1007/s10038-006-0011-7 ISSN 1435-232X Artikkelin verkkoversio. (englanniksi)

news-medical.net (Global: 8,069th place; Finnish: 3,714th place)

nih.gov (Global: 4th place; Finnish: 12th place)

pmc.ncbi.nlm.nih.gov

rarediseases.org (Global: 5,181st place; Finnish: low place)

uta.edu (Global: low place; Finnish: low place)

web.archive.org (Global: 1st place; Finnish: 1st place)

worldcat.org (Global: 5th place; Finnish: 9th place)

  • Debora R. Bertola, Henian Cao, Lilian M. J. Albano, Daniela P. Oliveira, Fernando Kok, Maria Joaquina Marques-Dias, Chong A. Kim, Robert A. Hegele: Cockayne syndrome type A: novel mutations in eight typical patients. Journal of Human Genetics, 2006-08, 51. vsk, nro 8, s. 701–705. doi:10.1007/s10038-006-0011-7 ISSN 1435-232X Artikkelin verkkoversio. (englanniksi)
  • Leslie B. Gordon, Heather Shappell, Joe Massaro, Ralph B. D’Agostino, Joan Brazier, Susan E. Campbell, Monica E. Kleinman, Mark W. Kieran: Association of Lonafarnib Treatment vs No Treatment With Mortality Rate in Patients With Hutchinson-Gilford Progeria Syndrome. JAMA, 24.4.2018, 319. vsk, nro 16, s. 1687. doi:10.1001/jama.2018.3264 ISSN 0098-7484 Artikkelin verkkoversio. (englanniksi)