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Terkkos Jarvela [15 articles]

Nylige artikler sendt til Terkkos bibliotek av forfatteren Jarvela. Du kan også see everyone s Jarvela.
  • Can primary hypolactasia manifest itself after the age of 20 years? A two-decade follow-up study.
    Scandinavian journal of gastroenterology (30 April 2008), pp. 1-6.
    by Leena Seppo, Tuula Tuure, Riitta Korpela, Irma Jarvela, Heli Rasinpera, Timo Sahi
    posted to no-tag by Terkko on 2008-07-30 09:31:12 as **
  • Analysis of X chromosome inactivation in autism spectrum disorders.
    Am J Med Genet B Neuropsychiatr Genet (24 March 2008)
    by Xiaohong Gong, Elena Bacchelli, Francesca Blasi, Claudio Toma, Catalina Betancur, Pauline Chaste, Richard Delorme, Christelle M M Durand, Fabien Fauchereau, Hany Goubran G Botros, Marion Leboyer, Marie-Christine C Mouren-Simeoni, Gudrun Nygren, Henrik Anckarsäter, Maria Rastam, I Carina C Gillberg, Christopher Gillberg, Daniel Moreno-De-Luca, Simona Carone, Ilona Nummela, Mari Rossi, Agatino Battaglia, Irma Jarvela, Elena Maestrini, Thomas Bourgeron,
    posted to no-tag by Terkko on 2008-03-27 09:37:56 as **
  • Submicroscopic Duplications of the Hydroxysteroid Dehydrogenase HSD17B10 and the E3 Ubiquitin Ligase HUWE1 Are Associated with Mental Retardation.
    Am J Hum Genet, Vol. 82, No. 2. (February 2008), pp. 432-443.
    by G Froyen, M Corbett, J Vandewalle, I Jarvela, O Lawrence, C Meldrum, M Bauters, K Govaerts, L Vandeleur, H Van Esch, J Chelly, D Sanlaville, H van Bokhoven, HH Ropers, F Laumonnier, E Ranieri, CE Schwartz, F Abidi, PS Tarpey, PA Futreal, A Whibley, FL Raymond, MR Stratton, JP Fryns, R Scott, M Peippo, M Sipponen, M Partington, D Mowat, M Field, A Hackett, P Marynen, G Turner, J Gécz
    posted to no-tag by Terkko on 2008-02-08 08:14:37 as **
  • The effect of complement factor H Y402H polymorphism on the outcome of photodynamic therapy in age-related macular degeneration.
    Eur J Ophthalmol, Vol. 17, No. 6. (c 2007), pp. 943-949.
    by SP Seitsonen, IE Jarvela, S Meri, PV Tommila, PH Ranta, IJ Immonen
    posted to no-tag by Terkko on 2007-12-03 08:27:32 as **
  • The T/G 13915 variant upstream of the lactase gene (LCT) is the founder allele of lactase persistence in an urban Saudi population
    J Med Genet, Vol. 44, No. 10. (1 October 2007), e89.
    by F Imtiaz, E Savilahti, A Sarnesto, D Trabzuni, K Al-Kahtani, Kagevi, MS Rashed, BF Meyer, Jarvela
    posted to no-tag by Terkko on 2007-10-11 13:08:50 as ** along with 1 person ryanraaum
  • Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans.
    Am J Hum Genet, Vol. 81, No. 3. (September 2007), pp. 615-625.
    by NS Enattah, A Trudeau, V Pimenoff, L Maiuri, S Auricchio, L Greco, M Rossi, M Lentze, JK Seo, S Rahgozar, I Khalil, M Alifrangis, S Natah, L Groop, N Shaat, A Kozlov, G Verschubskaya, D Comas, K Bulayeva, SQ Mehdi, JD Terwilliger, T Sahi, E Savilahti, M Perola, A Sajantila, I Jarvela, L Peltonen
    posted to no-tag by Terkko on 2007-08-20 09:45:43 as **
  • Correlation of intestinal disaccharidase activities with the C/T(-13910) variant and age.
    World J Gastroenterol, Vol. 13, No. 25. (7 July 2007), pp. 3508-3512.
    by NS Enattah, M Kuokkanen, C Forsblom, S Natah, A Oksanen, I Jarvela, L Peltonen, E Savilahti
    posted to no-tag by Terkko on 2007-08-01 08:18:08 as **
  • Exfoliation syndrome: prevalence and inheritance in a subisolate of the Finnish population
    Acta Ophthalmologica Scandinavica, Vol. 85, No. 5. (August 2007), pp. 500-507.
    by Forsman, Eva, Cantor, M Rita, Lu, Ake, Eriksson, Aldur, Fellman, Johan, Jarvela, Irma, Forsius, Henrik
    posted to no-tag by Terkko on 2007-07-30 10:43:58 as **
  • Investigation of founder effects for the Thr377Met Myocilin mutation in glaucoma families from differing ethnic backgrounds.
    Mol Vis, Vol. 13 (2007), pp. 487-492.
    by AW Hewitt, JR Samples, RR Allingham, I Jarvela, G Kitsos, SR Krishnadas, JE Richards, PR Lichter, MB Petersen, P Sundaresan, JL Wiggs, DA Mackey, MK Wirtz
    posted to no-tag by Terkko on 2007-04-11 10:02:16 as **
  • Juvenile-onset neuronal ceroid lipofuscinosis with infantile CLN1 mutation and palmitoyl-protein thioesterase deficiency
    European Journal of Neurology, Vol. 14, No. 4. (April 2007), pp. 369-372.
    by Kalviainen, , Eriksson, , Losekoot, , Sorri, , Harvima, , Santavuori, , Jarvela, , Autti, , Vanninen, , Salmenpera, , Van Diggelen,
    posted to no-tag by Terkko on 2007-04-02 10:28:52 as **
  • Analysis of variants in the complement factor H, the elongation of very long chain fatty acids-like 4 and the hemicentin 1 genes of age-related macular degeneration in the Finnish population.
    Mol Vis, Vol. 12 (2006), pp. 796-801.
    by S Seitsonen, S Lemmela, J Holopainen, P Tommila, P Ranta, A Kotamies, J Moilanen, T Palosaari, K Kaarniranta, S Meri, I Immonen, I Jarvela
    posted to no-tag by Terkko on 2006-08-08 09:19:03 as **
  • Sequence analysis of the genes encoding for H + /K + ATPase in autoimmune gastritis
    Annals of Medicine, Vol. 38, No. 4. (June 2006), pp. 287-293.
    by Oksanen, Aino, Lemmela, Susanna, Jarvela, Irma, Rautelin, Hilpi
    posted to no-tag by Terkko on 2006-07-28 11:36:37 as **
  • Molecularly defined adult-type hypolactasia in school-aged children with a previous history of cow's milk allergy.
    World J Gastroenterol, Vol. 12, No. 14. (14 April 2006), pp. 2264-2268.
    by H Rasinpera, K Saarinen, A Pelkonen, I Jarvela, E Savilahti, KL Kolho
    posted to no-tag by Terkko on 2006-05-17 09:32:29 as **
  • Molecular diagnosis of adulttype hypolactasia (lactase nonpersistence)
    Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 65, No. 7. (2005), pp. 535-540.
    by IE Jarvela
    posted to no-tag by Terkko on 2005-11-09 10:59:25 as **
  • Molecular genetics of adult-type hypolactasia
    Annals of Medicine, Vol. 37, No. 3. (May 2005), pp. 179-185.
    by Irma Jarvela
    posted to no-tag by Terkko on 2005-07-20 09:02:17 as **
    • NB: Du kan sitere denne siden som: http://www.citeulike.org/user/Terkko/author/Jarvela

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