Julkunen R - Search Results

1

Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21.

Paavola P, Heliö T, Kiuru M, Halme L, Turunen U, Terwilliger J, Karvonen AL, Julkunen R, Niemelä S, Nurmi H, Färkkilä M, Kontula K. Paavola P, et al. Among authors: julkunen r. Eur J Hum Genet. 2001 May;9(5):328-34. doi: 10.1038/sj.ejhg.5200626. Eur J Hum Genet. 2001. PMID: 11378820

2

Leukocyte interferon-alpha in the treatment of chronic hepatitis C in Finland.

Ebeling F, Lappalainen M, Vuoristo M, Nuutinen H, Leino R, Karvonen AL, Lehtola J, Julkunen R, Pohjanpelto P, Tölö H, Färkkilä M. Ebeling F, et al. Among authors: julkunen r. Scand J Gastroenterol. 2000 May;35(5):540-5. doi: 10.1080/003655200750023822. Scand J Gastroenterol. 2000. PMID: 10868459

3

Factors predicting interferon treatment response in patients with chronic hepatitis c: late viral clearance does not preclude a sustained response.

Ebeling F, Lappalainen M, Vuoristo M, Nuutinen H, Leino R, Karvonen AL, Lehtola J, Julkunen R, Pohjanpelto P, Färkkilä M. Ebeling F, et al. Among authors: julkunen r. Am J Gastroenterol. 2001 Apr;96(4):1237-42. doi: 10.1111/j.1572-0241.2001.03631.x. Am J Gastroenterol. 2001. PMID: 11316176 Clinical Trial.

4

Gene dose effect of the DQB1*0201 allele contributes to severity of coeliac disease.

Karinen H, Kärkkäinen P, Pihlajamäki J, Janatuinen E, Heikkinen M, Julkunen R, Kosma VM, Naukkarinen A, Laakso M. Karinen H, et al. Among authors: julkunen r. Scand J Gastroenterol. 2006 Feb;41(2):191-9. doi: 10.1080/00365520500206277. Scand J Gastroenterol. 2006. PMID: 16484124

5

HLA genotyping is useful in the evaluation of the risk for coeliac disease in the 1st-degree relatives of patients with coeliac disease.

Karinen H, Kärkkäinen P, Pihlajamäki J, Janatuinen E, Heikkinen M, Julkunen R, Kosma VM, Naukkarinen A, Laakso M. Karinen H, et al. Among authors: julkunen r. Scand J Gastroenterol. 2006 Nov;41(11):1299-304. doi: 10.1080/00365520600684548. Scand J Gastroenterol. 2006. PMID: 17060123

6

Population-based molecular detection of hereditary nonpolyposis colorectal cancer.

Salovaara R, Loukola A, Kristo P, Kääriäinen H, Ahtola H, Eskelinen M, Härkönen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, Järvinen H, Mecklin JP, Aaltonen LA, de la Chapelle A. Salovaara R, et al. Among authors: julkunen r. J Clin Oncol. 2000 Jun;18(11):2193-200. doi: 10.1200/JCO.2000.18.11.2193. J Clin Oncol. 2000. PMID: 10829038

7

Microsatellite instability in adenomas as a marker for hereditary nonpolyposis colorectal cancer.

Loukola A, Salovaara R, Kristo P, Moisio AL, Kääriäinen H, Ahtola H, Eskelinen M, Härkönen N, Julkunen R, Kangas E, Ojala S, Tulikoura J, Valkamo E, Järvinen H, Mecklin JP, de la Chapelle A, Aaltonen LA. Loukola A, et al. Among authors: julkunen r. Am J Pathol. 1999 Dec;155(6):1849-53. doi: 10.1016/S0002-9440(10)65503-4. Am J Pathol. 1999. PMID: 10595914 Free PMC article.

8

No support for endoscopic surveillance for gastric cancer in hereditary non-polyposis colorectal cancer.

Renkonen-Sinisalo L, Sipponen P, Aarnio M, Julkunen R, Aaltonen LA, Sarna S, Järvinen HJ, Mecklin JP. Renkonen-Sinisalo L, et al. Among authors: julkunen r. Scand J Gastroenterol. 2002 May;37(5):574-7. doi: 10.1080/00365520252903134. Scand J Gastroenterol. 2002. PMID: 12059060

9

Genomewide search and association studies in a Finnish celiac disease population: Identification of a novel locus and replication of the HLA and CTLA4 loci.

Rioux JD, Karinen H, Kocher K, McMahon SG, Kärkkäinen P, Janatuinen E, Heikkinen M, Julkunen R, Pihlajamäki J, Naukkarinen A, Kosma VM, Daly MJ, Lander ES, Laakso M. Rioux JD, et al. Among authors: julkunen r. Am J Med Genet A. 2004 Nov 1;130A(4):345-50. doi: 10.1002/ajmg.a.30072. Am J Med Genet A. 2004. PMID: 15386476

10

[Celiac disease, treatment guideline].

Collin P, Julkunen R, Lehtola J, Mäki M, Rasmussen M, Reunala T, Savilahti E, Uusitupa M, Vuoristo M. Collin P, et al. Among authors: julkunen r. Duodecim. 1997;113(1):82-7. Duodecim. 1997. PMID: 11370063 Finnish. No abstract available.

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