Výsledky vyhledávání

Incidence trends of vestibular schwannomas in Denmark, Finland, Norway and Sweden in 1987–2007

Autor: R Sankila, Lars Klaeboe, C. Johansen, Joachim Schüz, Maria Feychting, Anssi Auvinen, Suvi Larjavaara

Publikováno v: British Journal of Cancer

Background: The reported incidence rates of vestibular schwannomas (VS) vary substantially, but it is unclear as to what extent the variation reflects differences in risk or recording practices. Our aim was to describe the incidence rates of VS in De

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::950fd11bd43b17c80454303d754e922f
http://europepmc.org/articles/PMC3185956

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Does anyone survive pancreatic ductal adenocarcinoma? A nationwide study re-evaluating the data of the Finnish Cancer Registry

Autor: Stig Nordling, G Klöppel, Caj Haglund, Eero Pukkala, J Lüttges, Monika Carpelan-Holmström, R Sankila

Publikováno v: Gut. 54:385-387

Background: Worldwide survival data for ductal adenocarcinoma of the pancreas are the lowest among the 60 most frequent types of organ cancers. Hence published data on long time survivors of this disease are controversial. We performed a nationwide s

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::11d43cf346e423acab34385d6cc2da41
https://doi.org/10.1136/gut.2004.047191

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Evaluation of various treatments for carcinoma of the mandibular region

Autor: E. Pukkala, R. Sankila, A.-L. Söderholm, C. Lindyvist, Lyly Teppo

Publikováno v: British Journal of Oral and Maxillofacial Surgery. 29:223-229

Cancers of the mandibular region show the lowest survival rates of all oral cancers. In order to compare the effect of five different modes of treatment (including surgery and/or radiotherapy), a series of 159 patients was analysed. When adjustments

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef79c38a16a06b38658447106e6039c4
https://doi.org/10.1016/0266-4356(91)90188-b

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Analysis of p53 tumor suppressor gene in families with multiple glioma patients

Autor: N, Paunu, K, Syrjäkoski, R, Sankila, K O, Simola, P, Helén, M, Niemelä, M, Matikainen, J, Isola, H, Haapasalo

Publikováno v: Journal of neuro-oncology. 55(3)

The high incidence of gliomas in Li-Fraumeni families and the high frequency of somatic p53 mutations in sporadic glial tumors have raised the possibility that germline p53 mutations could play an important role in familial aggregation of gliomas. In

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fc0ff3f013c1080212e698f2e9258f52
https://pubmed.ncbi.nlm.nih.gov/11859970

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Risk of cancer in BRCA1 and BRCA2 mutation-positive and -negative breast cancer families (Finland)

Autor: H, Eerola, E, Pukkala, S, Pyrhönen, C, Blomqvist, R, Sankila, H, Nevanlinna

Publikováno v: Cancer causescontrol : CCC. 12(8)

To compare the risk of cancer between BRCA1 or BRCA2 mutation-positive and -negative families.We assessed standardized incidence ratios (SIR) in 107 Finnish breast cancer families (12 BRCA1, 11 BRCA2, 84 non-BRCA1/2) with confirmed genealogy. The obs

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ed4ef048b80e5efe306bd87396d4c987
https://pubmed.ncbi.nlm.nih.gov/11562114

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Relatives of prostate cancer patients have an increased risk of prostate and stomach cancers: a population-based, cancer registry study in Finland

Autor: M P, Matikaine, E, Pukkala, J, Schleutker, T L, Tammela, P, Koivisto, R, Sankila, O P, Kallioniemi

Publikováno v: Cancer causescontrol : CCC. 12(3)

Five to ten percent of prostate cancers may be caused by inherited genetic defects. In order to explore the nature of inherited cancer risks in the genetically homogeneous Finnish population, we investigated the incidence of prostate cancer and other

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b7947810279197642d7ef8988a4b3efd
https://pubmed.ncbi.nlm.nih.gov/11405327

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A genetic epidemiological study of hereditary prostate cancer (HPC) in Finland: frequent HPCX linkage in families with late-onset disease

Autor: J, Schleutker, M, Matikainen, J, Smith, P, Koivisto, A, Baffoe-Bonnie, T, Kainu, E, Gillanders, R, Sankila, E, Pukkala, J, Carpten, D, Stephan, T, Tammela, M, Brownstein, J, Bailey-Wilson, J, Trent, O P, Kallioniemi

Publikováno v: Clinical cancer research : an official journal of the American Association for Cancer Research. 6(12)

Several predisposition loci for hereditary prostate cancer (HPC) have been suggested, including HPC1 at 1q24-q25 (OMIM #601518) and HPCX at Xq27-q28 (OMIM #300147). Genetically homogeneous populations, such as that of Finland, and distinct subsets of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::b48c9d896718f1eb692953a5d6b44dd8
https://pubmed.ncbi.nlm.nih.gov/11156239

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Second malignant neoplasms after cancer in childhood and adolescence: a population-based case-control study in the 5 Nordic countries. The Nordic Society for Pediatric Hematology and Oncology. The Association of the Nordic Cancer Registries

Autor: S, Garwicz, H, Anderson, J H, Olsen, H, Døllner, H, Hertz, G, Jonmundsson, F, Langmark, M, Lanning, T, Möller, R, Sankila, H, Tulinius

Publikováno v: International journal of cancer. 88(4)

Our purpose was to assess the risk of developing a second malignant neoplasm (SMN) after cancer in childhood and adolescence associated with different treatment modalities. Our investigation was performed as a nested case-control study within a Nordi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::31496f350fdc8ec51b896f85ba91470d
https://pubmed.ncbi.nlm.nih.gov/11058888

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