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Characterization of ATM mutations in 41 Nordic families with ataxia telangiectasia.
Laake K, Jansen L, Hahnemann JM, Brondum-Nielsen K, Lönnqvist T, Kääriäinen H, Sankila R, Lähdesmäki A, Hammarström L, Yuen J, Tretli S, Heiberg A, Olsen JH, Tucker M, Kleinerman R, Børresen-Dale AL. Laake K, et al. Among authors: lahdesmaki a. Hum Mutat. 2000 Sep;16(3):232-46. doi: 10.1002/1098-1004(200009)16:3<232::AID-HUMU6>3.0.CO;2-L. Hum Mutat. 2000. PMID: 10980530
[Ataxia-telangiectasia surveyed in Sweden].
Lähdesmäki A, Arinbjarnarson K, Arvidsson J, el Segaier M, Fasth A, Fernell E, Gustafsson D, Oxelius VA, Risberg K, Yuen J, Zetterlund P, von Zweigbergk M, Ahsgren I, Hammarström L. Lähdesmäki A, et al. Lakartidningen. 2000 Oct 4;97(40):4461-5, 4467. Lakartidningen. 2000. PMID: 11068401 Swedish.
ATM mutations in B-cell chronic lymphocytic leukemia.
Lähdesmäki A, Kimby E, Duke V, Foroni L, Hammarström L. Lähdesmäki A, et al. Haematologica. 2004 Jan;89(1):109-10. Haematologica. 2004. PMID: 14754616 No abstract available.
Primary immunodeficiency mutation databases.
Vihinen M, Arredondo-Vega FX, Casanova JL, Etzioni A, Giliani S, Hammarström L, Hershfield MS, Heyworth PG, Hsu AP, Lähdesmäki A, Lappalainen I, Notarangelo LD, Puck JM, Reith W, Roos D, Schumacher RF, Schwarz K, Vezzoni P, Villa A, Väliaho J, Smith CI. Vihinen M, et al. Among authors: lahdesmaki a. Adv Genet. 2001;43:103-88. doi: 10.1016/s0065-2660(01)43005-7. Adv Genet. 2001. PMID: 11037300 Review.
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy.
Tyrmi JS, Kaartokallio T, Lokki AI, Jääskeläinen T, Kortelainen E, Ruotsalainen S, Karjalainen J, Ripatti S, Kivioja A, Laisk T, Kettunen J, Pouta A, Kivinen K, Kajantie E, Heinonen S, Kere J, Laivuori H; FINNPEC Study Group, FinnGen Project, and the Estonian Biobank Research Team. Tyrmi JS, et al. JAMA Cardiol. 2023 Jul 1;8(7):674-683. doi: 10.1001/jamacardio.2023.1312. JAMA Cardiol. 2023. PMID: 37285119 Free PMC article.
15 results