Lönnqvist TRI - Search Results

1

Early disc degeneration in radiotherapy-treated childhood brain tumor survivors.

Grahn P, Remes T, Kivisaari R, Suo-Palosaari MH, Arikoski PM, Koskenkorva PKT, Lähteenmäki PM, Lönnqvist TRI, Ojaniemi MK, Sirkiä KH, Sutela AK, Toiviainen-Salo SM, Rantala HMJ, Harila AH, Niinimäki J, Karppinen J, Ahonen M. Grahn P, et al. Among authors: lonnqvist tri. BMC Musculoskelet Disord. 2023 May 31;24(1):441. doi: 10.1186/s12891-023-06509-4. BMC Musculoskelet Disord. 2023. PMID: 37259117 Free PMC article.

2

Infantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and Twinky.

Nikali K, Suomalainen A, Saharinen J, Kuokkanen M, Spelbrink JN, Lönnqvist T, Peltonen L. Nikali K, et al. Hum Mol Genet. 2005 Oct 15;14(20):2981-90. doi: 10.1093/hmg/ddi328. Epub 2005 Aug 31. Hum Mol Genet. 2005. PMID: 16135556

3

[IOSCA - Infantile onset spinocerebellar ataxia].

Lönnqvist T. Lönnqvist T. Duodecim. 2011;127(14):1460-9. Duodecim. 2011. PMID: 21888047 Review. Finnish.

4

Toward cloning of a novel ataxia gene: refined assignment and physical map of the IOSCA locus (SCA8) on 10q24.

Nikali K, Isosomppi J, Lönnqvist T, Mao JI, Suomalainen A, Peltonen L. Nikali K, et al. Genomics. 1997 Jan 15;39(2):185-91. doi: 10.1006/geno.1996.4465. Genomics. 1997. PMID: 9027505

5

Tracing an ancestral mutation: genealogical and haplotype analysis of the infantile onset spinocerebellar ataxia locus.

Varilo T, Nikali K, Suomalainen A, Lönnqvist T, Peltonen L. Varilo T, et al. Genome Res. 1996 Sep;6(9):870-5. doi: 10.1101/gr.6.9.870. Genome Res. 1996. PMID: 8889554 Free article.

6

Motor development of infants with univentricular heart at the ages of 16 and 52 weeks.

Rajantie I, Laurila M, Pollari K, Lönnqvist T, Sarajuuri A, Jokinen E, Mälkiä E. Rajantie I, et al. Pediatr Phys Ther. 2013 Winter;25(4):444-50. doi: 10.1097/PEP.0b013e3182a31704. Pediatr Phys Ther. 2013. PMID: 23995669

7

[Post-infectious encephalomyelitis].

Linnankivi T, Valanne L, Lönnqvist T, Pihko H. Linnankivi T, et al. Duodecim. 2000;116(18):2019-24. Duodecim. 2000. PMID: 12017618 Finnish. No abstract available.

8

Diagnosis of the neuronal ceroid lipofuscinoses: an update.

Williams RE, Aberg L, Autti T, Goebel HH, Kohlschütter A, Lönnqvist T. Williams RE, et al. Biochim Biophys Acta. 2006 Oct;1762(10):865-72. doi: 10.1016/j.bbadis.2006.07.001. Epub 2006 Jul 12. Biochim Biophys Acta. 2006. PMID: 16930952 Free article. Review.

9

Mitochondrial encephalomyopathy and retinoblastoma explained by compound heterozygosity of SUCLA2 point mutation and 13q14 deletion.

Matilainen S, Isohanni P, Euro L, Lönnqvist T, Pihko H, Kivelä T, Knuutila S, Suomalainen A. Matilainen S, et al. Eur J Hum Genet. 2015 Mar;23(3):325-30. doi: 10.1038/ejhg.2014.128. Epub 2014 Jul 2. Eur J Hum Genet. 2015. PMID: 24986829 Free PMC article. Review.

10

Cancer in patients with ataxia-telangiectasia and in their relatives in the nordic countries.

Olsen JH, Hahnemann JM, Børresen-Dale AL, Brøndum-Nielsen K, Hammarström L, Kleinerman R, Kääriäinen H, Lönnqvist T, Sankila R, Seersholm N, Tretli S, Yuen J, Boice JD Jr, Tucker M. Olsen JH, et al. J Natl Cancer Inst. 2001 Jan 17;93(2):121-7. doi: 10.1093/jnci/93.2.121. J Natl Cancer Inst. 2001. PMID: 11208881

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