Lönnqvist T - Search Results

1

Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate.

Anttonen AK, Hilander T, Linnankivi T, Isohanni P, French RL, Liu Y, Simonović M, Söll D, Somer M, Muth-Pawlak D, Corthals GL, Laari A, Ylikallio E, Lähde M, Valanne L, Lönnqvist T, Pihko H, Paetau A, Lehesjoki AE, Suomalainen A, Tyynismaa H. Anttonen AK, et al. Among authors: lonnqvist t. Neurology. 2015 Jul 28;85(4):306-15. doi: 10.1212/WNL.0000000000001787. Epub 2015 Jun 26. Neurology. 2015. PMID: 26115735 Free PMC article.

2

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. Among authors: lonnqvist t. Genome Res. 1996 Sep;6(9):870-5. doi: 10.1101/gr.6.9.870. Genome Res. 1996. PMID: 8889554 Free article.

3

Infantile onset spinocerebellar ataxia with sensory neuropathy (IOSCA): neuropathological features.

Lönnqvist T, Paetau A, Nikali K, von Boguslawski K, Pihko H. Lönnqvist T, et al. J Neurol Sci. 1998 Nov 26;161(1):57-65. doi: 10.1016/s0022-510x(98)00249-4. J Neurol Sci. 1998. PMID: 9879682

4

Hematopoietic stem cell transplantation in infantile neuronal ceroid lipofuscinosis.

Lönnqvist T, Vanhanen SL, Vettenranta K, Autti T, Rapola J, Santavuori P, Saarinen-Pihkala UM. Lönnqvist T, et al. Neurology. 2001 Oct 23;57(8):1411-6. doi: 10.1212/wnl.57.8.1411. Neurology. 2001. PMID: 11673581 Clinical Trial.

5

[Post-infectious encephalomyelitis].

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

6

A case of Salla disease with involvement of the cerebellar white matter.

Linnankivi T, Lönnqvist T, Autti T. Linnankivi T, et al. Among authors: lonnqvist t. Neuroradiology. 2003 Feb;45(2):107-9. doi: 10.1007/s00234-002-0900-1. Epub 2003 Jan 16. Neuroradiology. 2003. PMID: 12592494

7

Hereditary neuropathy with liability to pressure palsies (HNPP) in a toddler presenting with toe-walking, pain and stiffness.

Lönnqvist T, Pihko H. Lönnqvist T, et al. Neuromuscul Disord. 2003 Dec;13(10):827-9. doi: 10.1016/s0960-8966(03)00134-2. Neuromuscul Disord. 2003. PMID: 14678806

8

Five new cases of a recently described leukoencephalopathy with high brain lactate.

Linnankivi T, Lundbom N, Autti T, Häkkinen AM, Koillinen H, Kuusi T, Lönnqvist T, Sainio K, Valanne L, Aärimaa T, Pihko H. Linnankivi T, et al. Among authors: lonnqvist t. Neurology. 2004 Aug 24;63(4):688-92. doi: 10.1212/01.wnl.0000134658.35601.41. Neurology. 2004. PMID: 15326244

9

Enrichment of the R77C alpha-sarcoglycan gene mutation in Finnish LGMD2D patients.

Hackman P, Juvonen V, Sarparanta J, Penttinen M, Aärimaa T, Uusitalo M, Auranen M, Pihko H, Alén R, Junes M, Lönnqvist T, Kalimo H, Udd B. Hackman P, et al. Among authors: lonnqvist t. Muscle Nerve. 2005 Feb;31(2):199-204. doi: 10.1002/mus.20267. Muscle Nerve. 2005. PMID: 15736300

10

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. Among authors: lonnqvist t. 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

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

100 results

Search Page

Filters