Lönnqvist T - Search Results

1

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

2

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

3

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.

4

[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.

5

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

6

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

7

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

8

Muscular dystonia and athetosis in six patients with congenital nephrotic syndrome of the Finnish type (NPHS1).

Laakkonen H, Lönnqvist T, Uusimaa J, Qvist E, Valanne L, Nuutinen M, Ala-Houhala M, Majamaa K, Jalanko H, Holmberg C. Laakkonen H, et al. Among authors: lonnqvist t. Pediatr Nephrol. 2006 Feb;21(2):182-9. doi: 10.1007/s00467-005-2116-1. Epub 2005 Dec 17. Pediatr Nephrol. 2006. PMID: 16362719

9

18q deletions: clinical, molecular, and brain MRI findings of 14 individuals.

Linnankivi T, Tienari P, Somer M, Kähkönen M, Lönnqvist T, Valanne L, Pihko H. Linnankivi T, et al. Among authors: lonnqvist t. Am J Med Genet A. 2006 Feb 15;140(4):331-9. doi: 10.1002/ajmg.a.31072. Am J Med Genet A. 2006. PMID: 16419126

10

Cerebroretinal microangiopathy with calcifications and cysts.

Linnankivi T, Valanne L, Paetau A, Alafuzoff I, Hakumäki JM, Kivelä T, Lönnqvist T, Mäkitie O, Pääkkönen L, Vainionpää L, Vanninen R, Herva R, Pihko H. Linnankivi T, et al. Among authors: lonnqvist t. Neurology. 2006 Oct 24;67(8):1437-43. doi: 10.1212/01.wnl.0000236999.63933.b0. Epub 2006 Aug 30. Neurology. 2006. PMID: 16943371

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 NCBI Filters

Text availability

Article attribute

Article type

Publication date

100 results

Search Page