Mononen I - Search Results

1

Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family.

Rantamäki M, Krahe R, Paetau A, Cormand B, Mononen I, Udd B. Rantamäki M, et al. Among authors: mononen i. Neurology. 2001 Sep 25;57(6):1043-9. doi: 10.1212/wnl.57.6.1043. Neurology. 2001. PMID: 11571332

2

[New adult-onset ataxia in a Finnish family].

Rantamäki M, Krahe R, Paetau A, Cormand B, Mononen I, Udd B. Rantamäki M, et al. Among authors: mononen i. Duodecim. 2002;118(20):2115-22. Duodecim. 2002. PMID: 12463002 Finnish. No abstract available.

3

A longitudinal study of serum 25-hydroxyvitamin D and intact parathyroid hormone levels indicate the importance of vitamin D and calcium homeostasis regulation in multiple sclerosis.

Soilu-Hänninen M, Laaksonen M, Laitinen I, Erälinna JP, Lilius EM, Mononen I. Soilu-Hänninen M, et al. Among authors: mononen i. J Neurol Neurosurg Psychiatry. 2008 Feb;79(2):152-7. doi: 10.1136/jnnp.2006.105320. Epub 2007 Jun 19. J Neurol Neurosurg Psychiatry. 2008. PMID: 17578859 Clinical Trial.

4

25-Hydroxyvitamin D levels in serum at the onset of multiple sclerosis.

Soilu-Hänninen M, Airas L, Mononen I, Heikkilä A, Viljanen M, Hänninen A. Soilu-Hänninen M, et al. Among authors: mononen i. Mult Scler. 2005 Jun;11(3):266-71. doi: 10.1191/1352458505ms1157oa. Mult Scler. 2005. PMID: 15957505

5

Detection of the Finnish-type congenital nephrotic syndrome by restriction fragment length polymorphism and dual-color oligonucleotide ligation assays.

Romppanen EL, Mononen I. Romppanen EL, et al. Among authors: mononen i. Clin Chem. 2000 Jun;46(6 Pt 1):811-6. Clin Chem. 2000. PMID: 10839769

6

Twenty-four-month alpha-galactosidase A replacement therapy in Fabry disease has only minimal effects on symptoms and cardiovascular parameters.

Koskenvuo JW, Hartiala JJ, Nuutila P, Kalliokoski R, Viikari JS, Engblom E, Penttinen M, Knuuti J, Mononen I, Kantola IM. Koskenvuo JW, et al. Among authors: mononen i. J Inherit Metab Dis. 2008 Jun;31(3):432-41. doi: 10.1007/s10545-008-0848-3. Epub 2008 May 23. J Inherit Metab Dis. 2008. PMID: 18509742

7

Carriers of the aspartylglucosaminuria genetic mutation and chronic arthritis.

Arvio M, Laiho K, Kauppi M, Peippo M, Leino P, Kautiainen H, Kaipiainen-Seppänen O, Mononen I. Arvio M, et al. Among authors: mononen i. Ann Rheum Dis. 2002 Feb;61(2):180-1. doi: 10.1136/ard.61.2.180. Ann Rheum Dis. 2002. PMID: 11796409 Free PMC article.

8

Vascular adhesion protein-1 in human ischaemic stroke.

Airas L, Lindsberg PJ, Karjalainen-Lindsberg ML, Mononen I, Kotisaari K, Smith DJ, Jalkanen S. Airas L, et al. Among authors: mononen i. Neuropathol Appl Neurobiol. 2008 Aug;34(4):394-402. doi: 10.1111/j.1365-2990.2007.00911.x. Epub 2007 Nov 14. Neuropathol Appl Neurobiol. 2008. PMID: 18005095

9

Molecular diagnosis of medium-chain acyl-CoA dehydrogenase deficiency by oligonucleotide ligation assay.

Romppanen EL, Mononen T, Mononen I. Romppanen EL, et al. Among authors: mononen t, mononen i. Clin Chem. 1998 Jan;44(1):68-71. Clin Chem. 1998. PMID: 9550560

10

PCR-oligonucleotide ligation assay from dried blood spots.

Romppanen EL, Mononen I. Romppanen EL, et al. Among authors: mononen i. Clin Chem. 1999 Nov;45(11):2022-5. Clin Chem. 1999. PMID: 10545079 No abstract available.

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