I Mononen
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Explore the profile of I Mononen including associated specialties, affiliations and a list of published articles.
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Articles
63
Citations
463
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Recent Articles
1.
Kelo E, Noronkoski T, Mononen I
Leukemia
. 2009 Jan;
23(6):1167-71.
PMID: 19158835
No abstract available.
2.
Koskenvuo J, Hartiala J, Nuutila P, Kalliokoski R, Viikari J, Engblom E, et al.
J Inherit Metab Dis
. 2008 May;
31(3):432-41.
PMID: 18509742
Fabry disease is an X-linked lysosomal storage disease caused by deficiency of alpha-galactosidase A enzyme activity. Decreased enzyme activity leads to accumulation of glycosphingolipids in different tissues including endothelial cells...
3.
Airas L, Lindsberg P, Karjalainen-Lindsberg M, Mononen I, Kotisaari K, Smith D, et al.
Neuropathol Appl Neurobiol
. 2007 Nov;
34(4):394-402.
PMID: 18005095
Aims: Leukocyte extravasation exacerbates tissue injury after ischaemic stroke. Vascular adhesion protein-1 (VAP-1) is an endothelial adhesion molecule with the potential capacity to guide transmigration of inflammatory cells into ischaemic...
4.
Soilu-Hanninen M, Laaksonen M, Laitinen I, Eralinna J, Lilius E, Mononen I
J Neurol Neurosurg Psychiatry
. 2007 Jun;
79(2):152-7.
PMID: 17578859
Background: Past sun exposure and vitamin D3 supplementation have been associated with a reduced risk of multiple sclerosis (MS). There are no previous longitudinal studies of vitamin D in MS....
5.
Soilu-Hanninen M, Airas L, Mononen I, Heikkila A, Viljanen M, Hanninen A
Mult Scler
. 2005 Jun;
11(3):266-71.
PMID: 15957505
Past sun exposure and vitamin D supplementation have been associated with a reduction in the risk of MS. We measured the serum concentration of 25-hydroxyvitamin D (25[OH]D) at the time...
6.
Arvio M, Laiho K, Kauppi M, Peippo M, Leino P, Kautiainen H, et al.
Ann Rheum Dis
. 2002 Jan;
61(2):180-1.
PMID: 11796409
Objective: To ascertain whether being a carrier of an autosomal recessive disease, aspartylglucosaminuria (AGU), predisposes to chronic arthritis, as does AGU disease. Methods: A group of 173 unrelated patients with...
7.
Rantamaki M, Krahe R, Paetau A, Cormand B, Mononen I, Udd B
Neurology
. 2001 Sep;
57(6):1043-9.
PMID: 11571332
Objective: To describe an unusual kindred with adult-onset ataxia and thalamic lesions detected by brain MRI. Methods: The authors characterized clinical, laboratory, and pathologic features of the disease and sought...
8.
Dunder U, Mononen I
FEBS Lett
. 2001 Jun;
499(1-2):77-81.
PMID: 11418116
Aspartylglycosaminuria (AGU), a severe lysosomal storage disease, is caused by the deficiency of the lysosomal enzyme, glycosylasparaginase (GA), and accumulation of aspartylglucosamine (GlcNAc-Asn) in tissues. Here we show that human...
9.
Hujakka H, Koistinen V, Eerikainen P, Kuronen I, Mononen I, Parviainen M, et al.
J Clin Microbiol
. 2001 May;
39(6):2146-50.
PMID: 11376049
A new immunochromatographic rapid test, POC PUUMALA (Erilab Ltd., Kuopio, Finland), for detection of acute-phase Puumala virus (PUUV) infection was developed based on a highly purified baculovirus-expressed PUUV nucleocapsid protein...
10.
Romppanen E, Mononen I
Clin Chem
. 2000 Jun;
46(6 Pt 1):811-6.
PMID: 10839769
Background: Congenital nephrotic syndrome of Finnish type (NPHS1) is an autosomal recessive disorder characterized by severe proteinuria of intrauterine onset. Ninety-four percent of the Finnish NPHS1 chromosomes have been reported...