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Items: 11

1.

Neurocognitive test profiles of extremely low birth weight five-year-old children differ according to neuromotor status.

Korkman M, Mikkola K, Ritari N, Tommiska V, Salokorpi T, Haataja L, Tammela O, Pääkkönen L, Olsén P, Fellman V.

Dev Neuropsychol. 2008;33(5):637-55. doi: 10.1080/87565640802254471.

PMID:
18788015
2.

More severe epilepsy and cognitive impairment in the offspring of a mother with mosaicism for the ring 20 chromosome.

Herrgård E, Mononen T, Mervaala E, Kuusela L, Aikiä M, Stenbäck U, Pääkkönen L, Airaksinen RL, Kälviäinen R.

Epilepsy Res. 2007 Jan;73(1):122-8. Epub 2006 Oct 31.

PMID:
17079116
3.

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.

Neurology. 2006 Oct 24;67(8):1437-43. Epub 2006 Aug 30.

PMID:
16943371
4.

Neurodevelopmental outcome at 5 years of age of a national cohort of extremely low birth weight infants who were born in 1996-1997.

Mikkola K, Ritari N, Tommiska V, Salokorpi T, Lehtonen L, Tammela O, Pääkkönen L, Olsen P, Korkman M, Fellman V.

Pediatrics. 2005 Dec;116(6):1391-400.

PMID:
16322163
5.

Striatal dopaminergic system in dopa-responsive dystonia: a multi-tracer PET study shows increased D2 receptors.

Rinne JO, Iivanainen M, Metsähonkala L, Vainionpää L, Pääkkönen L, Någren K, Helenius H.

J Neural Transm (Vienna). 2004 Jan;111(1):59-67.

PMID:
14714216
6.

[Itching legs and stiff neck].

Kröger L, Pääkkönen L.

Duodecim. 2001;117(8):825-7. Finnish. No abstract available.

PMID:
12116448
7.

Visual field constriction in children treated with vigabatrin.

Vanhatalo S, Pääkkönen L, Nousiainen I.

Neurology. 1999 May 12;52(8):1713-4. No abstract available. Erratum in: Neurology 2000 Jan 11;54(1):277.

PMID:
10331710
8.

Prenatal activity of a fetus with early-onset, severe spinal muscular atrophy.

Kirkinen P, Ryynänen M, Haring P, Torkkeli H, Pääkkönen L, Martikainen A.

Prenat Diagn. 1994 Nov;14(11):1074-6.

PMID:
7877956
9.

Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington disease.

Ikonen E, Salo A, Somer M, Somer H, Pääkkönen L, Peltonen L.

Am J Med Genet. 1992 Jul 1;43(4):753-8.

PMID:
1535752
10.

[3-Methylglutaconic aciduria].

Vakkuri P, Airaksinen E, Karttunen P, Ollikainen J, Pääkkönen L, Ruostesuo J, Ruotsalainen H, Ruokonen A.

Duodecim. 1987;103(2):87-91. Finnish. No abstract available.

PMID:
3608868
11.

Effects of taurine treatment on epileptic patients.

Airaksinen EM, Oja SS, Marnela KM, Leino E, Pääkkönen L.

Prog Clin Biol Res. 1980;39:157-66. No abstract available.

PMID:
7403183

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