Vainionpää L - Search Results

1

Effect of acetaminophen and of low intermittent doses of diazepam on prevention of recurrences of febrile seizures.

Uhari M, Rantala H, Vainionpää L, Kurttila R. Uhari M, et al. Among authors: vainionpaa l. J Pediatr. 1995 Jun;126(6):991-5. doi: 10.1016/s0022-3476(95)70231-8. J Pediatr. 1995. PMID: 7776115 Clinical Trial.

2

Molecular epidemiology of childhood mitochondrial encephalomyopathies in a Finnish population: sequence analysis of entire mtDNA of 17 children reveals heteroplasmic mutations in tRNAArg, tRNAGlu, and tRNALeu(UUR) genes.

Uusimaa J, Finnilä S, Remes AM, Rantala H, Vainionpää L, Hassinen IE, Majamaa K. Uusimaa J, et al. Among authors: vainionpaa l. Pediatrics. 2004 Aug;114(2):443-50. doi: 10.1542/peds.114.2.443. Pediatrics. 2004. PMID: 15286228

3

Childhood encephalopathies and myopathies: a prospective study in a defined population to assess the frequency of mitochondrial disorders.

Uusimaa J, Remes AM, Rantala H, Vainionpää L, Herva R, Vuopala K, Nuutinen M, Majamaa K, Hassinen IE. Uusimaa J, et al. Among authors: vainionpaa l. Pediatrics. 2000 Mar;105(3 Pt 1):598-603. doi: 10.1542/peds.105.3.598. Pediatrics. 2000. PMID: 10699115

4

Teaching evidence-based medicine using literature for problem solving.

Möttönen M, Tapanainen P, Nuutinen M, Rantala H, Vainionpää L, Uhari M. Möttönen M, et al. Among authors: vainionpaa l. Med Teach. 2001 Jan;23(1):90-91. doi: 10.1080/01421590150214645. Med Teach. 2001. PMID: 11260750 No abstract available.

5

A mutation in mitochondrial DNA-encoded cytochrome c oxidase II gene in a child with Alpers-Huttenlocher-like disease.

Uusimaa J, Finnilä S, Vainionpää L, Kärppä M, Herva R, Rantala H, Hassinen IE, Majamaa K. Uusimaa J, et al. Among authors: vainionpaa l. Pediatrics. 2003 Mar;111(3):e262-8. doi: 10.1542/peds.111.3.e262. Pediatrics. 2003. PMID: 12612282

6

Medical student abuse: an international phenomenon.

Uhari M, Kokkonen J, Nuutinen M, Vainionpaa L, Rantala H, Lautala P, Väyrynen M. Uhari M, et al. Among authors: vainionpaa l. JAMA. 1994 Apr 6;271(13):1049-51. doi: 10.1001/jama.271.13.1049. JAMA. 1994. PMID: 8139064

7

[Sandifer syndrome].

Norja R, Rantala H, Vainionpää L. Norja R, et al. Among authors: vainionpaa l. Duodecim. 1996;112(2):112-5. Duodecim. 1996. PMID: 10590615 Finnish. No abstract available.

8

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.

Uusimaa J, Moilanen JS, Vainionpää L, Tapanainen P, Lindholm P, Nuutinen M, Löppönen T, Mäki-Torkko E, Rantala H, Majamaa K. Uusimaa J, et al. Among authors: vainionpaa l. Ann Neurol. 2007 Sep;62(3):278-87. doi: 10.1002/ana.21196. Ann Neurol. 2007. PMID: 17823937

9

Visual field constriction in 91 Finnish children treated with vigabatrin.

Vanhatalo S, Nousiainen I, Eriksson K, Rantala H, Vainionpää L, Mustonen K, Aärimaa T, Alen R, Aine MR, Byring R, Hirvasniemi A, Nuutila A, Walden T, Ritanen-Mohammed UM, Karttunen-Lewandowski P, Pohjola LM, Kaksonen S, Jurvelin P, Granström ML. Vanhatalo S, et al. Among authors: vainionpaa l. Epilepsia. 2002 Jul;43(7):748-56. doi: 10.1046/j.1528-1157.2002.17801.x. Epilepsia. 2002. PMID: 12102679 Free article.

10

The effects of valproate, carbamazepine, and oxcarbazepine on growth and sexual maturation in girls with epilepsy.

Rättyä J, Vainionpää L, Knip M, Lanning P, Isojärvi JI. Rättyä J, et al. Among authors: vainionpaa l. Pediatrics. 1999 Mar;103(3):588-93. doi: 10.1542/peds.103.3.588. Pediatrics. 1999. PMID: 10049961

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