Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Pekka Nokelainen"'
Autor:
Marita Hovi, Hannu Heiskala, Eeva T. Aronen, Outi Saarenpää‐Heikkilä, Päivi Olsen, Pekka Nokelainen, Turkka Kirjavainen
Publikováno v:
Acta Paediatrica. 111:850-858
https://doi.org/10.1111/apa.16233 ABSTRACT Aim We assessed psychosocial burdens in children who developed narcolepsy after receiving the Pandemrix H1N1 vaccine during the 2009-2010 pandemic. Parental quality of life was also assessed. Methods This mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9481ba6bebb3fc6385ac700b81d1a10b
https://doi.org/10.1111/apa.16233
https://doi.org/10.1111/apa.16233
Publikováno v:
Child Neurology Open. 10:2329048X2311513
We present contactless technology measuring abnormal ventilation and compare it with polysomnography (PSG). A 13-years old girl with Pitt-Hopkins syndrome presented hyperpnoea periods with apneic spells. The PSG was conducted simultaneously with Emfi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd87582b9f76b410a2843c32bf861096
https://doi.org/10.1177/2329048x231151361
https://doi.org/10.1177/2329048x231151361
Autor:
Markku Partinen, Outi Saarenpää-Heikkilä, Ismo Ilveskoski, Christer Hublin, Miika Linna, Päivi Olsén, Pekka Nokelainen, Reija Alén, Tiina Wallden, Merimaaria Espo, Harri Rusanen, Jan Olme, Heli Sätilä, Harri Arikka, Pekka Kaipainen, Ilkka Julkunen, Turkka Kirjavainen
Publikováno v:
PLoS ONE, Vol 7, Iss 3, p e33723 (2012)
BackgroundNarcolepsy is a rare neurological sleep disorder especially in children who are younger than 10 years. In the beginning of 2010, an exceptionally large number of Finnish children suffered from an abrupt onset of excessive daytime sleepiness
Externí odkaz:
https://doaj.org/article/a4deaccd0d9c49a89c6aed6f2f59642a
Autor:
Mirja, HämäläInen, Laimi, Katri, Tanja, Laukkala, Pekka, Nokelainen, Mikael, Raisio, Heikki, Rantala, Pirjo, Aanttila, Heli, Sätilä
Publikováno v:
Duodecim; laaketieteellinen aikakauskirja. 132(2)
The majority of children with recurrent headaches can be effectively treated in the primary health care. Paracetamol and ibuprofen are the recommended first-line pain medications. Limited evidence is available on the effectiveness of triptans in chil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::94651caaf6138da40cf870ede9f5f4fd
https://pubmed.ncbi.nlm.nih.gov/26939493
https://pubmed.ncbi.nlm.nih.gov/26939493
Autor:
Pekka Nokelainen, Raili Raininko, Hannu Heiskala, Taina Autti, Anna-Maija Häkkinen, Kari Wirtavuori, Jonathan Flint
Publikováno v:
American Journal of Medical Genetics. 103:198-206
Two brothers with severe mental retardation of unknown origin were found to share several physical anomalies, including large round head, small concave nose, downslanted palpebral fissures, and gingival hyperplasia. In addition to relative macrocepha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e498c1e8e481b04b0ad38262250b0eef
https://doi.org/10.1002/ajmg.1536
https://doi.org/10.1002/ajmg.1536
Publikováno v:
Journal of the Neurological Sciences. 113:214-221
Late adult onset distal myopathies usually show vacuolar degeneration as a characteristic feature in muscle pathology. In this study vacuolar degeneration was not present in 12 patients with late adult onset distal myopathy. All patients were members
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b246cbaec633dfd0fbb7cd05481d5495
https://doi.org/10.1016/0022-510x(92)90249-k
https://doi.org/10.1016/0022-510x(92)90249-k
Publikováno v:
Muscle & Nerve. 14:451-456
Three DNA probes (APOC2, PSC11, and LDR152) detecting RFLP polymorphisms were used to test the usefulness of the RFLP approach in myotonic dystrophy (MD) families from the isolated Finnish population. The informativeness of these polymorphisms did no
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b62ad049b3fa5481186dd2f7be526618
https://doi.org/10.1002/mus.880140511
https://doi.org/10.1002/mus.880140511
Autor:
Jyrki T. Kuikka, Pekka Nokelainen, Kirsti I. Kumpulainen, Ritva-Liisa S. Vanninen, Raili Riikonen, Mervi Könönen, Kirsi Valkonen, Anni I. Kolehmainen
Publikováno v:
Biological psychiatry. 57(12)
In prenatally alcohol exposed children, the relationship between brain structure and function is highlighted to be important to study.We studied 12 children with fetal alcoholic syndrome (FAS) and fetal alcoholic effects (FAE) by magnetic resonance i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ffadf57871e3a69098bf47b65bb1b09
https://pubmed.ncbi.nlm.nih.gov/15953494
https://pubmed.ncbi.nlm.nih.gov/15953494
Autor:
Leena Peltonen, Ann-Christine Syvänen, Pertti Sistonen, Pekka Nokelainen, Antti Sajantila, Päivi Pacek, Matti Lukka, Bruce Budowle
Publikováno v:
Forensic science international. 68(2)
The allele frequencies at the tetranucleotide repeat (TCTA) vWA locus in the vWF gene were determined in the general Finnish population, in a population representing an internal isolate of Finland, in the Vologda-Russian population, and in US Black p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49d8bb741c06ca9971545027b2e4531f
https://pubmed.ncbi.nlm.nih.gov/7988968
https://pubmed.ncbi.nlm.nih.gov/7988968
Autor:
Björn Falck, Leena Alanen-Kurki, Leena Peltonen, Marja-Liisa Savontaus, Pekka Nokelainen, Hannu Somer, Keith J. Johnson, Jaakko Leisti, Robert Winqvist
Publikováno v:
Human genetics. 85(5)
Three polymorphic loci APOC2, CKMM and p134C were used to haplotype 15 Finnish dystrophia myotonica (DM) families representing about one third of all DM patients in this isolated population. Compound APOC2 and CKMM haplotypes reveal linkage disequili
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0197b360da950b12f9b0404f2edf3184
https://pubmed.ncbi.nlm.nih.gov/1977684
https://pubmed.ncbi.nlm.nih.gov/1977684