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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1971 2
1972 1
1973 2
1974 3
1975 3
1976 2
1977 1
1981 1
1985 1
1987 1
1988 1
1989 3
1990 4
1991 2
1992 6
1993 6
1994 6
1995 8
1996 8
1997 8
1998 8
1999 3
2000 3
2001 2
2002 5
2003 2
2004 5
2005 2
2006 3
2007 2
2008 3
2009 5
2010 4
2011 3
2012 2
2013 1
2014 5
2015 3
2016 2
2017 3
2022 0
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Article type
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Search Results

130 results
Results by year
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Page 1
[Mitochondrial diseases].
Pihko H, Suomalainen A, Somer H, Haltia M, Majander A. Pihko H, et al. Duodecim. 1992;108(6):578-90. Duodecim. 1992. PMID: 1366118 Review. Finnish. No abstract available.
POLG1 manifestations in childhood.
Isohanni P, Hakonen AH, Euro L, Paetau I, Linnankivi T, Liukkonen E, Wallden T, Luostarinen L, Valanne L, Paetau A, Uusimaa J, Lönnqvist T, Suomalainen A, Pihko H. Isohanni P, et al. Among authors: pihko h. Neurology. 2011 Mar 1;76(9):811-5. doi: 10.1212/WNL.0b013e31820e7b25. Neurology. 2011. PMID: 21357833
[Investments of research and treatment of brain diseases will pay of time].
Lindsberg PJ, Castrén E, Korkeila J, Alho H, Erkinjuntti T, Isometsä E, Kalso E, Marttunen M, Pihko H, Tienari P, Wartiovaara A, Jäkälä P, Kälviäinen R, Soininen H, Tiihonen J, Karlsson H, Rinne J, Roine RO, Elovaara I, Tamminen T, Ohman J, Majamaa K, Hari R. Lindsberg PJ, et al. Among authors: pihko h. Duodecim. 2014;130(17):1721-30. Duodecim. 2014. PMID: 25272783 Review. Finnish.
Dominant encephalopathy mimicking mitochondrial disease.
Lönnqvist T, Isohanni P, Valanne L, Olli-Lähdesmäki T, Suomalainen A, Pihko H. Lönnqvist T, et al. Among authors: pihko h. Neurology. 2011 Jan 4;76(1):101-3. doi: 10.1212/WNL.0b013e318203e908. Neurology. 2011. PMID: 21205700 No abstract available.
[Problematic brains of children].
Valanne L, Rautiainen P, Pihko H. Valanne L, et al. Among authors: pihko h. Duodecim. 1992;108(8):737-46. Duodecim. 1992. PMID: 1366287 Review. Finnish. No abstract available.
Partial 11q trisomy syndrome.
Pihko H, Therman E, Uchida IA. Pihko H, et al. Hum Genet. 1981;58(2):129-34. doi: 10.1007/BF00278696. Hum Genet. 1981. PMID: 7286998
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. Linnankivi T, et al. Among authors: pihko h. Neurology. 2006 Oct 24;67(8):1437-43. doi: 10.1212/01.wnl.0000236999.63933.b0. Epub 2006 Aug 30. Neurology. 2006. PMID: 16943371
Selenoprotein biosynthesis defect causes progressive encephalopathy with elevated lactate.
Anttonen AK, Hilander T, Linnankivi T, Isohanni P, French RL, Liu Y, Simonović M, Söll D, Somer M, Muth-Pawlak D, Corthals GL, Laari A, Ylikallio E, Lähde M, Valanne L, Lönnqvist T, Pihko H, Paetau A, Lehesjoki AE, Suomalainen A, Tyynismaa H. Anttonen AK, et al. Among authors: pihko h. Neurology. 2015 Jul 28;85(4):306-15. doi: 10.1212/WNL.0000000000001787. Epub 2015 Jun 26. Neurology. 2015. PMID: 26115735 Free PMC article.
130 results