Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Results by year

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

Year Number of Results
1975 1
1976 2
1979 2
1981 2
1982 2
1983 1
1984 5
1985 3
1986 2
1987 3
1988 1
1989 3
1990 5
1991 1
1992 7
1993 10
1994 8
1995 5
1996 5
1997 10
1998 3
1999 6
2000 6
2001 6
2002 3
2003 3
2004 7
2005 2
2006 3
2007 4
2008 3
2009 8
2010 5
2011 9
2012 1
2013 3
2014 5
2015 1
2016 4
2017 1
2018 5
2019 4
2021 1
2022 0
Text availability
Article attribute
Article type
Publication date

Search Results

159 results
Results by year
Filters applied: . Clear all
Page 1
LMNB1-Related Autosomal Dominant Leukodystrophy.
Raininko R, Gosky M, Padiath QS. Raininko R, et al. 2016 Jan 7 [updated 2021 Jul 15]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2016 Jan 7 [updated 2021 Jul 15]. In: Adam MP, Ardinger HH, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Mirzaa GM, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 26749591 Free Books & Documents. Review.
Infantile neuronal ceroid-lipofuscinosis (INCL): diagnostic criteria.
Santavuori P, Vanhanen SL, Sainio K, Nieminen M, Wallden T, Launes J, Raininko R. Santavuori P, et al. Among authors: raininko r. J Inherit Metab Dis. 1993;16(2):227-9. doi: 10.1007/BF00710250. J Inherit Metab Dis. 1993. PMID: 8411966 Review. No abstract available.
Re-evaluation of the dysequilibrium syndrome.
Melberg A, Orlén H, Raininko R, Entesarian M, Dahlqvist J, Gustavson KH, Dahl N. Melberg A, et al. Among authors: raininko r. Acta Neurol Scand. 2011 Jan;123(1):28-33. doi: 10.1111/j.1600-0404.2010.01335.x. Acta Neurol Scand. 2011. PMID: 20199520
Bone-marrow transplantation in aspartylglucosaminuria.
Autti T, Santavuori P, Raininko R, Renlund M, Rapola J, Saarinen-Pihkala U. Autti T, et al. Among authors: raininko r. Lancet. 1997 May 10;349(9062):1366-7. doi: 10.1016/S0140-6736(05)63202-3. Lancet. 1997. PMID: 9149703 No abstract available.
Brain MRI features and scoring of leukodystrophy in adult-onset Krabbe disease.
Cousyn L, Law-Ye B, Pyatigorskaya N, Debs R, Froissart R, Piraud M, Federico A, Salvatore S, Cerase A, Macário MC, Durães J, Kim SH, Adachi H, Audoin B, Ayrignac X, Da Y, Henderson R, La Piana R, Laule C, Nakamagoe K, Raininko R, Schols L, Sirrs SM, Viader F, Jastrzębski K, Leclercq D, Nadjar Y. Cousyn L, et al. Among authors: raininko r. Neurology. 2019 Aug 13;93(7):e647-e652. doi: 10.1212/WNL.0000000000007943. Epub 2019 Jul 23. Neurology. 2019. PMID: 31337714
Genomic deletions upstream of lamin B1 lead to atypical autosomal dominant leukodystrophy.
Nmezi B, Giorgio E, Raininko R, Lehman A, Spielmann M, Koenig MK, Adejumo R, Knight M, Gavrilova R, Alturkustani M, Sharma M, Hammond R, Gahl WA, Toro C, Brusco A, Padiath QS. Nmezi B, et al. Among authors: raininko r. Neurol Genet. 2019 Jan 24;5(1):e305. doi: 10.1212/NXG.0000000000000305. eCollection 2019 Feb. Neurol Genet. 2019. PMID: 30842973 Free PMC article.
159 results