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
1968 1
1969 3
1970 7
1972 3
1973 5
1974 6
1975 5
1976 6
1977 6
1978 5
1979 7
1980 8
1981 4
1982 9
1983 7
1984 5
1985 12
1986 6
1987 2
1988 10
1989 6
1990 9
1991 8
1992 11
1993 9
1994 4
1995 14
1996 12
1997 11
1998 8
1999 7
2000 10
2001 10
2002 8
2003 3
2004 4
2005 4
2006 4
2010 1
2012 1
2013 2
2020 3
2022 1
Text availability
Article attribute
Article type
Publication date

Search Results

263 results
Results by year
Filters applied: . Clear all
Page 1
Hereditary gelsolin amyloidosis.
Kiuru-Enari S, Haltia M. Kiuru-Enari S, et al. Among authors: haltia m. Handb Clin Neurol. 2013;115:659-81. doi: 10.1016/B978-0-444-52902-2.00039-4. Handb Clin Neurol. 2013. PMID: 23931809 Review.
Finnish neuroscience from past to present.
Korpi ER, Lindholm D, Panula P, Tienari PJ, Haltia M. Korpi ER, et al. Among authors: haltia m. Eur J Neurosci. 2020 Sep;52(5):3273-3289. doi: 10.1111/ejn.14693. Epub 2020 Feb 18. Eur J Neurosci. 2020. PMID: 32017266 No abstract available.
Polycystic Lipomembranous Osteodysplasia with Sclerosing Leukoencephalopathy.
Paloneva J, Autti T, Hakola P, Haltia MJ. Paloneva J, et al. Among authors: haltia mj. 2002 Jan 24 [updated 2020 Dec 10]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. 2002 Jan 24 [updated 2020 Dec 10]. In: Adam MP, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2022. PMID: 20301376 Free Books & Documents. Review.
The neuronal ceroid-lipofuscinoses.
Haltia M. Haltia M. J Neuropathol Exp Neurol. 2003 Jan;62(1):1-13. doi: 10.1093/jnen/62.1.1. J Neuropathol Exp Neurol. 2003. PMID: 12528813 Review.
Atelencephaly.
Iivanainen M, Haltia M, Lydecken K. Iivanainen M, et al. Among authors: haltia m. Dev Med Child Neurol. 1977 Oct;19(5):663-8. doi: 10.1111/j.1469-8749.1977.tb08000.x. Dev Med Child Neurol. 1977. PMID: 913906
Human prion diseases.
Haltia M. Haltia M. Ann Med. 2000 Oct;32(7):493-500. doi: 10.3109/07853890009002025. Ann Med. 2000. PMID: 11087170 Review.
Neuronal intranuclear inclusion disease is genetically heterogeneous.
Chen Z, Yan Yau W, Jaunmuktane Z, Tucci A, Sivakumar P, Gagliano Taliun SA, Turner C, Efthymiou S, Ibáñez K, Sullivan R, Bibi F, Athanasiou-Fragkouli A, Bourinaris T, Zhang D, Revesz T, Lashley T, DeTure M, Dickson DW, Josephs KA, Gelpi E, Kovacs GG, Halliday G, Rowe DB, Blair I, Tienari PJ, Suomalainen A, Fox NC, Wood NW, Lees AJ, Haltia MJ; Genomics England Research Consortium, Hardy J, Ryten M, Vandrovcova J, Houlden H. Chen Z, et al. Among authors: haltia mj. Ann Clin Transl Neurol. 2020 Sep;7(9):1716-1725. doi: 10.1002/acn3.51151. Epub 2020 Aug 10. Ann Clin Transl Neurol. 2020. PMID: 32777174 Free PMC article.
Creutzfeld-Jakob disease.
Tarkkanen A, Haltia M. Tarkkanen A, et al. Among authors: haltia m. Trans Ophthalmol Soc U K (1962). 1980 Apr;100(Pt 1):151-4. Trans Ophthalmol Soc U K (1962). 1980. PMID: 7022776
Pirkko Santavuori (1933-2004).
Tyynelä J, Autti T, Haltia M, Mole SE. Tyynelä J, et al. Among authors: haltia m. J Child Neurol. 2004 Jun;19(6):465-70. doi: 10.1177/088307380401900616. J Child Neurol. 2004. PMID: 15446399 No abstract available.
263 results