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

Year Number of Results
1997 1
1998 1
2001 1
2003 3
2004 1
2005 2
2006 3
2007 2
2008 1
2009 2
2010 2
2012 1
2013 1
2014 2
2015 1
2016 2
2017 3
2018 4
2019 1
2020 2
2021 3
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35 results
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Page 1
Screening for Fabry disease and Hereditary ATTR amyloidosis in idiopathic small-fiber and mixed neuropathy.
Samuelsson K, Radovic A, Press R, Auranen M, Ylikallio E, Tyynismaa H, KäRppä M, Veteläinen M, Peltola N, Mellgren SI, Mygland Å, Tallaksen C, Andersen H, Terkelsen AJ, Fontain F, Hietaharju A. Samuelsson K, et al. Among authors: karppa m. Muscle Nerve. 2019 Mar;59(3):354-357. doi: 10.1002/mus.26348. Epub 2018 Dec 4. Muscle Nerve. 2019. PMID: 30246259
Amyloid myopathy: a diagnostic challenge.
Tuomaala H, Kärppä M, Tuominen H, Remes AM. Tuomaala H, et al. Among authors: karppa m. Neurol Int. 2009 Nov 16;1(1):e7. doi: 10.4081/ni.2009.e7. Neurol Int. 2009. PMID: 21577365 Free PMC article.
Variants p.Q1236H and p.E1143G in mitochondrial DNA polymerase gamma POLG1 are not associated with increased risk for valproate-induced hepatotoxicity or pancreatic toxicity: A retrospective cohort study of patients with epilepsy.
Hynynen J, Pokka T, Komulainen-Ebrahim J, Myllynen P, Kärppä M, Pylvänen L, Kälviäinen R, Sokka A, Jyrkilä A, Lähdetie J, Haataja L, Mäkitalo A, Ylikotila P, Eriksson K, Haapala P, Ansakorpi H, Hinttala R, Vieira P, Majamaa K, Rantala H, Uusimaa J. Hynynen J, et al. Among authors: karppa m. Epilepsia. 2018 Nov;59(11):2125-2136. doi: 10.1111/epi.14568. Epub 2018 Sep 26. Epilepsia. 2018. PMID: 30255931
Atypical phenotypes in titinopathies explained by second titin mutations.
Evilä A, Vihola A, Sarparanta J, Raheem O, Palmio J, Sandell S, Eymard B, Illa I, Rojas-Garcia R, Hankiewicz K, Negrão L, Löppönen T, Nokelainen P, Kärppä M, Penttilä S, Screen M, Suominen T, Richard I, Hackman P, Udd B. Evilä A, et al. Among authors: karppa m. Ann Neurol. 2014 Feb;75(2):230-40. doi: 10.1002/ana.24102. Epub 2014 Feb 24. Ann Neurol. 2014. PMID: 24395473
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