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
2008 1
2009 1
2010 1
2014 2
2015 2
2016 2
2017 2
2018 1
2019 2
2021 0
Text availability
Article attribute
Article type
Publication date

Search Results

12 results
Results by year
Filters applied: . Clear all
Page 1
FGF-21 as a Potential Biomarker for Mitochondrial Diseases.
Scholle LM, Lehmann D, Deschauer M, Kraya T, Zierz S. Scholle LM, et al. Among authors: lehmann d. Curr Med Chem. 2018;25(18):2070-2081. doi: 10.2174/0929867325666180111094336. Curr Med Chem. 2018. PMID: 29332568 Review.
Camptocormia and shuffling gait due to a novel MT-TV mutation: Diagnostic pitfalls.
Reimann J, Lehmann D, Hardy SA, Falkous G, Knowles CV, Jones RL, Kunz WS, Taylor RW, Kornblum C. Reimann J, et al. Among authors: lehmann d. Neurol Genet. 2017 Apr 5;3(3):e147. doi: 10.1212/NXG.0000000000000147. eCollection 2017 Jun. Neurol Genet. 2017. PMID: 28396884 Free PMC article. No abstract available.
Expanded phenotypic spectrum of the m.8344A>G "MERRF" mutation: data from the German mitoNET registry.
Altmann J, Büchner B, Nadaj-Pakleza A, Schäfer J, Jackson S, Lehmann D, Deschauer M, Kopajtich R, Lautenschläger R, Kuhn KA, Karle K, Schöls L, Schulz JB, Weis J, Prokisch H, Kornblum C, Claeys KG, Klopstock T. Altmann J, et al. Among authors: lehmann d. J Neurol. 2016 May;263(5):961-972. doi: 10.1007/s00415-016-8086-3. Epub 2016 Mar 19. J Neurol. 2016. PMID: 26995359
12 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page