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
1999 1
2000 1
2003 1
2004 2
2005 2
2006 2
2007 7
2008 3
2009 8
2010 6
2011 6
2012 7
2013 4
2014 11
2015 6
2016 10
2017 6
2018 11
2019 7
2020 9
2021 4
Text availability
Article attribute
Article type
Publication date

Search Results

104 results
Results by year
Filters applied: . Clear all
Page 1
Mitochondrial diseases.
Molnar MJ, Kovacs GG. Molnar MJ, et al. Handb Clin Neurol. 2017;145:147-155. doi: 10.1016/B978-0-12-802395-2.00010-9. Handb Clin Neurol. 2017. PMID: 28987165 Review.
The Panomics Approach in Neurodegenerative Disorders.
Szatmari B, Balicza P, Nemeth G, Molnar MJ. Szatmari B, et al. Among authors: molnar mj. Curr Med Chem. 2019;26(10):1712-1720. doi: 10.2174/0929867324666170705120038. Curr Med Chem. 2019. PMID: 28685677 Review.
Wernicke-Korsakoff syndrome associated with mtDNA disease.
Jimoh IJ, Sebe B, Balicza P, Fedor M, Pataky I, Rudas G, Gal A, Inczedy-Farkas G, Nemeth G, Molnar MJ. Jimoh IJ, et al. Among authors: molnar mj. Ther Adv Neurol Disord. 2020 Jul 30;13:1756286420938972. doi: 10.1177/1756286420938972. eCollection 2020. Ther Adv Neurol Disord. 2020. PMID: 32821290 Free PMC article.
Ethnicity-related DMD Genotype Landscapes in European and Non-European Countries.
Selvatici R, Rossi R, Fortunato F, Trabanelli C, Sifi Y, Margutti A, Neri M, Gualandi F, Szabò L, Fekete B, Angelova L, Litvinenko I, Ivanov I, Vildan Y, Iuhas OA, Vintan M, Burloiu C, Lacramioara B, Visa G, Epure D, Rusu C, Vasile D, Sandu M, Vlodavets D, Mager M, Kyriakides T, Delin S, Lehman I, Fureš JS, Bojinova V, Militaru M, Guergueltcheva V, Burnyte B, Molnar MJ, Butoianu N, Bensemmane SD, Makri-Mokrane S, Herczegfalvi A, Panzaru M, Emandi AC, Lusakowska A, Potulska-Chromik A, Kostera-Pruszczyk A, Shatillo A, Khelladi DB, Dendane O, Fang M, Lu Z, Ferlini A. Selvatici R, et al. Among authors: molnar mj. Neurol Genet. 2020 Dec 24;7(1):e536. doi: 10.1212/NXG.0000000000000536. eCollection 2021 Feb. Neurol Genet. 2020. PMID: 33376799 Free PMC article.
A new family with transportinopathy: increased clinical heterogeneity.
Angelini C, Marozzo R, Pinzan E, Pegoraro V, Molnar MJ, Torella A, Nigro V. Angelini C, et al. Among authors: molnar mj. Ther Adv Neurol Disord. 2019 Jun 9;12:1756286419850433. doi: 10.1177/1756286419850433. eCollection 2019. Ther Adv Neurol Disord. 2019. PMID: 31217819 Free PMC article.
Broadening the phenotype of the TWNK gene associated Perrault syndrome.
Fekete B, Pentelényi K, Rudas G, Gál A, Grosz Z, Illés A, Idris J, Csukly G, Domonkos A, Molnar MJ. Fekete B, et al. Among authors: molnar mj. BMC Med Genet. 2019 Dec 18;20(1):198. doi: 10.1186/s12881-019-0934-4. BMC Med Genet. 2019. PMID: 31852434 Free PMC article.
104 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page