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

Year Number of Results
1984 1
1985 4
1986 4
1987 6
1988 6
1989 5
1990 4
1991 8
1992 14
1993 6
1994 1
1995 3
1996 6
1997 1
1998 8
1999 4
2000 3
2001 2
2002 1
2003 1
2005 1
2006 1
2007 2
2008 1
2009 3
2010 4
2011 6
2012 5
2013 7
2014 8
2015 6
2016 14
2017 6
2018 2
2019 3
2020 3
2022 0
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Article type
Publication date

Search Results

149 results
Results by year
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Page 1
Sporadic late-onset nemaline myopathy: clinico-pathological characteristics and review of 76 cases.
Schnitzler LJ, Schreckenbach T, Nadaj-Pakleza A, Stenzel W, Rushing EJ, Van Damme P, Ferbert A, Petri S, Hartmann C, Bornemann A, Meisel A, Petersen JA, Tousseyn T, Thal DR, Reimann J, De Jonghe P, Martin JJ, Van den Bergh PY, Schulz JB, Weis J, Claeys KG. Schnitzler LJ, et al. Among authors: ferbert a. Orphanet J Rare Dis. 2017 May 11;12(1):86. doi: 10.1186/s13023-017-0640-2. Orphanet J Rare Dis. 2017. PMID: 28490364 Free PMC article. Review.
[Hereditary Polyneuropathies].
Ferbert A, Roth C. Ferbert A, et al. Fortschr Neurol Psychiatr. 2020 Mar;88(3):198-209. doi: 10.1055/a-1009-2270. Epub 2020 Mar 31. Fortschr Neurol Psychiatr. 2020. PMID: 32232809 Review. German.
[Spontaneous intracranial hypotension and Marfan syndrome].
Apetroae A, Strenzke T, Ferbert A, Schellinger PD. Apetroae A, et al. Among authors: ferbert a. Nervenarzt. 2016 Aug;87(8):846-52. doi: 10.1007/s00115-016-0126-9. Nervenarzt. 2016. PMID: 27278058 Review. German.
[Diseases due to alcoholism].
Nagel M, Ferbert A. Nagel M, et al. Among authors: ferbert a. Fortschr Neurol Psychiatr. 2005 Aug;73(8):470-82; quiz 483-4. doi: 10.1055/s-2004-830191. Fortschr Neurol Psychiatr. 2005. PMID: 16052441 Review. German. No abstract available.
Differential diagnosis of vacuolar myopathies in the NGS era.
Mair D, Biskup S, Kress W, Abicht A, Brück W, Zechel S, Knop KC, Koenig FB, Tey S, Nikolin S, Eggermann K, Kurth I, Ferbert A, Weis J. Mair D, et al. Among authors: ferbert a. Brain Pathol. 2020 Sep;30(5):877-896. doi: 10.1111/bpa.12864. Epub 2020 Jun 15. Brain Pathol. 2020. PMID: 32419263 Free PMC article.
[Type I neurofibromatosis and megadolichobasilar artery].
Roth C, Gaiser T, Nagelmeier I, Rüschoff J, Ferbert A. Roth C, et al. Among authors: ferbert a. Nervenarzt. 2007 Oct;78(10):1195-9. doi: 10.1007/s00115-007-2263-7. Nervenarzt. 2007. PMID: 17492421 Review. German.
Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.
Lohmann K, Wilcox RA, Winkler S, Ramirez A, Rakovic A, Park JS, Arns B, Lohnau T, Groen J, Kasten M, Brüggemann N, Hagenah J, Schmidt A, Kaiser FJ, Kumar KR, Zschiedrich K, Alvarez-Fischer D, Altenmüller E, Ferbert A, Lang AE, Münchau A, Kostic V, Simonyan K, Agzarian M, Ozelius LJ, Langeveld AP, Sue CM, Tijssen MA, Klein C. Lohmann K, et al. Among authors: ferbert a. Ann Neurol. 2013 Apr;73(4):537-45. doi: 10.1002/ana.23829. Epub 2013 Apr 17. Ann Neurol. 2013. PMID: 23595291 Free PMC article.
149 results