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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
2023 1
2024 2

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151 results

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Page 1
[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.
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.
[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.
Large-Scale Screening: Phenotypic and Mutational Spectrum in Isolated and Combined Dystonia Genes.
Thomsen M, Marth K, Loens S, Everding J, Junker J, Borngräber F, Ott F, Jesús S, Gelderblom M, Odorfer T, Kuhlenbäumer G, Kim HJ, Schaeffer E, Becktepe J, Kasten M, Brüggemann N, Pfister R, Kollewe K, Krauss JK, Lohmann E, Hinrichs F, Berg D, Jeon B, Busch H, Altenmüller E, Mir P, Kamm C, Volkmann J, Zittel S, Ferbert A, Zeuner KE, Rolfs A, Bauer P, Kühn AA, Bäumer T, Klein C, Lohmann K. Thomsen M, et al. Among authors: ferbert a. Mov Disord. 2024 Mar;39(3):526-538. doi: 10.1002/mds.29693. Epub 2024 Jan 12. Mov Disord. 2024. PMID: 38214203
Myelin protein zero mutation-related hereditary neuropathies: Neuropathological insight from a new nerve biopsy cohort.
Bremer J, Meinhardt A, Katona I, Senderek J, Kämmerer-Gassler EK, Roos A, Ferbert A, Schröder JM, Nikolin S, Nolte K, Sellhaus B, Popzhelyazkova K, Tacke F, Schara-Schmidt U, Neuen-Jacob E, de Groote CC, de Jonghe P, Timmerman V, Baets J, Weis J. Bremer J, et al. Among authors: ferbert a. Brain Pathol. 2024 Jan;34(1):e13200. doi: 10.1111/bpa.13200. Epub 2023 Aug 15. Brain Pathol. 2024. PMID: 37581289 Free PMC article.
The complete apallic syndrome--a case report.
Biniek R, Ferbert A, Rimpel J, Paepke U, Berns TH, Schuchardt V, Heitmann R. Biniek R, et al. Among authors: ferbert a. Intensive Care Med. 1989;15(3):212-5. doi: 10.1007/BF01058577. Intensive Care Med. 1989. PMID: 2661617 Review.
Role of ANO3 mutations in dystonia: A large-scale mutational screening study.
Olschewski L, Jesús S, Kim HJ, Tunc S, Löns S, Junker J, Zeuner KE, Kühn AA, Kuhlenbäumer G, Schäffer E, Berg D, Kasten M, Ferbert A, Altenmüller E, Brüggemann N, Bauer P, Rolfs A, Jeon B, Bäumer T, Mir P, Klein C, Lohmann K. Olschewski L, et al. Among authors: ferbert a. Parkinsonism Relat Disord. 2019 May;62:196-200. doi: 10.1016/j.parkreldis.2018.12.030. Epub 2019 Jan 2. Parkinsonism Relat Disord. 2019. PMID: 30712998
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.
151 results