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Results by year

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

Year Number of Results
1950 1
1954 1
1955 3
1956 7
1957 7
1958 4
1960 2
1962 1
1966 1
1968 3
1969 1
1970 2
1971 1
1972 2
1975 1
1978 2
1979 4
1980 6
1981 3
1982 9
1983 6
1984 2
1985 5
1986 3
1987 1
1988 4
1990 4
1992 4
1993 1
1994 2
1996 1
1997 1
1998 2
1999 3
2000 1
2001 1
2002 3
2003 1
2004 3
2005 3
2006 6
2007 10
2008 8
2009 5
2010 7
2011 6
2012 3
2013 1
2014 8
2015 8
2016 2
2017 3
2018 2
2019 4
2020 6
2021 2
2022 7
2023 3
2024 1

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Article type

Publication date

Search Results

194 results

Results by year

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Page 1
The genetic landscape of axonal neuropathies in the middle-aged and elderly: Focus on MME.
Senderek J, Lassuthova P, Kabzińska D, Abreu L, Baets J, Beetz C, Braathen GJ, Brenner D, Dalton J, Dankwa L, Deconinck T, De Jonghe P, Dräger B, Eggermann K, Ellis M, Fischer C, Stojkovic T, Herrmann DN, Horvath R, Høyer H, Iglseder S, Kennerson M, Kinslechner K, Kohler JN, Kurth I, Laing NG, Lamont PJ, Wolfgang N L, Ludolph A, Marques W Jr, Nicholson G, Ong R, Petri S, Ravenscroft G, Rebelo A, Ricci G, Rudnik-Schöneborn S, Schirmacher A, Schlotter-Weigel B, Schoels L, Schüle R, Synofzik M, Francou B, Strom TM, Wagner J, Walk D, Wanschitz J, Weinmann D, Weishaupt J, Wiessner M, Windhager R, Young P, Züchner S, Toegel S, Seeman P, Kochański A, Auer-Grumbach M. Senderek J, et al. Among authors: hoyer h. Neurology. 2020 Dec 15;95(24):e3163-e3179. doi: 10.1212/WNL.0000000000011132. Epub 2020 Nov 3. Neurology. 2020. PMID: 33144514 Free PMC article.
[A.H. Ali et al. respond].
Ali AH, Høyer H, Rugland E, Holmøy T. Ali AH, et al. Among authors: hoyer h. Tidsskr Nor Laegeforen. 2022 Sep 26;142(13). doi: 10.4045/tidsskr.22.0560. Print 2022 Sep 27. Tidsskr Nor Laegeforen. 2022. PMID: 36164790 Free article. Norwegian. No abstract available.
Ca2+-sensitisers--a promising option to treat heart failure?
Brixius K, Hoyer HK, Schwinger RH. Brixius K, et al. Among authors: hoyer hk. Cardiovasc Drugs Ther. 2005 Dec;19(6):423-8. doi: 10.1007/s10557-005-6128-7. Cardiovasc Drugs Ther. 2005. PMID: 16453087 Review.
A woman in her fifties with progressive walking difficulties.
Ali AH, Høyer H, Rugland E, Holmøy T. Ali AH, et al. Among authors: hoyer h. Tidsskr Nor Laegeforen. 2022 Jul 28;142(11). doi: 10.4045/tidsskr.21.0522. Print 2022 Aug 16. Tidsskr Nor Laegeforen. 2022. PMID: 35997187 Free article. English, Norwegian.
Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders.
Olsen CG, Busk ØL, Holla ØL, Tveten K, Holmøy T, Tysnes OB, Høyer H. Olsen CG, et al. Among authors: hoyer h. Amyotroph Lateral Scler Frontotemporal Degener. 2024 Feb;25(1-2):177-187. doi: 10.1080/21678421.2023.2270705. Epub 2024 Jan 23. Amyotroph Lateral Scler Frontotemporal Degener. 2024. PMID: 37849306
Clinical trials in pediatric ALS: a TRICALS feasibility study.
Kliest T, Van Eijk RPA, Al-Chalabi A, Albanese A, Andersen PM, Amador MDM, BrÅthen G, Brunaud-Danel V, Brylev L, Camu W, De Carvalho M, Cereda C, Cetin H, Chaverri D, Chiò A, Corcia P, Couratier P, De Marchi F, Desnuelle C, Van Es MA, Esteban J, Filosto M, GarcÍa Redondo A, Grosskreutz J, Hanemann CO, HolmØy T, HØyer H, Ingre C, Koritnik B, Kuzma-Kozakiewicz M, Lambert T, Leigh PN, Lunetta C, Mandrioli J, Mcdermott CJ, Meyer T, Mora JS, Petri S, Povedano M, Reviers E, Riva N, Roes KCB, Rubio MÁ, Salachas F, Sarafov S, SorarÙ G, Stevic Z, Svenstrup K, MØller AT, Turner MR, Van Damme P, Van Leeuwen LAG, Varona L, VÁzquez Costa JF, Weber M, Hardiman O, Van Den Berg LH. Kliest T, et al. Among authors: hoyer h. Amyotroph Lateral Scler Frontotemporal Degener. 2022 Nov;23(7-8):481-488. doi: 10.1080/21678421.2021.2024856. Epub 2022 Feb 16. Amyotroph Lateral Scler Frontotemporal Degener. 2022. PMID: 35172656 Free PMC article.
HINT1 neuropathy in Norway: clinical, genetic and functional profiling.
Amor-Barris S, Høyer H, Brauteset LV, De Vriendt E, Strand L, Jordanova A, Braathen GJ, Peeters K. Amor-Barris S, et al. Among authors: hoyer h. Orphanet J Rare Dis. 2021 Mar 4;16(1):116. doi: 10.1186/s13023-021-01746-z. Orphanet J Rare Dis. 2021. PMID: 33663550 Free PMC article.
A polymorphic AT-repeat causes frequent allele dropout for an MME mutational hotspot exon.
Høyer H, Hilmarsen HT, Sunder-Plassmann R, Braathen GJ, Andersen PM, Beetz C, Hacker S, Holla ØL, Kurth I, Löscher WN, Reiter SBCF, Rudnik-Schöneborn S, Strand L, Windhager R, Witsch-Baumgartner M, Senderek J, Auer-Grumbach M. Høyer H, et al. J Med Genet. 2022 Oct;59(10):1024-1026. doi: 10.1136/jmedgenet-2021-108281. Epub 2022 Mar 22. J Med Genet. 2022. PMID: 35318247 Free PMC article. No abstract available.
194 results