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
1990 2
1995 1
1996 1
1997 2
2000 1
2001 3
2003 2
2004 2
2006 2
2007 1
2008 3
2009 1
2010 4
2011 2
2012 3
2013 3
2014 3
2015 4
2016 1
2017 1
2018 2
2019 4
2020 2
2021 1
Text availability
Article attribute
Article type
Publication date

Search Results

45 results
Results by year
Filters applied: . Clear all
Page 1
The clinical, histologic, and genotypic spectrum of SEPN1-related myopathy: A case series.
Villar-Quiles RN, von der Hagen M, Métay C, Gonzalez V, Donkervoort S, Bertini E, Castiglioni C, Chaigne D, Colomer J, Cuadrado ML, de Visser M, Desguerre I, Eymard B, Goemans N, Kaindl A, Lagrue E, Lütschg J, Malfatti E, Mayer M, Merlini L, Orlikowski D, Reuner U, Salih MA, Schlotter-Weigel B, Stoetter M, Straub V, Topaloglu H, Urtizberea JA, van der Kooi A, Wilichowski E, Romero NB, Fardeau M, Bönnemann CG, Estournet B, Richard P, Quijano-Roy S, Schara U, Ferreiro A. Villar-Quiles RN, et al. Among authors: reuner u. Neurology. 2020 Sep 15;95(11):e1512-e1527. doi: 10.1212/WNL.0000000000010327. Epub 2020 Aug 13. Neurology. 2020. PMID: 32796131
Pregnancy in Wilson's disease: Management and outcome.
Pfeiffenberger J, Beinhardt S, Gotthardt DN, Haag N, Freissmuth C, Reuner U, Gauss A, Stremmel W, Schilsky ML, Ferenci P, Weiss KH. Pfeiffenberger J, et al. Among authors: reuner u. Hepatology. 2018 Apr;67(4):1261-1269. doi: 10.1002/hep.29490. Epub 2018 Feb 18. Hepatology. 2018. PMID: 28859232
Efficacy and safety of oral chelators in treatment of patients with Wilson disease.
Weiss KH, Thurik F, Gotthardt DN, Schäfer M, Teufel U, Wiegand F, Merle U, Ferenci-Foerster D, Maieron A, Stauber R, Zoller H, Schmidt HH, Reuner U, Hefter H, Trocello JM, Houwen RH, Ferenci P, Stremmel W; EUROWILSON Consortium. Weiss KH, et al. Among authors: reuner u. Clin Gastroenterol Hepatol. 2013 Aug;11(8):1028-35.e1-2. doi: 10.1016/j.cgh.2013.03.012. Epub 2013 Mar 28. Clin Gastroenterol Hepatol. 2013. PMID: 23542331
The interesting case-orphan diseases-double trouble.
Reuner U, Stremmel W, Weiskirchen R. Reuner U, et al. Ann Transl Med. 2019 Apr;7(Suppl 2):S74. doi: 10.21037/atm.2019.04.31. Ann Transl Med. 2019. PMID: 31179311 Free PMC article.
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C gene.
Bonne G, Mercuri E, Muchir A, Urtizberea A, Bécane HM, Recan D, Merlini L, Wehnert M, Boor R, Reuner U, Vorgerd M, Wicklein EM, Eymard B, Duboc D, Penisson-Besnier I, Cuisset JM, Ferrer X, Desguerre I, Lacombe D, Bushby K, Pollitt C, Toniolo D, Fardeau M, Schwartz K, Muntoni F. Bonne G, et al. Among authors: reuner u. Ann Neurol. 2000 Aug;48(2):170-80. Ann Neurol. 2000. PMID: 10939567
Cardiac and autonomic function in patients with Wilson's disease.
Quick S, Reuner U, Weidauer M, Hempel C, Heidrich FM, Mues C, Sveric KM, Ibrahim K, Reichmann H, Linke A, Speiser U. Quick S, et al. Among authors: reuner u. Orphanet J Rare Dis. 2019 Jan 28;14(1):22. doi: 10.1186/s13023-019-1007-7. Orphanet J Rare Dis. 2019. PMID: 30691535 Free PMC article.
Cardiac Manifestation of Wilson's Disease.
Quick S, Weidauer M, Heidrich FM, Sveric K, Reichmann H, Ibrahim K, Strasser RH, Linke A, Speiser U, Reuner U. Quick S, et al. Among authors: reuner u. J Am Coll Cardiol. 2018 Dec 4;72(22):2808-2809. doi: 10.1016/j.jacc.2018.08.2197. J Am Coll Cardiol. 2018. PMID: 30497569 Free article. No abstract available.
Left ventricular clefts - incidental finding or pathologic sign of Wilson's disease?
Zhang K, Reuner U, Weidauer M, Speiser U, Ibrahim K, Christoph M, Heinzel FR, Pieske B, Heidrich FM, Quick S. Zhang K, et al. Among authors: reuner u. Orphanet J Rare Dis. 2019 Nov 7;14(1):244. doi: 10.1186/s13023-019-1238-7. Orphanet J Rare Dis. 2019. PMID: 31699127 Free PMC article. Clinical Trial.
Generation of two induced pluripotent stem cell lines from a female adult homozygous for the Wilson disease associated ATP7B variant p.H1069Q (AKOSi008-A) and a healthy control (AKOSi009-A).
Petters J, Völkner C, Krohn S, Murua Escobar H, Bullerdiek J, Reuner U, Frech MJ, Hermann A, Lukas J. Petters J, et al. Among authors: reuner u. Stem Cell Res. 2020 Dec;49:102079. doi: 10.1016/j.scr.2020.102079. Epub 2020 Nov 5. Stem Cell Res. 2020. PMID: 33197697 Free article.
45 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page