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

Year Number of Results
2004 1
2005 4
2006 5
2007 3
2008 2
2009 2
2010 3
2011 2
2012 4
2013 3
2014 4
2015 2
2016 3
2017 7
2018 6
2019 5
2020 2
2021 4
2022 1
2023 7
2024 2

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62 results

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Page 1
Analysis of Inherited Optic Neuropathies.
Lazdinyte S, Schorderet DF, Schaller A, Valmaggia C, Todorova MG. Lazdinyte S, et al. Among authors: schaller a. Klin Monbl Augenheilkd. 2019 Apr;236(4):451-461. doi: 10.1055/a-0829-6828. Epub 2019 Mar 4. Klin Monbl Augenheilkd. 2019. PMID: 30831606 English.
Late-onset severe long QT syndrome.
Asatryan B, Schaller A, Bartholdi D, Medeiros-Domingo A. Asatryan B, et al. Among authors: schaller a. Ann Noninvasive Electrocardiol. 2018 Jul;23(4):e12517. doi: 10.1111/anec.12517. Epub 2017 Nov 30. Ann Noninvasive Electrocardiol. 2018. PMID: 29194874 Free PMC article.
Biallelic variants in DNA2 cause poikiloderma with congenital cataracts and severe growth failure reminiscent of Rothmund-Thomson syndrome.
Di Lazzaro Filho R, Yamamoto GL, Silva TJ, Rocha LA, Linnenkamp BDW, Castro MAA, Bartholdi D, Schaller A, Leeb T, Kelmann S, Utagawa CY, Steiner CE, Steinmetz L, Honjo RS, Kim CA, Wang L, Abourjaili-Bilodeau R, Campeau PM, Warman M, Passos-Bueno MR, Hoch NC, Bertola DR. Di Lazzaro Filho R, et al. Among authors: schaller a. J Med Genet. 2023 Nov;60(11):1127-1132. doi: 10.1136/jmg-2022-109119. Epub 2023 Apr 13. J Med Genet. 2023. PMID: 37055165
Phenotypic Spectrum of HCN4 Mutations: A Clinical Case.
Servatius H, Porro A, Pless SA, Schaller A, Asatryan B, Tanner H, de Marchi SF, Roten L, Seiler J, Haeberlin A, Baldinger SH, Noti F, Lam A, Fuhrer J, Moroni A, Medeiros-Domingo A. Servatius H, et al. Among authors: schaller a. Circ Genom Precis Med. 2018 Feb;11(2):e002033. doi: 10.1161/CIRCGEN.117.002033. Circ Genom Precis Med. 2018. PMID: 29440115 Free article. No abstract available.
Triheptanoin - Novel therapeutic approach for the ultra-rare disease mitochondrial malate dehydrogenase deficiency.
Laemmle A, Steck AL, Schaller A, Kurth S, Perret Hoigné E, Felser AD, Slavova N, Salvisberg C, Atencio M, Mochel F, Nuoffer JM, Gautschi M. Laemmle A, et al. Among authors: schaller a. Mol Genet Metab Rep. 2021 Oct 19;29:100814. doi: 10.1016/j.ymgmr.2021.100814. eCollection 2021 Dec. Mol Genet Metab Rep. 2021. PMID: 34712577 Free PMC article.
62 results