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Page 1
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Wein N, Vulin A, Falzarano MS, Szigyarto CA, Maiti B, Findlay A, Heller KN, Uhlén M, Bakthavachalu B, Messina S, Vita G, Passarelli C, Gualandi F, Wilton SD, Rodino-Klapac LR, Yang L, Dunn DM, Schoenberg DR, Weiss RB, Howard MT, Ferlini A, Flanigan KM. Wein N, et al. Among authors: szigyarto ca. Nat Med. 2015 Apr;21(4):414. doi: 10.1038/nm0415-414b. Nat Med. 2015. PMID: 25849273 No abstract available.
Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Wein N, Vulin A, Falzarano MS, Szigyarto CA, Maiti B, Findlay A, Heller KN, Uhlén M, Bakthavachalu B, Messina S, Vita G, Passarelli C, Brioschi S, Bovolenta M, Neri M, Gualandi F, Wilton SD, Rodino-Klapac LR, Yang L, Dunn DM, Schoenberg DR, Weiss RB, Howard MT, Ferlini A, Flanigan KM. Wein N, et al. Among authors: szigyarto ca. Nat Med. 2014 Sep;20(9):992-1000. doi: 10.1038/nm.3628. Epub 2014 Aug 10. Nat Med. 2014. PMID: 25108525 Free PMC article.
Corrigendum: Translation from a DMD exon 5 IRES results in a functional dystrophin isoform that attenuates dystrophinopathy in humans and mice.
Wein N, Vulin A, Falzarano MS, Szigyarto CA, Maiti B, Findlay A, Heller KN, Uhlén M, Bakthavachalu B, Messina S, Vita G, Passarelli C, Brioschi S, Bovolenta M, Neri M, Gualandi F, Wilton SD, Rodino-Klapac LR, Yang L, Dunn DM, Schoenberg DR, Weiss RB, Howard MT, Ferlini A, Flanigan KM. Wein N, et al. Among authors: szigyarto ca. Nat Med. 2015 May;21(5):537. doi: 10.1038/nm0515-537c. Nat Med. 2015. PMID: 25951531 No abstract available.
Rimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy.
Previtali SC, Gidaro T, Díaz-Manera J, Zambon A, Carnesecchi S, Roux-Lombard P, Spitali P, Signorelli M, Szigyarto CA, Johansson C, Gray J, Labolle D, Porte Thomé F, Pitchforth J, Domingos J, Muntoni F. Previtali SC, et al. Among authors: szigyarto ca. Pharmacol Res. 2020 Sep;159:104999. doi: 10.1016/j.phrs.2020.104999. Epub 2020 Jun 12. Pharmacol Res. 2020. PMID: 32535224 Free PMC article. Clinical Trial.
Blood-derived biomarkers correlate with clinical progression in Duchenne muscular dystrophy.
Strandberg K, Ayoglu B, Roos A, Reza M, Niks E, Signorelli M, Fasterius E, Pontén F, Lochmüller H, Domingos J, Ala P, Muntoni F, Aartsma-Rus A, Spitali P, Nilsson P, Szigyarto CA. Strandberg K, et al. Among authors: szigyarto ca. J Neuromuscul Dis. 2020;7(3):231-246. doi: 10.3233/JND-190454. J Neuromuscul Dis. 2020. PMID: 32390640 Free PMC article.
Enhanced validation of antibodies for research applications.
Edfors F, Hober A, Linderbäck K, Maddalo G, Azimi A, Sivertsson Å, Tegel H, Hober S, Szigyarto CA, Fagerberg L, von Feilitzen K, Oksvold P, Lindskog C, Forsström B, Uhlen M. Edfors F, et al. Among authors: szigyarto ca. Nat Commun. 2018 Oct 8;9(1):4130. doi: 10.1038/s41467-018-06642-y. Nat Commun. 2018. PMID: 30297845 Free PMC article.
Biomarkers of Duchenne muscular dystrophy: current findings.
Szigyarto CA, Spitali P. Szigyarto CA, et al. Degener Neurol Neuromuscul Dis. 2018 Jan 25;8:1-13. doi: 10.2147/DNND.S121099. eCollection 2018. Degener Neurol Neuromuscul Dis. 2018. PMID: 30050384 Free PMC article. Review.
226th ENMC International Workshop:: Towards validated and qualified biomarkers for therapy development for Duchenne muscular dystrophy 20-22 January 2017, Heemskerk, The Netherlands.
Aartsma-Rus A, Ferlini A, McNally EM, Spitali P, Sweeney HL; workshop participants. Aartsma-Rus A, et al. Neuromuscul Disord. 2018 Jan;28(1):77-86. doi: 10.1016/j.nmd.2017.10.002. Epub 2017 Oct 26. Neuromuscul Disord. 2018. PMID: 29203356 Free PMC article. No abstract available.
22 results