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

Year Number of Results
1998 1
2002 1
2003 2
2004 2
2005 5
2006 4
2008 1
2009 5
2010 4
2011 5
2012 6
2013 4
2014 1
2015 3
2016 3
2017 4
2018 7
2019 8
2020 4
2021 8
2022 6
2023 7
2024 1

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84 results

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Page 1
Obituary.
Romero NB, Urtizberea JA, Quijano-Roy S. Romero NB, et al. Among authors: urtizberea ja. Neuromuscul Disord. 2024 Apr 1;38:42-43. doi: 10.1016/j.nmd.2024.03.008. Online ahead of print. Neuromuscul Disord. 2024. PMID: 38564999 No abstract available.
The new missense G376V-TDP-43 variant induces late-onset distal myopathy but not amyotrophic lateral sclerosis.
Zibold J, Lessard LER, Picard F, da Silva LG, Zadorozhna Y, Streichenberger N, Belotti E, Osseni A, Emerit A, Errazuriz-Cerda E, Michel-Calemard L, Menassa R, Coudert L, Wiessner M, Stucka R, Klopstock T, Simonetti F, Hutten S, Nonaka T, Hasegawa M, Strom TM, Bernard E, Ollagnon E, Urtizberea A, Dormann D, Petiot P, Schaeffer L, Senderek J, Leblanc P. Zibold J, et al. Among authors: urtizberea a. Brain. 2023 Dec 11:awad410. doi: 10.1093/brain/awad410. Online ahead of print. Brain. 2023. PMID: 38079474
Gene therapies in pediatrics.
Andoni Urtizberea J. Andoni Urtizberea J. Arch Pediatr. 2023 Nov;30(8S1):8S1. doi: 10.1016/S0929-693X(23)00220-8. Arch Pediatr. 2023. PMID: 38043976 No abstract available.
[The Schwartz-Jampel syndrome].
Urtizberea JA, Severa G, Ropars J, Malfatti E. Urtizberea JA, et al. Med Sci (Paris). 2023 Nov;39 Hors série n° 1:37-46. doi: 10.1051/medsci/2023133. Epub 2023 Nov 17. Med Sci (Paris). 2023. PMID: 37975769 French.
[The Second Baltic School of Neuromyology].
Andoni Urtizberea J, Malfatti E, Carlier PG. Andoni Urtizberea J, et al. Med Sci (Paris). 2022 Dec;38 Hors série n° 1:49-51. doi: 10.1051/medsci/2022183. Epub 2023 Jan 16. Med Sci (Paris). 2022. PMID: 36649638 Free article. French.
[Therapeutic innovation at all costs?].
Andoni Urtizberea J. Andoni Urtizberea J. Med Sci (Paris). 2022 Dec;38 Hors série n° 1:5. doi: 10.1051/medsci/2022174. Epub 2023 Jan 16. Med Sci (Paris). 2022. PMID: 36649627 Free article. French. No abstract available.
STAC3 related congenital myopathy: A case series of seven Comorian patients.
Gromand M, Gueguen P, Pervillé A, Ferroul F, Morel G, Harouna A, Doray B, Urtizberea JA, Alessandri JL, Robin S. Gromand M, et al. Among authors: urtizberea ja. Eur J Med Genet. 2022 Oct;65(10):104598. doi: 10.1016/j.ejmg.2022.104598. Epub 2022 Aug 25. Eur J Med Genet. 2022. PMID: 36030003
84 results