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

Year Number of Results
2002 4
2003 1
2004 3
2005 2
2006 2
2007 5
2008 3
2009 4
2010 1
2011 2
2012 2
2013 4
2014 4
2015 5
2016 3
2017 2
2018 5
2019 2
2020 5
2021 2
2022 10
2023 5
2024 4

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69 results

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Page 1
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita.
Laquerriere A, Jaber D, Abiusi E, Maluenda J, Mejlachowicz D, Vivanti A, Dieterich K, Stoeva R, Quevarec L, Nolent F, Biancalana V, Latour P, Sternberg D, Capri Y, Verloes A, Bessieres B, Loeuillet L, Attie-Bitach T, Martinovic J, Blesson S, Petit F, Beneteau C, Whalen S, Marguet F, Bouligand J, Héron D, Viot G, Amiel J, Amram D, Bellesme C, Bucourt M, Faivre L, Jouk PS, Khung S, Sigaudy S, Delezoide AL, Goldenberg A, Jacquemont ML, Lambert L, Layet V, Lyonnet S, Munnich A, Van Maldergem L, Piard J, Guimiot F, Landrieu P, Letard P, Pelluard F, Perrin L, Saint-Frison MH, Topaloglu H, Trestard L, Vincent-Delorme C, Amthor H, Barnerias C, Benachi A, Bieth E, Boucher E, Cormier-Daire V, Delahaye-Duriez A, Desguerre I, Eymard B, Francannet C, Grotto S, Lacombe D, Laffargue F, Legendre M, Martin-Coignard D, Mégarbané A, Mercier S, Nizon M, Rigonnot L, Prieur F, Quélin C, Ranjatoelina-Randrianaivo H, Resta N, Toutain A, Verhelst H, Vincent M, Colin E, Fallet-Bianco C, Granier M, Grigorescu R, Saada J, Gonzales M, Guiochon-Mantel A, Bessereau JL, Tawk M, Gut I, Gitiaux C, Melki J. Laquerriere A, et al. Among authors: sternberg d. J Med Genet. 2022 Jun;59(6):559-567. doi: 10.1136/jmedgenet-2020-107595. Epub 2021 Apr 5. J Med Genet. 2022. PMID: 33820833 Free PMC article.
Beta-blocker-induced quadriparesis.
Izzedine H, Launay-Vacher V, Hulot JS, Sternberg D, Deray G. Izzedine H, et al. Among authors: sternberg d. Ann Intern Med. 2004 Aug 17;141(4):W62. doi: 10.7326/0003-4819-141-4-200408170-00028-w1. Ann Intern Med. 2004. PMID: 15313766 No abstract available.
Physiological and Pathophysiological Insights of Nav1.4 and Nav1.5 Comparison.
Loussouarn G, Sternberg D, Nicole S, Marionneau C, Le Bouffant F, Toumaniantz G, Barc J, Malak OA, Fressart V, Péréon Y, Baró I, Charpentier F. Loussouarn G, et al. Among authors: sternberg d. Front Pharmacol. 2016 Jan 14;6:314. doi: 10.3389/fphar.2015.00314. eCollection 2015. Front Pharmacol. 2016. PMID: 26834636 Free PMC article. Review.
[The high phenotypic variability of RYR1 gene mutations].
Islam Kediha M, Nouioua S, Tazir M, Sternberg D, Lunardi J, Ali Pacha L. Islam Kediha M, et al. Among authors: sternberg d. Med Sci (Paris). 2022 Dec;38 Hors série n° 1:46-48. doi: 10.1051/medsci/2022178. Epub 2023 Jan 16. Med Sci (Paris). 2022. PMID: 36649637 Free article. French.
New mutation in the β1 propeller domain of LRP4 responsible for congenital myasthenic syndrome associated with Cenani-Lenz syndrome.
Masingue M, Cattaneo O, Wolff N, Buon C, Sternberg D, Euchparmakian M, Boex M, Behin A, Mamchaouhi K, Maisonobe T, Nougues MC, Isapof A, Fontaine B, Messéant J, Eymard B, Strochlic L, Bauché S. Masingue M, et al. Among authors: sternberg d. Sci Rep. 2023 Aug 28;13(1):14054. doi: 10.1038/s41598-023-41008-5. Sci Rep. 2023. PMID: 37640745 Free PMC article.
Severe congenital myasthenic syndromes caused by agrin mutations affecting secretion by motoneurons.
Jacquier A, Risson V, Simonet T, Roussange F, Lacoste N, Ribault S, Carras J, Theuriet J, Girard E, Grosjean I, Le Goff L, Kröger S, Meltoranta J, Bauché S, Sternberg D, Fournier E, Kostera-Pruszczyk A, O'Connor E, Eymard B, Lochmüller H, Martinat C, Schaeffer L. Jacquier A, et al. Among authors: sternberg d. Acta Neuropathol. 2022 Oct;144(4):707-731. doi: 10.1007/s00401-022-02475-8. Epub 2022 Aug 10. Acta Neuropathol. 2022. PMID: 35948834 Free PMC article.
Brody myopathy demonstrates a pseudo-increment on repetitive nerve stimulation.
Masingue M, Arzel M, Sternberg D, Stojkovic T, Behin A, Bassez G, Vicart S, Péréon Y, Magot A, Kuntzer T, Eymard B, Fournier E. Masingue M, et al. Among authors: sternberg d. Muscle Nerve. 2020 Apr;61(4):491-495. doi: 10.1002/mus.26809. Epub 2020 Jan 22. Muscle Nerve. 2020. PMID: 31944327
[Congenital myasthenic syndromes; French experience].
Eymard B, Hantaï D, Fournier E, Nicole S, Sternberg D, Richard P, Fardeau M. Eymard B, et al. Among authors: sternberg d. Bull Acad Natl Med. 2014 Feb;198(2):257-70; discussion 270-1. Bull Acad Natl Med. 2014. PMID: 26263703 Review. French.
Diagnostic yield of a practical electrodiagnostic protocol discriminating between different congenital myasthenic syndromes.
Stojkovic T, Masingue M, Turmel H, Hezode-Arzel M, Béhin A, Leonard-Louis S, Bassez G, Bauché S, Blondy P, Richard P, Sternberg D, Eymard B, Fournier E, Villar-Quiles RN. Stojkovic T, et al. Among authors: sternberg d. Neuromuscul Disord. 2022 Dec;32(11-12):870-878. doi: 10.1016/j.nmd.2022.10.001. Epub 2022 Oct 9. Neuromuscul Disord. 2022. PMID: 36522822
69 results