Nasser GA - Search Results

1

An unstable triplet repeat in a gene related to myotonic muscular dystrophy.

Fu YH, Pizzuti A, Fenwick RG Jr, King J, Rajnarayan S, Dunne PW, Dubel J, Nasser GA, Ashizawa T, de Jong P, et al. Fu YH, et al. Among authors: nasser ga. Science. 1992 Mar 6;255(5049):1256-8. doi: 10.1126/science.1546326. Science. 1992. PMID: 1546326

2

Nicotine patch therapy in smoking cessation reduces the extent of exercise-induced myocardial ischemia.

Mahmarian JJ, Moyé LA, Nasser GA, Nagueh SF, Bloom MF, Benowitz NL, Verani MS, Byrd WG, Pratt CM. Mahmarian JJ, et al. Among authors: nasser ga. J Am Coll Cardiol. 1997 Jul;30(1):125-30. doi: 10.1016/s0735-1097(97)00128-9. J Am Coll Cardiol. 1997. PMID: 9207632 Free article.

3

Acute-Onset Ataxia and Transient Cerebellar Diffusion Restriction Associated with a PRRT2 Mutation.

Legris N, Chassin O, Nasser G, Riant F, Tournier-Lasserve E, Denier C. Legris N, et al. J Stroke Cerebrovasc Dis. 2019 Feb;28(2):e3-e4. doi: 10.1016/j.jstrokecerebrovasdis.2018.10.021. Epub 2018 Nov 28. J Stroke Cerebrovasc Dis. 2019. PMID: 30501978

4

Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature review.

Osman O, Labrune P, Reiner P, Sarov M, Nasser G, Riant F, Tournier-Lasserve E, Chabriat H, Denier C. Osman O, et al. Rev Neurol (Paris). 2020 Mar;176(3):170-179. doi: 10.1016/j.neurol.2019.06.006. Epub 2019 Sep 11. Rev Neurol (Paris). 2020. PMID: 31521395 Review.

5

Familial acute necrotizing encephalopathy due to mutation in the RANBP2 gene.

Denier C, Balu L, Husson B, Nasser G, Burglen L, Rodriguez D, Labauge P, Chevret L. Denier C, et al. J Neurol Sci. 2014 Oct 15;345(1-2):236-8. doi: 10.1016/j.jns.2014.07.025. Epub 2014 Jul 18. J Neurol Sci. 2014. PMID: 25128471

6

Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1.

Rerat K, Parker F, Nasser G, Vidaud D, Riant F, Tournier-Lasserve E, Denier C. Rerat K, et al. J Neurol Sci. 2015 Mar 15;350(1-2):98-100. doi: 10.1016/j.jns.2015.02.023. Epub 2015 Feb 18. J Neurol Sci. 2015. PMID: 25702150

7

Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene.

Bisserbe A, Tertian G, Buffet C, Turhan A, Lambotte O, Nasser G, Alvin P, Tardieu M, Riant F, Bergametti F, Tournier-Lasserve E, Denier C. Bisserbe A, et al. Rev Neurol (Paris). 2015 May;171(5):445-9. doi: 10.1016/j.neurol.2015.01.566. Epub 2015 Apr 2. Rev Neurol (Paris). 2015. PMID: 25843205

8

Congenital vertebral duplication: a predisposing risk factor for dissection.

Melki E, Nasser G, Vandendries C, Adams D, Ducreux D, Denier C. Melki E, et al. J Neurol Sci. 2012 Mar 15;314(1-2):161-2. doi: 10.1016/j.jns.2011.10.030. Epub 2011 Nov 16. J Neurol Sci. 2012. PMID: 22093143

9

Can developmental venous anomalies cause seizures?

Dussaule C, Masnou P, Nasser G, Archambaud F, Cauquil-Michon C, Gagnepain JP, Bouilleret V, Denier C. Dussaule C, et al. J Neurol. 2017 Dec;264(12):2495-2505. doi: 10.1007/s00415-017-8456-5. Epub 2017 Mar 17. J Neurol. 2017. PMID: 28314978 Review.

10

[Coats Plus: Coats disease with systemic features].

Troumani Y, Ackermann F, Cohen S, Touhami S, Nasser G, Denier C, Labetoulle M, Rousseau A. Troumani Y, et al. J Fr Ophtalmol. 2016 Sep;39(7):e167-70. doi: 10.1016/j.jfo.2015.06.015. Epub 2016 Aug 18. J Fr Ophtalmol. 2016. PMID: 27546161 French. No abstract available.

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