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Functional and Molecular Characterization of New SPTLC1 Missense Variants in Patients with Hereditary Sensory and Autonomic Neuropathy Type 1 (HSAN1).
Rochat J, Blavier A, Ruet S, Vasseur S, Puma A, Desnous B, Chan V, Delmont E, Attarian S, Juntas Morales R, Quadrio I, Vidoni L, Bonello-Palot N, Cheillan D. Rochat J, et al. Among authors: attarian s. Genes (Basel). 2024 May 26;15(6):692. doi: 10.3390/genes15060692. Genes (Basel). 2024. PMID: 38927628 Free PMC article.
Predictive factors of efficacy of rituximab in patients with anti-MAG neuropathy.
Gazzola S, Delmont E, Franques J, Boucraut J, Salort-Campana E, Verschueren A, Sagui E, Hubert AM, Pouget J, Attarian S. Gazzola S, et al. Among authors: attarian s. J Neurol Sci. 2017 Jun 15;377:144-148. doi: 10.1016/j.jns.2017.04.015. Epub 2017 Apr 12. J Neurol Sci. 2017. PMID: 28477685
Motor unit number index (MUNIX) in patients with anti-MAG neuropathy.
Fatehi F, Delmont E, Grapperon AM, Salort-Campana E, Sévy A, Verschueren A, Boucraut J, Attarian S. Fatehi F, et al. Among authors: attarian s. Clin Neurophysiol. 2017 Jul;128(7):1264-1269. doi: 10.1016/j.clinph.2017.04.022. Epub 2017 May 9. Clin Neurophysiol. 2017. PMID: 28545015
The utility of motor unit number index: A systematic review.
Fatehi F, Grapperon AM, Fathi D, Delmont E, Attarian S. Fatehi F, et al. Among authors: attarian s. Neurophysiol Clin. 2018 Oct;48(5):251-259. doi: 10.1016/j.neucli.2018.09.001. Epub 2018 Oct 2. Neurophysiol Clin. 2018. PMID: 30287192 Review.
346 results