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Page 1
Non-Motor Symptoms and Quality of Life in Patients with PRRT2-Related Paroxysmal Kinesigenic Dyskinesia.
Ekmen A, Doulazmi M, Méneret A, Jegatheesan P, Hervé A, Damier P, Gras D, Roubertie A, Piard J, Mutez E, Tarrano C, Welniarz Q, Vidailhet M, Worbe Y, Gallea C, Roze E. Ekmen A, et al. Among authors: doulazmi m. Mov Disord Clin Pract. 2023 Jun 5;10(7):1082-1089. doi: 10.1002/mdc3.13795. eCollection 2023 Jul. Mov Disord Clin Pract. 2023. PMID: 37476308 Free PMC article.
Low-intensity electromagnetic fields induce human cryptochrome to modulate intracellular reactive oxygen species.
Sherrard RM, Morellini N, Jourdan N, El-Esawi M, Arthaut LD, Niessner C, Rouyer F, Klarsfeld A, Doulazmi M, Witczak J, d'Harlingue A, Mariani J, Mclure I, Martino CF, Ahmad M. Sherrard RM, et al. Among authors: doulazmi m. PLoS Biol. 2018 Oct 2;16(10):e2006229. doi: 10.1371/journal.pbio.2006229. eCollection 2018 Oct. PLoS Biol. 2018. PMID: 30278045 Free PMC article.
Non cell-autonomous role of DCC in the guidance of the corticospinal tract at the midline.
Welniarz Q, Morel MP, Pourchet O, Gallea C, Lamy JC, Cincotta M, Doulazmi M, Belle M, Méneret A, Trouillard O, Ruiz M, Brochard V, Meunier S, Trembleau A, Vidailhet M, Chédotal A, Dusart I, Roze E. Welniarz Q, et al. Among authors: doulazmi m. Sci Rep. 2017 Mar 24;7(1):410. doi: 10.1038/s41598-017-00514-z. Sci Rep. 2017. PMID: 28341853 Free PMC article.
Mutations in the netrin-1 gene cause congenital mirror movements.
Méneret A, Franz EA, Trouillard O, Oliver TC, Zagar Y, Robertson SP, Welniarz Q, Gardner RJM, Gallea C, Srour M, Depienne C, Jasoni CL, Dubacq C, Riant F, Lamy JC, Morel MP, Guérois R, Andreani J, Fouquet C, Doulazmi M, Vidailhet M, Rouleau GA, Brice A, Chédotal A, Dusart I, Roze E, Markie D. Méneret A, et al. Among authors: doulazmi m. J Clin Invest. 2017 Nov 1;127(11):3923-3936. doi: 10.1172/JCI95442. Epub 2017 Sep 25. J Clin Invest. 2017. PMID: 28945198 Free PMC article.
A randomized, controlled, double-blind, crossover trial of triheptanoin in alternating hemiplegia of childhood.
Hainque E, Caillet S, Leroy S, Flamand-Roze C, Adanyeguh I, Charbonnier-Beaupel F, Retail M, Le Toullec B, Atencio M, Rivaud-Péchoux S, Brochard V, Habarou F, Ottolenghi C, Cormier F, Méneret A, Ruiz M, Doulazmi M, Roubergue A, Corvol JC, Vidailhet M, Mochel F, Roze E. Hainque E, et al. Among authors: doulazmi m. Orphanet J Rare Dis. 2017 Oct 2;12(1):160. doi: 10.1186/s13023-017-0713-2. Orphanet J Rare Dis. 2017. PMID: 28969699 Free PMC article. Clinical Trial.
Health-Related Quality of Life Is Severely Affected in Primary Orthostatic Tremor.
Maugest L, McGovern EM, Mazalovic K, Doulazmi M, Apartis E, Anheim M, Bourdain F, Benchetrit E, Czernecki V, Broussolle E, Bonnet C, Falissard B, Jahanshahi M, Vidailhet M, Roze E. Maugest L, et al. Among authors: doulazmi m. Front Neurol. 2018 Jan 15;8:747. doi: 10.3389/fneur.2017.00747. eCollection 2017. Front Neurol. 2018. PMID: 29379467 Free PMC article.
Long-term follow-up in an open-label trial of triheptanoin in GLUT1 deficiency syndrome: a sustained dramatic effect.
Hainque E, Gras D, Meneret A, Atencio M, Luton MP, Barbier M, Doulazmi M, Habarou F, Ottolenghi C, Roze E, Mochel F. Hainque E, et al. Among authors: doulazmi m. J Neurol Neurosurg Psychiatry. 2019 Nov;90(11):1291-1293. doi: 10.1136/jnnp-2018-320283. Epub 2019 Apr 4. J Neurol Neurosurg Psychiatry. 2019. PMID: 30948626 Free PMC article. Clinical Trial. No abstract available.
Descriptive analysis of the French NS-Park registry: Towards a nation-wide Parkinson's disease cohort?
Mariani LL, Doulazmi M, Chaigneau V, Brefel-Courbon C, Carrière N, Danaila T, Defebvre L, Defer G, Dellapina E, Doé de Maindreville A, Geny C, Maltête D, Meissner WG, Rascol O, Thobois S, Torny F, Tranchant C, Vidailhet M, Corvol JC, Degos B; NS-Park/F-CRIN Network study group. Mariani LL, et al. Among authors: doulazmi m. Parkinsonism Relat Disord. 2019 Jul;64:226-234. doi: 10.1016/j.parkreldis.2019.04.012. Epub 2019 Apr 25. Parkinsonism Relat Disord. 2019. PMID: 31047798
50 results