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Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays.
J Neurol. 2011 Jan;258(1):56-67. doi: 10.1007/s00415-010-5682-5. Epub 2010 Aug 27.
J Neurol. 2011.
PMID: 20798953
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
Hamza W, Ali Pacha L, Hamadouche T, Muller J, Drouot N, Ferrat F, Makri S, Chaouch M, Tazir M, Koenig M, Benhassine T.
Hamza W, et al. Among authors: ferrat f.
BMC Med Genet. 2015 Jun 12;16:36. doi: 10.1186/s12881-015-0180-3.
BMC Med Genet. 2015.
PMID: 26068213
Free PMC article.
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Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
Renaud M, Moreira MC, Ben Monga B, Rodriguez D, Debs R, Charles P, Chaouch M, Ferrat F, Laurencin C, Vercueil L, Mallaret M, M'Zahem A, Pacha LA, Tazir M, Tilikete C, Ollagnon E, Ochsner F, Kuntzer T, Jung HH, Beis JM, Netter JC, Djamshidian A, Bower M, Bottani A, Walsh R, Murphy S, Reiley T, Bieth É, Roelens F, Poll-The BT, Lourenço CM, Jardim LB, Straussberg R, Landrieu P, Roze E, Thobois S, Pouget J, Guissart C, Goizet C, Dürr A, Tranchant C, Koenig M, Anheim M.
Renaud M, et al. Among authors: ferrat f.
JAMA Neurol. 2018 Apr 1;75(4):495-502. doi: 10.1001/jamaneurol.2017.4373.
JAMA Neurol. 2018.
PMID: 29356829
Free PMC article.
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Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.
Sayad M, Zouambia M, Chaouch M, Ferrat F, Nebbal M, Bendini M, Lesage S, Brice A, Brahim Errahmani M, Asselah B.
Sayad M, et al. Among authors: ferrat f.
BMC Neurosci. 2016 Feb 1;17:6. doi: 10.1186/s12868-016-0240-4.
BMC Neurosci. 2016.
PMID: 26831335
Free PMC article.
Clinical Trial.
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