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Senda Ajroud-Driss

Affiliations: 
Neurology Northwestern University, Evanston, IL 
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"Senda Ajroud-Driss"
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Parents

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Fayçal Hentati grad student Institut National de Neurologie

Children

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Faisal Fecto research scientist 2007-2012 Northwestern

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Publications

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Berger A, Locatelli M, Arcila-Londono X, et al. (2023) The natural history of ALS: Baseline characteristics from a multicenter clinical cohort. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-9
Kacem I, Sghaier I, Bougatef S, et al. (2019) Epidemiological and clinical features of amyotrophic lateral sclerosis in a Tunisian cohort. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-9
Lange DJ, Shahbazi M, Silani V, et al. (2017) Pyrimethamine Significantly Lowers CSF/SOD1 in ALS Patients With SOD1 Mutations. Annals of Neurology
Sufit RL, Ajroud-Driss S, Casey P, et al. (2017) Open label study to assess the safety of VM202 in subjects with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-10
Ajroud-Driss S, Fecto F, Ajroud K, et al. (2015) Mutation in the novel nuclear-encoded mitochondrial protein CHCHD10 in a family with autosomal dominant mitochondrial myopathy. Neurogenetics. 16: 1-9
Ajroud-Driss S, Siddique T. (2015) Sporadic and hereditary amyotrophic lateral sclerosis (ALS). Biochimica Et Biophysica Acta. 1852: 679-684
Edens BM, Ajroud-Driss S, Ma L, et al. (2015) Molecular mechanisms and animal models of spinal muscular atrophy. Biochimica Et Biophysica Acta. 1852: 685-692
Allen JA, Chen R, Ajroud-Driss S, et al. (2013) Gastrostomy tube placement by endoscopy versus radiologic methods in patients with ALS: a retrospective study of complications and outcome. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 14: 308-14
Allen J, Hall M, Wallery S, et al. (2012) Gastrostomy Tube Placement by Endoscopy Versus Radiologic Methods in Patients with ALS: A Retrospective Review of Complications and Outcome (P01.101) Neurology. 78: P01.101-P01.101
Ajroud-Driss S, Fecto F, Ajroud K, et al. (2012) Mutations in the Nuclear Encoded Novel Mitochondrial Protein CHCHD10 Cause an Autosomal Dominant Mitochondrial Myopathy (IN7-2.002) Neurology. 78: IN7-2.002-IN7-2.002
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