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Sonia Nouioua

Observed names: Nouioua Sonia, Nouioua, Sonia, S Nouioua, S. Nouioua, Sonia NOUIOUA, Sonia NOUIOUA
Observed institutions: Université de Bordeaux, Inserm, University of Algiers Benyoucef Benkhedda, Centre Hospitalier Universitaire de Bordeaux, Assistance Publique – Hôpitaux de Paris, Hôpital Pellegrin, Centre de Neurophysique Physiologie et Pathologie, Pitié-Salpêtrière Hospital, Centre Hospitalo-Universitaire Bab El Oued, Hôpital Mustapha Pacha, Laboratoire Physiopathologie et Génétique du Neurone et du Muscle, Centre Universitaire Morsli Abdellah de Tipaza, Université Pierre-et-Marie-Curie, Youcef El Khatib University of Health Sciences, University of Blida
ORCID: 0009-0003-3396-6637
Observed ORCID: 0009-0003-3396-6637
OpenAlex ID: A5034780126
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations
2006 · H. Azzedine, N. Ravisé, et al. · Neurology · 111
Hereditary motor and sensory neuropathies or Charcot–Marie–Tooth diseases: An update
2014 · Meriem Tazir, Tarik Hamadouche, et al. · Journal of the Neurological Sciences · 96
Autosomal recessive Charcot‐Marie‐Tooth disease: from genes to phenotypes
2013 · Meriem Tazir, Mounia Bellatache, et al. · Journal of the Peripheral Nervous System · 83
Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide
2015 · Sylvia Stockler-Ipsiroglu, Delia Apatean, et al. · Molecular Genetics and Metabolism · 71
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Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients
2009 · M. Tazir, L. Ali-Pacha, et al. · Journal of the Neurological Sciences · 68
Phenotypic variability in giant axonal neuropathy
2009 · Meriem Tazir, Sonia Nouioua, et al. · Neuromuscular Disorders · 65
The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa
2008 · P. Richard, K. Gaudon, et al. · Neurology · 42
Creatine deficiency syndrome. A treatable myopathy due to arginine–glycine amidinotransferase (AGAT) deficiency
2013 · S. Nouioua, D. Cheillan, et al. · Neuromuscular Disorders · 39
Founder Effect and Estimation of the Age of the c.892C>T (p.Arg298Cys) Mutation in LMNA Associated to Charcot‐Marie‐Tooth Subtype CMT2B1 in Families from North Western Africa
2008 · T. Hamadouche, Y. Poitelon, et al. · Annals of Human Genetics · 34
Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypes
2011 · Sonia Nouioua, Tarik Hamadouche, et al. · Neuromuscular Disorders · 32
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling
2023 · Nika Schuermans, Salima El Chehadeh, et al. · Nature Genetics · 30
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Nerve Biopsy Is Still Useful in Some Inherited Neuropathies
2017 · Mathilde Duchesne, Stéphane Mathis, et al. · Journal of Neuropathology & Experimental Neurology · 29
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1
2002 · M Tazir, J.M Vallat, et al. · Neuromuscular Disorders · 28
Multicenter Transversal Two-Phase Study to Determine a National Prevalence of Epilepsy in Algeria
2012 · Dalila Moualek, Lamia Ali Pacha, et al. · Neuroepidemiology · 16
Multiple sclerosis: Progression rate and severity in a multicenter cohort from Algeria
2014 · Nassima Hecham, Sonia Nouioua, et al. · Multiple Sclerosis Journal · 14
A TOR1AIP1 variant segregating with an early onset limb girdle myasthenia—Support for the role of LAP1 in NMJ function and disease
2021 · Edoardo Malfatti, Tara Catchpool, et al. · Neuropathology and Applied Neurobiology · 12
Distal hereditary motor neuropathies
2024 · Meriem Tazir, Sonia Nouioua · Revue Neurologique · 10
Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations
2011 · Salima Assami, Hamid Azzedine, et al. · Movement Disorders · 8
NEUROMYODredger : Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven Countries
2025 · Edoardo Malfatti, Alexandru Caramizaru, et al. · Clinical Genetics · 5
Description d’une famille algérienne associant une dysferlinopathie et une merosinopathie primaires
2017 · Sonia Nouioua, Amira Cherallah, et al. · Revue Neurologique · 3
Disease Progression in Charcot‐Marie‐Tooth Disease Type 4B ( CMT4B ) Associated With Mutations in Myotubularin‐Related Proteins 2 and 13
2025 · Alessandro Bertini, Mary M. Reilly, et al. · European Journal of Neurology · 2
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Un cas de myasthénie congénitale des ceintures résolu grâce à une collaboration tripartite
2021 · Sonia Nouioua, Edoardo Malfatti, et al. · médecine/sciences · 2
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Intragenic deletion patterns of dystrophin gene in Duchenne and Becker muscular dystrophy patients from Algeria
2013 · Amira Cherrallah, Traki Benhassine, et al. · Genes & Genomics · 2
Neuromyélite optique de Devic séropositive à neuro-imagerie normale
2018 · Maria Merazga, Lamia Alipacha, et al. · Revue Neurologique · 1
G.P.4.04 A new MTMR2 mutation is responsible for a congenital form of Charcot-Marie-Tooth disease (CMT4B1) and vocal cord paresis
2009 · M. Tazir, S. Nouioua, et al. · Neuromuscular Disorders · 1
Works count: 85
Citation count: 804
H-index: 14
I10-index: 17
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