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Ali Benomar
Affiliation : Mohammed V University · Centre Hospitalier Ibn Sina · Université Internationale Abulcasis des Sciences de la Santé
- 77Publications (affiliation in Morocco)
- 145Total publications
- 4492Citations
- 29h-index
Research profile
Ali Benomar has 77 indexed publications (1996–2026). Their work appears mainly in “Revue Neurologique”, “World Journal of Neuroscience” and “Frontiers in Neurology”. Their most cited article, “Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders” (2014), has been cited 540 times. 8 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France.
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Create my free profile Add my publicationsResearch areas
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Peripheral Neuropathies and Disorders
- Neurological disorders and treatments
- Metabolism and Genetic Disorders
Publications (77)
- Primary costovertebral hydatidosis revealed by compressive myelitis: a case report
- Neurocysticercosis in a Non-endemic Setting: A Report of Three Cases
- Focal Temporal Lobe Seizures with Preserved Consciousness Revealed by Psychiatric Manifestations: A Case Study
- Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome
- Headache and Status Epilepticus Reveal Paget’s Disease of the Bone
- Recurrent Transient Ischemic Attacks Revealing Cerebral Amyloid Angiopathy: A Comprehensive Case
- Mutations GBA et TMEM175 et dystonie généralisée : à propos d’un cas
- Leber’s Disease or Multiple Sclerosis: When Diagnosis is not the Real Challenge
- Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson’s Disease in Sporadic Moroccan Patients
- Trends in the consumption and cost of antiepileptics in Morocco between 2008 and 2018
- Manifestations neurologiques de la maladie cœliaque
- Polyradiculonévrite aiguë et Covid-19 : à propos de 3 observations
- Encéphalite limbique et infection aiguë au virus hépatite A
- Méningo-encéphalite tuberculeuse compliquée de mouvements anormaux multiples par atteinte bilatérale des noyaux gris centraux
- Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease
- 5PSQ-079 Immunotherapy in metastatic melanoma: a miracle or poison
- A case of bilateral thalamic infarct complicating tuberculous meningoencephalitis
- 4CPS-037 The impact of multidisciplinary collaboration in optimising the prescription of antibiotics in a paediatric hospital
- Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients
- Stroke and syphilis: A retrospective study of 53 patients
- Association of vitamin D status with multiple sclerosis in a case-control study from Morocco
- Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat
- Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing
- Myasthénie et dilatation de bronches : défi diagnostique et thérapeutique
- 5PSQ-099 Cytotoxic preparation unit: evaluation of clinical services satisfaction in three hospitals
- LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease
- Mutation Analysis of Consanguineous Moroccan Patients with Parkinson’s Disease Combining Microarray and Gene Panel
- Evidence for prehistoric origins of the G2019S mutation in the North African Berber population
- Association Study of Two Polymorphisms in Vitamin D Pathway with Multiple Sclerosis in the Moroccan Population
- A case of neurosyphilis presenting with essential-like tremor
- Dystonie et myasthénie
- Étude des symptômes non moteurs de la maladie de Parkinson dans une cohorte de 100 patients marocains
- Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia
- Vitamin D deficiency and its role in neurological conditions: A review
- Clinical and genetic data of Huntington disease in Moroccan patients
- A Novel Homozygous p.L539F Mutation Identified inPINK1Gene in a Moroccan Patient with Parkinsonism
- Is there any difference in the overall cost of care and the cost of pharmaceutical products between patients with ruptured and unruptured aneurysms?
- Les paramètres influençant le coût des produits pharmaceutiques dans la prise en charge des anévrismes intracrâniens par embolisation
- Syndrome de Tolosa-Hunt récidivant à bascule
- La « déréalisation » et la « dépersonnalisation » : un trouble dissociatif révélateur d’une sclérose en plaques
- Évolution des dépenses de l’Assurance maladie obligatoire attribuées aux affections de longue durée au Maroc
- Evaluation of retinal nerve fiber layer thickness measured by optical coherence tomography in Moroccan patients with multiple sclerosis
- Amyloses rénales AA : corrélations anatomocliniques dans une série marocaine de 30 cas
- Measles in Morocco: Epidemiological Profile and Impact of Vaccination Strategy
- Myokymia revealing multiple sclerosis
- Amyotrophic lateral sclerosis in Moroccan population: environmental and clinical aspects
- Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders
- Profile of idiopathic parkinson’s disease in Moroccan patients
- Multiple sclerosis: Clinical characteristics and disability progression in Moroccan children
- Complications neurologiques de la sarcoïdose : série de 14 cas
- Clinical and Genetic Study of Friedreich’s Ataxia and Ataxia with Vitamin E Deficiency in 44 Moroccan Families
- Myasthénie auto-immune juvénile associée à un thymome
- KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction
- Genetic factors and multiple sclerosis in the Moroccan population: A role for HLA class II
- LA MALADIE DE GILLES DE LA TOURETTE
- A clinical study of non-parkinsonian tremor in Moroccan patients
- Infarctus de l’artère spinale antérieure simulant une sclérose latérale amyotrophique
- Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia
- Profile of multiple system atrophy in Moroccan patients attending a movement disorders outpatient clinic in Rabat university hospital
- Localisations métastatiques inhabituelles d’adénocarcinome pulmonaire
- CLN6 p.I154del Mutation Causing Late Infantile Neuronal Ceroid Lipofuscinosis in a Large Consanguineous Moroccan Family
- Vitamin E in ataxia and neurodegenerative diseases: A review
- An autosomal recessive leucoencephalopathy with ischemic stroke, dysmorphic syndrome and retinitis pigmentosa maps to chromosome 17q24.2-25.3
- Les tuberculomes intra-duraux et extramédullaires : à propos de trois cas
- Prevalence of human papillomavirus genotype among Moroccan women during a local screening program
- Accident vasculaire cérébral révélant une granulomatose
- Efficacité et tolérance du cyclophosphamide dans le traitement de fond des formes progressives de la sclérose en plaques
- A locus for bilateral occipital polymicrogyria maps to chromosome 6q16–q22
- A novel locus for autosomal recessive spastic ataxia on chromosome 17p
- Les urgences hypertensives: épidémiologie, prise en charge et pronostic
- Autosomal recessive axonal Charcot-Marie-Tooth disease (ARCMT2): phenotype-genotype correlations in 13 Moroccan families
- Vitamin E deficiency ataxia with (744 del A) mutation on α-TTP gene: genetic and clinical peculiarities in Moroccan patients
- Vitamin E deficiency ataxia associated with adenoma
- Refinement of the locus for autosomal dominant cerebellar ataxia type II to chromosome 3p21.1-14.1
- Infarctus cérébral, syndrome pseudolupique et myxome de l'oreillette gauche
- An expanded CAG repeat sequence in spinocerebellar ataxia type 7.
- Autosomal dominant cerebellar ataxia type I in Morocco: presence of the SCA1 and SCA3/MJD mutations
Publication venues
- Revue Neurologique × 20
- World Journal of Neuroscience × 4
- Frontiers in Neurology × 3
- Journal of the Neurological Sciences × 3
- Pan African Medical Journal × 2
- Cureus × 2
Publications per year
- 20262
- 20251
- 20245
- 20231
- 20223
- 20212
- 20202
- 20192
- 20187
- 20177
Collaborations
Partner institutions : Centre Hospitalier Universitaire de Rabat-Salé · Centre Hospitalier Universitaire Ibn Rochd · Inserm · Pitié-Salpêtrière Hospital · Université Pierre-et-Marie-Curie
Co-authors’ countries : France
Co-authors
- Wafa Regragui
- Mohamed Yahyaoui
- Houyam Tibar
- Ahmed Bouhouche
- El Hachmia Ait Ben Haddou
- Naïma Bouslam
- Rachid Razıne
- M. Yahyaoui
- Wafaa Regragui
- Hajar Naciri Darai
- Rédouane Abouqal
- Dahab Ouhabi
Bibliographic data from OpenAlex (open database).
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