الرئيسية › دليل الباحثين › Ali Benomar
Ali Benomar
الانتماء : Mohammed V University · Centre Hospitalier Ibn Sina · Université Internationale Abulcasis des Sciences de la Santé
- 77منشورات (انتماء مغربي)
- 145مجموع المنشورات
- 4492الاستشهادات
- 29مؤشر h
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Peripheral Neuropathies and Disorders
- Neurological disorders and treatments
- Metabolism and Genetic Disorders
المنشورات (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
المؤلفون المشاركون
- 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
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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