Author

Salima Assami

Observed names: S Assami, S. Assami

Observed institutions: University of Algiers Benyoucef Benkhedda, Hôpital Mustapha Pacha

OpenAlex ID: A5029816032

LRRK2 G2019S mutation in Parkinson’s disease: A neuropsychological and neuropsychiatric study in a large Algerian cohort

2010 · Soreya Belarbi, Nassima Hecham, et al. · Parkinsonism & Related Disorders · 94

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

Identification of seven novel mutations in theGAN gene

2003 · P. Bomont, C. Ioos, et al. · Human Mutation · 51

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Charcot–Marie–Tooth 2-like presentation of an Algerian family with giant axonal neuropathy

2000 · R. Zemmouri, H. Azzedine, et al. · Neuromuscular Disorders · 37

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

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

Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain: Abstracts of Symposia and free communications

1994 · The European Velnacrine Study Group, L. Harms, et al. · Journal of Neurology · 13

Pantothenate kinase–associated neurodegeneration: Clinical description of 10 patients and identification of new mutations

2011 · Salima Assami, Hamid Azzedine, et al. · Movement Disorders · 8

Encéphalites autoimmunes à autoanticorps : diversité clinique et immunologique

2017 · Tahar Amine Bakhti, Sonia Nouioua, et al. · Revue Neurologique

Les dystonies primitives non liées au gène DYT1 : variabilité phénotypique et difficultés diagnostiques

2017 · Dalila Moualek, Brahim Merrouche, et al. · Revue Neurologique

Étude clinique et génétique d’une cohorte de 46 patients atteints d’ataxie de Friedreich

2017 · Lamia Ali Pacha, Traki Benhassine, et al. · journal algérien de médecine

Variabilité phénotypique de deux familles AR CMT avec une mutation du gène GDAP1

2015 · Mounia Bellatache, Sonia Nouioua, et al. · Revue Neurologique

Paraplégies spastiques familiales : étude d’une série de 70 familles et corrélations phénotype/génotype

2014 · M.I. Kediha, S. Nouioua, et al. · Revue Neurologique

Autosomal recessive cerebellar ataxia: A clinical and genetic study

2013 · L. Ali-Pacha, W. Hamza, et al. · Journal of the Neurological Sciences

Front & Back Matter

2012 · Ruth Ann Marrie, Bo Nancy Yu, et al. · Neuroepidemiology

G.P.10.09 Description of a family associating a calpainopathy and a Duchenne myopathy

2009 · S. Nouioua, A.M. Cobo, et al. · Neuromuscular Disorders

P.P.1 04 Algerian FKRP mutations causing MDC1C congenital muscular dystrophy with mental retardation

2006 · S. Makri, P. Richard, et al. · Neuromuscular Disorders

P.P.1 03 A clinical, morphological and genetic study of congenital muscular dystrophies in Algeria

2006 · S. Makri, N. Terki, et al. · Neuromuscular Disorders

Works count: 21

Citation count: 426

H-index: 10

I10-index: 10