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CICP: Cluster Iterative Closest Point for sparse–dense point cloud registration

Robotics and autonomous systems, 2018-10, Vol.108, p.66-86

2018

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P118 Évolution de la flore microbienne et de l’antibiorésistance chez le diabétique

Diabetes & metabolism, 2012-03, Vol.38, p.A59-A59

2012

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COMPARISON OF UAV LIDAR ODOMETRY OF ROTATING AND FIXED VELODYNE PLATFORMS

International archives of the photogrammetry, remote sensing and spatial information sciences., 2020, Vol.XLIII-B1-2020, p.527-534

2020

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Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families

Revue neurologique, 2024-10

2024

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Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families

Revue neurologique, 2023-06, Vol.179 (6), p.570-575

2023

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High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in Algiers

Clinical microbiology and infection, 2011-04, Vol.17 (4), p.526-532

2011

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Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

Brain (London, England : 1878), 2009-10, Vol.132 (10), p.2688-2698

2009

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Classifications of neurogenetic diseases: An increasingly complex problem

Revue neurologique, 2016-06, Vol.172 (6-7), p.339-349

2016

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Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa

Neurology, 2011-01, Vol.76 (3), p.301-303

2011

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Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

Neurology, 2006-08, Vol.67 (4), p.602-606

2006

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Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients

Journal of the neurological sciences, 2009-03, Vol.278 (1), p.77-81

2009

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Evolution of antimicrobial resistance and serotype distribution of Streptococcus pneumoniae isolated from children with invasive and noninvasive pneumococcal diseases in Algeria from 2005 to 2012

New microbes and new infections, 2015-07, Vol.6 (C), p.42-48

2015

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Autosomal recessive cerebellar ataxia: A clinical and genetic study

Journal of the neurological sciences, 2013-10, Vol.333, p.e468-e468

2013

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Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

Neuromolecular medicine, 2006-03, Vol.8 (1-2), p.75-85

2006

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Diagnostic de l’ataxie spastique autosomique récessive de Charlevoix-Saguenay (ARSACS) chez des patients algériens

Revue neurologique, 2014-04, Vol.170, p.A147-A147

2014

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

Revue neurologique, 2014-04, Vol.170, p.A151-A151

2014

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Low disease risk in relatives of north african lrrk2 Parkinson disease patients

Neurology, 2010-09, Vol.75 (12), p.1118-1119

2010

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DETECTING AND ANALYZING CORROSION SPOTS ON THE HULL OF LARGE MARINE VESSELS USING COLORED 3D LIDAR POINT CLOUDS

ISPRS annals of the photogrammetry, remote sensing and spatial information sciences, 2016-06, Vol.III-3, p.153-160

2016

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The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

Neurology, 2008-12, Vol.71 (24), p.1967-1972

2008

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Diagnostic génétique de la forme PARK8 de la maladie de Parkinson en Algérie par recherche de la mutation c 6055G>A (p gly2019ser) dans le gène LRRK2

Revue neurologique, 2013-04, Vol.169, p.A122-A123

2013

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P070 IL-17 and nitric oxide pathways are involved in inflammatory response during Alzheimer’s disease: A study in Algerian patients

Cytokine (Philadelphia, Pa.), 2012-09, Vol.59 (3), p.541-541

2012

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Prevalence and characterization of extended-spectrum β-lactamases in Klebsiella pneumoniae in Algiers hospitals (Algeria)

Pathologie biologie (Paris), 2008-07, Vol.56 (5), p.319-325

2008

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LRRK2 G2019S as a Cause of Parkinson's Disease in North African Arabs

The New England journal of medicine, 2006-01, Vol.354 (4), p.422-423

2006

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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

Annals of human genetics, 2008-09, Vol.72 (5), p.590-597

2008

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CICP: Cluster Iterative Closest Point for sparse–dense point cloud registration

P118 Évolution de la flore microbienne et de l’antibiorésistance chez le diabétique

COMPARISON OF UAV LIDAR ODOMETRY OF ROTATING AND FIXED VELODYNE PLATFORMS

Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families

Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families

High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in Algiers

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

Classifications of neurogenetic diseases: An increasingly complex problem

Mutations in the glucocerebrosidase gene confer a risk for Parkinson disease in North Africa

Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations

Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients

Evolution of antimicrobial resistance and serotype distribution of Streptococcus pneumoniae isolated from children with invasive and noninvasive pneumococcal diseases in Algeria from 2005 to 2012

Autosomal recessive cerebellar ataxia: A clinical and genetic study

Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease

Diagnostic de l’ataxie spastique autosomique récessive de Charlevoix-Saguenay (ARSACS) chez des patients algériens

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

Low disease risk in relatives of north african lrrk2 Parkinson disease patients

DETECTING AND ANALYZING CORROSION SPOTS ON THE HULL OF LARGE MARINE VESSELS USING COLORED 3D LIDAR POINT CLOUDS

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

Diagnostic génétique de la forme PARK8 de la maladie de Parkinson en Algérie par recherche de la mutation c 6055G>A (p gly2019ser) dans le gène LRRK2

P070 IL-17 and nitric oxide pathways are involved in inflammatory response during Alzheimer’s disease: A study in Algerian patients

Prevalence and characterization of extended-spectrum β-lactamases in Klebsiella pneumoniae in Algiers hospitals (Algeria)

Phenotype, genotype, and worldwide genetic penetrance of LRRK2 -associated Parkinson's disease: a case-control study

LRRK2 G2019S as a Cause of Parkinson's Disease in North African Arabs

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

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