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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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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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Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Neurology, 2008-11, Vol.71 (19), p.1550-1552

2008

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Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C

Brain (London, England : 1878), 2004-01, Vol.127 (1), p.154-163

2004

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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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Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism

American journal of human genetics, 2010-09, Vol.87 (3), p.410-417

2010

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Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays

Journal of neurology, 2011, Vol.258 (1), p.56-67

2011

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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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Antimicrobial Resistance of Respiratory Pathogens in North African Countries

Journal of chemotherapy (Florence), 2009-12, Vol.21 (6), p.627-632

2009

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Identification of seven novel mutations in the GAN gene

Human mutation, 2003-04, Vol.21 (4), p.446-446

2003

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Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

American journal of human genetics, 2002-03, Vol.70 (3), p.726-736

2002

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G2019S LRRK2 mutation in French and North African families with Parkinson's disease

Annals of neurology, 2005-11, Vol.58 (5), p.784-787

2005

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Immunogenicity of Toxins during Staphylococcus aureus Infection

Clinical infectious diseases, 2010-01, Vol.50 (1), p.61-68

2010

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Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1

Neuromuscular disorders : NMD, 2002-11, Vol.12 (9), p.849-852

2002

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

Neuromuscular disorders : NMD, 2000-12, Vol.10 (8), p.592-598

2000

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Use of two methods of analysis to estimate the annual rate of tuberculosis infection in Southern Algeria

Tubercle and lung disease, 1996-06, Vol.77 (3), p.207-214

1996

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High prevalence of community- and hospital-acquired infections of methicillin-resistant Staphylococcus aureus containing Panton-Valentine leukocidin gene in Algiers

Pathologie biologie (Paris), 2010-04, Vol.58 (2), p.e15-e20

2010

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Hereditary sensory neuropathy with neurotrophic keratitis: description of an autosomal recessive disorder with a selective reduction of small myelinated nerve fibres and a discussion of the classification of the hereditary sensory neuropathies

Brain (London, England : 1878), 1987-06, Vol.110 (3), p.563-583

1987

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Chronic childhood spinal muscular atrophies in Algeria: A genetic study

Journal of the neurological sciences, 1990-04, Vol.96 (1), p.89-101

1990

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Genetic study of the autosomal recessive form of Charcot-Marie-Tooth in an Algerian family

Archives de l'Institut Pasteur d'Algérie, 1998, Vol.62, p.268

1998

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Comparison of 3 6-month chemotherapy regimes in pulmonary tuberculosis in routine practice in Algiers. 18th-month results

Revue francaise des maladies respiratoires, 1983, Vol.11 (5), p.667

1983

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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

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

Is the common LRRK2 G2019S mutation related to dyskinesias in North African Parkinson disease?

Phenotypic variability in autosomal recessive axonal Charcot–Marie–Tooth disease due to the R298C mutation in lamin A/C

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

Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism

Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays

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

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

Antimicrobial Resistance of Respiratory Pathogens in North African Countries

Identification of seven novel mutations in the GAN gene

Homozygous Defects in LMNA, Encoding Lamin A/C Nuclear-Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy in Human (Charcot-Marie-Tooth Disorder Type 2) and Mouse

G2019S LRRK2 mutation in French and North African families with Parkinson's disease

Immunogenicity of Toxins during Staphylococcus aureus Infection

Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1

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

Use of two methods of analysis to estimate the annual rate of tuberculosis infection in Southern Algeria

High prevalence of community- and hospital-acquired infections of methicillin-resistant Staphylococcus aureus containing Panton-Valentine leukocidin gene in Algiers

Hereditary sensory neuropathy with neurotrophic keratitis: description of an autosomal recessive disorder with a selective reduction of small myelinated nerve fibres and a discussion of the classification of the hereditary sensory neuropathies

Chronic childhood spinal muscular atrophies in Algeria: A genetic study

Genetic study of the autosomal recessive form of Charcot-Marie-Tooth in an Algerian family

Comparison of 3 6-month chemotherapy regimes in pulmonary tuberculosis in routine practice in Algiers. 18th-month results

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