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Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation

Human genetics, 2005-11, Vol.118 (1), p.45-48

2005

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Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing

Revue neurologique, 2008-12, Vol.164 (12), p.995-1009

2008

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MECP2 is highly mutated in X-linked mental retardation

Human molecular genetics, 2001-04, Vol.10 (9), p.941

2001

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So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation

Seizure (London, England), 2002-06, Vol.11 (4), p.273-277

2002

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MECP2 is highly mutated in X-linked mental retardation

Human molecular genetics, 2001-04, Vol.10 (9), p.941-946

2001

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Malformations cérébrales et épilepsie : présentations radiocliniques et implications pour le diagnostic génétique

Revue neurologique, 2008-12, Vol.164 (12), p.995-1009

2008

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So-called ‘cryptogenic’ partial seizures resulting from a subtle cortical dysgenesis due to adoublecortin gene mutation

Seizure (London, England), 2002-06, Vol.11 (4), p.273-277

2002

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Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy

Human mutation, 2001-09, Vol.18 (3), p.251-252

2001

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Interference of P1290 P polymorphism (4002 A--> G) in molecular diagnosis of mucoviscidosis using the cystic fibrosis assay: an example of a diagnostic trap

Annales de biologie clinique (Paris), 1999-11, Vol.57 (6), p.741-742

1999

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The wide spectrum of tubulinopathies: what are the key features for the diagnosis?

Brain (London, England : 1878), 2014-06, Vol.137 (Pt 6), p.1676-1700

2014

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Simple Wastewater Preparation Protocol Applied to Monitor the Emergence of the Omicron 21L/BA.2 Variant by Genome Sequencing

Viruses, 2023-01, Vol.15 (2), p.268

2023

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Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria

European journal of human genetics : EJHG, 2013-04, Vol.21 (4), p.381-385

2013

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Adherence to highly active antiretroviral therapies (HAART) in HIV-infected patients: from a predictive to a dynamic approach

Social science & medicine (1982), 2002-05, Vol.54 (10), p.1481-1496

2002

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Roles of Political Orientation and Social Representations of Social Order on Socio-Representational Construction Towards Universal Basic Income in France

Basic income studies, 2023-12, Vol.18 (2), p.187-213

2023

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Relationship between emotional experience and resilience: An fMRI study in fire-fighters

Neuropsychologia, 2013-04, Vol.51 (5), p.845-849

2013

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N’Kheïla (Maroc)

Encyclopédie berbère, 2012-10 (34), p.5559-5560

Souville, Georges

2012

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New insights into genotype―phenotype correlations for the doublecortin-related lissencephaly spectrum

Brain (London, England : 1878), 2013, Vol.136 (Pt 1), p.223-244

2013

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Detection of Aspergillus Galactomannan Antigenemia To Determine Biological and Clinical Implications of Beta-Lactam Treatments

Journal of Clinical Microbiology, 2005-10, Vol.43 (10), p.5214-5220

2005

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Different reporting patterns for occupational diseases among physicians: a study of French general practitioners, pulmonologists and rheumatologists

International archives of occupational and environmental health, 2010-03, Vol.83 (3), p.251-258

2010

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Management of excreta from elderly treated with antineoplastic drugs

La Presse médicale (1983), 2016-05, Vol.45 (5), p.532-537

2016

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Definitions and measures of exercise dependence

Addiction research & theory, 2006-12, Vol.14 (6), p.631-646

2006

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Mellah (stations de l’oued)

Encyclopédie berbère, 2010-12 (31), p.4856-4857

Souville, G.

2010

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Madene El-Mellah (mine de sel, Maroc)

Encyclopédie berbère, 2010-12 (30), p.4479-4482

Souville, G.

2010

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Maaziz

Encyclopédie berbère, 2010-12 (30), p.4453-4454

Souville, G.

2010

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Data interoperability in the future of middleware

Journal of internet services and applications, 2012-05, Vol.3 (1), p.127-131

2012

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Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardation

Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing

MECP2 is highly mutated in X-linked mental retardation

So-called 'cryptogenic' partial seizures resulting from a subtle cortical dysgenesis due to a doublecortin gene mutation

MECP2 is highly mutated in X-linked mental retardation

Malformations cérébrales et épilepsie : présentations radiocliniques et implications pour le diagnostic génétique

So-called ‘cryptogenic’ partial seizures resulting from a subtle cortical dysgenesis due to adoublecortin gene mutation

Five novel frameshift mutations in exon 3 and 4 of the MECP2 gene identified in Rett patients: Consequences for the molecular diagnosis strategy

Interference of P1290 P polymorphism (4002 A--> G) in molecular diagnosis of mucoviscidosis using the cystic fibrosis assay: an example of a diagnostic trap

The wide spectrum of tubulinopathies: what are the key features for the diagnosis?

Simple Wastewater Preparation Protocol Applied to Monitor the Emergence of the Omicron 21L/BA.2 Variant by Genome Sequencing

Expanding the spectrum of TUBA1A-related cortical dysgenesis to Polymicrogyria

Adherence to highly active antiretroviral therapies (HAART) in HIV-infected patients: from a predictive to a dynamic approach

Roles of Political Orientation and Social Representations of Social Order on Socio-Representational Construction Towards Universal Basic Income in France

Relationship between emotional experience and resilience: An fMRI study in fire-fighters

N’Kheïla (Maroc)

New insights into genotype―phenotype correlations for the doublecortin-related lissencephaly spectrum

Detection of Aspergillus Galactomannan Antigenemia To Determine Biological and Clinical Implications of Beta-Lactam Treatments

Different reporting patterns for occupational diseases among physicians: a study of French general practitioners, pulmonologists and rheumatologists

Management of excreta from elderly treated with antineoplastic drugs

Definitions and measures of exercise dependence

Mellah (stations de l’oued)

Madene El-Mellah (mine de sel, Maroc)

Maaziz

Data interoperability in the future of middleware

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