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Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis

European journal of haematology, 2018-10, Vol.101 (4), p.566-569

2018

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A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11

American journal of medical genetics. Part A, 2008-03, Vol.146A (5), p.578-584

2008

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Loss of heterozygosity on chromosome 9 and p16 (MTS1, CDKN2) gene mutations in esophageal cancers

International journal of cancer, 1997-07, Vol.72 (1), p.27-30

1997

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Supporting Fathers and Supported Mothers in Families with Disruptive Boys: Who are they?

Journal of child psychology and psychiatry, 1995-09, Vol.36 (6), p.1003-1018

1995

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Can Spouse Support be Accurately and Reliably Rated? A Generalizability Study of Families with Disruptive Boys

Journal of child psychology and psychiatry, 1993-07, Vol.34 (5), p.689-714

1993

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Long‐term safety and efficacy of rituximab in 248 adults with immune thrombocytopenia: Results at 5 years from the French prospective registry ITP‐ritux

American journal of hematology, 2019-12, Vol.94 (12), p.1314-1324

2019

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Factors associated with verbal fluency in older adults living with HIV in West Africa: A longitudinal study

Tropical medicine & international health, 2023-01, Vol.28 (1), p.35-42

2023

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Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies

Annals of neurology, 2020-04, Vol.87 (4), p.584-598

2020

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The graphemic/motor frontal area Exner's area revisited

Annals of neurology, 2009-10, Vol.66 (4), p.537-545

2009

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Asynchrony of the early maturation of white matter bundles in healthy infants: Quantitative landmarks revealed noninvasively by diffusion tensor imaging

Human brain mapping, 2008-01, Vol.29 (1), p.14-27

2008

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Analysis of the DYSF mutational spectrum in a large cohort of patients

Human mutation, 2009-02, Vol.30 (2), p.E345-E375

2009

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Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy

Movement disorders, 2019-07, Vol.34 (7), p.1049-1059

2019

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Improved performance and safety from Argus II retinal prosthesis post‐approval study in France

Acta ophthalmologica (Oxford, England), 2021-11, Vol.99 (7), p.e1212-e1221

2021

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The mechanisms underlying MMR deficiency in immunodeficiency‐related non‐Hodgkin lymphomas are different from those in other sporadic microsatellite instable neoplasms

International journal of cancer, 2009-11, Vol.125 (10), p.2360-2366

2009

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Differential 1-year clinical outcomes for ST-segment elevation myocardial infarction related to stent thrombosis or saphenous vein graft thrombosis

Catheterization and cardiovascular interventions, 2013-08, Vol.82 (2), p.193-200

2013

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A study of cortical morphology in children with fetal alcohol spectrum disorders

Human brain mapping, 2014-05, Vol.35 (5), p.2285-2296

2014

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Genetic Characterization of a French Cohort of GNE‐mutation negative inclusion body myopathy patients with exome sequencing

Muscle & nerve, 2017-11, Vol.56 (5), p.993-997

2017

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Obstetrical Complications and Violent Delinquency: Testing Two Developmental Pathways

Child development, 2002-03, Vol.73 (2), p.496-508

2002

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Family income and youths' symptoms of depression and anxiety: a longitudinal study of the French GAZEL Youth cohort

Depression and anxiety, 2010-12, Vol.27 (12), p.1095-1103

2010

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Fertility Limitation and Child Schooling in Ouagadougou: Selective Fertility or Resource Dilution?

Studies in family planning, 2015-06, Vol.46 (2), p.177-199

2015

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ANXIETY AND 10-YEAR RISK OF INCIDENT AND RECURRENT DEPRESSIVE SYMPTOMATOLOGY IN OLDER ADULTS

Depression and anxiety, 2013-06, Vol.30 (6), p.554-563

2013

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Prevalence, severity, and clinical correlates of pain in patients with systemic sclerosis

Arthritis care & research (2010), 2010-03, Vol.62 (3), p.409-417

2010

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Inherited or acquired modifiers of iron status may dramatically affect the phenotype in dehydrated hereditary stomatocytosis

A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11

Loss of heterozygosity on chromosome 9 and p16 (MTS1, CDKN2) gene mutations in esophageal cancers

Supporting Fathers and Supported Mothers in Families with Disruptive Boys: Who are they?

Can Spouse Support be Accurately and Reliably Rated? A Generalizability Study of Families with Disruptive Boys

Long‐term safety and efficacy of rituximab in 248 adults with immune thrombocytopenia: Results at 5 years from the French prospective registry ITP‐ritux

Factors associated with verbal fluency in older adults living with HIV in West Africa: A longitudinal study

Fine‐Mapping of SNCA in Rapid Eye Movement Sleep Behavior Disorder and Overt Synucleinopathies

The graphemic/motor frontal area Exner's area revisited

Asynchrony of the early maturation of white matter bundles in healthy infants: Quantitative landmarks revealed noninvasively by diffusion tensor imaging

Analysis of the DYSF mutational spectrum in a large cohort of patients

Genome‐wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy

Diagnostic accuracy of the Multistix 8 SG reagent strip in diagnosis of spontaneous bacterial peritonitis

Improved performance and safety from Argus II retinal prosthesis post‐approval study in France

The mechanisms underlying MMR deficiency in immunodeficiency‐related non‐Hodgkin lymphomas are different from those in other sporadic microsatellite instable neoplasms

Whole‐genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140

Differential 1-year clinical outcomes for ST-segment elevation myocardial infarction related to stent thrombosis or saphenous vein graft thrombosis

A study of cortical morphology in children with fetal alcohol spectrum disorders

Genetic Characterization of a French Cohort of GNE‐mutation negative inclusion body myopathy patients with exome sequencing

Obstetrical Complications and Violent Delinquency: Testing Two Developmental Pathways

Family income and youths' symptoms of depression and anxiety: a longitudinal study of the French GAZEL Youth cohort

REEP1 mutations in SPG31: Frequency, mutational spectrum, and potential association with mitochondrial morpho-functional dysfunction

Fertility Limitation and Child Schooling in Ouagadougou: Selective Fertility or Resource Dilution?

ANXIETY AND 10-YEAR RISK OF INCIDENT AND RECURRENT DEPRESSIVE SYMPTOMATOLOGY IN OLDER ADULTS

Prevalence, severity, and clinical correlates of pain in patients with systemic sclerosis

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