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Natural history of Crohn's disease: Comparison between childhood‐ and adult‐onset disease

Inflammatory bowel diseases, 2010-06, Vol.16 (6), p.953-961

2010

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Presence of increased stiffness of the common carotid artery and endothelial dysfunction in severely obese children: a prospective study

The Lancet (British edition), 2001-10, Vol.358 (9291), p.1400-1404

2001

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Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia

Human mutation, 2005-11, Vol.26 (5), p.497-497

2005

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Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France[S]

Journal of lipid research, 2016-03, Vol.57 (3), p.482-491

2016

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Intractable Diarrhea With Tufting Enteropathy: A Favorable Outcome Is Possible

Journal of pediatric gastroenterology and nutrition, 2011-06, Vol.52 (6), p.734-739

2011

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Intermediate-Term Efficacy and Tolerance of Statins in Children

The Journal of pediatrics, 2019-07, Vol.210, p.161-165

2019

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Review of the nutritional benefits and risks related to intense sweeteners

Archives of public health = Archives belges de santé publique, 2015-10, Vol.73 (1), p.41, Article 41

2015

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Association of Arterial Stiffness and Endothelial Dysfunction with Metabolic Syndrome in Obese Children

The Journal of pediatrics, 2008-07, Vol.153 (1), p.65-70.e1

2008

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Religious dietary rules and their potential nutritional and health consequences

International journal of epidemiology, 2021-03, Vol.50 (1), p.12-26

2021

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Long-Term Follow-Up of Statin Treatment in a Cohort of Children with Familial Hypercholesterolemia: Efficacy and Tolerability

Paediatric drugs, 2011-08, Vol.13 (4), p.267-275

2011

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Pediatric Jejunal Gastrointestinal Stromal Tumor Diagnosed by Wireless Capsule Endoscopy

Journal of pediatric gastroenterology and nutrition, 2007-09, Vol.45 (3), p.358-360

2007

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Plasma Citrulline Concentration Reflects Enterocyte Mass in Children With Short Bowel Syndrome

Pediatric research, 2009-05, Vol.65 (5), p.559-563

2009

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Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

The Journal of pediatrics, 2001-08, Vol.139 (2), p.204-209

2001

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Distribution of Human Rotavirus G Types Circulating in Paris, France, during the 1997–1998 Epidemic: High Prevalence of Type G4

Journal of Clinical Microbiology, 1999-07, Vol.37 (7), p.2373-2375

1999

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Role of the DGAT Gene C79T Single‐Nucleotide Polymorphism in French Obese Subjects

Obesity (Silver Spring, Md.), 2003-10, Vol.11 (10), p.1163-1167

2003

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Pulmonary function and sleep-related breathing disorders in severely obese children

Clinical nutrition (Edinburgh, Scotland), 2006-10, Vol.25 (5), p.803-809

2006

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Obesity in Children and Adolescents Worldwide: Current Views and Future Directions—Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition

Journal of pediatric gastroenterology and nutrition, 2002-08, Vol.35, p.S205-S212

2002

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Efficacy of cyclosporin A in children with type 2 autoimmune hepatitis

The Journal of pediatrics, 1999-07, Vol.135 (1), p.111-114

1999

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Efficacy and tolerability of racecadotril in acute diarrhea in children

Gastroenterology (New York, N.Y. 1943), 2001-03, Vol.120 (4), p.799-805

2001

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Dépister la dénutrition de l’enfant

Nutrition clinique et métabolisme, 2013-09, Vol.27 (3), p.156-159

2013

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Dépister la dénutrition de l’enfant en pratique courante

Cahiers de nutrition et de diététique, 2013-09, Vol.48 (4), p.201-208

2013

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Molecular Spectrum of Autosomal Dominant Hypercholesterolemia in France

Human mutation, 2010-11, Vol.31 (11), p.E1811-E1824

2010

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Les médicaments hypocholestérolémiants chez l’enfant

Therapie, 2003-01, Vol.58 (1), p.63-67

Girardet, Jean-Philippe

2003

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Erratum: Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia

Human mutation, 2005-12, Vol.26 (6), p.592-592

2005

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Insulin resistance and ferritin as major determinants of abnormal serum aminotransferase in severely obese children

International journal of pediatric obesity, 2006-01, Vol.1 (2), p.77-82

2006

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Natural history of Crohn's disease: Comparison between childhood‐ and adult‐onset disease

Presence of increased stiffness of the common carotid artery and endothelial dysfunction in severely obese children: a prospective study

Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia

Global molecular analysis and APOE mutations in a cohort of autosomal dominant hypercholesterolemia patients in France[S]

Intractable Diarrhea With Tufting Enteropathy: A Favorable Outcome Is Possible

Intermediate-Term Efficacy and Tolerance of Statins in Children

Review of the nutritional benefits and risks related to intense sweeteners

Association of Arterial Stiffness and Endothelial Dysfunction with Metabolic Syndrome in Obese Children

Religious dietary rules and their potential nutritional and health consequences

Long-Term Follow-Up of Statin Treatment in a Cohort of Children with Familial Hypercholesterolemia: Efficacy and Tolerability

Pediatric Jejunal Gastrointestinal Stromal Tumor Diagnosed by Wireless Capsule Endoscopy

Plasma Citrulline Concentration Reflects Enterocyte Mass in Children With Short Bowel Syndrome

Mutational analysis of melanocortin-4 receptor, agouti-related protein, and α-melanocyte-stimulating hormone genes in severely obese children

Distribution of Human Rotavirus G Types Circulating in Paris, France, during the 1997–1998 Epidemic: High Prevalence of Type G4

Role of the DGAT Gene C79T Single‐Nucleotide Polymorphism in French Obese Subjects

Pulmonary function and sleep-related breathing disorders in severely obese children

Obesity in Children and Adolescents Worldwide: Current Views and Future Directions—Working Group Report of the First World Congress of Pediatric Gastroenterology, Hepatology, and Nutrition

Efficacy of cyclosporin A in children with type 2 autoimmune hepatitis

Efficacy and tolerability of racecadotril in acute diarrhea in children

Dépister la dénutrition de l’enfant

Dépister la dénutrition de l’enfant en pratique courante

Molecular Spectrum of Autosomal Dominant Hypercholesterolemia in France

Les médicaments hypocholestérolémiants chez l’enfant

Erratum: Novel mutations of the PCSK9 gene cause variable phenotype of autosomal dominant hypercholesterolemia

Insulin resistance and ferritin as major determinants of abnormal serum aminotransferase in severely obese children

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