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Screening of esophageal varices in children using esophageal capsule endoscopy: a multicenter prospective study

Endoscopy, 2019-01, Vol.51 (1), p.10-17

2019

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Cholic acid for primary bile acid synthesis defects: a life-saving therapy allowing a favorable outcome in adulthood

Orphanet journal of rare diseases, 2018-10, Vol.13 (1), p.190-190, Article 190

2018

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Characteristics and management of congenital esophageal stenosis: findings from a multicenter study

Orphanet journal of rare diseases, 2013-12, Vol.8 (1), p.186-186, Article 186

2013

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Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis

Diagnostics (Basel), 2022-05, Vol.12 (5), p.1169

2022

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Contribution of capsule endoscopy to Peutz-Jeghers syndrome management in children

Digestive and liver disease, 2012-10, Vol.44 (10), p.839-843

2012

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Long-term outcomes and predictors of disabling disease in a population-based cohort of patients with incident Crohn's disease diagnosed between 1994 and 1997

Clinics and research in hepatology and gastroenterology, 2022-11, Vol.46 (9), p.101974-101974, Article 101974

2022

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Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities

Clinics and research in hepatology and gastroenterology, 2021-09, Vol.45 (5), p.101562, Article 101562

2021

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Chylomicron retention disease

Digestive and liver disease, 2013-02, Vol.45 (2), p.e3-e3

2013

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Maternal uniparental disomy 14 revealed by alpha 1 antitrypsin deficiency

Clinics and research in hepatology and gastroenterology, 2014-10, Vol.38 (5), p.604-606

2014

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Astrovirus and digestive disorders in neonatal units

Acta Paediatrica, 2012-05, Vol.101 (5), p.e208-e212

2012

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Vaccination coverage of children with inflammatory bowel disease after an awareness campaign on the risk of infection

Digestive and liver disease, 2015-06, Vol.47 (6), p.460-464

2015

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Tufted angioma with Kasabach–Merritt syndrome mistaken for child abuse

Forensic science international, 2014-12, Vol.245, p.e15-e17

2014

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Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities

Clinics and research in hepatology and gastroenterology, 2021, Vol.45 (5), p.101562-101562

2021

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Incidence of inflammatory bowel disease (IBD) in Western France (1994–1997)

Gastroenterology (New York, N.Y. 1943), 2000-04, Vol.118 (4), p.A1339-A1339

2000

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A follow-up is necessary to accurately assess the incidence rate of inflammatory bowel diseases (IBD) in population registries

Gastroenterology (New York, N.Y. 1943), 2000-04, Vol.118 (4), p.A1339-A1339

2000

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SRD5B1 (AKR1D1) gene analysis in delta(4)-3-oxosteroid 5beta-reductase deficiency: evidence for primary genetic defect

Journal of hepatology, 2004, Vol.40 (4), p.716-718

2004

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Diagnosis and neonatal screening of cystic fibrosis

La revue du praticien, 2003-01, Vol.53 (2), p.135

2003

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Intérêt de l'élastométrie impulsionnelle dans l'évaluation non invasive du stade de fibrose hépatique chez l'enfant. [Value of transient elastography in noninvasive assessment in children's hepatic fibrosis]

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2009-07, Vol.16 (7), p.1005-10

2009

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Screening of esophageal varices in children using esophageal capsule endoscopy: a multicenter prospective study

Cholic acid for primary bile acid synthesis defects: a life-saving therapy allowing a favorable outcome in adulthood

Characteristics and management of congenital esophageal stenosis: findings from a multicenter study

Targeted-Capture Next-Generation Sequencing in Diagnosis Approach of Pediatric Cholestasis

Contribution of capsule endoscopy to Peutz-Jeghers syndrome management in children

Clinical similarities and differences of patients with X-linked lymphoproliferative syndrome type 1 (XLP-1/SAP deficiency) versus type 2 (XLP-2/XIAP deficiency)

Long-term outcomes and predictors of disabling disease in a population-based cohort of patients with incident Crohn's disease diagnosed between 1994 and 1997

Functional abdominal pain disorders and patient- and parent-reported outcomes in children with inflammatory bowel disease in remission

Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities

Chylomicron retention disease

Maternal uniparental disomy 14 revealed by alpha 1 antitrypsin deficiency

Astrovirus and digestive disorders in neonatal units

Vaccination coverage of children with inflammatory bowel disease after an awareness campaign on the risk of infection

Tufted angioma with Kasabach–Merritt syndrome mistaken for child abuse

Antenatal finding of 16q24.1 duplication including FOXF1, revealing an autosomal dominant familial pathology with congenital short bowel, malrotation and renal abnormalities

Incidence of inflammatory bowel disease (IBD) in Western France (1994–1997)

A follow-up is necessary to accurately assess the incidence rate of inflammatory bowel diseases (IBD) in population registries

SRD5B1 (AKR1D1) gene analysis in delta(4)-3-oxosteroid 5beta-reductase deficiency: evidence for primary genetic defect

Diagnosis and neonatal screening of cystic fibrosis

Intérêt de l'élastométrie impulsionnelle dans l'évaluation non invasive du stade de fibrose hépatique chez l'enfant. [Value of transient elastography in noninvasive assessment in children's hepatic fibrosis]

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