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Christel Chalouhi

Necker-Enfants Malades Hospital

13

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120

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Safety of Cyproheptadine, an Orexigenic Drug. Analysis of the French National Pharmacovigilance Data-Base and Systematic Review

2021 Frontiers in Pediatrics
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Heterozygous ANKRD17 loss-of-function variants cause a syndrome with intellectual disability, speech delay, and dysmorphism

2021 American Journal of Human Genetics
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Scurvy: A New Old Cause of Skeletal Pain in Young Children

2020 Frontiers in Pediatrics
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Frequency of Abnormal Glucose Tolerance Test Suggestive of Dumping Syndrome Following œsophageal Atresia Repair

2020 Journal of Pediatric Gastroenterology and Nutrition
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Chromosome 14q32.2 Imprinted Region Disruption as an Alternative Molecular Diagnosis of Silver-Russell Syndrome

2018 The Journal of Clinical Endocrinology and Metabolism
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Efficiency of prenatal diagnosis in Pierre Robin sequence.

2017 Prenatal Diagnosis
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Prenatal diagnosis of Pierre Robin Sequence: accuracy and ability to predict phenotype and functional severity

2015 Prenatal Diagnosis
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Developmental outcome in Pierre Robin sequence: a longitudinal and prospective study of a consecutive series of severe phenotypes.

2013 American Journal of Medical Genetics Part A
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