Search Results - "Pham, Aurélie"
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Diagnosis and management of postnatal fetal growth restriction
Published in Baillière's best practice & research. Clinical endocrinology & metabolism (01-08-2018)“…Fetal growth restriction (FGR) can result from multiple causes, such as genetic, epigenetic, environment, hormonal regulation, or vascular troubles and their…”
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Screening of patients born small for gestational age with the Silver-Russell syndrome phenotype for DLK1 variants
Published in European journal of human genetics : EJHG (01-12-2021)“…Silver-Russell syndrome (SRS) is a rare imprinting disorder associated with prenatal and postnatal growth retardation. Loss of methylation (LOM) on chromosome…”
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Usefulness of routine early œsophagogram after primary repair of œsophageal atresia: a multicenter study
Published in Pediatric research (01-11-2023)“…Background Advances in surgical and neonatal care have led to improved survival of patients with œsophageal atresia (OA) over time. Morbidity remains…”
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Dental pulp stem cells as a promising model to study imprinting diseases
Published in International journal of oral science (02-04-2022)“…Parental imprinting is an epigenetic process leading to monoallelic expression of certain genes depending on their parental origin. Imprinting diseases are…”
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Prokaryotic abundance, cell size and extracellular enzymatic activity in a human impacted and mangrove dominated tropical estuary (Can Gio, Vietnam)
Published in Estuarine, coastal and shelf science (05-04-2021)“…Extracellular enzymatic activities constitute the first and limiting step of the whole process of organic matter (OM) cycling in aquatic ecosystems. This study…”
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Perinatal features of children with Silver-Russell syndrome due to 11p15 loss of methylation
Published in Frontiers in pediatrics (04-04-2024)“…A diagnosis of Silver-Russell syndrome (SRS), a rare imprinting disorder responsible for foetal growth restriction, is considered for patients presenting at…”
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A Case of Scrotoschisis with Exteriorization of Both Testes
Published in Fetal and pediatric pathology (02-11-2022)“…Scrotoschisis is a congenital malformation characterized by testicular exstrophy through a scrotal defect. We report a full-term baby boy with exteriorization…”
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Feeding disorders in children with oesophageal atresia: a cross-sectional study
Published in Archives of disease in childhood (01-01-2022)“…IntroductionWith advances in surgical and neonatal care, the survival of patients with oesophageal atresia (OA) has improved over time. Whereas a number of…”
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Real-world effectiveness of nirsevimab immunisation against bronchiolitis in infants: a case-control study in Paris, France
Published in The lancet child & adolescent health (01-10-2024)“…Respiratory syncytial virus (RSV) is the most common cause of bronchiolitis in infants. Nirsevimab, an RSV-neutralising monoclonal antibody, was approved for…”
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Low Maternal DLK1 Levels at 26 Weeks Is Associated With Small for Gestational Age at Birth
Published in Frontiers in endocrinology (Lausanne) (28-02-2022)“…Detecting SGA (small for gestational age) during pregnancy improves the fetal and neonatal prognosis. To date, there is no valid antenatal biomarker of SGA…”
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Dental pulp stem cells as a promising model to study imprinting diseases
Published in 国际口腔科学杂志(英文版) (2022)Get full text
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Acute respiratory distress in children
Published in La Revue du praticien (01-04-2020)Get more information
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