Search Results - "Reynaud, R."
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Human skin penetration of hyaluronic acid of different molecular weights as probed by Raman spectroscopy
Published in Skin research and technology (01-02-2016)“…Topical delivery of molecules into the human skin is one of the main issues in dermatology and cosmetology. Several techniques were developed to study…”
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Synergistic use of bioactive agents for the management of different skin conditions: an overview of biological activities
Published in European review for medical and pharmacological sciences (01-02-2023)“…Recently, many plant-derived bioactive agents have been included in dermo-cosmetics formulations. This leads to an extensive portfolio of innovative products…”
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3
Two cases of fractures in neonates associated with maternofetal vitamin D deficiency
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-09-2019)“…Vitamin D supplementation is essential for the entire population, especially during pregnancy and in the pediatric period. We report two case studies of…”
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4
Prevalence of overweight, obesity, and early adiposity rebound in nursery school children in southeastern France
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-07-2022)“…The aim of the present study was to assess the prevalence of overweight, obesity, and early adiposity rebound in nursery school children aged 3.5–4.5 years and…”
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Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms
Published in European journal of endocrinology (01-04-2011)“…BackgroundPituitary stalk interruption syndrome (PSIS) is a particular entity in the population of patients with hypopituitarism. Only rare cases have a known…”
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Clinical, radiological, and molecular diagnosis of congenital pituitary diseases causing short stature
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-02-2022)“…Short stature in children can be caused by congenital pituitary disorders involving at least one form of growth hormone deficiency. Clinical and radiological…”
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X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood
Published in European journal of endocrinology (01-06-2019)“…Objective Turner Syndrome is associated with several phenotypic conditions associated with a higher risk of subsequent comorbidity. We aimed to evaluate the…”
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Conformation changes in human hair keratin observed using confocal Raman spectroscopy after active ingredient application
Published in International journal of cosmetic science (01-06-2019)“…Objective In hair care cosmetic products’ evaluation, one commonly used method is to evaluate the hair appearance as a gold standard in order to determine the…”
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Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-04-2020)“…Acute liver failure (ALF) in childhood is a life-threatening emergency. ALF is often caused by drug toxicity, autoimmune hepatitis, inherited metabolic…”
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Combined pituitary hormone deficiency: current and future status
Published in Journal of endocrinological investigation (01-01-2015)“…Over the last two decades, the understanding of the mechanisms involved in pituitary ontogenesis has largely increased. Since the first description of POU1F1…”
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Impact of continuous glucose monitoring on everyday life of young children with type 1 diabetes and their parents: An evaluation of 114 families
Published in Primary care diabetes (01-02-2024)“…The prevalence of type 1 diabetes is increasing worldwide. The advent of new monitoring devices has enabled tighter glycemic control. To study the impact of…”
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Investigation of tall stature in children: Diagnostic work-up, review of the main causes
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-02-2018)“…Tall stature is not a common motive for medical consultation, even though by definition 2.5 % of children in the general population are concerned. It is…”
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Limited Value of 18F-F-DOPA PET to Localize Pancreatic Insulin-Secreting Tumors in Adults with Hyperinsulinemic Hypoglycemia
Published in The journal of clinical endocrinology and metabolism (01-01-2010)“…Context: Fluorine-18-l-dihydroxyphenylalanine positron emission tomography (18F-FDOPA PET) imaging is increasingly used in the workup of neuroendocrine tumors…”
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14
Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-05-2022)“…Neonatal screening for congenital hypothyroidism (CH) is based on the measurement of thyroid-stimulating hormone (TSH) in whole dried blood samples on filter…”
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Hospital-based home care for young children newly diagnosed with type 1 diabetes: Assessing expectations and obstacles in families and general practitioners
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-09-2019)“…This study aimed to evaluate whether hospital-based home care was desired by the parents of children diagnosed with type 1 diabetes (T1D) under the age of 5…”
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Infant food diversification. Assessment of practices in relation to French recommendations in pediatricians and pediatric residents in southern France
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-10-2016)“…Infant food diversification has undergone a rapid succession of good practice recommendations in France, but there has been no assessment of pediatrician…”
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Untersuchung des nasalen Metabolismus von Aroma‐ und Geruchsstoffen
Published in Lebensmittelchemie (01-09-2022)Get full text
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GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency
Published in Hormone and metabolic research (01-06-2016)“…Patients with Xq26.3 microduplication present with X-linked acrogigantism (X-LAG) syndrome, an early-childhood form of gigantism due to marked growth hormone…”
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Nasaler Metabolismus: Warum Kaffee auf einmal nach Knoblauch riecht?
Published in Lebensmittelchemie (01-03-2022)Get full text
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Rapid differential diagnosis of diabetes insipidus in a 7-month-old infant: The copeptin approach
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01-01-2018)“…Diabetes insipidus is characterized by hypoosmotic polyuria related to deficiency of arginine–vasopressin (AVP) secretion (central diabetes insipidus, CDI) or…”
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