Search Results - "Reynaud, R."

Human skin penetration of hyaluronic acid of different molecular weights as probed by Raman spectroscopy by Essendoubi, M., Gobinet, C., Reynaud, R., Angiboust, J. F., Manfait, M., Piot, O.

“…Background Topical delivery of molecules into the human skin is one of the main issues in dermatology and cosmetology. Several techniques were developed to…”
Get full text

Poorly described phenotypes add to the misfortune of rare diseases by A, Fabre, K, Aouchiche, R, Reynaud

“…An often overlooked problem in the characterization of rare diseases is the contingent and evolving nature of accepted phenotypes. In the era of…”
Get full text

Synergistic use of bioactive agents for the management of different skin conditions: an overview of biological activities by Baldi, M, Reynaud, R, Lefevre, F, Fleury, M, Scandolera, A, Maramaldi, G

“…Recently, many plant-derived bioactive agents have been included in dermo-cosmetics formulations. This leads to an extensive portfolio of innovative products…”
Get more information

Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review by Chavany, J., Cano, A., Roquelaure, B., Bourgeois, P., Boubnova, J., Gaignard, P., Hoebeke, C., Reynaud, R., Rhomer, B., Slama, A., Badens, C., Chabrol, B., Fabre, A.

“…Acute liver failure (ALF) in childhood is a life-threatening emergency. ALF is often caused by drug toxicity, autoimmune hepatitis, inherited metabolic…”
Get full text

Prevalence of overweight, obesity, and early adiposity rebound in nursery school children in southeastern France by Roth, B., Reynaud, R., Nègre, V., Gentile, S., Pauly, V., Bernard, O.

“…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…”
Get full text

Two cases of fractures in neonates associated with maternofetal vitamin D deficiency by Albertini, F., Marquant, E., Reynaud, R., Lacroze, V.

“…Vitamin D supplementation is essential for the entire population, especially during pregnancy and in the pediatric period. We report two case studies of…”
Get full text

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 by Fiot, Elodie, Zénaty, Delphine, Boizeau, Priscilla, Haignere, Jeremie, Dos Santos, Sophie, Leger, Juliane

“…Objective Turner Syndrome is associated with several phenotypic conditions associated with a higher risk of subsequent comorbidity. We aimed to evaluate the…”
Get more information

Pituitary stalk interruption syndrome in 83 patients: novel HESX1 mutation and severe hormonal prognosis in malformative forms by Reynaud, R, Albarel, F, Saveanu, A, Kaffel, N, Castinetti, F, Lecomte, P, Brauner, R, Simonin, G, Gaudart, J, Carmona, E, Enjalbert, A, Barlier, A, Brue, T

“…Pituitary stalk interruption syndrome (PSIS) is a particular entity in the population of patients with hypopituitarism. Only rare cases have a known genetic…”
Get more information

Clinical, radiological, and molecular diagnosis of congenital pituitary diseases causing short stature by Castets, S., Villanueva, C., Vergier, J., Brue, T., Saveanu, A., Reynaud, R.

“…Short stature in children can be caused by congenital pituitary disorders involving at least one form of growth hormone deficiency. Clinical and radiological…”
Get full text

Impact of continuous glucose monitoring on everyday life of young children with type 1 diabetes and their parents: An evaluation of 114 families by Aouchiche, K., Bernoux, D., Baechler Sadoul, E., Haine, E., Joubert, F., Epstein, S., Faure Galon, N., Dalla-Vale, F., Combe, J.C., Samper, M., Simonin, G., Castets, S., Marquant, E., Vergier, J., Reynaud, R.

“…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…”
Get full text

Conformation changes in human hair keratin observed using confocal Raman spectroscopy after active ingredient application by Essendoubi, M., Meunier, M., Scandolera, A., Gobinet, C., Manfait, M., Lambert, C., Auriol, D., Reynaud, R., Piot, O.

“…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…”
Get full text

Treatment of pediatric heterozygous familial hypercholesterolemia: Where do we stand in real-world study in France seven years after the recommendations of the european atherosclerosis society (EAS)? by Peretti, N., Vimont, A., Mas, E., Lemale, J., Reynaud, R., Tounian, P., Poinsot, P., Bruckert, E., Gallo, A., Beliard, S.

Get full text

Combined pituitary hormone deficiency: current and future status by Castinetti, F., Reynaud, R., Quentien, M.-H., Jullien, N., Marquant, E., Rochette, C., Herman, J.-P., Saveanu, A., Barlier, A., Enjalbert, A., Brue, T.

“…Over the last two decades, the understanding of the mechanisms involved in pituitary ontogenesis has largely increased. Since the first description of POU1F1…”
Get full text

Hospital-based home care for young children newly diagnosed with type 1 diabetes: Assessing expectations and obstacles in families and general practitioners by Moulin, J., Castets, S., Galon-Faure, N., Jego, M., Reynaud, R.

“…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…”
Get full text

Neonatal screening for congenital hypothyroidism: Time to lower the TSH threshold in France by Levaillant, L., Huet, F., Bretones, P., Corne, C., Dupuis, C., Reynaud, R., Somma, C., Barat, P., Corcuff, J.B., Bouhours-Nouet, N., Gauthereau, V., Polak, M., Leger, J., Cheillan, D., Coutant, R.

“…Neonatal screening for congenital hypothyroidism (CH) is based on the measurement of thyroid-stimulating hormone (TSH) in whole dried blood samples on filter…”
Get full text

Investigation of tall stature in children: Diagnostic work-up, review of the main causes by Vergier, J, Marquant, E, Busa, T, Reynaud, R

“…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…”
Get full text

Analyse phénotypique et génotypique de 21 patients porteurs de mutation de GLI2 : expérience du réseau GENHYPOPIT by Charmensat, C., Saveanu, A., Reynaud, R.

“…Description phénotypique des patients atteints d’une mutation de GLI2. Sélection de la base de données GENHYPOPIT des patients avec déficit somatotrope ou…”
Get full text

Limited value of 18F-F-DOPA PET to localize pancreatic insulin-secreting tumors in adults with hyperinsulinemic hypoglycemia by Tessonnier, L, Sebag, F, Ghander, C, De Micco, C, Reynaud, R, Palazzo, F F, Conte-Devolx, B, Henry, J F, Mundler, O, Taïeb, D

“…Fluorine-18-L-dihydroxyphenylalanine positron emission tomography (18F-FDOPA PET) imaging is increasingly used in the workup of neuroendocrine tumors. It has…”
Get more information

Infant food diversification. Assessment of practices in relation to French recommendations in pediatricians and pediatric residents in southern France by Banti, T, Carsin, A, Chabrol, B, Reynaud, R, Fabre, A

“…Infant food diversification has undergone a rapid succession of good practice recommendations in France, but there has been no assessment of pediatrician…”
Get full text

GPR101 Mutations are not a Frequent Cause of Congenital Isolated Growth Hormone Deficiency by Castinetti, F, Daly, A F, Stratakis, C A, Caberg, J-H, Castermans, E, Trivellin, G, Rostomyan, L, Saveanu, A, Jullien, N, Reynaud, R, Barlier, A, Bours, V, Brue, T, Beckers, A

“…Patients with Xq26.3 microduplication present with X-linked acrogigantism (X-LAG) syndrome, an early-childhood form of gigantism due to marked growth hormone…”
Get more information