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18 results on '"Viaud, Magali"'

1. Long-Term Weight Gain in Children with Craniopharyngioma

Author

Rovani, Sibylle, primary, Butler, Victoria, additional, Samara-Boustani, Dinane, additional, Pinto, Graziella, additional, Gonzalez-Briceno, Laura, additional, Nguyen Quoc, Adrien, additional, Vermillac, Gaëlle, additional, Stoupa, Athanasia, additional, Besançon, Alix, additional, Beltrand, Jacques, additional, Thalassinos, Caroline, additional, Flechtner, Isabelle, additional, Dassa, Yamina, additional, Viaud, Magali, additional, Arrom-Branas, Maria Beatriz, additional, Boddaert, Nathalie, additional, Puget, Stéphanie, additional, Blauwblomme, Thomas, additional, Alapetite, Claire, additional, Bolle, Stéphanie, additional, Doz, François, additional, Grill, Jacques, additional, Dufour, Christelle, additional, Bourdeaut, Franck, additional, Abbou, Samuel, additional, Guerrini-Rousseau, Léa, additional, Leruste, Amaury, additional, Beccaria, Kévin, additional, Polak, Michel, additional, and Kariyawasam, Dulanjalee, additional

Published
2024
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2. Quand le féminin est mis à mal … À propos d’une prise de poids significative chez des jeunes femmes en post-annonce diagnostique d’une agénésie utéro-vaginale

Author

Ouallouche, Chloé, Nataf, Nicole, Bidet, Maud, Cheikhelard, Alaa, Paniel, Jean-Bertrand, Louis-Sylvestre, Christine, Morcel, Karine, Viaud, Magali, Elie, Caroline, Baptiste, Amandine, Aigrain, Yves, Darai, Emile, Rouzier, Roman, Descamps, Philippe, Brun, Jean-Luc, Ranke, Aline, Lopes, Patrice, Pienkowski, Catherine, Leguevaque, Pierre, Gueniche, Karinne, Vibert, Sarah, Guinard, Maïa, and Polak, Michel

Published
2020
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4. Age at diagnosis in patients with chronic congenital endocrine conditions: a regional cohort study from a reference center for rare diseases

Author

Kallali, Wafa, Messiaen, Claude, Saïdi, Roumaisah, Lessim, Soucounda, Viaud, Magali, Dulon, Jerome, Nedelcu, Mariana, Samara, Dinane, Houang, Muriel, Donadille, Bruno, Courtillot, Carine, de Filippo, GianPaolo, Carel, Jean-Claude, Christin-Maitre, Sophie, Touraine, Philippe, Netchine, Irene, Polak, Michel, and Léger, Juliane

Published
2021
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5. GH and Childhood-onset Craniopharyngioma: When to Initiate GH Replacement Therapy?

Author

Nguyen Quoc, Adrien, primary, Beccaria, Kévin, additional, González Briceño, Laura, additional, Pinto, Graziella, additional, Samara-Boustani, Dinane, additional, Stoupa, Athanasia, additional, Beltrand, Jacques, additional, Besançon, Alix, additional, Thalassinos, Caroline, additional, Puget, Stéphanie, additional, Blauwblomme, Thomas, additional, Alapetite, Claire, additional, Bolle, Stéphanie, additional, Doz, François, additional, Grill, Jacques, additional, Dufour, Christelle, additional, Bourdeaut, Franck, additional, Abbou, Samuel, additional, Guerrini-Rousseau, Léa, additional, Leruste, Amaury, additional, Brabant, Séverine, additional, Cavadias, Iphigénie, additional, Viaud, Magali, additional, Boddaert, Nathalie, additional, Polak, Michel, additional, and Kariyawasam, Dulanjalee, additional

Published
2023
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9. Puberty and fertility in classic galactosemia

Author

Flechtner, Isabelle, primary, Viaud, Magali, additional, Kariyawasam, Dulanjalee, additional, Perrissin-Fabert, Marie, additional, Bidet, Maud, additional, Bachelot, Anne, additional, Touraine, Philippe, additional, Labrune, Philippe, additional, de Lonlay, Pascale, additional, and Polak, Michel, additional

Published
2021
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10. Glucose pattern in children with classical congenital adrenal hyperplasia: evidence from continuous glucose monitoring.

Author

Galderisi, Alfonso, Kariyawasam, Dulanjalee, Stoupa, Atanasia, Quoc, Adrien Nguyen, Pinto, Graziella, Viaud, Magali, Brabant, Séverine, Beltrand, Jacques, Polak, Michel, and Samara-Boustani, Dinane

Subjects
CONTINUOUS glucose monitoring, ADRENOGENITAL syndrome, GLUCOSE
Abstract

This article discusses the use of continuous glucose monitoring (CGM) in children with classical congenital adrenal hyperplasia (CAH). The authors acknowledge a comment from another study that was published shortly after their own, highlighting some differences between the two studies. They emphasize the need for further investigation in this area and identify three major gaps in knowledge: the absence of control groups for CGM-based studies, the lack of consensus on reporting CGM outcomes, and the heterogeneity of reporting CGM data. The authors also suggest the need for validating diabetes-validated metrics in people with CAH. Overall, this article aims to contribute to the ongoing debate on CGM use in people with CAH. [Extracted from the article]

Published
2024
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11. Quand le féminin est mis à mal … À propos d’une prise de poids significative chez des jeunes femmes en post-annonce diagnostique d’une agénésie utéro-vaginale

Author

Gueniche, Karinne, primary, Vibert, Sarah, additional, Guinard, Maïa, additional, Polak, Michel, additional, Ouallouche, Chloé, additional, Nataf, Nicole, additional, Bidet, Maud, additional, Cheikhelard, Alaa, additional, Paniel, Jean-Bertrand, additional, Louis-Sylvestre, Christine, additional, Morcel, Karine, additional, Viaud, Magali, additional, Elie, Caroline, additional, Baptiste, Amandine, additional, Aigrain, Yves, additional, Darai, Emile, additional, Rouzier, Roman, additional, Descamps, Philippe, additional, Brun, Jean-Luc, additional, Ranke, Aline, additional, Lopes, Patrice, additional, Pienkowski, Catherine, additional, and Leguevaque, Pierre, additional

Published
2020
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12. Pituitary deficiency and precocious puberty after childhood severe traumatic brain injury: a long-term follow-up prospective study

Author

Dassa, Yamina, primary, Crosnier, Hélène, additional, Chevignard, Mathilde, additional, Viaud, Magali, additional, Personnier, Claire, additional, Flechtner, Isabelle, additional, Meyer, Philippe, additional, Puget, Stéphanie, additional, Boddaert, Nathalie, additional, Breton, Sylvain, additional, and Polak, Michel, additional

Published
2019
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13. Improved General and Height-Specific Quality of Life in Children With Short Stature After 1 Year on Growth Hormone

Author

González Briceño, Laura G, primary, Viaud, Magali, additional, Beltrand, Jacques, additional, Flechtner, Isabelle, additional, Dassa, Yamina, additional, Samara-Boustani, Dinane, additional, Thalassinos, Caroline, additional, Pauwels, Christian, additional, Busiah, Kanetee, additional, Pinto, Graziella, additional, Jaquet, Delphine, additional, and Polak, Michel, additional

Published
2019
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14. Surgery is not superior to dilation for the management of vaginal agenesis in Mayer-Rokitansky-Küster-Hauser syndrome: a multicenter comparative observational study in 131 patients

Author

Cheikhelard, Alaa, primary, Bidet, Maud, additional, Baptiste, Amandine, additional, Viaud, Magali, additional, Fagot, Christine, additional, Khen-Dunlop, Naziha, additional, Louis-Sylvestre, Christine, additional, Sarnacki, Sabine, additional, Touraine, Philippe, additional, Elie, Caroline, additional, Aigrain, Yves, additional, Polak, Michel, additional, Brun, Jean-Luc, additional, Darai, Emile, additional, Descamps, Philippe, additional, Gueniche, Karinne, additional, Leguevaque, Pierre, additional, Lopes, Patrice, additional, Louis-Borrione, Claude, additional, Morcel, Karine, additional, Ouallouche, Chloe, additional, Paniel, Bernard-Jean, additional, Ranke, Aline, additional, Rouzier, Romain, additional, and Pienkowski, Catherine, additional

Published
2018
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16. Efficacy and Safety of Growth Hormone Treatment in Children with Hypochondroplasia: Comparison with an Historical Cohort

Author

Pinto, Graziella, primary, Cormier-Daire, Valérie, additional, Le Merrer, Martine, additional, Samara-Boustani, Dinane, additional, Baujat, Geneviève, additional, Fresneau, Laurence, additional, Viaud, Magali, additional, Souberbielle, Jean Claude, additional, Pineau, Jean Claude, additional, and Polak, Michel, additional

Published
2014
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17. Efficacy and Safety of Growth Hormone Treatment in Children with Hypochondroplasia: Comparison with an Historical Cohort.

Author

Pinto, Graziella, Cormier-Daire, Valérie, Le Merrer, Martine, Samara-Boustani, Dinane, Baujat, Geneviève, Fresneau, Laurence, Viaud, Magali, Souberbielle, Jean Claude, Pineau, Jean Claude, and Polak, Michel

Subjects
HUMAN growth hormone, RECOMBINANT human somatotropin, SKELETAL dysplasia, STATURE, PEDIATRIC endocrinology
Abstract

Background/Aims: Hypochondroplasia (HCH) is a skeletal dysplasia characterized by disproportionate short stature. The aims of the study are to evaluate efficacy and safety of recombinant human growth hormone (r-hGH) therapy in HCH children, when compared with a historical cohort of untreated HCH children. Methods: Nineteen HCH patients with an initial height standard deviation score (SDS) ≤-2 and a mean age of 9.3 ± 3.1 years were treated with a mean r-hGH dose of 0.053 mg/kg/day over 3 years. Growth charts were derived from the historical cohort (n = 40). Results: Height gain in the treated population was +0.62 ± 0.81 SDS greater than in the general population, and +1.39 ± 0.9 SDS greater than in the historical untreated HCH cohort (mean gain of 7.4 ± 6.6 cm gain). A negative correlation between height gain and age at treatment initiation was reported (p = 0.04). There was no significant difference in response between patients with fibroblast growth factor receptor 3 mutations and those without. No treatment-related serious adverse events were reported. Conclusions: r-hGH treatment is well tolerated and effective in improving growth in HCH patients, particularly when started early. The treatment effect varies greatly and must be evaluated for each patient during treatment to determine the value of continued therapy. © 2014 S. Karger AG, Basel [ABSTRACT FROM AUTHOR]

Published
2015
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18. Clinical and Preliminary Molecular Description of a Cohort of Patients with Growth Retardation Due to Severe Primary IGF1 Deficiency (GROWPATI Study)

Author

Stoupa, Athanasia, Viaud, Magali, Flechtner, Isabelle, Pinto, Graziella, Samara-Boustani, Dinane, Thalassinos, Caroline, Gonzalez Briceno, Laura Gabriela, Beltrand, Jacques, Netchine, Irene, Brioude, Frederic, Marie Legendre, Amselem, Serge, Polak, Michel, CHU Necker - Enfants Malades [AP-HP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Imagine - Institut des maladies génétiques (IHU) (Imagine - U1163), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Paris Cité (UPCité), Institut Cochin (IC UM3 (UMR 8104 / U1016)), Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-Université Paris Cité (UPCité), Service d'endocrinologie, gynécologie et diabétologie pédiatriques [CHU Necker], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP), Imagine - Institut des maladies génétiques (IMAGINE - U1163), Université Paris Descartes - Paris 5 (UPD5)-Institut National de la Santé et de la Recherche Médicale (INSERM), Centre de Recherche Saint-Antoine (UMRS893), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut National de la Santé et de la Recherche Médicale (INSERM), UF de Génétique moléculaire [CHU Trousseau], CHU Trousseau [APHP], Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU)-Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Maladies génétiques d'expression pédiatrique [CHU Trousseau] (Inserm U933), Institut National de la Santé et de la Recherche Médicale (INSERM)-CHU Trousseau [APHP], Université Pierre et Marie Curie - Paris 6 - UFR de Médecine Pierre et Marie Curie (UPMC), Université Pierre et Marie Curie - Paris 6 (UPMC), and Couvet, Sandrine

Subjects
[SDV.MHEP.EM] Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics, [SDV.MHEP.EM]Life Sciences [q-bio]/Human health and pathology/Endocrinology and metabolism, [SDV.GEN.GH] Life Sciences [q-bio]/Genetics/Human genetics
Abstract

Background: Severe primary insulin-growth factor-1 (IGF1) deficiency (SPIGF1D) is a rare cause of growth retardation. Diagnostic criteria include age- and sex-dependent low basal IGF1 levels (

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