Search Results - "Passone, Caroline de Gouveia Buff"

Growth hormone treatment in Prader-Willi syndrome patients: systematic review and meta-analysis by Passone, Caroline de Gouveia Buff, Franco, Ruth Rocha, Ito, Simone Sakura, Trindade, Evelinda, Polak, Michel, Damiani, Durval, Bernardo, Wanderley Marques

“…BackgroundGrowth hormone (GH) treatment is currently recommended in Prader-Willi syndrome (PWS) patients.ObjectivesTo evaluate the impact (efficacy and safety)…”
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Translation and validation of Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0 Diabetes Module) in Brazil-Portuguese language by Garcia, Leila F. dos S., Manna, Thais Della, Passone, Caroline de Gouveia Buff, Oliveira, Lygia Spassapan de

“…The aim of the present study was to create a translated version of the Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0 Diabetes Module)…”
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Sulfonylurea for improving neurological features in neonatal diabetes: A systematic review and meta‐analyses by Gouveia Buff Passone, Caroline, Giani, Elisa, Vaivre‐Douret, Laurence, Kariyawasam, Dulanjalee, Berdugo, Marianne, Garcin, Laure, Beltrand, Jacques, Bernardo, Wanderley Marques, Polak, Michel

“…Objective In monogenic diabetes due to KCNJ11 and ABCC8 mutations that impair KATP‐ channel function, sulfonylureas improve long‐term glycemic control…”
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Mitchell–Riley Syndrome: Improving Clinical Outcomes and Searching for Functional Impact of RFX-6 Mutations by Passone, Caroline de Gouveia Buff, Vermillac, Gaëlle, Staels, Willem, Besancon, Alix, Kariyawasam, Dulanjalee, Godot, Cécile, Lambe, Cécile, Talbotec, Cécile, Girard, Muriel, Chardot, Christophe, Berteloot, Laureline, Hachem, Taymme, Lapillonne, Alexandre, Poidvin, Amélie, Storey, Caroline, Neve, Mathieu, Stan, Cosmina, Dugelay, Emmanuelle, Fauret-Amsellem, Anne-Laure, Capri, Yline, Cavé, Hélène, Ybarra, Marina, Chandra, Vikash, Scharfmann, Raphaël, Bismuth, Elise, Polak, Michel, Carel, Jean Claude, Pigneur, Bénédicte, Beltrand, Jacques

“…Aims/HypothesisCaused by biallelic mutations of the gene encoding the transcription factor RFX6, the rare Mitchell-Riley syndrome (MRS) comprises neonatal…”
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Correction notice: Growth hormone treatment in Prader-Willi syndrome patients: systematic review and meta-analysis

“…Passone CDGB, Franco RR, Ito SS, et al. Growth hormone treatment in Prader-Willi syndrome patients:systematic review and meta-analysis. BMJ Paediatrics Open…”
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Sulphonylurea for Improving Neurological Features in Neonatal Diabetes: a systematic review and meta-analyses by Passone, Caroline de Gouveia Buff, Giani, Elisa, Vaivre-Douret, Laurence, Kariyawasam, Dulanjalee, Berdugo, Marianne, Garcin, Laure, Beltrand, Jacques, Bernardo, Wanderley Marques, Polak, Michel

“…In monogenic diabetes due to KCNJ11 and ABCC8 mutations that impair KATP- channel function, sulphonylureas improve long-term glycaemic control. Although KATP…”
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Translation and validation of Pediatric Quality of Life InventoryTM 3.0 Diabetes Module (PedsQLTM 3.0 Diabetes Module) in Brazil-Portuguese language by Garcia, Leila F. dos S., Manna, Thais Della, Passone, Caroline de Gouveia Buff, Oliveira, Lygia Spassapan de

“…Abstract Objective: The aim of the present study was to create a translated version of the Pediatric Quality of Life InventoryTM 3.0 Diabetes Module (PedsQLTM…”
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Translation and validation of Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0 Diabetes Module) in Brazil‐Portuguese language by Garcia, Leila F. dos S., Manna, Thais Della, Passone, Caroline de Gouveia Buff, Oliveira, Lygia Spassapan de

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Programa de Qualidade na Interação Familiar (PQIF) para manejo de comportamentos na síndrome Prader-Willi by Pacheco Gomide, Cibele, Mendes Aguiar, Thays, Sakura Ito, Simone, Rocha Franco, Ruth, De Gouveia Buff Passone, Caroline, Damiani, Durval, Moreira Pereira, Clarissa

“…Pais e cuidadores de crianças com a síndrome Prader-Willi (SPW) enfrentam desafios no manejo dos comportamentos característicos do fenótipo comportamental…”
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Programa de Qualidade na Interação Familiar (PQIF) para manejo de comportamentos na síndrome Prader-Willi by Pacheco Gomide, Cibele, Mendes Aguiar, Thays, Sakura Ito, Simone, Rocha Franco, Ruth, De Gouveia Buff Passone, Caroline, Damiani, Durval, Moreira Pereira, Clarissa

“…Pais e cuidadores de crianças com a síndrome Prader-Willi (SPW) enfrentam desafios no manejo dos comportamentos característicos do fenótipo comportamental…”
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Translation and validation of Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0 Diabetes Module) in Brazil‐Portuguese language by Leila F. dos S. Garcia, Thais Della Manna, Caroline de Gouveia Buff Passone, Lygia Spassapan de Oliveira

“…Objective: The aim of the present study was to create a translated version of the Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0…”
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