Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Béatrice THOUVENIN"'
Autor:
Béatrice Thouvenin, Véronique Soupre, Marie-Anne Caillaud, Charlotte Henry-Mestelan, Christel Chalouhi, Bachar Houssamo, Cécile Chapuis, Katia Lind, Aurélie Royer, Nancy Vegas, Jeanne Amiel, Gérard Couly, Arnaud Picard, Laurence Vaivre-Douret, Véronique Abadie
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Abstract Background Pierre Robin sequence (PRS) is a heterogeneous condition involving retro(micro)gnathia, glossoptosis and upper airway obstruction, very often with posterior cleft palate. Patients with PRS, either isolated or associated with Stick
Externí odkaz:
https://doaj.org/article/c1621709acc0475a988a4f5d87c333a3
Autor:
Justine Mirete, Béatrice Thouvenin, Gaelle Malecot, Morgane Le-Gouëz, Christel Chalouhi, Catherine du Fraysseix, Aurélie Royer, Anais Leon, Clément Vachey, Véronique Abadie
Publikováno v:
Frontiers in Pediatrics, Vol 6 (2018)
ObjectiveTo describe a series of children who were hospitalized for a tube-weaning program in the general pediatric ward of a pediatric tertiary university hospital: describe our method, to determine the success rate of our inpatient pediatric tube w
Externí odkaz:
https://doaj.org/article/70c6e7c60f014889919c045ffa776ebb
Autor:
Jeanne Amiel, Katia Lind, Aurélie Royer, Cécile Chapuis, Béatrice Thouvenin, Laurence Vaivre-Douret, Christel Chalouhi, Gérard Couly, Marie-Anne Caillaud, Véronique Abadie, Nancy Vegas, Arnaud Picard, Charlotte Henry-Mestelan, Bachar Houssamo, Véronique Soupre
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-15 (2021)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Pierre Robin sequence (PRS) is a heterogeneous condition involving retro(micro)gnathia, glossoptosis and upper airway obstruction, very often with posterior cleft palate. Patients with PRS, either isolated or associated with Stickler syndr
Autor:
Béatrice THOUVENIN, Véronique SOUPRE, Marie-Anne CAILLAUD, Charlotte Henry-Mestelan, Christel CHALOUHI, Bachar HOUSSAMO, Cécile Chapuis, Katia LIND, Aurélie ROYER, Nancy VEGAS, Jeanne AMIEL, Gérard COULY, Arnaud PICARD, Laurence VAIVRE-DOURET, Véronique Abadie
We assessed the phonatory and morphological outcome of 72 cognitively unimpaired adolescents with Pierre Robin Sequence (PRS), studied their generic (Kidscreen-52), oral (COHIP-SF19) and vocal (VHI-9i) qualities of life (QoL), and sought to identify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::349c15f371f7f2dc78e0a04203e41f32
https://doi.org/10.21203/rs.3.rs-532688/v1
https://doi.org/10.21203/rs.3.rs-532688/v1
Autor:
Véronique Abadie, Christel Chalouhi, Laure Soulez-la-Rivière, Christine Rastel, Gaëlle Malécot-Le Meur, Béatrice Thouvenin
Publikováno v:
Soins Pédiatrie/Puériculture. 37:37-42
To support children and their families with weaning off artificial nutrition, a psychomotor therapist and speech therapist from the 'Pierre Robin syndrome and congenital sucking-swallowing disorders' specialist rare disease centre at Necker-Enfant Ma
Autor:
Gaëlle, Malécot-Le Meur, Laure, Soulez-Larivière, Véronique, Abadie, Béatrice, Thouvenin, Christine, Rastel, Christel, Chalouhi
Publikováno v:
Soins. Pediatrie, puericulture. 37(293)
To support children and their families with weaning off artificial nutrition, a psychomotor therapist and speech therapist from the 'Pierre Robin syndrome and congenital sucking-swallowing disorders' specialist rare disease centre at Necker-Enfant Ma
Publikováno v:
L'Évolution Psychiatrique. 75:123-137
Resume Comment comprendre la violence soudainement auto-infligee par l’adolescent qui tente de se suicider ? Les imagos parentales font-elles inconsciemment partie de ce scenario violent ? Telles sont les questions auxquelles les auteurs vont tente
Autor:
Christel Chalouhi, Juliette Djadi-Prat, Béatrice Thouvenin, Véronique Abadie, Gérard Couly, S. Pierrot, Stanislas Lyonnet
Publikováno v:
American journal of medical genetics. Part A. (2)
Pierre Robin sequence (PRS) is a congenital condition with a heterogeneous and imprecise developmental prognosis. We conducted a longitudinal prospective study analyzing the long-term developmental outcome of a consecutive series of 39 children with