Stéphanie Pannier
Necker-Enfants Malades Hospital
89 Papers
192 Citations
Stéphanie Pannier is an academic researcher from Necker-Enfants Malades Hospital. The author has contributed to research in topics: Medicine & Internal medicine. The author has an hindex of 19, co-authored 73 publications. Previous affiliations of Stéphanie Pannier include Paris Descartes University.
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Papers
Targeted therapy in patients with PIK3CA-related overgrowth syndrome
Quitterie Venot,Thomas Blanc,Thomas Blanc,Thomas Blanc,Smail Hadj Rabia,Smail Hadj Rabia,Laureline Berteloot,Sophia Ladraa,J P Duong,J P Duong,Estelle Blanc,Simon C. Johnson,Clément Hoguin,Olivia Boccara,Sabine Sarnacki,Sabine Sarnacki,Nathalie Boddaert,Nathalie Boddaert,Stéphanie Pannier,Stéphanie Pannier,Frank Martinez,Sato Magassa,Junna Yamaguchi,Bertrand Knebelmann,Bertrand Knebelmann,Bertrand Knebelmann,Pierre Merville,Nicolas Grenier,Dominique Joly,Dominique Joly,Dominique Joly,Valérie Cormier-Daire,Valérie Cormier-Daire,Caroline Michot,Caroline Michot,Christine Bole-Feysot,Arnaud Picard,Arnaud Picard,Véronique Soupre,Stanislas Lyonnet,Stanislas Lyonnet,Jérémy Sadoine,Lotfi Slimani,Catherine Chaussain,Cécile Laroche-Raynaud,Laurent Guibaud,Christine Broissand,Jeanne Amiel,Jeanne Amiel,Christophe Legendre,Christophe Legendre,Christophe Legendre,Fabiola Terzi,Fabiola Terzi,Guillaume Canaud,Guillaume Canaud,Guillaume Canaud +56 more
TL;DR: This study provides the first direct evidence supporting PIK3CA inhibition as a promising therapeutic strategy in patients with PROS, by reversing symptoms in a mouse model of PROS/CLOVES syndrome, which results from gain-of-function mutations in PI3KCA.
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Congenital pseudarthrosis of the tibia
TL;DR: Treatment of CPT is still challenging in pediatric orthopedics because of bone union difficulties, persistant angulation, joint stiffness and sometimes severe limb length discrepancy sequellae, so combining these new techniques with existing treatments may improve the final prognosis, which nevertheless remains poor.
176
Hereditary multiple exostoses and enchondromatosis.
TL;DR: Hereditary multiple exostoses (HME) is an autosomal-dominant disorder characterized by the development of benign tumours, multiple osteochondromas (exostoses), growing outward from the metaphyses of long bones, and the severity of the disease is variable.
132
Success rate and risk factors of failure of the induced membrane technique in children: a systematic review.
TL;DR: The induced membrane technique is suitable for bone defects of critical size in children and is a reliable technique with no need of micro vascular surgery, however, several risk factors of failure are found.
54
Primary aneurysmal bone cysts in children: percutaneous sclerotherapy with absolute alcohol and proposal of a vascular classification
K. Lambot-Juhan,Stéphanie Pannier,David Grevent,Zagorka Pejin,Sylvain Breton,Laureline Berteloot,S. Emond-Gonsard,Nathalie Boddaert,Christophe Glorion,Francis Brunelle +9 more
TL;DR: Sclerotherapy with absolute alcohol is a safe and effective treatment of ABC and a vascular classification of ABC is proposed as lymphatic or venous and considering ABC intraosseous slow-flow vascular malformations is suggested.
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