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Thomas Edouard

Toulouse University Hospital

France

Research Interests

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Professors in France

Articles (24)

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Collaborators (19)

Philippe Chanson

Professeur d'Endocrinologie

Université Paris-Saclay

FRANCE

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Agnes Bloch-Zupan

Subgroup LEADER : Craniofacial and oral developments, and their associated abnormalities; Teams : Pathophysiology of Down's syndrome and rare dose-effect diseases causing intellectual disabilities (ID) or autism spectrum disorders (ASD) and other comorbidities

University of Strasbourg

FRANCE

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Roberto Mendoza‐Londono

CANADA

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Marie-Eve Robinson

Associate Professor

McGill University

CANADA

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Eric Pasmant

Head

Institut Curie

FRANCE

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Peter Clayton

The University of Manchester

UNITED KINGDOM

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Agnès Linglart

Professor of Pediatrics

Université Paris-Saclay

FRANCE

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Ola Nilsson

Professor of Pediatric Endocrinology

Karolinska Institutet

SWEDEN

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Philippe Campeau

Professor

faculty of medicine university of montréal montréal canada

CANADA

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Armelle Yart

Research Director

INSERM

FRANCE

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Catherine Chaussain

Prof

Université Paris Cité

FRANCE

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Giedre Grigelioniene

Karolinska Institutet

SWEDEN

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Massimiliano Rossi

Université Claude Bernard Lyon 1

FRANCE

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Alexandru SAVEANU

Aix-Marseille Université Faculté de Medecine

FRANCE

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Justin Davies

Professor of Paediatric Endocrinology

University of Southampton

UNITED KINGDOM

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Michael Tansey

Iowa State University

UNITED STATES

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Louise Cheryl GREGORY PhD

Senior Research Fellow

University College London

UNITED KINGDOM

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Caroline Andrique

Associate professor

Université Paris Descartes

FRANCE

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Philippe F Backeljauw

University of Cincinnati College of Medicine

UNITED STATES

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Thomas Edouard

Research Interests

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Articles (24)

Confirmation of frameshift variants in the last exon of FGFR1 as a cause of multiple epiphyseal dysplasia

A Phase 3 Trial of Vosoritide in Children with Hypochondroplasia.

Phase 3 Trial of Oral Infigratinib in Children with Achondroplasia.

RAS/MAPK pathway modulation with simvastatin in children with Noonan syndrome: a multicentre, randomised, double-blind, placebo-controlled phase 3 trial

Abnormal Enamel Mineralization and Hypercalcemia due to <i>GNA11</i> Variants

French national diagnosis and care protocol (PNDS) for infantile idiopathic hypercalcemia (IIH)

Once-weekly somapacitan in children with Noonan syndrome: randomized controlled phase 3 trial

A personalized home-based exercise training program in children with Marfan and Loeys-Dietz syndromes improves aerobic exercise capacity and health-related quality of life

International guideline on genetic testing of children with short stature

Vitamin D supplementation during pregnancy: Position statement of the Groupe de Recherche et d’Information sur les Ostéoporoses (GRIO)

Expanding the molecular spectrum of aggrecanopathies: exploring 24 patients with ACAN significant variants

Real-World Safety and Effectiveness of Vosoritide in Children with Achondroplasia: French Early Access Program

Survey on vitamin D supplementation in children in France: Evaluation of real-life practices following the new 2022 French recommendations

Chapter 7: The different forms of primary hyperparathyroidism at different ages of life: Childhood, pregnancy, lactation, old age

EndoCompass Project: Research Roadmap for Growth Disorders

Growth hormone treatment outcomes in children with genetic isolated growth hormone deficiency

Shprintzen-Goldberg syndrome: Follow-up of the cardiovascular features in an international cohort of 29 patients with SGS

Orofacial Features, Oral Health-Related Quality of Life, and Exposure to Bullying in Osteogenesis Imperfecta: A Cross-Sectional Study

Health-related quality of life in children and adolescents with Marfan syndrome or related disorders: a controlled cross-sectional study

Novel therapeutic perspectives in Noonan syndrome and RASopathies

Novel therapeutic perspectives in Noonan syndrome and RASopathies

Adult height improved over decades in patients with X-linked hypophosphatemia: a cohort study

Clinical heterogeneity of <i>NADSYN1</i>-associated VCRL syndrome

Editorial: Endocrine aspects of Noonan syndrome and related syndromes

Collaborators (19)

Philippe Chanson

Agnes Bloch-Zupan

Roberto Mendoza‐Londono

Marie-Eve Robinson

Eric Pasmant

Peter Clayton

Agnès Linglart

Ola Nilsson

Philippe Campeau

Armelle Yart

Catherine Chaussain

Giedre Grigelioniene

Massimiliano Rossi

Alexandru SAVEANU

Justin Davies

Michael Tansey

Louise Cheryl GREGORY PhD

Caroline Andrique

Philippe F Backeljauw

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