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Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature

Proceedings of the National Academy of Sciences - PNAS, 2012-03, Vol.109 (11), p.4257-4262

2012

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Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature

American journal of medical genetics. Part A, 2017-04, Vol.173 (4), p.1061-1065

2017

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A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone

Nature genetics, 2004-07, Vol.36 (7), p.720-724

2004

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Contribution of LHX4 Mutations to Pituitary Deficits in a Cohort of 417 Unrelated Patients

The journal of clinical endocrinology and metabolism, 2017-01, Vol.102 (1), p.290-301

2017

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Quality of Life Determinants in Young Women with Turner’s Syndrome after Growth Hormone Treatment: Results of the StaTur Population-Based Cohort Study

The journal of clinical endocrinology and metabolism, 2005-04, Vol.90 (4), p.1992-1997

2005

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Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome

European journal of medical genetics, 2020-12, Vol.63 (12), p.104064-104064, Article 104064

2020

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Adult Height and Pubertal Growth in Turner Syndrome after Treatment with Recombinant Growth Hormone

The journal of clinical endocrinology and metabolism, 2005-09, Vol.90 (9), p.5197-5204

2005

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Implication of the Pro12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French population

BMC medical genetics, 2005-03, Vol.6 (1), p.11-11

2005

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Genetic Study of the Melanin-Concentrating Hormone Receptor 2 in Childhood and Adulthood Severe Obesity

The journal of clinical endocrinology and metabolism, 2007-11, Vol.92 (11), p.4403-4409

2007

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Associations of glucocorticoid receptor and corticosteroid-binding globulin gene polymorphisms on fat mass and fat mass distribution in prepubertal obese children

Journal of physiology and biochemistry, 2012-12, Vol.68 (4), p.645-650

2012

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Necdin Plays a Role in the Serotonergic Modulation of the Mouse Respiratory Network: Implication for Prader-Willi Syndrome

The Journal of neuroscience, 2008-02, Vol.28 (7), p.1745-1755

2008

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Incidence and risk factors for dupilumab associated ocular adverse events: a real‐life prospective study

Journal of the European Academy of Dermatology and Venereology, 2021-01, Vol.35 (1), p.172-179

2021

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Latent class analysis categorizes chronic hand eczema patients according to skin barrier impairment

Journal of the European Academy of Dermatology and Venereology, 2020-07, Vol.34 (7), p.1529-1535

2020

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Growth hormone in combination with leuprorelin in pubertal children with idiopathic short stature

Endocrine Connections, 2018-05, Vol.7 (5), p.708-718

2018

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Growth hormone treatment in children with Prader-Willi syndrome: safety and effectiveness data from the PATRO Children study

Therapeutic advances in endocrinology and metabolism, 2024-01, Vol.15, p.20420188241264343

2024

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Dysautonomie cardiovasculaire au cours du sommeil : un éclairage sur les morts subites dans le syndrome de Prader-Willi

Revue neurologique, 2020-09, Vol.176, p.S42-S42

2020

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Study of decision-making capacity in Prader-Willi syndrome with a Gambling Task

Journal of intellectual & developmental disability, 2022-01, Vol.47 (1), p.18-26

2022

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Association of Melanin-Concentrating Hormone Receptor 1 5′ Polymorphism With Early-Onset Extreme Obesity

Diabetes (New York, N.Y.), 2005-10, Vol.54 (10), p.3049-3055

2005

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Breathing deficits of the Prader-Willi syndrome

Respiratory physiology & neurobiology, 2009-08, Vol.168 (1), p.119-124

2009

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Cardiovascular abnormalities in Turner's syndrome: What prevention?

Archives of cardiovascular diseases, 2008-07, Vol.101 (7), p.485-490

2008

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OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels

Human mutation, 2010, Vol.31 (1), p.20-26

2010

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Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

European journal of human genetics : EJHG, 2011-10, Vol.19 (10), p.1082-1089

2011

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Subtle Health Impairment and Socioeducational Attainment in Young Adult Patients with Congenital Hypothyroidism Diagnosed by Neonatal Screening: A Longitudinal Population-Based Cohort Study

The journal of clinical endocrinology and metabolism, 2011-06, Vol.96 (6), p.1771-1782

2011

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Effect of Nutritional Intervention on Food Choices of French Students in Middle School Cafeterias, Using an Interactive Educational Software Program ( Nutri-Advice )

Journal of nutrition education and behavior, 2016-02, Vol.48 (2), p.131-137.e1

2016

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Early Developmental Regression in Autism Spectrum Disorder: Evidence from an International Multiplex Sample

Journal of autism and developmental disorders, 2011-03, Vol.41 (3), p.332-340

2011

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Noonan syndrome-causing SHP2 mutants inhibit insulin-like growth factor 1 release via growth hormone-induced ERK hyperactivation, which contributes to short stature

Noonan syndrome, PTPN11 mutations, and brain tumors. A clinical report and review of the literature

A common polymorphism of the growth hormone receptor is associated with increased responsiveness to growth hormone

Contribution of LHX4 Mutations to Pituitary Deficits in a Cohort of 417 Unrelated Patients

Quality of Life Determinants in Young Women with Turner’s Syndrome after Growth Hormone Treatment: Results of the StaTur Population-Based Cohort Study

Associations between cognitive performance and the rehabilitation, medical care and social support provided to French children with Prader-Willi syndrome

Adult Height and Pubertal Growth in Turner Syndrome after Treatment with Recombinant Growth Hormone

Implication of the Pro12Ala polymorphism of the PPAR-gamma 2 gene in type 2 diabetes and obesity in the French population

Genetic Study of the Melanin-Concentrating Hormone Receptor 2 in Childhood and Adulthood Severe Obesity

Associations of glucocorticoid receptor and corticosteroid-binding globulin gene polymorphisms on fat mass and fat mass distribution in prepubertal obese children

Necdin Plays a Role in the Serotonergic Modulation of the Mouse Respiratory Network: Implication for Prader-Willi Syndrome

Incidence and risk factors for dupilumab associated ocular adverse events: a real‐life prospective study

Latent class analysis categorizes chronic hand eczema patients according to skin barrier impairment

Growth hormone in combination with leuprorelin in pubertal children with idiopathic short stature

Growth hormone treatment in children with Prader-Willi syndrome: safety and effectiveness data from the PATRO Children study

Dysautonomie cardiovasculaire au cours du sommeil : un éclairage sur les morts subites dans le syndrome de Prader-Willi

Study of decision-making capacity in Prader-Willi syndrome with a Gambling Task

Association of Melanin-Concentrating Hormone Receptor 1 5′ Polymorphism With Early-Onset Extreme Obesity

Breathing deficits of the Prader-Willi syndrome

Cardiovascular abnormalities in Turner's syndrome: What prevention?

OBSL1 mutations in 3-M syndrome are associated with a modulation of IGFBP2 and IGFBP5 expression levels

Gene-ontology enrichment analysis in two independent family-based samples highlights biologically plausible processes for autism spectrum disorders

Subtle Health Impairment and Socioeducational Attainment in Young Adult Patients with Congenital Hypothyroidism Diagnosed by Neonatal Screening: A Longitudinal Population-Based Cohort Study

Effect of Nutritional Intervention on Food Choices of French Students in Middle School Cafeterias, Using an Interactive Educational Software Program ( Nutri-Advice )

Early Developmental Regression in Autism Spectrum Disorder: Evidence from an International Multiplex Sample

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