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Increasing knowledge in IGF1R defects: lessons from 35 new patients

Journal of medical genetics, 2020-03, Vol.57 (3), p.160

2020

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Forum theater staging of difficult encounters with patients to increase empathy in students: evaluation of efficacy at The University of Angers Medical School

BMC medical education, 2020-02, Vol.20 (1), p.58-58, Article 58

2020

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Effectiveness and Overall Safety of NutropinAq ® for Growth Hormone Deficiency and Other Paediatric Growth Hormone Disorders: Completion of the International Cooperative Growth Study, NutropinAq ® European Registry (iNCGS)

Frontiers in endocrinology (Lausanne), 2021-05, Vol.12, p.676083-676083

2021

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The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing

The journal of clinical endocrinology and metabolism, 2023-08, Vol.108 (9), p.e779-e788

2023

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Gene expression signatures predict response to therapy with growth hormone

The pharmacogenomics journal, 2021-10, Vol.21 (5), p.594-607

2021

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Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study

The journal of clinical endocrinology and metabolism, 2022-02, Vol.107 (3), p.e1136-e1147

2022

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Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome

Annales d'endocrinologie, 2022-04, Vol.83 (2), p.119-141

2022

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Increased incidence of congenital hypothyroidism in France from 1982 to 2012: a nationwide multicenter analysis

Annals of epidemiology, 2016-02, Vol.26 (2), p.100-105.e4

2016

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A New Case of PCSK1 Pathogenic Variant With Congenital Proprotein Convertase 1/3 Deficiency and Literature Review

The journal of clinical endocrinology and metabolism, 2019-04, Vol.104 (4), p.985-993

2019

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Executive functioning in adolescents and adults with Silver-Russell syndrome

PloS one, 2023-01, Vol.18 (1), p.e0279745-e0279745

2023

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Heterozygous gain of function variant in GUCY1A2 may cause autonomous ovarian hyperfunction

European journal of endocrinology, 2024-03, Vol.190 (4), p.266

2024

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Trends in childhood type 1 diabetes incidence in France, 2010–2015

Diabetes research and clinical practice, 2019-03, Vol.149, p.200-207

2019

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GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty

Human reproduction (Oxford), 2020-10, Vol.35 (10), p.2312-2322

2020

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Baseline Inhibin B and Anti-Mullerian Hormone Measurements for Diagnosis of Hypogonadotropic Hypogonadism (HH) in Boys with Delayed Puberty

The journal of clinical endocrinology and metabolism, 2010-12, Vol.95 (12), p.5225-5232

2010

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Prevalence and Determinants of Transient Congenital Hypothyroidism in Children With Eutopic Gland in France: A Retrospective Cohort Study

The journal of clinical endocrinology and metabolism, 2022-03, Vol.107 (4), p.e1501-e1509

2022

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Identification of novel compound heterozygous variants in the SLC30A7 (ZNT7) gene in two French brothers with stunted growth, testicular hypoplasia and bone marrow failure

Human molecular genetics, 2023-06, Vol.32 (12), p.2016-2031

2023

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Growth pattern in children with X-linked hypophosphatemia treated with burosumab and growth hormone

Orphanet journal of rare diseases, 2022-11, Vol.17 (1), p.412-412, Article 412

2022

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Risk of low birth weight and micronutrient deficiencies in neonates from mothers after gastric bypass: A case control study

Surgery for obesity and related diseases, 2017-08, Vol.13 (8), p.1384-1391

2017

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Executive Functions in Children and Adolescents with Turner Syndrome: A Systematic Review and Meta-Analysis

Neuropsychology review, 2018-06, Vol.28 (2), p.188-215

2018

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Clinically Symptomatic Resistance to Thyroid Hormone β Syndrome Because of THRB Gene Mosaicism

The journal of clinical endocrinology and metabolism, 2022-08, Vol.107 (9), p.e3548-e3552

2022

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Association of maternal nutrition with transient neonatal hyperinsulinism

PloS one, 2018-05, Vol.13 (5), p.e0195383-e0195383

2018

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Graves’ disease in children

Annales d'endocrinologie, 2018-12, Vol.79 (6), p.647-655

2018

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Combination of osteogenesis imperfecta and hypophosphatasia in three children with multiple fractures, low bone mass and severe osteomalacia, a challenge for therapeutic management

European journal of medical genetics, 2023-11, Vol.66 (11), p.104856-104856, Article 104856

2023

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Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disability

Clinical genetics, 2019-10, Vol.96 (4), p.354-358

2019

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Neonatal and neurodevelopmental outcomes in preterm infants according to maternal body mass index: A prospective cohort study

PloS one, 2019, Vol.14 (12), p.e0225027-e0225027

2019

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Increasing knowledge in IGF1R defects: lessons from 35 new patients

Forum theater staging of difficult encounters with patients to increase empathy in students: evaluation of efficacy at The University of Angers Medical School

Effectiveness and Overall Safety of NutropinAq ® for Growth Hormone Deficiency and Other Paediatric Growth Hormone Disorders: Completion of the International Cooperative Growth Study, NutropinAq ® European Registry (iNCGS)

The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing

Gene expression signatures predict response to therapy with growth hormone

Long-Term Efficacy of T3 Analogue Triac in Children and Adults With MCT8 Deficiency: A Real-Life Retrospective Cohort Study

Consensus statement by the French Society of Endocrinology (SFE) and French Society of Pediatric Endocrinology & Diabetology (SFEDP) on diagnosis of Cushing's syndrome

Increased incidence of congenital hypothyroidism in France from 1982 to 2012: a nationwide multicenter analysis

A New Case of PCSK1 Pathogenic Variant With Congenital Proprotein Convertase 1/3 Deficiency and Literature Review

Executive functioning in adolescents and adults with Silver-Russell syndrome

Heterozygous gain of function variant in GUCY1A2 may cause autonomous ovarian hyperfunction

Trends in childhood type 1 diabetes incidence in France, 2010–2015

GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty

Baseline Inhibin B and Anti-Mullerian Hormone Measurements for Diagnosis of Hypogonadotropic Hypogonadism (HH) in Boys with Delayed Puberty

Prevalence and Determinants of Transient Congenital Hypothyroidism in Children With Eutopic Gland in France: A Retrospective Cohort Study

Identification of novel compound heterozygous variants in the SLC30A7 (ZNT7) gene in two French brothers with stunted growth, testicular hypoplasia and bone marrow failure

Growth pattern in children with X-linked hypophosphatemia treated with burosumab and growth hormone

Risk of low birth weight and micronutrient deficiencies in neonates from mothers after gastric bypass: A case control study

Executive Functions in Children and Adolescents with Turner Syndrome: A Systematic Review and Meta-Analysis

Clinically Symptomatic Resistance to Thyroid Hormone β Syndrome Because of THRB Gene Mosaicism

Association of maternal nutrition with transient neonatal hyperinsulinism

Graves’ disease in children

Combination of osteogenesis imperfecta and hypophosphatasia in three children with multiple fractures, low bone mass and severe osteomalacia, a challenge for therapeutic management

Confirmation that variants in TTI2 are responsible for autosomal recessive intellectual disability

Neonatal and neurodevelopmental outcomes in preterm infants according to maternal body mass index: A prospective cohort study

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