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Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism

Diabetes & metabolism, 2015-09, Vol.41 (4), p.331-337

2015

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Corrigendum to “Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism” [Diabetes Metab. 41 (2015) 331–337]

Diabetes & metabolism, 2016-12, Vol.42 (6), p.e1-e1

2016

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Impact of OMNIPOD® on the quality of life of adolescents with type 1 diabetes

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2022-01, Vol.29 (1), p.21-26

2022

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Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples

European journal of medical genetics, 2023-06, Vol.66 (6), p.104748-104748, Article 104748

2023

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Les mutations du gène NNT : principales causes de déficits familiaux isolés en glucocorticoïdes (FGD)

Annales d'endocrinologie, 2012-09, Vol.73 (4), p.264-264

2012

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Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature

The Journal of clinical investigation, 2006-03, Vol.116 (3), p.760-768

2006

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Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations

Diabetes care, 2015-11, Vol.38 (11), p.2033-2041

2015

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Treatment of an infantile acne with oral isotretinoin

EJD. European journal of dermatology, 2004, Vol.14 (1), p.71-72

2004

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Positive Impact of Long-Term Antithyroid Drug Treatment on the Outcome of Children with Graves' Disease: National Long-Term Cohort Study

The journal of clinical endocrinology and metabolism, 2012-01, Vol.97 (1), p.110-119

2012

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Markers of Recurrence and Long-Term Morbidity in Craniopharyngioma: A Systematic Analysis of 171 Patients

The journal of clinical endocrinology and metabolism, 2012-04, Vol.97 (4), p.1258-1267

2012

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True hermaphroditism: Genetic variants and clinical management

The Journal of pediatrics, 1994-11, Vol.125 (5), p.738-744

1994

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La corrélation phénotype-génotype pousse les explorations et révèle un nouveau mécanisme moléculaire impliqué dans le déficit en 21-hydroxylase

Annales d'endocrinologie, 2024-10, Vol.85 (5), p.458-458

2024

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Predictors of Autoimmune Hyperthyroidism Relapse in Children after Discontinuation of Antithyroid Drug Treatment

The journal of clinical endocrinology and metabolism, 2008-10, Vol.93 (10), p.3817-3826

2008

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Pigmentation photodistribuée révélatrice d’une mitochondropathie

Annales de Dermatologie et de Vénéréologie - FMC, 2023-12, Vol.3 (8), p.A197

2023

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X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome

European journal of endocrinology, 2016-03, Vol.174 (3), p.281-288

2016

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Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndrome

European journal of endocrinology, 2011-06, Vol.164 (6), p.891-897

2011

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Nonparallel changes of growth hormone (GH) and insulin-like growth factor-I, insulin-like growth factor binding protein-3, and GH-binding protein, after craniospinal irradiation and chemotherapy

The journal of clinical endocrinology and metabolism, 1994-03, Vol.78 (3), p.597-601

1994

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Efficacité et effets indésirables de la protonthérapie chez les enfants et adolescents porteurs d’adénomes hypophysaires

Annales d'endocrinologie, 2022-10, Vol.83 (5), p.313

2022

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X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

European journal of endocrinology, 2019-06, Vol.180 (6), p.397-406

2019

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True hermaphroditism: Genetic variants and clinical management

The Journal of pediatrics, 1994-11, Vol.125 (5), p.738-744

1994

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Access of children and adolescents with type 1 diabetes to insulin pump therapy has greatly increased in France since 2001

Diabetes & metabolism, 2011-02, Vol.37 (1), p.59-63

2011

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A 5-year prospective study of growth hormone (GH)-deficient children treated with GH before the age of 3 years

The journal of clinical endocrinology and metabolism, 1997-02, Vol.82 (2), p.452-456

1997

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Cloning of cDNA for a cell wall-bound acid invertase from tomato (Lycopersicon esculentum) and expression of soluble and cell wall-bound invertases in plants and wounded leaves of L. esculentum and L. peruvianum

Genes & Genetic Systems, 1998, Vol.73(3), pp.149-157

1998

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Nonparallel changes of growth hormone (GH) and insulin-like growth factor-I, insulin-like growth factor binding protein-3, and GH-binding protein, after craniospinal irradiation and chemotherapy

The journal of clinical endocrinology and metabolism, 1994-03, Vol.78 (3), p.597-601

1994

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Clinical aspects of gonadal dysgenesis

Bulletin de l'Association des anatomistes, 1991-03, Vol.75 (228), p.39

1991

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Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism

Corrigendum to “Ten-year improvement of insulin resistance and growth with recombinant human insulin-like growth factor 1 in a patient with insulin receptor mutations resulting in leprechaunism” [Diabetes Metab. 41 (2015) 331–337]

Impact of OMNIPOD® on the quality of life of adolescents with type 1 diabetes

Role of chromosomal imbalances in the pathogenesis of DSD: A retrospective analysis of 115 prenatal samples

Les mutations du gène NNT : principales causes de déficits familiaux isolés en glucocorticoïdes (FGD)

Loss of constitutive activity of the growth hormone secretagogue receptor in familial short stature

Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations

Treatment of an infantile acne with oral isotretinoin

Positive Impact of Long-Term Antithyroid Drug Treatment on the Outcome of Children with Graves' Disease: National Long-Term Cohort Study

Markers of Recurrence and Long-Term Morbidity in Craniopharyngioma: A Systematic Analysis of 171 Patients

True hermaphroditism: Genetic variants and clinical management

La corrélation phénotype-génotype pousse les explorations et révèle un nouveau mécanisme moléculaire impliqué dans le déficit en 21-hydroxylase

Predictors of Autoimmune Hyperthyroidism Relapse in Children after Discontinuation of Antithyroid Drug Treatment

Pigmentation photodistribuée révélatrice d’une mitochondropathie

X-chromosome gene dosage as a determinant of impaired pre and postnatal growth and adult height in Turner syndrome

Growth hormone treatment before the age of 4 years prevents short stature in young girls with Turner syndrome

Nonparallel changes of growth hormone (GH) and insulin-like growth factor-I, insulin-like growth factor binding protein-3, and GH-binding protein, after craniospinal irradiation and chemotherapy

Efficacité et effets indésirables de la protonthérapie chez les enfants et adolescents porteurs d’adénomes hypophysaires

X chromosome gene dosage as a determinant of congenital malformations and of age-related comorbidity risk in patients with Turner syndrome, from childhood to early adulthood

True hermaphroditism: Genetic variants and clinical management

Access of children and adolescents with type 1 diabetes to insulin pump therapy has greatly increased in France since 2001

A 5-year prospective study of growth hormone (GH)-deficient children treated with GH before the age of 3 years

Cloning of cDNA for a cell wall-bound acid invertase from tomato (Lycopersicon esculentum) and expression of soluble and cell wall-bound invertases in plants and wounded leaves of L. esculentum and L. peruvianum

Nonparallel changes of growth hormone (GH) and insulin-like growth factor-I, insulin-like growth factor binding protein-3, and GH-binding protein, after craniospinal irradiation and chemotherapy

Clinical aspects of gonadal dysgenesis

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