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Child Health, Developmental Plasticity, and Epigenetic Programming

Endocrine reviews, 2011-04, Vol.32 (2), p.159-224

2011

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Conditional and Specific NF-κB Blockade Protects Pancreatic Beta Cells from Diabetogenic Agents

Proceedings of the National Academy of Sciences - PNAS, 2006-03, Vol.103 (13), p.5072-5077

2006

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Continuous subcutaneous insulin infusion allows tolerance induction and diabetes treatment in a type 1 diabetic child with insulin allergy

Diabetes & metabolism, 2013-04, Vol.39 (2), p.174-177

2013

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Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with TPIT Gene Mutations

The journal of clinical endocrinology and metabolism, 2012-03, Vol.97 (3), p.E486-E495

2012

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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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Leydig-Cell Tumors Caused by an Activating Mutation of the Gene Encoding the Luteinizing Hormone Receptor

The New England journal of medicine, 1999-12, Vol.341 (23), p.1731-1736

1999

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Medullary thyroid carcinoma identified within the first year of life in children with hereditary multiple endocrine neoplasia type 2A (codon 634) and 2B

European journal of endocrinology, 2009-05, Vol.160 (5), p.807-813

2009

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Hypogonadotropic Hypogonadism Due to Loss of Function of the KiSS1-Derived Peptide Receptor GPR54

Proceedings of the National Academy of Sciences - PNAS, 2003-09, Vol.100 (19), p.10972-10976

2003

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Soluble leptin receptor in serum of subjects with complete resistance to leptin: relation to fat mass

Diabetes (New York, N.Y.), 2000-08, Vol.49 (8), p.1347-1352

2000

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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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Risk of autoimmune diabetes in APECED: association with short alleles of the 5′insulin VNTR

Genes and immunity, 2010-10, Vol.11 (7), p.590-597

2010

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Near normalization of final height with adapted doses of growth hormone in Turner's syndrome

The journal of clinical endocrinology and metabolism, 1998-05, Vol.83 (5), p.1462-1466

1998

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Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Kidney international, 1998-09, Vol.54 (3), p.720-730

1998

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Breast Inflammatory Gigantomastia in a Context of Immune-Mediated Diseases

The journal of clinical endocrinology and metabolism, 2005-09, Vol.90 (9), p.5287-5294

2005

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Long-term mortality after childhood growth hormone treatment: the SAGhE cohort study

The lancet. Diabetes & endocrinology, 2020-08, Vol.8 (8), p.683-692

2020

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Zinc transporter (ZnT)8186–194 is an immunodominant CD8+ T cell epitope in HLA-A2+ type 1 diabetic patients

Diabetologia, 2012-07, Vol.55 (7), p.2026-2031

2012

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Precocious puberty and statural growth

Human reproduction update, 2004-03, Vol.10 (2), p.135-147

2004

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Four families with loss of function mutations of the thyrotropin receptor

The journal of clinical endocrinology and metabolism, 1996-12, Vol.81 (12), p.4229-4235

1996

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Zinc transporter (ZnT)8(186-194) is an immunodominant CD8+ T cell epitope in HLA-A2+ type 1 diabetic patients

Diabetologia, 2012-07, Vol.55 (7), p.2026-2031

2012

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Pharmacokinetics and pharmacodynamics of GnRH agonists: clinical implications in pediatrics

Journal of Pediatric Endocrinology and Metabolism, 2000, Vol.13 Suppl 1 (Supplement), p.723

2000

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Dental Caries and Enamelin Haplotype

Journal of dental research, 2014-04, Vol.93 (4), p.360-365

2014

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Effect of gonadotropin-releasing hormone agonist treatment in boys with central precocious puberty: final height results

Hormone research, 2002, Vol.58 (1), p.1-7

2002

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Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib

Journal of medical genetics, 2011-01, Vol.48 (1), p.55-63

2011

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Low dose linomide in Type I juvenile diabetes of recent onset : a randomised placebo-controlled double blind trial

Diabetologia, 1998-09, Vol.41 (9), p.1040-1046

1998

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Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

Human molecular genetics, 1993-04, Vol.2 (4), p.373-377

1993

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Child Health, Developmental Plasticity, and Epigenetic Programming

Conditional and Specific NF-κB Blockade Protects Pancreatic Beta Cells from Diabetogenic Agents

Continuous subcutaneous insulin infusion allows tolerance induction and diabetes treatment in a type 1 diabetic child with insulin allergy

Phenotypic Homogeneity and Genotypic Variability in a Large Series of Congenital Isolated ACTH-Deficiency Patients with TPIT Gene Mutations

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

Leydig-Cell Tumors Caused by an Activating Mutation of the Gene Encoding the Luteinizing Hormone Receptor

Medullary thyroid carcinoma identified within the first year of life in children with hereditary multiple endocrine neoplasia type 2A (codon 634) and 2B

Hypogonadotropic Hypogonadism Due to Loss of Function of the KiSS1-Derived Peptide Receptor GPR54

Soluble leptin receptor in serum of subjects with complete resistance to leptin: relation to fat mass

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

Risk of autoimmune diabetes in APECED: association with short alleles of the 5′insulin VNTR

Near normalization of final height with adapted doses of growth hormone in Turner's syndrome

Novel mutations in the thiazide-sensitive NaCl cotransporter gene in patients with Gitelman syndrome with predominant localization to the C-terminal domain

Breast Inflammatory Gigantomastia in a Context of Immune-Mediated Diseases

Long-term mortality after childhood growth hormone treatment: the SAGhE cohort study

Zinc transporter (ZnT)8186–194 is an immunodominant CD8+ T cell epitope in HLA-A2+ type 1 diabetic patients

Precocious puberty and statural growth

Four families with loss of function mutations of the thyrotropin receptor

Zinc transporter (ZnT)8(186-194) is an immunodominant CD8+ T cell epitope in HLA-A2+ type 1 diabetic patients

Pharmacokinetics and pharmacodynamics of GnRH agonists: clinical implications in pediatrics

Dental Caries and Enamelin Haplotype

Effect of gonadotropin-releasing hormone agonist treatment in boys with central precocious puberty: final height results

Quantification of the methylation at the GNAS locus identifies subtypes of sporadic pseudohypoparathyroidism type Ib

Low dose linomide in Type I juvenile diabetes of recent onset : a randomised placebo-controlled double blind trial

Heterogeneity in the mutations responsible for X chromosome-linked Kallmann syndrome

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