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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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Mutant WD-repeat protein in triple-A syndrome

Nature genetics, 2000-11, Vol.26 (3), p.332-335

2000

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Aetiological diagnosis of male sex ambiguity: a collaborative study

European journal of pediatrics, 2002-01, Vol.161 (1), p.49-59

2002

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Self-Esteem and Social Adjustment in Young Women with Turner Syndrome—Influence of Pubertal Management and Sexuality: Population-Based Cohort Study

The journal of clinical endocrinology and metabolism, 2006-08, Vol.91 (8), p.2972-2979

2006

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Growth hormone (GH) treatment to final height in children with idiopathic short stature: Evidence for a dose effect

The Journal of pediatrics, 2005, Vol.146 (1), p.45-53

2005

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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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Improvement in Adult Height after Growth Hormone Treatment in Adolescents with Short Stature Born Small for Gestational Age: Results of a Randomized Controlled Study

The journal of clinical endocrinology and metabolism, 2003-04, Vol.88 (4), p.1587-1593

2003

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Postnatal Changes of T, LH, and FSH in 46,XY Infants with Mutations in the AR Gene

The journal of clinical endocrinology and metabolism, 2002-01, Vol.87 (1), p.29-32

2002

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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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Séance dédiée à l'hormone de croissance

Bulletin de l'Académie nationale de médecine, 2012-01, Vol.196 (1), p.115-116

Chaussain, Jean-Louis

2012

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45,X/46,XY mosaicism: report of 27 cases

Pediatrics (Evanston), 1999-08, Vol.104 (2 Pt 1), p.304-308

1999

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Reversal of Early Neurologic and Neuroradiologic Manifestations of X-Linked Adrenoleukodystrophy by Bone Marrow Transplantation

The New England journal of medicine, 1990-06, Vol.322 (26), p.1860-1866

1990

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Final height after long-term growth hormone treatment in Turner syndrome

The Journal of pediatrics, 1995-11, Vol.127 (5), p.729-735

1995

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Puberty in subjects with complete androgen insensitivity syndrome

Hormone research, 2006-01, Vol.65 (3), p.126-131

2006

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Final Height after Long-Term Treatment with Triptorelin Slow Release for Central Precocious Puberty: Importance of Statural Growth after Interruption of Treatment

The journal of clinical endocrinology and metabolism, 1999-06, Vol.84 (6), p.1973-1978

1999

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Human Prop-1: cloning, mapping, genomic structure: Mutations in familial combined pituitary hormone deficiency

FEBS letters, 1998-10, Vol.437 (3), p.216-220

1998

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Long-acting lanreotide in adolescent girls with constitutional tall stature

Hormone research, 2009-01, Vol.71 (4), p.228-236

2009

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Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome

European journal of human genetics : EJHG, 2000-08, Vol.8 (8), p.613-620

2000

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Short Stature Associated with Intrauterine Growth Retardation: Final Height of Untreated and Growth Hormone-Treated Children

The journal of clinical endocrinology and metabolism, 1998-04, Vol.83 (4), p.1070-1074

1998

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Adult height of prepubertal short children born small for gestational age treated with GH

European journal of endocrinology, 2005-06, Vol.152 (6), p.835-843

2005

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Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11β-hydroxylase) and CYP11B2 (aldosterone synthase) cause steroid 11β-hydroxylase deficiency and congenital adrenal hyperplasia

The journal of clinical endocrinology and metabolism, 2001-07, Vol.86 (7), p.3197-3201

2001

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Sur la fiabilité des examens médicaux visant à déterminer l'âge à des fins judiciaires et la possibilité d'amélioration en la matière pour les mineurs étrangers isolés

Bulletin de l'Académie nationale de médecine, 2007, Vol.191 (1), p.139-142

2007

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Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious puberty

Human molecular genetics, 1995-02, Vol.4 (2), p.183-188

1995

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Amplitude of pubertal growth in short stature children with intrauterine growth retardation

Hormone research, 2002-01, Vol.57 Suppl 2 (Suppl. 2), p.88-94

2002

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Adrenoleukodystrophy: the most frequent genetic cause of Addison's disease

Hormone research, 2003, Vol.59 Suppl 1 (1), p.104-105

2003

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

Mutant WD-repeat protein in triple-A syndrome

Aetiological diagnosis of male sex ambiguity: a collaborative study

Self-Esteem and Social Adjustment in Young Women with Turner Syndrome—Influence of Pubertal Management and Sexuality: Population-Based Cohort Study

Growth hormone (GH) treatment to final height in children with idiopathic short stature: Evidence for a dose effect

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

Improvement in Adult Height after Growth Hormone Treatment in Adolescents with Short Stature Born Small for Gestational Age: Results of a Randomized Controlled Study

Postnatal Changes of T, LH, and FSH in 46,XY Infants with Mutations in the AR Gene

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

Séance dédiée à l'hormone de croissance

45,X/46,XY mosaicism: report of 27 cases

Reversal of Early Neurologic and Neuroradiologic Manifestations of X-Linked Adrenoleukodystrophy by Bone Marrow Transplantation

Final height after long-term growth hormone treatment in Turner syndrome

Puberty in subjects with complete androgen insensitivity syndrome

Final Height after Long-Term Treatment with Triptorelin Slow Release for Central Precocious Puberty: Importance of Statural Growth after Interruption of Treatment

Human Prop-1: cloning, mapping, genomic structure: Mutations in familial combined pituitary hormone deficiency

Long-acting lanreotide in adolescent girls with constitutional tall stature

Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndrome

Short Stature Associated with Intrauterine Growth Retardation: Final Height of Untreated and Growth Hormone-Treated Children

Adult height of prepubertal short children born small for gestational age treated with GH

Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11β-hydroxylase) and CYP11B2 (aldosterone synthase) cause steroid 11β-hydroxylase deficiency and congenital adrenal hyperplasia

Sur la fiabilité des examens médicaux visant à déterminer l'âge à des fins judiciaires et la possibilité d'amélioration en la matière pour les mineurs étrangers isolés

Characterization of heterogeneous mutations causing constitutive activation of the luteinizing hormone receptor in familial male precocious puberty

Amplitude of pubertal growth in short stature children with intrauterine growth retardation

Adrenoleukodystrophy: the most frequent genetic cause of Addison's disease

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