Search Results - "Chaussain, JL"
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Hypogonadotropic Hypogonadism Due to Loss of Function of the KiSS1-Derived Peptide Receptor GPR54
Published in Proceedings of the National Academy of Sciences - PNAS (16-09-2003)“…Hypogonadotropic hypogonadism is defined as a deficiency of the pituitary secretion of follicle-stimulating hormone and luteinizing hormone, which results in…”
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2
Precocious puberty and statural growth
Published in Human reproduction update (01-03-2004)“…Precocious puberty results mostly from the precocious activation of the gonadotropic axis. Although the age limits have recently been discussed, most…”
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3
Growth hormone (GH) treatment to final height in children with idiopathic short stature: Evidence for a dose effect
Published in The Journal of pediatrics (2005)“…To investigate in an open-label randomized study, the effect of two doses of growth hormone (GH) on final height and height velocity during the first 2 years…”
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4
Adult Height and Pubertal Growth in Turner Syndrome after Treatment with Recombinant Growth Hormone
Published in The journal of clinical endocrinology and metabolism (01-09-2005)“…Objective: The objective of this study was to evaluate factors affecting adult height (AH) in patients with Turner syndrome treated with GH. Design: The study…”
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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
Published in The journal of clinical endocrinology and metabolism (01-04-2003)“…The efficacy of GH for increasing adult height (AH) in short adolescents born small for gestational age (SGA) is unclear, due to the lack of long-term…”
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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
Published in The journal of clinical endocrinology and metabolism (01-04-2005)“…GH is used to increase adult height in children with Turner’s syndrome with little knowledge of the impact on quality of life. We carried out a…”
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7
Mutant WD-repeat protein in triple-A syndrome
Published in Nature genetics (01-11-2000)“…Triple-A syndrome (MIM 231550; also known as Allgrove syndrome) is an autosomal recessive disorder characterized by adrenocorticotropin hormone…”
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Postnatal changes of T, LH, and FSH in 46,XY infants with mutations in the AR gene
Published in The journal of clinical endocrinology and metabolism (2002)“…Androgen insensitivity syndromes (AIS) result from the incapacity for T and dihydrotestosterone to virilize male embryos and is mainly attributable to…”
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PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency
Published in The journal of clinical endocrinology and metabolism (01-09-2001)“…Alterations of the gene encoding the pituitary transcription factor PROP1 were associated with congenital forms of multiple pituitary hormone deficiencies in…”
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10
Adult Height after Ketoconazole Treatment in Patients with Familial Male-Limited Precocious Puberty
Published in The journal of clinical endocrinology and metabolism (01-01-2005)“…Familial male-limited precocious puberty is a rare cause of precocious puberty due to activating mutations of the LH receptor, leading to early onset…”
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Growth hormone treatment of short children born small for gestational age : Growth responses with continuous and discontinuous regimens over 6 years
Published in The journal of clinical endocrinology and metabolism (01-08-2000)“…We report an epi-analysis of 6-yr growth responses obtained with GH treatment in short children born small for gestational age (SGA). Four randomized,…”
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12
45,X/46,XY Mosaicism: Report of 27 Cases
Published in Pediatrics (Evanston) (01-08-1999)“…There exist substantial differences between prenatally and postnatally diagnosed cases of 45,X/46,XY mosaicism. Ninety percent of prenatally diagnosed cases…”
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13
Puberty in subjects with complete androgen insensitivity syndrome
Published in Hormone research (01-01-2006)“…Androgen receptor defects affect the regulation of the gonadotropic axis. However, little is known about the timing of pubertal maturation in complete androgen…”
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14
Treatment of Central Precocious Puberty by Subcutaneous Injections of Leuprorelin 3-Month Depot (11.25 mg)
Published in The journal of clinical endocrinology and metabolism (01-09-2002)“…Depot GnRH agonists are widely used for the treatment of precocious puberty. Leuprorelin 3-month depot is currently used in adults but has not been evaluated…”
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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
Published in The journal of clinical endocrinology and metabolism (01-06-1999)“…The impact of treatment of central precocious puberty (CPP) with GnRH agonists on final statural height (FH) remains controversial, and guidelines on the…”
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Human Prop-1: cloning, mapping, genomic structure: Mutations in familial combined pituitary hormone deficiency
Published in FEBS letters (23-10-1998)“…Prop-1 is a newly isolated pituitary-specific paired-like homeodomain transcription factor whose cDNA sequence is well known in mouse. To study its involvement…”
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Lack of effect of GnRH agonists on final height in girls with advanced puberty : A randomized long-term pilot study
Published in The journal of clinical endocrinology and metabolism (01-10-1999)“…GnRH agonists improve final height in girls with "true" precocious puberty. To test if a comparable effect can be obtained in older girls, we performed a…”
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18
Aetiological diagnosis of male sex ambiguity: a collaborative study
Published in European journal of pediatrics (01-01-2002)“…A collaborative study, supported by the Biomed2 Programme of the European Community, was initiated to optimise the aetiological diagnosis in genetic or gonadal…”
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Effect of gonadotropin-releasing hormone agonist treatment in boys with central precocious puberty: final height results
Published in Hormone research (2002)“…The small number of boys present in most studies on final height (FH) after gonadotropin-releasing hormone agonist (GnRHa) treatment for central precocious…”
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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
Published in The journal of clinical endocrinology and metabolism (01-07-2001)Get full text
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