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Clinical Management of Congenital Hypogonadotropic Hypogonadism

Endocrine reviews, 2019-04, Vol.40 (2), p.669-710

2019

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MANAGEMENT OF ENDOCRINE DISEASE: Cushing's syndrome due to ectopic ACTH secretion: an expert operational opinion

European journal of endocrinology, 2020-04, Vol.182 (4), p.R29

2020

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Non-invasive Diagnostic Strategy in ACTH-dependent Cushing’s Syndrome

The journal of clinical endocrinology and metabolism, 2020-10, Vol.105 (10), p.3273-3284

2020

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Treatment of acromegaly has substantial effects on body composition: a long-term follow-up study

European journal of endocrinology, 2022-02, Vol.186 (2), p.173

2022

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Exome Sequencing as a Tool for Detecting Point Mutations and Deletions in Patients With Hypogonadotropic Hypogonadism

The journal of clinical endocrinology and metabolism, 2022-10, Vol.107 (10), p.e4254-e4255

Young, Jacques

2022

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ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure

Genetics in medicine, 2019-04, Vol.21 (4), p.930-938

2019

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Hyperprolactinemia-induced ovarian acyclicity is reversed by kisspeptin administration

The Journal of clinical investigation, 2012-10, Vol.122 (10), p.3791-3795

2012

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Approach to the Male Patient with Congenital Hypogonadotropic Hypogonadism

The journal of clinical endocrinology and metabolism, 2012-03, Vol.97 (3), p.707-718

Young, Jacques

2012

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Does Genetic Susceptibility of the Gonadotropic Axis Explain the Variable Impact of Stressors Causing Functional Hypothalamic Amenorrhea?

The journal of clinical endocrinology and metabolism, 2021-03, Vol.106 (3), p.e1473-e1475

Young, Jacques

2021

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Female Gonadal Function before and after Treatment of Acromegaly

The journal of clinical endocrinology and metabolism, 2010-10, Vol.95 (10), p.4518-4525

2010

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X-linked acrogigantism syndrome: clinical profile and therapeutic responses

Endocrine-related cancer, 2015-06, Vol.22 (3), p.353-367

2015

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Germline AIP Mutations in Apparently Sporadic Pituitary Adenomas: Prevalence in a Prospective Single-Center Cohort of 443 Patients

The journal of clinical endocrinology and metabolism, 2012-04, Vol.97 (4), p.E663-E670

2012

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Doping with testosterone and androgenic/anabolic steroids: Impact on health, screening tools and medical care

Annales d'endocrinologie, 2023-05, Vol.84 (3), p.401-405

Young, Jacques

2023

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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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SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome

PLoS genetics, 2012-08, Vol.8 (8), p.e1002896-e1002896

2012

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Factors predicting relapse of nonfunctioning pituitary macroadenomas after neurosurgery: a study of 142 patients

European journal of endocrinology, 2010-08, Vol.163 (2), p.193

2010

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Lack of Androgen Receptor Expression in Sertoli Cells Accounts for the Absence of Anti-Mullerian Hormone Repression during Early Human Testis Development

The journal of clinical endocrinology and metabolism, 2009-05, Vol.94 (5), p.1818-1825

2009

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Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2

PLoS genetics, 2006-10, Vol.2 (10), p.e175-e175

2006

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Evidence for DNA-Binding Domain–Ligand-Binding Domain Communications in the Androgen Receptor

Molecular and Cellular Biology, 2012-08, Vol.32 (15), p.3033-3043

2012

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Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations

PloS one, 2011-10, Vol.6 (10), p.e25614-e25614

2011

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Acromegaly

Best Practice & Research Clinical Endocrinology & Metabolism, 2009-10, Vol.23 (5), p.555-574

2009

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Impairment in insulin secretion without changes in insulin resistance explains hyperglycemia in patients with acromegaly treated with pasireotide LAR

Endocrine Connections, 2022-12, Vol.11 (12), p.1-9

2022

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Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5

Diabetes (New York, N.Y.), 2005-11, Vol.54 (11), p.3126-3132

2005

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Transient pituitary ACTH-dependent Cushing syndrome caused by an immune checkpoint inhibitor combination

Melanoma research, 2017-12, Vol.27 (6), p.649-652

2017

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Androgens and spermatogenesis

Annales d'endocrinologie, 2022-06, Vol.83 (3), p.155-158

2022

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Clinical Management of Congenital Hypogonadotropic Hypogonadism

MANAGEMENT OF ENDOCRINE DISEASE: Cushing's syndrome due to ectopic ACTH secretion: an expert operational opinion

Non-invasive Diagnostic Strategy in ACTH-dependent Cushing’s Syndrome

Treatment of acromegaly has substantial effects on body composition: a long-term follow-up study

Exome Sequencing as a Tool for Detecting Point Mutations and Deletions in Patients With Hypogonadotropic Hypogonadism

ATG7 and ATG9A loss-of-function variants trigger autophagy impairment and ovarian failure

Hyperprolactinemia-induced ovarian acyclicity is reversed by kisspeptin administration

Approach to the Male Patient with Congenital Hypogonadotropic Hypogonadism

Does Genetic Susceptibility of the Gonadotropic Axis Explain the Variable Impact of Stressors Causing Functional Hypothalamic Amenorrhea?

Female Gonadal Function before and after Treatment of Acromegaly

X-linked acrogigantism syndrome: clinical profile and therapeutic responses

Germline AIP Mutations in Apparently Sporadic Pituitary Adenomas: Prevalence in a Prospective Single-Center Cohort of 443 Patients

Doping with testosterone and androgenic/anabolic steroids: Impact on health, screening tools and medical care

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

SEMA3A, a gene involved in axonal pathfinding, is mutated in patients with Kallmann syndrome

Factors predicting relapse of nonfunctioning pituitary macroadenomas after neurosurgery: a study of 142 patients

Lack of Androgen Receptor Expression in Sertoli Cells Accounts for the Absence of Anti-Mullerian Hormone Repression during Early Human Testis Development

Kallmann syndrome: mutations in the genes encoding prokineticin-2 and prokineticin receptor-2

Evidence for DNA-Binding Domain–Ligand-Binding Domain Communications in the Androgen Receptor

Normosmic congenital hypogonadotropic hypogonadism due to TAC3/TACR3 mutations: characterization of neuroendocrine phenotypes and novel mutations

Acromegaly

Impairment in insulin secretion without changes in insulin resistance explains hyperglycemia in patients with acromegaly treated with pasireotide LAR

Large Genomic Rearrangements in the Hepatocyte Nuclear Factor-1β (TCF2) Gene Are the Most Frequent Cause of Maturity-Onset Diabetes of the Young Type 5

Transient pituitary ACTH-dependent Cushing syndrome caused by an immune checkpoint inhibitor combination

Androgens and spermatogenesis

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