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A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

The journal of clinical endocrinology and metabolism, 2010-02, Vol.95 (2), p.659-669

2010

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Impact of clinical, hormonal, radiological, and immunohistochemical studies on the diagnosis of postmenopausal hyperandrogenism

European journal of endocrinology, 2011-11, Vol.165 (5), p.779

2011

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Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients

European journal of endocrinology, 2013-12, Vol.169 (6), p.805

2013

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Kallmann Syndrome Caused by Mutations in the PROK2 and PROKR2 Genes: Pathophysiology and Genotype-Phenotype Correlations

Frontiers of hormone research, 2010-01, Vol.39, p.121-132

2010

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Impact of combined and progestogen-only contraceptives on bone mineral density

Joint, bone, spine : revue du rhumatisme, 2009-03, Vol.76 (2), p.134-138

2009

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Reproductive Phenotypes in Men With Acquired or Congenital Hypogonadotropic Hypogonadism: A Comparative Study

The journal of clinical endocrinology and metabolism, 2022-07, Vol.107 (7), p.e2812-e2824

2022

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Sex Steroids, Precursors, and Metabolite Deficiencies in Men With Isolated Hypogonadotropic Hypogonadism and Panhypopituitarism: A GCMS-Based Comparative Study

The journal of clinical endocrinology and metabolism, 2015-02, Vol.100 (2), p.E292-E296

2015

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SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

Human reproduction (Oxford), 2012-05, Vol.27 (5), p.1460-1465

2012

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Hyperandrogenism after menopause : ovarian or adrenal origin?

Gynécologie, obstétrique, fertilité & sénologie, 2022-10

2022

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Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies

Endocrine, 2015-08, Vol.49 (3), p.865-866

2015

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Efficacy and safety of dopamine agonists in patients treated with antipsychotics and presenting a macroprolactinoma

European journal of endocrinology, 2020-08, Vol.183 (2), p.221

2020

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Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life

Orphanet journal of rare diseases, 2015-06, Vol.10 (1), p.71-71, Article 71

2015

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Heterogeneous Prognoses for pT3 Papillary Thyroid Carcinomas and Impact of Delayed Risk Stratification

Thyroid (New York, N.Y.), 2017-06, Vol.27 (6), p.778

2017

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The Prevalence of CHD7 Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients

The journal of clinical endocrinology and metabolism, 2014-10, Vol.99 (10), p.E2138-E2143

2014

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Insulin-like Peptide 3 (INSL3) in Men With Congenital Hypogonadotropic Hypogonadism/Kallmann Syndrome and Effects of Different Modalities of Hormonal Treatment: A Single-Center Study of 281 Patients

The journal of clinical endocrinology and metabolism, 2014-02, Vol.99 (2), p.E268-E275

2014

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Pituitary Adenoma Recurrence Suspected on Central Hyperthyroidism Despite Empty Sella and Confirmed by 68Ga-DOTA-TOC PET/CT

Clinical nuclear medicine, 2017-06, Vol.42 (6), p.454-455

2017

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Severe Congenital Adrenal Hyperplasia Presenting as Bilateral Testicular Tumors and Azoospermia in the Third Decade of Life

Journal of the Endocrine Society, 2018-09, Vol.2 (9), p.997-1000

2018

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Impact of Clinical, Hormonal, Radiological, and Immunohistochemical Studies on the Diagnosis of Postmenopausal Hyperandrogenism

Obstetrical & gynecological survey, 2012-07, Vol.67 (7), p.411-412

2012

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Congenital hypogonadotropic hypogonadism and Kallmann syndrome as models for studying hormonal regulation of human testicular endocrine functions

Annales d'endocrinologie, 2014-05, Vol.75 (2), p.79-87

2014

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SUN-444 Efficacy and Safety of Dopamine Agonists in Psychiatric Patients Treated with Antipsychotics and Presenting a Macroprolactinoma

Journal of the Endocrine Society, 2019-04, Vol.3 (Supplement_1)

2019

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Hypertrophic Osteoarthropathy and Follicular Thyroid Cancer: A Rare Paraneoplastic Syndrome

European thyroid journal, 2015-12, Vol.4 (4), p.266-270

2015

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Impact de la contraception estroprogestative et progestative sur la densité minérale osseuse

Revue du rhumatisme (Ed. française : 1993), 2009-03, Vol.76 (3), p.222-226

2009

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A Comparative Phenotypic Study of Kalimann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

The journal of clinical endocrinology and metabolism, 2010, Vol.95 (2), p.659-669

2010

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Pituitary Adenoma Recurrence Suspected on Central Hyperthyroidism Despite Empty Sella and Confirmed by 68 Ga-DOTA-TOC PET/CT

Clinical nuclear medicine, 2017-03

2017

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Severe Congenital Adrenal Hyperplasia Presenting as Bilateral Testicular Tumors and Azoospermia in the Third Decade of Life

Journal of the Endocrine Society, 2018, Vol.2 (9), p.997-1000

2018

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A Comparative Phenotypic Study of Kallmann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

Impact of clinical, hormonal, radiological, and immunohistochemical studies on the diagnosis of postmenopausal hyperandrogenism

Greater prevalence of PROKR2 mutations in Kallmann syndrome patients from the Maghreb than in European patients

Kallmann Syndrome Caused by Mutations in the PROK2 and PROKR2 Genes: Pathophysiology and Genotype-Phenotype Correlations

Impact of combined and progestogen-only contraceptives on bone mineral density

Reproductive Phenotypes in Men With Acquired or Congenital Hypogonadotropic Hypogonadism: A Comparative Study

Sex Steroids, Precursors, and Metabolite Deficiencies in Men With Isolated Hypogonadotropic Hypogonadism and Panhypopituitarism: A GCMS-Based Comparative Study

SEMA3A deletion in a family with Kallmann syndrome validates the role of semaphorin 3A in human puberty and olfactory system development

Hyperandrogenism after menopause : ovarian or adrenal origin?

Pituitary stalk interruption and olfactory bulbs aplasia/hypoplasia in a man with Kallmann syndrome and reversible gonadotrope and somatotrope deficiencies

Efficacy and safety of dopamine agonists in patients treated with antipsychotics and presenting a macroprolactinoma

Kallmann syndrome with FGFR1 and KAL1 mutations detected during fetal life

Heterogeneous Prognoses for pT3 Papillary Thyroid Carcinomas and Impact of Delayed Risk Stratification

The Prevalence of CHD7 Missense Versus Truncating Mutations Is Higher in Patients With Kallmann Syndrome Than in Typical CHARGE Patients

Insulin-like Peptide 3 (INSL3) in Men With Congenital Hypogonadotropic Hypogonadism/Kallmann Syndrome and Effects of Different Modalities of Hormonal Treatment: A Single-Center Study of 281 Patients

Pituitary Adenoma Recurrence Suspected on Central Hyperthyroidism Despite Empty Sella and Confirmed by 68Ga-DOTA-TOC PET/CT

Severe Congenital Adrenal Hyperplasia Presenting as Bilateral Testicular Tumors and Azoospermia in the Third Decade of Life

Impact of Clinical, Hormonal, Radiological, and Immunohistochemical Studies on the Diagnosis of Postmenopausal Hyperandrogenism

Congenital hypogonadotropic hypogonadism and Kallmann syndrome as models for studying hormonal regulation of human testicular endocrine functions

SUN-444 Efficacy and Safety of Dopamine Agonists in Psychiatric Patients Treated with Antipsychotics and Presenting a Macroprolactinoma

Hypertrophic Osteoarthropathy and Follicular Thyroid Cancer: A Rare Paraneoplastic Syndrome

Impact de la contraception estroprogestative et progestative sur la densité minérale osseuse

A Comparative Phenotypic Study of Kalimann Syndrome Patients Carrying Monoallelic and Biallelic Mutations in the Prokineticin 2 or Prokineticin Receptor 2 Genes

Pituitary Adenoma Recurrence Suspected on Central Hyperthyroidism Despite Empty Sella and Confirmed by 68 Ga-DOTA-TOC PET/CT

Severe Congenital Adrenal Hyperplasia Presenting as Bilateral Testicular Tumors and Azoospermia in the Third Decade of Life

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