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Human Reproduction (Oxford, England)
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August 31, 2020
GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty
Héléna Mosbah, Claire Bouvattier, Luigi Maione, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 19, 2013
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
Séverine Trabado, Luigi Maione, Hélène Bry-Gauillard, et al.
Human Reproduction (Oxford, England)
|
September 24, 2023
Impact of Cushing's syndrome on the gonadotrope axis and testicular functions in men
Georgios E Papadakis, Benedicte de Kalbermatten, Alexandre Dormoy, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 22, 2017
Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH
Hélène Bry-Gauillard, Florence Larrat-Ledoux, Jean-Marc Levaillant, et al.
Human Reproduction (Oxford, England)
|
November 25, 2022
Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing
Guillaume Bachelot, Anne Bachelot, Marion Bonnier, et al.
European Journal of Endocrinology
|
August 13, 2024
Plasma 21-deoxycortisone: a sensitive additive tool in 21-hydroxylase deficiency in newborns
Jean Fiet, Guillaume Bachelot, Coumba Sow, et al.
Endocrine Connections
|
January 13, 2025
Mineralocorticoid axis activity and cardiac remodeling in patients with ACTH-dependent Cushing's syndrome
Peter Wolf, Simon Travers, Oliver Domenig, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 6, 2014
Cardiac structure and function in Cushing's syndrome: a cardiac magnetic resonance imaging study
Peter Kamenický, Alban Redheuil, Charles Roux, et al.
The Lancet. Diabetes & Endocrinology
|
June 6, 2025
Reversal of congenital hypogonadotropic hypogonadism in two brothers carrying a homozygous KISS1 frameshift mutation
Régis Coutant, Nadia Zaegel, Frédéric Illouz, et al.
Chemical Communications (Cambridge, England)
|
November 30, 2019
Selective modification of a native protein in a patient tissue homogenate using palladium nanoparticles
Arnaud Peramo, Anaëlle Dumas, Hynd Remita, et al.
Page
of 21
Search research articles
Search
Showing results (141-150 of 208) with videos related to
Sort By:
Page
of 21
Human Reproduction (Oxford, England)
|
August 31, 2020
GnRH stimulation testing and serum inhibin B in males: insufficient specificity for discriminating between congenital hypogonadotropic hypogonadism from constitutional delay of growth and puberty
Héléna Mosbah, Claire Bouvattier, Luigi Maione, et al.
The Journal of Clinical Endocrinology and Metabolism
|
November 19, 2013
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
Séverine Trabado, Luigi Maione, Hélène Bry-Gauillard, et al.
Human Reproduction (Oxford, England)
|
September 24, 2023
Impact of Cushing's syndrome on the gonadotrope axis and testicular functions in men
Georgios E Papadakis, Benedicte de Kalbermatten, Alexandre Dormoy, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 22, 2017
Anti-Müllerian Hormone and Ovarian Morphology in Women With Isolated Hypogonadotropic Hypogonadism/Kallmann Syndrome: Effects of Recombinant Human FSH
Hélène Bry-Gauillard, Florence Larrat-Ledoux, Jean-Marc Levaillant, et al.
Human Reproduction (Oxford, England)
|
November 25, 2022
Combining metabolomics and machine learning models as a tool to distinguish non-classic 21-hydroxylase deficiency from polycystic ovary syndrome without adrenocorticotropic hormone testing
Guillaume Bachelot, Anne Bachelot, Marion Bonnier, et al.
European Journal of Endocrinology
|
August 13, 2024
Plasma 21-deoxycortisone: a sensitive additive tool in 21-hydroxylase deficiency in newborns
Jean Fiet, Guillaume Bachelot, Coumba Sow, et al.
Endocrine Connections
|
January 13, 2025
Mineralocorticoid axis activity and cardiac remodeling in patients with ACTH-dependent Cushing's syndrome
Peter Wolf, Simon Travers, Oliver Domenig, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 6, 2014
Cardiac structure and function in Cushing's syndrome: a cardiac magnetic resonance imaging study
Peter Kamenický, Alban Redheuil, Charles Roux, et al.
The Lancet. Diabetes & Endocrinology
|
June 6, 2025
Reversal of congenital hypogonadotropic hypogonadism in two brothers carrying a homozygous KISS1 frameshift mutation
Régis Coutant, Nadia Zaegel, Frédéric Illouz, et al.
Chemical Communications (Cambridge, England)
|
November 30, 2019
Selective modification of a native protein in a patient tissue homogenate using palladium nanoparticles
Arnaud Peramo, Anaëlle Dumas, Hynd Remita, et al.
Page
of 21