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European Journal of Endocrinology
|
March 12, 2025
Reassessing the role of the p.(Arg304Gln) missense AIP variant in pituitary tumorigenesis
Paul Benjamin Loughrey, Nadira B Mothojakan, Donato Iacovazzo, et al.
European Journal of Endocrinology
|
March 25, 2016
Growth Hormone Research Society perspective on the development of long-acting growth hormone preparations
Jens Sandahl Christiansen, Philippe F Backeljauw, Martin Bidlingmaier, et al.
The New England Journal of Medicine
|
December 4, 2014
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation
Giampaolo Trivellin, Adrian F Daly, Fabio R Faucz, et al.
The Lancet. Diabetes & Endocrinology
|
October 23, 2021
Consensus on diagnosis and management of Cushing's disease: a guideline update
Maria Fleseriu, Richard Auchus, Irina Bancos, et al.
Endocrine-Related Cancer
|
July 19, 2015
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
Liliya Rostomyan, Adrian F Daly, Patrick Petrossians, et al.
Nature Reviews. Endocrinology
|
August 13, 2025
Consensus on acromegaly therapeutic outcomes: an update
Shlomo Melmed, Luigi di Filippo, Maria Fleseriu, et al.
Orphanet Journal of Rare Diseases
|
July 12, 2022
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
Elodie Fiot, Bertille Alauze, Bruno Donadille, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 6, 2010
Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: an international collaborative study
Adrian F Daly, Maria A Tichomirowa, Patrick Petrossians, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 29, 2012
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
Nelly Burnichon, Alberto Cascón, Francesca Schiavi, et al.
Annales D'Endocrinologie
|
July 13, 2024
Diagnosis and management of children and adult craniopharyngiomas: A French Endocrine Society/French Society for Paediatric Endocrinology & Diabetes Consensus Statement
Thomas Cuny, Rachel Reynaud, Gérald Raverot, et al.
Page
of 37
Search research articles
Search
Showing results (351-360 of 363) with videos related to
Sort By:
Page
of 37
European Journal of Endocrinology
|
March 12, 2025
Reassessing the role of the p.(Arg304Gln) missense AIP variant in pituitary tumorigenesis
Paul Benjamin Loughrey, Nadira B Mothojakan, Donato Iacovazzo, et al.
European Journal of Endocrinology
|
March 25, 2016
Growth Hormone Research Society perspective on the development of long-acting growth hormone preparations
Jens Sandahl Christiansen, Philippe F Backeljauw, Martin Bidlingmaier, et al.
The New England Journal of Medicine
|
December 4, 2014
Gigantism and acromegaly due to Xq26 microduplications and GPR101 mutation
Giampaolo Trivellin, Adrian F Daly, Fabio R Faucz, et al.
The Lancet. Diabetes & Endocrinology
|
October 23, 2021
Consensus on diagnosis and management of Cushing's disease: a guideline update
Maria Fleseriu, Richard Auchus, Irina Bancos, et al.
Endocrine-Related Cancer
|
July 19, 2015
Clinical and genetic characterization of pituitary gigantism: an international collaborative study in 208 patients
Liliya Rostomyan, Adrian F Daly, Patrick Petrossians, et al.
Nature Reviews. Endocrinology
|
August 13, 2025
Consensus on acromegaly therapeutic outcomes: an update
Shlomo Melmed, Luigi di Filippo, Maria Fleseriu, et al.
Orphanet Journal of Rare Diseases
|
July 12, 2022
Turner syndrome: French National Diagnosis and Care Protocol (NDCP; National Diagnosis and Care Protocol)
Elodie Fiot, Bertille Alauze, Bruno Donadille, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 6, 2010
Clinical characteristics and therapeutic responses in patients with germ-line AIP mutations and pituitary adenomas: an international collaborative study
Adrian F Daly, Maria A Tichomirowa, Patrick Petrossians, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 29, 2012
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
Nelly Burnichon, Alberto Cascón, Francesca Schiavi, et al.
Annales D'Endocrinologie
|
July 13, 2024
Diagnosis and management of children and adult craniopharyngiomas: A French Endocrine Society/French Society for Paediatric Endocrinology & Diabetes Consensus Statement
Thomas Cuny, Rachel Reynaud, Gérald Raverot, et al.
Page
of 37