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Pathology
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January 20, 2026
Heritable metabolic bone disorders: a guide to current genetic testing and clinical management for adult endocrinologists
Shejil Kumar, Emma L Duncan, Lisa Hayes, et al.
Pancreas
|
December 15, 2015
Synchronous Nesidioblastosis, Endocrine Microadenoma, and Intraductal Papillary Mucinous Neoplasia in a Man Presenting With Hyperinsulinemic Hypoglycemia
Sunita M C De Sousa, Koroush S Haghighi, Min Ru Qiu, et al.
Physical Review. E
|
February 17, 2024
Isochronous island bifurcations driven by resonant magnetic perturbations in tokamaks
B B Leal, I L Caldas, M C de Sousa, et al.
Acta Diabetologica
|
February 27, 2025
Correction: Improving detection of monogenic diabetes through reanalysis of GCK variants of uncertain significance
Sunita M C De Sousa, Jennifer M N Phan, Amanda Wells, et al.
Acta Diabetologica
|
January 17, 2025
Improving detection of monogenic diabetes through reanalysis of GCK variants of uncertain significance
Sunita M C De Sousa, Jennifer M N Phan, Amanda Wells, et al.
Pituitary
|
August 23, 2017
Vasculogenic hyperprolactinemia: severe prolactin excess in association with internal carotid artery aneurysms
Sunita M C De Sousa, Emily J Meyer, Wayne Rankin, et al.
Endocrine Oncology (Bristol, England)
|
May 25, 2026
A contemporary overview of multiple endocrine neoplasia syndromes: MEN syndromes 1-5 and beyond
Raquel A Maggacis, Alexandra Sorvina, Lisa J Hayes, et al.
The Medical Journal of Australia
|
May 14, 2026
Primary Hyperparathyroidism in Adults: Recent Developments in Diagnosis and Management
Elizabeth Wootton, Sunita M C De Sousa, Richard L Prince, et al.
BMC Endocrine Disorders
|
January 31, 2020
A putative role for the aryl hydrocarbon receptor (AHR) gene in a patient with cyclical Cushing's disease
Sunita M C De Sousa, Jim Manavis, Jinghua Feng, et al.
BMC Endocrine Disorders
|
November 9, 2016
Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome
Sunita M C De Sousa, Karin S Kassahn, Liam C McIntyre, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 63) with videos related to
Sort By:
Page
of 7
Pathology
|
January 20, 2026
Heritable metabolic bone disorders: a guide to current genetic testing and clinical management for adult endocrinologists
Shejil Kumar, Emma L Duncan, Lisa Hayes, et al.
Pancreas
|
December 15, 2015
Synchronous Nesidioblastosis, Endocrine Microadenoma, and Intraductal Papillary Mucinous Neoplasia in a Man Presenting With Hyperinsulinemic Hypoglycemia
Sunita M C De Sousa, Koroush S Haghighi, Min Ru Qiu, et al.
Physical Review. E
|
February 17, 2024
Isochronous island bifurcations driven by resonant magnetic perturbations in tokamaks
B B Leal, I L Caldas, M C de Sousa, et al.
Acta Diabetologica
|
February 27, 2025
Correction: Improving detection of monogenic diabetes through reanalysis of GCK variants of uncertain significance
Sunita M C De Sousa, Jennifer M N Phan, Amanda Wells, et al.
Acta Diabetologica
|
January 17, 2025
Improving detection of monogenic diabetes through reanalysis of GCK variants of uncertain significance
Sunita M C De Sousa, Jennifer M N Phan, Amanda Wells, et al.
Pituitary
|
August 23, 2017
Vasculogenic hyperprolactinemia: severe prolactin excess in association with internal carotid artery aneurysms
Sunita M C De Sousa, Emily J Meyer, Wayne Rankin, et al.
Endocrine Oncology (Bristol, England)
|
May 25, 2026
A contemporary overview of multiple endocrine neoplasia syndromes: MEN syndromes 1-5 and beyond
Raquel A Maggacis, Alexandra Sorvina, Lisa J Hayes, et al.
The Medical Journal of Australia
|
May 14, 2026
Primary Hyperparathyroidism in Adults: Recent Developments in Diagnosis and Management
Elizabeth Wootton, Sunita M C De Sousa, Richard L Prince, et al.
BMC Endocrine Disorders
|
January 31, 2020
A putative role for the aryl hydrocarbon receptor (AHR) gene in a patient with cyclical Cushing's disease
Sunita M C De Sousa, Jim Manavis, Jinghua Feng, et al.
BMC Endocrine Disorders
|
November 9, 2016
Case report of whole genome sequencing in the XY female: identification of a novel SRY mutation and revision of a misdiagnosis of androgen insensitivity syndrome
Sunita M C De Sousa, Karin S Kassahn, Liam C McIntyre, et al.
Page
of 7