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Endocrinology and Metabolism Clinics of North America
|
November 14, 2021
Hereditary Primary Hyperparathyroidism
Paul J Newey
Clinical Endocrinology
|
June 30, 2019
Clinical genetic testing in endocrinology: Current concepts and contemporary challenges
Paul J Newey
Clinical Endocrinology
|
August 23, 2022
Approach to the patient with a variant of uncertain significance on genetic testing
Paul J Newey
Journal of the Endocrine Society
|
January 26, 2022
MEN1 Surveillance Guidelines: Time to (Re)Think?
Paul J Newey, John Newell-Price
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
|
April 2, 2011
Role of multiple endocrine neoplasia type 1 mutational analysis in clinical practice
Paul J Newey, Rajesh V Thakker
Journal of Molecular Endocrinology
|
November 29, 2022
Identification of prolactin receptor variants with diverse effects on receptor signalling
Caroline M Gorvin, Paul J Newey, Rajesh V Thakker
The Journal of Clinical Endocrinology and Metabolism
|
April 6, 2023
Stable Incidence and Increasing Prevalence of Primary Hyperparathyroidism in a Population-based Study in Scotland
Enrique Soto-Pedre, Paul J Newey, Graham P Leese
The Lancet. Diabetes & Endocrinology
|
July 14, 2015
Challenges and controversies in management of pancreatic neuroendocrine tumours in patients with MEN1
Christopher J Yates, Paul J Newey, Rajesh V Thakker
Clinical Endocrinology
|
December 22, 2021
Genetics of monogenic disorders of calcium and bone metabolism
Paul J Newey, Fadil M Hannan, Abbie Wilson, et al.
Human Mutation
|
January 7, 2010
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors
Paul J Newey, Michael R Bowl, Treena Cranston, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 26) with videos related to
Sort By:
Page
of 3
Endocrinology and Metabolism Clinics of North America
|
November 14, 2021
Hereditary Primary Hyperparathyroidism
Paul J Newey
Clinical Endocrinology
|
June 30, 2019
Clinical genetic testing in endocrinology: Current concepts and contemporary challenges
Paul J Newey
Clinical Endocrinology
|
August 23, 2022
Approach to the patient with a variant of uncertain significance on genetic testing
Paul J Newey
Journal of the Endocrine Society
|
January 26, 2022
MEN1 Surveillance Guidelines: Time to (Re)Think?
Paul J Newey, John Newell-Price
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
|
April 2, 2011
Role of multiple endocrine neoplasia type 1 mutational analysis in clinical practice
Paul J Newey, Rajesh V Thakker
Journal of Molecular Endocrinology
|
November 29, 2022
Identification of prolactin receptor variants with diverse effects on receptor signalling
Caroline M Gorvin, Paul J Newey, Rajesh V Thakker
The Journal of Clinical Endocrinology and Metabolism
|
April 6, 2023
Stable Incidence and Increasing Prevalence of Primary Hyperparathyroidism in a Population-based Study in Scotland
Enrique Soto-Pedre, Paul J Newey, Graham P Leese
The Lancet. Diabetes & Endocrinology
|
July 14, 2015
Challenges and controversies in management of pancreatic neuroendocrine tumours in patients with MEN1
Christopher J Yates, Paul J Newey, Rajesh V Thakker
Clinical Endocrinology
|
December 22, 2021
Genetics of monogenic disorders of calcium and bone metabolism
Paul J Newey, Fadil M Hannan, Abbie Wilson, et al.
Human Mutation
|
January 7, 2010
Cell division cycle protein 73 homolog (CDC73) mutations in the hyperparathyroidism-jaw tumor syndrome (HPT-JT) and parathyroid tumors
Paul J Newey, Michael R Bowl, Treena Cranston, et al.
Page
of 3