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Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 5, 2002
Hyperparathyroidism in hereditary syndromes: special expressions and special managements
Stephen J Marx, William F Simonds, Sunita K Agarwal, et al.
Journal of the Endocrine Society
|
September 16, 2022
Metastatic Grade 3 Neuroendocrine Tumor in Multiple Endocrine Neoplasia Type 1 Expressing Somatostatin Receptors
Akua Graf, James Welch, Rashika Bansal, et al.
Journal of Community Hospital Internal Medicine Perspectives
|
May 3, 2019
Retrospective study of inpatient diabetes management service, length of stay and 30-day readmission rate of patients with diabetes at a community hospital
Samantha R Mandel, Susan Langan, Nestoras Nicolas Mathioudakis, et al.
Surgery
|
December 5, 2009
Reoperation for parathyroid adenoma: a contemporary experience
Anathea C Powell, H Richard Alexander, Richard Chang, et al.
Cancers
|
March 25, 2022
Parathyroid Carcinoma: Incidence, Survival Analysis, and Management: A Study from the SEER Database and Insights into Future Therapeutic Perspectives
Asad Ullah, Jaffar Khan, Abdul Waheed, et al.
American Journal of Human Genetics
|
February 14, 2024
The association of GNB5 with Alzheimer disease revealed by genomic analysis restricted to variants impacting gene function
Jianhua Zhang, Mritunjay Pandey, Adam Awe, et al.
The New England Journal of Medicine
|
November 17, 2021
Parathyroid Hormone Resistance and Autoantibodies to the PTH1 Receptor
Adel Mandl, Peter D Burbelo, Giovanni Di Pasquale, et al.
Journal of Medical Genetics
|
November 11, 2020
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome
Pasquelena De Nittis, Stephanie Efthymiou, Alexandre Sarre, et al.
Annals of the New York Academy of Sciences
|
May 22, 2004
Molecular pathology of the MEN1 gene
Sunita K Agarwal, A Lee Burns, Karen E Sukhodolets, et al.
American Journal of Human Genetics
|
September 3, 2016
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
Elisabeth M Lodder, Pasquelena De Nittis, Charlotte D Koopman, et al.
Page
of 10
Search research articles
Search
Showing results (81-90 of 91) with videos related to
Sort By:
Page
of 10
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
November 5, 2002
Hyperparathyroidism in hereditary syndromes: special expressions and special managements
Stephen J Marx, William F Simonds, Sunita K Agarwal, et al.
Journal of the Endocrine Society
|
September 16, 2022
Metastatic Grade 3 Neuroendocrine Tumor in Multiple Endocrine Neoplasia Type 1 Expressing Somatostatin Receptors
Akua Graf, James Welch, Rashika Bansal, et al.
Journal of Community Hospital Internal Medicine Perspectives
|
May 3, 2019
Retrospective study of inpatient diabetes management service, length of stay and 30-day readmission rate of patients with diabetes at a community hospital
Samantha R Mandel, Susan Langan, Nestoras Nicolas Mathioudakis, et al.
Surgery
|
December 5, 2009
Reoperation for parathyroid adenoma: a contemporary experience
Anathea C Powell, H Richard Alexander, Richard Chang, et al.
Cancers
|
March 25, 2022
Parathyroid Carcinoma: Incidence, Survival Analysis, and Management: A Study from the SEER Database and Insights into Future Therapeutic Perspectives
Asad Ullah, Jaffar Khan, Abdul Waheed, et al.
American Journal of Human Genetics
|
February 14, 2024
The association of GNB5 with Alzheimer disease revealed by genomic analysis restricted to variants impacting gene function
Jianhua Zhang, Mritunjay Pandey, Adam Awe, et al.
The New England Journal of Medicine
|
November 17, 2021
Parathyroid Hormone Resistance and Autoantibodies to the PTH1 Receptor
Adel Mandl, Peter D Burbelo, Giovanni Di Pasquale, et al.
Journal of Medical Genetics
|
November 11, 2020
Inhibition of G-protein signalling in cardiac dysfunction of intellectual developmental disorder with cardiac arrhythmia (IDDCA) syndrome
Pasquelena De Nittis, Stephanie Efthymiou, Alexandre Sarre, et al.
Annals of the New York Academy of Sciences
|
May 22, 2004
Molecular pathology of the MEN1 gene
Sunita K Agarwal, A Lee Burns, Karen E Sukhodolets, et al.
American Journal of Human Genetics
|
September 3, 2016
GNB5 Mutations Cause an Autosomal-Recessive Multisystem Syndrome with Sinus Bradycardia and Cognitive Disability
Elisabeth M Lodder, Pasquelena De Nittis, Charlotte D Koopman, et al.
Page
of 10