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Author Details
Full Name
Stephen J Marx
Affiliation
National Institutes of Digestive Disease and Kidney, National Institutes of Health
ORCID
Career Start Year
1971
Papers
321
H Index
83
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
31778168
Neonatal Severe Hyperparathyroidism: Novel Insights From Calcium, PTH, and the CASR Gene.
J Clin Endocrinol Metab
2020
31782130
Long-term remission of disseminated parathyroid cancer following immunotherapy.
Endocrine
2020
31778168
Neonatal Severe Hyperparathyroidism: Novel Insights From Calcium, PTH, and the CASR Gene.
J Clin Endocrinol Metab
2020
31782130
Long-term remission of disseminated parathyroid cancer following immunotherapy.
Endocrine
2020
30414705
High prevalence of chronic kidney disease in patients with multiple endocrine neoplasia type 1 and improved kidney function after parathyroidectomy.
Surgery
2019
30536424
Evolution of Our Understanding of the Hyperparathyroid Syndromes: A Historical Perspective.
J Bone Miner Res
2019
30414705
High prevalence of chronic kidney disease in patients with multiple endocrine neoplasia type 1 and improved kidney function after parathyroidectomy.
Surgery
2019
30848815
New Concepts About Familial Isolated Hyperparathyroidism.
J Clin Endocrinol Metab
2019
30848815
New Concepts About Familial Isolated Hyperparathyroidism.
J Clin Endocrinol Metab
2019
30536424
Evolution of Our Understanding of the Hyperparathyroid Syndromes: A Historical Perspective.
J Bone Miner Res
2019
29115694
Familial Hypocalciuric Hypercalcemia as an Atypical Form of Primary Hyperparathyroidism.
J Bone Miner Res
2018
30065698
Questions and Controversies About Parathyroid Pathophysiology in Children With Multiple Endocrine Neoplasia Type 1.
Front Endocrinol (Lausanne)
2018
29927501
Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease.
Clin Endocrinol (Oxf)
2018
30324798
Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing.
Eur J Endocrinol
2018
29897580
Recent Topics Around Multiple Endocrine Neoplasia Type 1.
J Clin Endocrinol Metab
2018
29115694
Familial Hypocalciuric Hypercalcemia as an Atypical Form of Primary Hyperparathyroidism.
J Bone Miner Res
2018
29155309
Prognostic Utility of Total <sup>68</sup>Ga-DOTATATE-Avid Tumor Volume in Patients With Neuroendocrine Tumors.
Gastroenterology
2018
29108698
Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure.
Surgery
2018
29408534
Probability of Positive Genetic Testing Results in Patients with Family History of Primary Hyperparathyroidism.
J Am Coll Surg
2018
30065698
Questions and Controversies About Parathyroid Pathophysiology in Children With Multiple Endocrine Neoplasia Type 1.
Front Endocrinol (Lausanne)
2018
29927501
Children with MEN1 gene mutations may present first (and at a young age) with Cushing disease.
Clin Endocrinol (Oxf)
2018
29897580
Recent Topics Around Multiple Endocrine Neoplasia Type 1.
J Clin Endocrinol Metab
2018
30324798
Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing.
Eur J Endocrinol
2018
29408534
Probability of Positive Genetic Testing Results in Patients with Family History of Primary Hyperparathyroidism.
J Am Coll Surg
2018
29108698
Familial isolated primary hyperparathyroidism associated with germline GCM2 mutations is more aggressive and has a lesser rate of biochemical cure.
Surgery
2018
29155309
Prognostic Utility of Total <sup>68</sup>Ga-DOTATATE-Avid Tumor Volume in Patients With Neuroendocrine Tumors.
Gastroenterology
2018
29136674
Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
Horm Metab Res
2017
28945857
Calcimimetic Use in Familial Hypocalciuric Hypercalcemia-A Perspective in Endocrinology.
J Clin Endocrinol Metab
2017
29879737
Correction: Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
Horm Metab Res
2017
29264504
Ethnicity of Patients With Germline <i>GCM2</i>-Activating Variants and Primary Hyperparathyroidism.
J Endocr Soc
2017
29136674
Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
Horm Metab Res
2017
28289088
Association between neuroendocrine tumors biomarkers and primary tumor site and disease type based on total <sup>68</sup>Ga-DOTATATE-Avid tumor volume measurements.
Eur J Endocrinol
2017
29879737
Correction: Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue.
Horm Metab Res
2017
28289088
Association between neuroendocrine tumors biomarkers and primary tumor site and disease type based on total <sup>68</sup>Ga-DOTATATE-Avid tumor volume measurements.
Eur J Endocrinol
2017
29264504
Ethnicity of Patients With Germline <i>GCM2</i>-Activating Variants and Primary Hyperparathyroidism.
J Endocr Soc
2017
28945857
Calcimimetic Use in Familial Hypocalciuric Hypercalcemia-A Perspective in Endocrinology.
J Clin Endocrinol Metab
2017
26712231
Prospective Study of 68Ga-DOTATATE Positron Emission Tomography/Computed Tomography for Detecting Gastro-Entero-Pancreatic Neuroendocrine Tumors and Unknown Primary Sites.
J Clin Oncol
2016
27464610
Reoperative Surgery in Patients with Multiple Endocrine Neoplasia Type 1 Associated Primary Hyperparathyroidism.
Ann Surg Oncol
2016
26542588
Limited Parathyroidectomy in Multiple Endocrine Neoplasia Type 1-Associated Primary Hyperparathyroidism: A Setup for Failure.
Ann Surg Oncol
2016
26712231
Prospective Study of 68Ga-DOTATATE Positron Emission Tomography/Computed Tomography for Detecting Gastro-Entero-Pancreatic Neuroendocrine Tumors and Unknown Primary Sites.
J Clin Oncol
2016
26407873
Hyperplasia in glands with hormone excess.
Endocr Relat Cancer
2016
27745835
GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
Am J Hum Genet
2016
27594983
A patient with MEN1 typical features and MEN2-like features.
Int J Endocr Oncol
2016
26542588
Limited Parathyroidectomy in Multiple Endocrine Neoplasia Type 1-Associated Primary Hyperparathyroidism: A Setup for Failure.
Ann Surg Oncol
2016
26407873
Hyperplasia in glands with hormone excess.
Endocr Relat Cancer
2016
27745835
GCM2-Activating Mutations in Familial Isolated Hyperparathyroidism.
Am J Hum Genet
2016
27594983
A patient with MEN1 typical features and MEN2-like features.
Int J Endocr Oncol
2016
27464610
Reoperative Surgery in Patients with Multiple Endocrine Neoplasia Type 1 Associated Primary Hyperparathyroidism.
Ann Surg Oncol
2016
25658165
Letter to the editor: Distinguishing typical primary hyperparathyroidism from familial hypocalciuric hypercalcemia by using an index of urinary calcium.
J Clin Endocrinol Metab
2015
25658165
Letter to the editor: Distinguishing typical primary hyperparathyroidism from familial hypocalciuric hypercalcemia by using an index of urinary calcium.
J Clin Endocrinol Metab
2015
1 - 50 of 642
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Center for Cancer Research, National Cancer Institute, National Institutes of Health
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Center for Cancer Research, National Cancer Institute
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Rhode Island Hospital
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