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Disease-Specific Survival by Treatment Modality in Patients with Stage IE Primary Thyroid Lymphoma: Discussion of Risks and Benefits

Annals of surgical oncology, 2024-03, Vol.31 (3), p.1436-1437

Nilubol, Naris

2024

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ASO Author Reflections: Predicting Postoperative Resolution of Hypertension in Primary Hyperaldosteronism

Annals of surgical oncology, 2021-11, Vol.28 (12), p.7496-7496

2021

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MiR-34a and miR-483-5p are candidate serum biomarkers for adrenocortical tumors

Surgery, 2013-12, Vol.154 (6), p.1224-1229

2013

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Hyperparathyroidism-jaw tumor syndrome: Results of operative management

Surgery, 2014-12, Vol.156 (6), p.1315-1325

2014

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Malignant-functioning neuroendocrine tumors of the pancreas: A survival analysis

Surgery, 2016-05, Vol.159 (5), p.1382-1389

2016

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Resection of primary tumor site is associated with prolonged survival in metastatic nonfunctioning pancreatic neuroendocrine tumors

Surgery, 2016, Vol.159 (1), p.311-319

2016

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Contralateral Suppression Index Does Not Predict Clinical Cure in Patients Undergoing Surgery for Primary Aldosteronism

Annals of surgical oncology, 2021-11, Vol.28 (12), p.7487-7495

2021

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SDHB mutation status and tumor size but not tumor grade are important predictors of clinical outcome in pheochromocytoma and abdominal paraganglioma

Surgery, 2017-01, Vol.161 (1), p.230-239

2017

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Clinical characteristics and outcomes of SDHB-related pheochromocytoma and paraganglioma in children and adolescents

Journal of cancer research and clinical oncology, 2020-04, Vol.146 (4), p.1051-1063

2020

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Immune signature of pheochromocytoma and paraganglioma in context of neuroendocrine neoplasms associated with prognosis

Endocrine, 2023-01, Vol.79 (1), p.171-179

2023

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Surgical Resection of Pheochromocytomas and Paragangliomas is Associated with Lower Cholesterol Levels

World journal of surgery, 2020-02, Vol.44 (2), p.552-560

2020

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Pediatric patients with pheochromocytoma and paraganglioma should have routine preoperative genetic testing for common susceptibility genes in addition to imaging to detect extra-adrenal and metastatic tumors

Surgery, 2017-01, Vol.161 (1), p.220-227

2017

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P115: Identification of a novel SDHB c.638T>G, p.M213R likely pathogenic variant accountable for hereditary paraganglioma-pheochromocytoma syndrome: A case report

Genetics in Medicine Open, 2024, Vol.2, p.100996, Article 100996

2024

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FDG PET/CT Scan and Functional Adrenal Tumors: A Pilot Study for Lateralization

World journal of surgery, 2016-03, Vol.40 (3), p.683-689

2016

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Incidence and management of postoperative hyperglycemia in patients undergoing insulinoma resection

Endocrine, 2018-09, Vol.61 (3), p.422-427

2018

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Multiple Endocrine Neoplasia Type 1 Syndrome Pancreatic Neuroendocrine Tumor Genotype/Phenotype: Is There Any Advance on Predicting or Preventing?

Surgical oncology clinics of North America, 2023-04, Vol.32 (2), p.315-325

2023

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MEN1 PNET Genotype/Phenotype- Is there any advance on predicting or preventing?

Surgical oncology clinics of North America, 2023-04, Vol.32 (2), p.315-325

2023

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Multiple Endocrine Neoplasia Type 1 Syndrome Pancreatic Neuroendocrine Tumor Genotype/Phenotype

Surgical oncology clinics of North America, 2023-04, Vol.32 (2), p.315-325

2023

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Detection of Grade 2/3 Von Hippel-Lindau Associated Pancreatic Lesions by 18-FDG PET/CT Volumetric Parameters

Journal of the American College of Surgeons, 2015-10, Vol.221 (4), p.S59-S59

2015

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Assessment of Tumor Growth in Pancreatic Neuroendocrine Tumors in von Hippel Lindau Syndrome

Journal of the American College of Surgeons, 2014-02, Vol.218 (2), p.163-169

2014

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Response after Surgical Resection of Metastatic Pheochromocytoma and Paraganglioma: Can Postoperative Biochemical Remission Be Predicted?

Journal of the American College of Surgeons, 2013-09, Vol.217 (3), p.489-496

2013

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Prospective screening in familial nonmedullary thyroid cancer

Surgery, 2013-12, Vol.154 (6), p.1194-1198

2013

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Combination Therapy with Sorafenib and Vemurafenib Is Effective in Anaplastic Thyroid Cancer

Journal of the American College of Surgeons, 2016-10, Vol.223 (4), p.S45-S45

2016

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Role of 18F-FDG PET/CT in management of adrenocortical carcinoma: a comprehensive review of the literature

Clinical and translational imaging : reviews in nuclear medicine and molecular imaging, 2022, Vol.10 (3), p.285-299

2022

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Urinary Metabolomics Analyses Identify Novel Markers of Malignant Adrenocortical Neoplasms

Journal of the American College of Surgeons, 2015-10, Vol.221 (4), p.S61-S62

2015

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Disease-Specific Survival by Treatment Modality in Patients with Stage IE Primary Thyroid Lymphoma: Discussion of Risks and Benefits

ASO Author Reflections: Predicting Postoperative Resolution of Hypertension in Primary Hyperaldosteronism

MiR-34a and miR-483-5p are candidate serum biomarkers for adrenocortical tumors

Hyperparathyroidism-jaw tumor syndrome: Results of operative management

Malignant-functioning neuroendocrine tumors of the pancreas: A survival analysis

Resection of primary tumor site is associated with prolonged survival in metastatic nonfunctioning pancreatic neuroendocrine tumors

Contralateral Suppression Index Does Not Predict Clinical Cure in Patients Undergoing Surgery for Primary Aldosteronism

SDHB mutation status and tumor size but not tumor grade are important predictors of clinical outcome in pheochromocytoma and abdominal paraganglioma

Clinical characteristics and outcomes of SDHB-related pheochromocytoma and paraganglioma in children and adolescents

Immune signature of pheochromocytoma and paraganglioma in context of neuroendocrine neoplasms associated with prognosis

Surgical Resection of Pheochromocytomas and Paragangliomas is Associated with Lower Cholesterol Levels

Pediatric patients with pheochromocytoma and paraganglioma should have routine preoperative genetic testing for common susceptibility genes in addition to imaging to detect extra-adrenal and metastatic tumors

P115: Identification of a novel SDHB c.638T>G, p.M213R likely pathogenic variant accountable for hereditary paraganglioma-pheochromocytoma syndrome: A case report

FDG PET/CT Scan and Functional Adrenal Tumors: A Pilot Study for Lateralization

Incidence and management of postoperative hyperglycemia in patients undergoing insulinoma resection

Multiple Endocrine Neoplasia Type 1 Syndrome Pancreatic Neuroendocrine Tumor Genotype/Phenotype: Is There Any Advance on Predicting or Preventing?

MEN1 PNET Genotype/Phenotype- Is there any advance on predicting or preventing?

Multiple Endocrine Neoplasia Type 1 Syndrome Pancreatic Neuroendocrine Tumor Genotype/Phenotype

Detection of Grade 2/3 Von Hippel-Lindau Associated Pancreatic Lesions by 18-FDG PET/CT Volumetric Parameters

Assessment of Tumor Growth in Pancreatic Neuroendocrine Tumors in von Hippel Lindau Syndrome

Response after Surgical Resection of Metastatic Pheochromocytoma and Paraganglioma: Can Postoperative Biochemical Remission Be Predicted?

Prospective screening in familial nonmedullary thyroid cancer

Combination Therapy with Sorafenib and Vemurafenib Is Effective in Anaplastic Thyroid Cancer

Role of 18F-FDG PET/CT in management of adrenocortical carcinoma: a comprehensive review of the literature

Urinary Metabolomics Analyses Identify Novel Markers of Malignant Adrenocortical Neoplasms

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