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Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma

Clinics (São Paulo, Brazil), 2009-01, Vol.64 (7), p.699-706

2009

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Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy

Clinical endocrinology (Oxford), 2010-04, Vol.72 (4), p.462-468

2010

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Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1

Clinics (São Paulo, Brazil), 2012-01, Vol.67 (suppl 1), p.99-108

2012

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A differential diagnosis of inherited endocrine tumors and their tumor counterparts

Clinics (São Paulo, Brazil), 2013-07, Vol.68 (7), p.1039-1056

2013

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Assessing the emerging oncogene protein kinase C epsilon as a candidate gene in families with Carney complex-2

Clinical endocrinology (Oxford), 2012-01, Vol.76 (1), p.147-148

2012

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Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing

European journal of endocrinology, 2018-12, Vol.179 (6), p.391

2018

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Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil

Clinics (São Paulo, Brazil), 2012-01, Vol.67 (suppl 1), p.3-6

2012

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Isolated familial somatotropinoma: 11q13-loh and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis

Clinics (São Paulo, Brazil), 2010-04, Vol.65 (4), p.407-415

2010

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Sporadic Medullary Thyroid Carcinoma: Clinical Data From A University Hospital

Clinics (São Paulo, Brazil), 2009-05, Vol.64 (5), p.379-386

2009

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New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations

Journal of the Endocrine Society, 2019-09, Vol.3 (9), p.1682-1692

2019

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EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease

The New England journal of medicine, 2018-03, Vol.378 (13), p.1259-1261

2018

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Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1

Clinics (São Paulo, Brazil), 2012-01, Vol.67 (Suppl 1), p.169-172

2012

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Editorial: Early Genetic and Clinical Diagnosis in MEN1

Frontiers in endocrinology (Lausanne), 2020-04, Vol.11, p.218-218

2020

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Assessment of Depression, Anxiety, Quality of Life, and Coping in Long-Standing Multiple Endocrine Neoplasia Type 2 Patients

Thyroid (New York, N.Y.), 2017-05, Vol.27 (5), p.693

2017

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Preventive medicine of von Hippel–Lindau disease-associated pancreatic neuroendocrine tumors

Endocrine-related cancer, 2018-09, Vol.25 (9), p.783-793

2018

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Early‐onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1–associated primary hyperparathyroidism

Journal of bone and mineral research, 2010-11, Vol.25 (11), p.2382-2391

2010

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Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation

The journal of clinical endocrinology and metabolism, 2015-02, Vol.100 (2), p.E308-E318

2015

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Penetrance of Functioning and Nonfunctioning Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 in the Second Decade of Life

The journal of clinical endocrinology and metabolism, 2014-01, Vol.99 (1), p.E89-E96

2014

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Questions and Controversies About Parathyroid Pathophysiology in Children With Multiple Endocrine Neoplasia Type 1

Frontiers in endocrinology (Lausanne), 2018-07, Vol.9, p.359-359

2018

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Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma

The journal of clinical endocrinology and metabolism, 2007-05, Vol.92 (5), p.1934-1937

2007

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Complete resolution of hypercortisolism with sorafenib in a patient with advanced medullary thyroid carcinoma and ectopic ACTH (adrenocorticotropic hormone) syndrome

Thyroid (New York, N.Y.), 2014-06, Vol.24 (6), p.1062

2014

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Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility

Endocrine-related cancer, 2015-02, Vol.22 (1), p.65-76

2015

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High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene

The journal of clinical endocrinology and metabolism, 2010-03, Vol.95 (3), p.1318-1327

2010

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Hypercalcitoninemia is not Pathognomonic of Medullary Thyroid Carcinoma

Bone mineral density analysis in patients with primary hyperparathyroidism associated with multiple endocrine neoplasia type 1 after total parathyroidectomy

Biochemical, bone and renal patterns in hyperparathyroidism associated with multiple endocrine neoplasia type 1

A differential diagnosis of inherited endocrine tumors and their tumor counterparts

65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytoma

Assessing the emerging oncogene protein kinase C epsilon as a candidate gene in families with Carney complex-2

Germline mutation landscape of multiple endocrine neoplasia type 1 using full gene next-generation sequencing

Narrowing the gap of personalized medicine in emerging countries: the case of multiple endocrine neoplasias in Brazil

Isolated familial somatotropinoma: 11q13-loh and gene/protein expression analysis suggests a possible involvement of aip also in non-pituitary tumorigenesis

Sporadic Medullary Thyroid Carcinoma: Clinical Data From A University Hospital

New Insights Into Pheochromocytoma Surveillance of Young Patients With VHL Missense Mutations

EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease

Post-surgical follow-up of primary hyperparathyroidism associated with multiple endocrine neoplasia type 1

Editorial: Early Genetic and Clinical Diagnosis in MEN1

Assessment of Depression, Anxiety, Quality of Life, and Coping in Long-Standing Multiple Endocrine Neoplasia Type 2 Patients

Preventive medicine of von Hippel–Lindau disease-associated pancreatic neuroendocrine tumors

Early‐onset, progressive, frequent, extensive, and severe bone mineral and renal complications in multiple endocrine neoplasia type 1–associated primary hyperparathyroidism

Penetrance and Clinical Features of Pheochromocytoma in a Six-Generation Family Carrying a Germline TMEM127 Mutation

Penetrance of Functioning and Nonfunctioning Pancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 in the Second Decade of Life

Questions and Controversies About Parathyroid Pathophysiology in Children With Multiple Endocrine Neoplasia Type 1

Germline Mutation in the Aryl Hydrocarbon Receptor Interacting Protein Gene in Familial Somatotropinoma

Complete resolution of hypercortisolism with sorafenib in a patient with advanced medullary thyroid carcinoma and ectopic ACTH (adrenocorticotropic hormone) syndrome

Comprehensive assessment of the disputed RET Y791F variant shows no association with medullary thyroid carcinoma susceptibility

High Penetrance of Pheochromocytoma Associated with the Novel C634Y/Y791F Double Germline Mutation in the RET Protooncogene

Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations

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