Lista de obras -

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

artículo científico publicado en 2018

A differential diagnosis of inherited endocrine tumors and their tumor counterparts

artículo científico publicado en 2013

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

artículo científico publicado en 2017

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

artículo científico publicado en 2014

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

artículo científico publicado el 1 de enero de 2012

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

artículo científico publicado en 2009

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

artículo científico publicado en 2014

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

artículo científico publicado en 2014

Correction: Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue

artículo científico publicado en 2017

EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease.

artículo científico publicado en 2018

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

artículo científico publicado en 2010

Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue

artículo científico publicado en 2017

Familial isolated pituitary adenoma: evidence for genetic heterogeneity.

artículo científico publicado en 2010

Germline mutation in the aryl hydrocarbon receptor interacting protein gene in familial somatotropinoma

artículo científico publicado en 2007

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

article

Guidelines for the management of neuroendocrine tumours by the Brazilian gastrointestinal tumour group

artículo científico publicado en 2017

High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene

artículo científico publicado en 2010

Hypercalcitoninemia is not pathognomonic of medullary thyroid carcinoma

scientific article published on January 2009

Insulinoma: A retrospective study analyzing the differences between benign and malignant tumors

artículo científico publicado en 2018

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

artículo científico publicado en 2010

Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile

scientific article published on 04 June 2008

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

artículo científico publicado el 1 de enero de 2012

Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study

artículo científico publicado en 2019

Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1

artículo científico publicado en 2007

Penetrance of functioning and nonfunctioning pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 in the second decade of life.

artículo científico

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

artículo científico publicado en 2018

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

scientific article published on 17 July 2018

RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma.

artículo científico publicado en 2015

Successful parathyroid tissue autograft after 3 years of cryopreservation: a case report.

artículo científico publicado en 2014

Supernumerary parathyroid glands in hyperparathyroidism associated with multiple endocrine neoplasia type 1

artículo científico publicado en 2012

The parathyroids and the kidney: Fuller Albright revisited.

artículo científico publicado en 2009

Total parathyroidectomy in a large cohort of cases with hyperparathyroidism associated with multiple endocrine neoplasia type 1: experience from a single academic center ⬇️

artículo científico publicado el 1 de enero de 2012

Transitory increase in creatinine levels after parathyroidectomy: evidence of another action of the parathyroid glands?

artículo científico publicado en 2011

Lista de obras de

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

A differential diagnosis of inherited endocrine tumors and their tumor counterparts

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

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

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

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

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

Correction: Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue

EPAS1 Mutations and Paragangliomas in Cyanotic Congenital Heart Disease.

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

Familial Hyperparathyroidism - Disorders of Growth and Secretion in Hormone-Secretory Tissue

Familial isolated pituitary adenoma: evidence for genetic heterogeneity.

Germline mutation in the aryl hydrocarbon receptor interacting protein gene in familial somatotropinoma

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

Guidelines for the management of neuroendocrine tumours by the Brazilian gastrointestinal tumour group

High penetrance of pheochromocytoma associated with the novel C634Y/Y791F double germline mutation in the RET protooncogene

Hypercalcitoninemia is not pathognomonic of medullary thyroid carcinoma

Insulinoma: A retrospective study analyzing the differences between benign and malignant tumors

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

Multiple endocrine neoplasia type 1 in Brazil: MEN1 founding mutation, clinical features, and bone mineral density profile

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

Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study

Novel MEN1 germline mutations in Brazilian families with multiple endocrine neoplasia type 1

Penetrance of functioning and nonfunctioning pancreatic neuroendocrine tumors in multiple endocrine neoplasia type 1 in the second decade of life.

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

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

RET Y791F Variant Does Not Increase the Risk for Medullary Thyroid Carcinoma.

Successful parathyroid tissue autograft after 3 years of cryopreservation: a case report.

Supernumerary parathyroid glands in hyperparathyroidism associated with multiple endocrine neoplasia type 1

The parathyroids and the kidney: Fuller Albright revisited.

Total parathyroidectomy in a large cohort of cases with hyperparathyroidism associated with multiple endocrine neoplasia type 1: experience from a single academic center ⬇️

Transitory increase in creatinine levels after parathyroidectomy: evidence of another action of the parathyroid glands?