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Biochemical Diagnosis of Chromaffin Cell Tumors in Patients at High and Low Risk of Disease: Plasma versus Urinary Free or Deconjugated O -Methylated Catecholamine Metabolites

Clinical chemistry (Baltimore, Md.), 2018-11, Vol.64 (11), p.1646-1656

2018

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Peri-procedural intravascular ultrasound monitoring during bi-caval valve implantation in the treatment of carcinoid-induced tricuspid regurgitation

European heart journal cardiovascular imaging, 2024-01, Vol.25 (2), p.e98-e98

2024

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Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

JAMA : the journal of the American Medical Association, 2004-08, Vol.292 (8), p.943

2004

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Carcinoid heart disease: An immense challenge despite medical and surgical advances

Kardiologia polska (1957), 2022-11, Vol.80 (11), p.1163-1164

2022

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Chromogranin A (CgA) as a biomarker in carcinoid heart disease and NETG1/G2 neuroendocrine neoplasms of the small intestine (SI-NENs) related carcinoid syndrome

Medicina clínica, 2022-07, Vol.159 (2), p.85-89

2022

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Cardiac paraganglioma: A challenging diagnostic and treatment dilemma

Kardiologia polska (1957), 2022-03, Vol.80 (3), p.378-379

2022

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Functional significance of germline EPAS1 variants

Endocrine-related cancer, 2021-02, Vol.28 (2), p.97-109

2021

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Eleven-year follow-up of cardiac paraganglioma in a patient with SDHD C11X gene mutation

Kardiologia polska, 2021-11, Vol.79 (11), p.1276-1277

2021

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Left Ventricular Structural and Functional Alterations in Patients With Pheochromocytoma/Paraganglioma Before and After Surgery

JACC. Cardiovascular imaging, 2020-12, Vol.13 (12), p.2498-2509

2020

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GROWTH RATE OF PARAGANGLIOMAS RELATED TO GERMLINE MUTATIONS OF THE SDHX GENES

Endocrine practice, 2017-03, Vol.23 (3), p.342-352

2017

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A Clinical Efficacy of PRRT in Patients with Advanced, Nonresectable, Paraganglioma-Pheochromocytoma, Related to SDHx Gene Mutation

Journal of clinical medicine, 2019-06, Vol.8 (7), p.952

2019

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Analysis of Patients with NET G1/G2 Neuroendocrine Tumors of the Small Intestine in the Course of Carcinoid Heart Disease-A Retrospective Study

Journal of clinical medicine, 2023-01, Vol.12 (3), p.790

2023

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What do we know about carcinoid heart disease in the present era?

Kardiologia polska (1957), 2022-10, Vol.80 (10), p.990-1001

2022

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Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma

European journal of endocrinology, 2015-02, Vol.172 (2), p.89

2015

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Early-Onset Renal Cell Carcinoma as a Novel Extraparaganglial Component of SDHB-Associated Heritable Paraganglioma

American journal of human genetics, 2004-01, Vol.74 (1), p.153-159

2004

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Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

Nature clinical practice. Endocrinology & metabolism, 2008-02, Vol.4 (2), p.111-115

2008

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Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes

Clinical endocrinology (Oxford), 2013-12, Vol.79 (6), p.817-823

2013

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A 51-year-old patient with carcinoid heart disease and severe tricuspid regurgitation

Kardiologia polska, 2017-01, Vol.75 (2), p.183-183

2017

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Outcomes of cardiac surgical treatment for carcinoid heart disease

Kardiologia polska, 2022-01, Vol.80 (2), p.202-204

2022

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Clinical Predictors and Algorithm for the Genetic Diagnosis of Pheochromocytoma Patients

Clinical cancer research, 2009-10, Vol.15 (20), p.6378-6385

2009

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Impact of Screening Kindreds for SDHD p.Cys11X as a Common Mutation Associated with Paraganglioma Syndrome Type 1

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4818-4825

2008

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Abstract 3391: Next generation sequencing paves the way for personalized medicine in pheochromocytoma and paraganglioma patients and their families

Cancer research (Chicago, Ill.), 2017-07, Vol.77 (13_Supplement), p.3391-3391

2017

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Right and left-sided carcinoid heart disease

Cardiology journal, 2018-01, Vol.25 (3), p.417-417

2018

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Chromogranin A (CgA) as a biomarker in carcinoid heart disease and NETG1/G2 neuroendocrine neoplasms of the small intestine (SI-NENs) related carcinoid syndrome

Medicina clínica (English ed.), 2022-07, Vol.159 (2), p.85-89

2022

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Biochemical Diagnosis of Chromaffin Cell Tumors in Patients at High and Low Risk of Disease: Plasma versus Urinary Free or Deconjugated O -Methylated Catecholamine Metabolites

Peri-procedural intravascular ultrasound monitoring during bi-caval valve implantation in the treatment of carcinoid-induced tricuspid regurgitation

Distinct clinical features of paraganglioma syndromes associated with SDHB and SDHD gene mutations

Carcinoid heart disease: An immense challenge despite medical and surgical advances

Chromogranin A (CgA) as a biomarker in carcinoid heart disease and NETG1/G2 neuroendocrine neoplasms of the small intestine (SI-NENs) related carcinoid syndrome

Cardiac paraganglioma: A challenging diagnostic and treatment dilemma

Functional significance of germline EPAS1 variants

Eleven-year follow-up of cardiac paraganglioma in a patient with SDHD C11X gene mutation

Left Ventricular Structural and Functional Alterations in Patients With Pheochromocytoma/Paraganglioma Before and After Surgery

GROWTH RATE OF PARAGANGLIOMAS RELATED TO GERMLINE MUTATIONS OF THE SDHX GENES

A Clinical Efficacy of PRRT in Patients with Advanced, Nonresectable, Paraganglioma-Pheochromocytoma, Related to SDHx Gene Mutation

Analysis of Patients with NET G1/G2 Neuroendocrine Tumors of the Small Intestine in the Course of Carcinoid Heart Disease-A Retrospective Study

Intrarenal hemodynamics and kidney function in pheochromocytoma and paraganglioma before and after surgical treatment

What do we know about carcinoid heart disease in the present era?

Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma

Early-Onset Renal Cell Carcinoma as a Novel Extraparaganglial Component of SDHB-Associated Heritable Paraganglioma

Extra-adrenal and adrenal pheochromocytomas associated with a germline SDHC mutation

Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromes

A 51-year-old patient with carcinoid heart disease and severe tricuspid regurgitation

Outcomes of cardiac surgical treatment for carcinoid heart disease

Clinical Predictors and Algorithm for the Genetic Diagnosis of Pheochromocytoma Patients

Impact of Screening Kindreds for SDHD p.Cys11X as a Common Mutation Associated with Paraganglioma Syndrome Type 1

Abstract 3391: Next generation sequencing paves the way for personalized medicine in pheochromocytoma and paraganglioma patients and their families

Right and left-sided carcinoid heart disease

Chromogranin A (CgA) as a biomarker in carcinoid heart disease and NETG1/G2 neuroendocrine neoplasms of the small intestine (SI-NENs) related carcinoid syndrome

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