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

7D.07: RETINAL ARTERIOLAR STRUCTURE IN PATIENTS WITH PHEOCHROMOCYTOMA.

artículo científico publicado en 2015

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

artículo científico publicado en 2017

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

artículo científico publicado en 2019

A registry-based study of thyroid paraganglioma: histological and genetic characteristics

artículo científico publicado en 2015

Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation.

artículo científico publicado en 2008

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

scientific article published on 10 August 2018

Biochemical diagnosis of phaeochromocytoma using plasma-free normetanephrine, metanephrine and methoxytyramine: importance of supine sampling under fasting conditions

artículo científico publicado en 2013

Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention

artículo científico publicado en 2017

Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients

artículo científico publicado en 2009

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out

artículo científico publicado en 2009

Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy.

artículo científico publicado en 2019

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

artículo científico publicado en 2004

Evaluation of Head and Neck Paragangliomas by Computed Tomography in Patients with Pheochromocytoma-Paraganglioma Syndromes

artículo científico publicado en 2016

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

artículo científico publicado en 2008

Functional significance of germline EPAS1 variants

artículo científico publicado en 2020

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

artículo científico publicado en 2016

Genetic screening for glucocorticoid-remediable aldosteronism (GRA): experience of three clinical centres in Poland

scientific article published on 01 January 2005

Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas

artículo científico publicado en 2010

Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1.

artículo científico publicado en 2007

Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1

artículo científico publicado en 2008

Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset

artículo científico publicado en 2003

Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma

scientific article published on 01 February 2015

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

scientific article published on 11 September 2020

Long-term prognosis of patients with pediatric pheochromocytoma.

artículo científico publicado en 2013

Mediastinal paragangliomas related to SDHx gene mutations.

artículo científico publicado en 2016

Multiple endocrine neoplasia type 2.

artículo científico publicado en 2005

Multiple phaeochromocytoma with renal artery stenosis or occlusion: report of two cases

artículo científico publicado en 1993

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

Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study

artículo científico publicado en 2014

Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome

artículo científico publicado en 2009

Pheochromocytoma of the urinary bladder coexisting with another extra-adrenal tumour--case report of a 19-year-old male patient

scientific article published on 01 January 2002

Pheochromocytoma presenting as takotsubo-like cardiomyopathy following delivery.

artículo científico publicado en 2014

Pheochromocytoma-related 'classic' takotsubo cardiomyopathy.

artículo científico publicado en 2010

Pheochromocytoma: presentation, diagnosis and treatment

artículo científico publicado en 2006

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

artículo científico publicado en 2018

Primary aldosteronism - recent progress and current concepts.

artículo científico publicado en 2013

Primary hyperparathyroidism as first manifestation in MEN 2A: an international multicenter study

artículo científico publicado en 2020

Retinal arterial remodeling in patients with pheochromocytoma or paraganglioma and its reversibility following surgical treatment

artículo científico publicado en 2020

Right and left-sided carcinoid heart disease

artículo científico publicado en 2018

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10.

artículo científico publicado en 2011

Systematic and Multidisciplinary Evaluation of Fibromuscular Dysplasia Patients Reveals High Prevalence of Previously Undetected Fibromuscular Dysplasia Lesions and Affects Clinical Decisions: The ARCADIA-POL Study

scientific article published on 09 March 2020

Systematic comparison of sporadic and syndromic pancreatic islet cell tumors

artículo científico publicado en 2010

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

artículo científico publicado en 2013

The clinical utility of circulating neuroendocrine gene transcript analysis in well-differentiated paragangliomas and pheochromocytomas

artículo científico publicado en 2016

The coexistence of acute aortic dissection with autosomal dominant polycystic kidney disease--description of two hypertensive patients

scientific article published on 01 January 2004

The penetrance of MEN2 pheochromocytoma is not only determined by RET mutations.

artículo científico publicado en 2017

The role of biochemical tests and clinical symptoms in differential diagnosis of primary aldosteronism

artículo científico publicado en 2003

The role of calcium in the pathogenesis of arterial hypertension

artículo científico publicado en 1988

Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography

artículo científico publicado en 2015

[Doxazosin (alpha 1-adrenoreceptor antagonist) used in primary hypertension and it's beneficial effect on lipid metabolism]

artículo científico publicado en 1993

[Evaluation of selected parameters of zinc metabolism in patients with primary hypertension].

artículo científico publicado en 1996

[Influence of angiotensin I converting enzyme inhibitors on selected parameters of zinc metabolism]

artículo científico publicado en 1996

[New therapeutic perspectives associated with the introduction of angiotensin II receptor antagonists]

artículo científico publicado en 1997

[Plasma renin activity, aldosterone and adrenergic activity in patients with hypertension and in normotensives with a family history of hypertension]

artículo científico publicado en 1996

[Secondary hypertension in year 2002: current trends in diagnosis and treatment]

artículo científico publicado en 2002

Lista de obras de

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

7D.07: RETINAL ARTERIOLAR STRUCTURE IN PATIENTS WITH PHEOCHROMOCYTOMA.

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

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

A registry-based study of thyroid paraganglioma: histological and genetic characteristics

Age-related neoplastic risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germ line RET Cys634Trp (TGC>TGG) mutation.

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

Biochemical diagnosis of phaeochromocytoma using plasma-free normetanephrine, metanephrine and methoxytyramine: importance of supine sampling under fasting conditions

Clinical Characterization of the Pheochromocytoma and Paraganglioma Susceptibility Genes SDHA, TMEM127, MAX, and SDHAF2 for Gene-Informed Prevention

Clinical predictors and algorithm for the genetic diagnosis of pheochromocytoma patients

Clinical predictors for germline mutations in head and neck paraganglioma patients: cost reduction strategy in genetic diagnostic process as fall-out

Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy.

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

Evaluation of Head and Neck Paragangliomas by Computed Tomography in Patients with Pheochromocytoma-Paraganglioma Syndromes

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

Functional significance of germline EPAS1 variants

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

Genetic screening for glucocorticoid-remediable aldosteronism (GRA): experience of three clinical centres in Poland

Germinal mutations of RET, SDHB, SDHD, and VHL genes in patients with apparently sporadic pheochromocytomas and paragangliomas

Germline NF1 mutational spectra and loss-of-heterozygosity analyses in patients with pheochromocytoma and neurofibromatosis type 1.

Impact of screening kindreds for SDHD p.Cys11X as a common mutation associated with paraganglioma syndrome type 1

Intronic single nucleotide polymorphisms in the RET protooncogene are associated with a subset of apparently sporadic pheochromocytoma and may modulate age of onset

Lack of utility of SDHB mutation testing in adrenergic metastatic phaeochromocytoma

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

Long-term prognosis of patients with pediatric pheochromocytoma.

Mediastinal paragangliomas related to SDHx gene mutations.

Multiple endocrine neoplasia type 2.

Multiple phaeochromocytoma with renal artery stenosis or occlusion: report of two cases

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

Outcomes of adrenal-sparing surgery or total adrenalectomy in phaeochromocytoma associated with multiple endocrine neoplasia type 2: an international retrospective population-based study

Pathogenicity of DNA variants and double mutations in multiple endocrine neoplasia type 2 and von Hippel-Lindau syndrome

Pheochromocytoma of the urinary bladder coexisting with another extra-adrenal tumour--case report of a 19-year-old male patient

Pheochromocytoma presenting as takotsubo-like cardiomyopathy following delivery.

Pheochromocytoma-related 'classic' takotsubo cardiomyopathy.

Pheochromocytoma: presentation, diagnosis and treatment

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

Primary aldosteronism - recent progress and current concepts.

Primary hyperparathyroidism as first manifestation in MEN 2A: an international multicenter study

Retinal arterial remodeling in patients with pheochromocytoma or paraganglioma and its reversibility following surgical treatment

Right and left-sided carcinoid heart disease

Risk profiles and penetrance estimations in multiple endocrine neoplasia type 2A caused by germline RET mutations located in exon 10.

Systematic and Multidisciplinary Evaluation of Fibromuscular Dysplasia Patients Reveals High Prevalence of Previously Undetected Fibromuscular Dysplasia Lesions and Affects Clinical Decisions: The ARCADIA-POL Study

Systematic comparison of sporadic and syndromic pancreatic islet cell tumors

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

The clinical utility of circulating neuroendocrine gene transcript analysis in well-differentiated paragangliomas and pheochromocytomas

The coexistence of acute aortic dissection with autosomal dominant polycystic kidney disease--description of two hypertensive patients

The penetrance of MEN2 pheochromocytoma is not only determined by RET mutations.

The role of biochemical tests and clinical symptoms in differential diagnosis of primary aldosteronism

The role of calcium in the pathogenesis of arterial hypertension

Usefulness of Somatostatin Receptor Scintigraphy (Tc-[HYNIC, Tyr3]-Octreotide) and 123I-Metaiodobenzylguanidine Scintigraphy in Patients with SDHx Gene-Related Pheochromocytomas and Paragangliomas Detected by Computed Tomography

[Doxazosin (alpha 1-adrenoreceptor antagonist) used in primary hypertension and it's beneficial effect on lipid metabolism]

[Evaluation of selected parameters of zinc metabolism in patients with primary hypertension].

[Influence of angiotensin I converting enzyme inhibitors on selected parameters of zinc metabolism]

[New therapeutic perspectives associated with the introduction of angiotensin II receptor antagonists]

[Plasma renin activity, aldosterone and adrenergic activity in patients with hypertension and in normotensives with a family history of hypertension]

[Secondary hypertension in year 2002: current trends in diagnosis and treatment]