Lista de obras -

A novel life-threatening mutation in long QT2 syndrome

artículo científico publicado en 2015

Administration of colony stimulating factor-1 corrects some macrophage, dental, and skeletal defects in an osteopetrotic mutation (toothless, tl) in the rat

artículo científico publicado el 1 de enero de 1992

Alteration of myocardial sarcoplasmic reticulum Ca2+-ATPase and Na+-Ca2+ exchanger expression in human left ventricular volume overload

scientific article published on 07 March 2007

Alterations in calcium regulatory protein expression in patients with preserved left ventricle systolic function and mitral valve stenosis

scientific article published on 12 September 2008

Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene

artículo científico publicado en 2017

Associations of the eNOS G894T gene polymorphism with target organ damage in children with newly diagnosed primary hypertension

artículo científico publicado en 2015

Cardiac rhabdomyoma in tuberous sclerosis: hyperactive Erk signaling

artículo científico publicado en 2007

Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family

artículo científico publicado en 2015

Colony-stimulating factor 1-dependent resident macrophages play a regulatory role in fighting Escherichia coli fecal peritonitis

artículo científico publicado en 1996

Combination Testing Using a Single MSH5 Variant alongside HLA Haplotypes Improves the Sensitivity of Predicting Coeliac Disease Risk in the Polish Population.

artículo científico publicado en 2015

Combined renin-angiotensin system gene polymorphisms and outcomes in coronary artery disease - a preliminary report

artículo científico publicado en 2011

Correction by CSF-1 of defects in the osteopetrotic op/op mouse suggests local, developmental, and humoral requirements for this growth factor

artículo científico publicado en 1991

Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene

artículo científico publicado en 2009

Distinct in vivo functions of two macrophage subpopulations as evidenced by studies using macrophage-deficient op/op mouse

artículo científico publicado el 1 de julio de 1992

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

artículo científico publicado en 2016

Expression of cellular retinoic acid-binding protein I and II (CRABP I and II) in embryonic mouse hearts treated with retinoic acid

artículo científico publicado el 16 de marzo de 2011

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

artículo científico publicado en 2016

Genetic variants in hypertensive patients with coronary artery disease and coexisting atheromatous renal artery stenosis.

artículo científico publicado en 2008

Granulocyte-macrophage colony-stimulating factor accelerates growth of Lewis lung carcinoma in mice

artículo científico publicado en 1996

Granulocyte-macrophage colony-stimulating factor corrects macrophage deficiencies, but not osteopetrosis, in the colony-stimulating factor-1-deficient op/op mouse

artículo científico publicado en 1994

Identification novel LQT syndrome-associated variants in Polish population and genotype-phenotype correlations in eight families

scientific article published on 22 September 2018

Identification of a novel inherited ALK variant M1199L in the WNT type of medulloblastoma

artículo científico publicado en 2016

Identification of a novel inherited ALK variant M1199L in the WNT type of medulloblastoma

Impact of genetic and clinical factors on dose requirements and quality of anticoagulation therapy in Polish patients receiving acenocoumarol: dosing calculation algorithm.

artículo científico publicado en 2013

Increased resistance of CSF-1-deficient, macrophage-deficient, TNF alpha-deficient, and IL-1 alpha-deficient op/op mice to endotoxin.

artículo científico publicado en 1995

Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors

artículo científico publicado en 2011

Is evaluation of complex polymorphism helpful in the assessment of prognosis after percutaneous coronary intervention. A prospective study.

artículo científico publicado en 2011

MB-04A NOVEL GERMLINE MUTATION IN ALK GENE (M1199L) IDENTYFIED IN THE WNT TYPE OF MEDULLOBLASTOMA.

artículo científico publicado en 2016

Mediastinal paragangliomas related to SDHx gene mutations.

artículo científico publicado en 2016

Myocardial iron homeostasis in advanced chronic heart failure patients

scientific article published on 06 September 2011

Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.

artículo científico publicado en 2016

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

Pheochromocytoma presenting as takotsubo-like cardiomyopathy following delivery.

artículo científico publicado en 2014

Polymorphisms of angiotensin II type 1 receptor gene and those of angiotensinogen point at culprit artery in ST-segment elevation myocardial infarction ⬇️

artículo científico publicado el 27 de marzo de 2012

Polymorphisms of the beta-1 and beta-2 adrenergic receptors in Polish patients with idiopathic dilated cardiomyopathy.

artículo científico publicado en 2009

QTc prolongation in patients with hearing loss: Electrocardiographic and genetic study

artículo científico publicado en 2015

The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease

artículo científico publicado el 1 de julio de 2003

Titin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations

artículo científico publicado en 2017

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

Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation

artículo científico publicado en 2012

[Calreticulin, Ca2+-binding chaperon of the endoplasmic reticulum]

artículo científico publicado en 2005

Lista de obras de

A novel life-threatening mutation in long QT2 syndrome

Administration of colony stimulating factor-1 corrects some macrophage, dental, and skeletal defects in an osteopetrotic mutation (toothless, tl) in the rat

Alteration of myocardial sarcoplasmic reticulum Ca2+-ATPase and Na+-Ca2+ exchanger expression in human left ventricular volume overload

Alterations in calcium regulatory protein expression in patients with preserved left ventricle systolic function and mitral valve stenosis

Andersen-Tawil syndrome: Clinical presentation and predictors of symptomatic arrhythmias - Possible role of polymorphisms K897T in KCNH2 and H558R in SCN5A gene

Associations of the eNOS G894T gene polymorphism with target organ damage in children with newly diagnosed primary hypertension

Cardiac rhabdomyoma in tuberous sclerosis: hyperactive Erk signaling

Coexistence of Andersen-Tawil Syndrome with Polymorphisms in hERG1 Gene (K897T) and SCN5A Gene (H558R) in One Family

Colony-stimulating factor 1-dependent resident macrophages play a regulatory role in fighting Escherichia coli fecal peritonitis

Combination Testing Using a Single MSH5 Variant alongside HLA Haplotypes Improves the Sensitivity of Predicting Coeliac Disease Risk in the Polish Population.

Combined renin-angiotensin system gene polymorphisms and outcomes in coronary artery disease - a preliminary report

Correction by CSF-1 of defects in the osteopetrotic op/op mouse suggests local, developmental, and humoral requirements for this growth factor

Dilated cardiomyopathy with profound segmental wall motion abnormalities and ventricular arrhythmia caused by the R541C mutation in the LMNA gene

Distinct in vivo functions of two macrophage subpopulations as evidenced by studies using macrophage-deficient op/op mouse

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

Expression of cellular retinoic acid-binding protein I and II (CRABP I and II) in embryonic mouse hearts treated with retinoic acid

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

Genetic variants in hypertensive patients with coronary artery disease and coexisting atheromatous renal artery stenosis.

Granulocyte-macrophage colony-stimulating factor accelerates growth of Lewis lung carcinoma in mice

Granulocyte-macrophage colony-stimulating factor corrects macrophage deficiencies, but not osteopetrosis, in the colony-stimulating factor-1-deficient op/op mouse

Identification novel LQT syndrome-associated variants in Polish population and genotype-phenotype correlations in eight families

Identification of a novel inherited ALK variant M1199L in the WNT type of medulloblastoma

Identification of a novel inherited ALK variant M1199L in the WNT type of medulloblastoma

Impact of genetic and clinical factors on dose requirements and quality of anticoagulation therapy in Polish patients receiving acenocoumarol: dosing calculation algorithm.

Increased resistance of CSF-1-deficient, macrophage-deficient, TNF alpha-deficient, and IL-1 alpha-deficient op/op mice to endotoxin.

Influence of renin-angiotensin system gene polymorphisms on the risk of ST-segment-elevation myocardial infarction and association with coronary artery disease risk factors

Is evaluation of complex polymorphism helpful in the assessment of prognosis after percutaneous coronary intervention. A prospective study.

MB-04A NOVEL GERMLINE MUTATION IN ALK GENE (M1199L) IDENTYFIED IN THE WNT TYPE OF MEDULLOBLASTOMA.

Mediastinal paragangliomas related to SDHx gene mutations.

Myocardial iron homeostasis in advanced chronic heart failure patients

Next-generation sequencing for diagnosis of thoracic aortic aneurysms and dissections: diagnostic yield, novel mutations and genotype phenotype correlations.

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

Pheochromocytoma presenting as takotsubo-like cardiomyopathy following delivery.

Polymorphisms of angiotensin II type 1 receptor gene and those of angiotensinogen point at culprit artery in ST-segment elevation myocardial infarction ⬇️

Polymorphisms of the beta-1 and beta-2 adrenergic receptors in Polish patients with idiopathic dilated cardiomyopathy.

QTc prolongation in patients with hearing loss: Electrocardiographic and genetic study

The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease

Titin Truncating Variants in Dilated Cardiomyopathy - Prevalence and Genotype-Phenotype Correlations

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

Variants of the lamin A/C (LMNA) gene in non-valvular atrial fibrillation patients: a possible pathogenic role of the Thr528Met mutation

[Calreticulin, Ca2+-binding chaperon of the endoplasmic reticulum]