Lista de obras - Zofia Bilińska - Dominio Público Uruguay

A Novel DSP Truncating Variant in a Family with Episodic Myocardial Injury in the Course of Arrhythmogenic Cardiomyopathy-A Possible Role of a Low Penetrance NLRP3 Variant

artículo científico publicado en 2020

A Recurrent Exertional Syncope and Sudden Cardiac Arrest in a Young Athlete with Known Pathogenic p.Arg420Gln Variant in the RYR2 Gene

artículo científico publicado en 2020

A combination of quinidine/mexiletine reduces arrhythmia in dilated cardiomyopathy in two patients with R814W SCN5A mutation

scientific article published on 20 October 2020

A different background of arrhythmia in siblings with a positive family history of sudden death at young age

scientific article published on 14 October 2019

A fatal outcome of thoracic aortic aneurysm in a male patient with bicuspid aortic valve

artículo científico publicado en 2013

A new c.1621 C>G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype–phenotype correlation

artículo científico publicado en 2010

A new missense mutation, p.Arg719Leu, of the beta-myosin heavy chain gene in a patient with familial hypertrophic cardiomyopathy

artículo científico publicado en 2017

A novel HCN4 variant related to familial sinus bradycardia, left ventricular noncompaction and thoracic aortic aneurysm

artículo científico publicado en 2020

A novel truncating variant in the LAMP2 gene in a young woman with hypertrophic cardiomyopathy and variable clinical course in the family

artículo científico publicado en 2019

A study in Polish patients with cardiomyopathy emphasizes pathogenicity of phospholamban (PLN) mutations at amino acid position 9 and low penetrance of heterozygous null PLN mutations

artículo científico publicado en 2015

Acoustic quantification assessment of left atrial area and function in patients with dilated nonischaemic cardiomyopathy with and without restriction in Doppler study

scientific article published on 01 February 2002

Active lymphocytic myocarditis treated with murine OKT3 monoclonal antibody in a patient presenting with intractable ventricular tachycardia.

artículo científico publicado en 2002

Adrenergic beta receptor blockaders in congestive heart failure: potential mechanisms of their action

artículo científico publicado en 1988

Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes

artículo científico publicado en 2020

Antibody response to influenza vaccine in coronary artery disease: a substudy of the FLUCAD study

artículo científico publicado en 2009

Assessment of the inflammatory process by endomyocardial biopsy in patients with dilated cardiomyopathy based on pathological and immunohistochemical methods.

artículo científico publicado en 2006

Atypical forms of hypertrophic cardiomyopathy

artículo científico publicado el 1 de enero de 1991

Autophagy in transition from hypertrophic cardiomyopathy to heart failure

artículo científico publicado en 2009

Autosomal recessive, familial, isolated dilated cardiomyopathy due to compound desmoplakin gene mutations

article

Baseline clinical characteristics and midterm prognosis of STE-ACS and NSTE-ACS patients with normal coronary arteries.

artículo científico publicado en 2009

Brain natriuretic peptide plasma levels in ischemic and nonischemic advanced heart failure.

artículo científico publicado en 2004

Cardiac amyloidosis diagnosed by endomyocardial biopsy. Clinical, histopathological, immunohistochemical and ultrastructural studies

artículo científico publicado en 2005

Cardiovascular complication of cocaine abuse

artículo científico publicado el 1 de enero de 2012

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases

artículo científico publicado en 2007

Clinical Applications for Next Generation Sequencing in Cardiology

Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis

scientific article published on 01 July 2020

Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene

artículo científico publicado en 2020

Coincidence of Andersen-Tawil syndrome and Marfan syndrome: A case report

scientific article published on 23 January 2019

Coronary computed tomographic angiography for prediction of procedural and intermediate outcome of bypass grafting to left anterior descending artery occlusion with failed visualization on conventional angiography.

artículo científico publicado en 2012

Cumulative incidence of coronary lesions with vulnerable characteristics in patients with stable angina pectoris: an intravascular ultrasound and angiographic study

artículo científico publicado en 2005

Determinants of prognosis in nonischemic dilated cardiomyopathy

artículo científico publicado en 1996

Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations

scientific article published on 01 November 2018

Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies

artículo científico publicado en 2006

Dilated cardiomyopathy in children and adolescents. Diagnostic problems, clinical course and prognosis

artículo científico publicado el 1 de enero de 1991

Dilated cardiomyopathy in children: clinical course and prognosis

artículo científico publicado en 1994

Dilated cardiomyopathy in the postgenomic era

artículo científico publicado en 2009

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

Dilated cardiomyopathy: clinical problems evaluated on the basis of our data

artículo científico publicado en 1986

Does p.Q247X in TRIM63 cause human hypertrophic cardiomyopathy?

artículo científico publicado en 2014

ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients

artículo científico publicado en 2020

Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy.

artículo científico publicado en 2016

Familial dilated cardiomyopathy: evidence for clinical and immunogenetic heterogeneity

artículo científico publicado en 2003

Familial thoracic aortic aneurysms and dissections (FTAAD)

artículo científico publicado en 2011

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

scientific article published on 03 February 2010

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

artículo científico publicado en 2010

Genetic muscle disorder mimicking atrial arrhythmias with conduction defects requiring pacemaker implantation

artículo científico publicado en 2019

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

artículo científico publicado en 2021

Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy.

artículo científico publicado en 2017

Hypertrophic cardiomyopathy--a new look at the significance of hypertrophy

artículo científico publicado el 1 de enero de 1991

Impact of cardiac magnetic resonance on the diagnosis of hypertrophic cardiomyopathy - a 10-year experience with over 1000 patients

artículo científico publicado en 2020

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

In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients

artículo científico publicado en 2005

Increased frequency of organ-specific cardiac antibodies in healthy relatives of patients with dilated cardiomyopathy: evidence for autoimmunity in Polish families

scientific article published on 01 October 1996

Influenza vaccination in secondary prevention from coronary ischaemic events in coronary artery disease: FLUCAD study

scientific article published on 10 January 2008

Intrafamilial variability of cardiovascular abnormalities in relation to p.R460H TGFBR2 mutation

scientific article published on 18 May 2020

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies

artículo científico publicado en 2013

Lamin A/C mutations in dilated cardiomyopathy

artículo científico

Lamin missense mutations-the spectrum of phenotype variability is increasing

artículo científico publicado en 2018

Late results of immunosuppressive therapy in patients with heart failure and biopsy proven myocarditis

artículo científico publicado en 1989

Left ventricular enlargement is common in relatives of patients with dilated cardiomyopathy

scientific article published on 01 December 1995

Level of angiotensin II and aldosterone in plasma is often elevated in patients with heart failure treated with converting enzyme inhibitors--preliminary results

artículo científico publicado en 2002

Myocarditis: diagnostic problems

artículo científico publicado el 1 de mayo de 2003

New therapeutic goals--new drugs in heart failure treatment

artículo científico publicado en 2007

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

artículo científico publicado en 2016

Novel truncating desmoplakin mutation as a potential cause of sudden cardiac death in a family.

artículo científico publicado en 2016

Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation.

artículo científico publicado en 2008

Organ-specific cardiac autoantibodies in dilated cardiomyopathy. Frequency and clinical correlates in Polish patients.

artículo científico publicado en 1995

Plasma concentrations of N-terminal atrial natriuretic peptide are raised in asymptomatic relatives of dilated cardiomyopathy patients with left ventricular enlargement

artículo científico publicado en 2002

Platelet reactivity on aspirin, clopidogrel and abciximab in patients with acute coronary syndromes and reduced estimated glomerular filtration rate.

artículo científico publicado en 2009

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

artículo científico publicado en 2009

Prognostic value of the electrocardiogram in dilated cardiomyopathy

artículo científico publicado en 1988

Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies

scientific article published on 31 October 2020

Quantification of mitral regurgitation in patients with hypertrophic cardiomyopathy using aortic and pulmonary flow data: impacts of left ventricular outflow tract obstruction and different left ventricular segmentation methods.

artículo científico publicado en 2017

Rapid and effective response of the R222Q SCN5A to quinidine treatment in a patient with Purkinje-related ventricular arrhythmia and familial dilated cardiomyopathy: a case report.

artículo científico publicado en 2018

Recurrent ventricular fibrillation during a febrile illness as the first manifestation of Brugada syndrome--a case report

artículo científico publicado en 2004

Restrictive cardiomyopathy due to novel desmin gene mutation

artículo científico publicado en 2017

Severe Course of Peripartum Cardiomyopathy and Subsequent Recovery in a Patient with a Novel TTN Gene-Truncating Mutation

article

Significance of dyslipidaemia in patients with heart failure of unexplained aetiology.

artículo científico publicado en 2008

Specific contribution of lamin A and lamin C in the development of laminopathies.

artículo científico publicado en 2008

Spectrum of transthyretin gene mutations and clinical characteristics of Polish patients with cardiac transthyretin amyloidosis

artículo científico publicado en 2020

Sudden cardiac arrest in patients without overt heart disease: limited value of next generation sequencing

artículo científico publicado en 2018

Superior early diagnostic performance of a sensitive cardiac troponin assay as compared to a standard troponin test in the diagnosis of acute myocardial infarction

artículo científico publicado el 1 de enero de 2012

The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation

artículo científico publicado en 2014

The new European definition of cardiomyopathies: which space for muscle dystrophies?: reply

Therapeutic challenges and management of heart failure during pregnancy (part 2).

artículo científico publicado en 2012

Therapeutic challenges and management of heart failure during pregnancy (part I)

artículo científico publicado en 2012

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

artículo científico publicado en 2017

Ultrastructural evidence of myocardial capillary remodeling in peripartum cardiomyopathy

artículo científico publicado en 2010

Unexpected eosinophilic myocarditis in a young woman with rapidly progressive dilated cardiomyopathy

artículo científico publicado en 2002

Usefulness of 1H MR spectroscopy in the evaluation of myocardial metabolism in patients with dilated idiopathic cardiomyopathy: pilot study.

artículo científico publicado en 2003

Variable clinical presentation of glycogen storage disease type IV: from severe hepatosplenomegaly to cardiac insufficiency. Some discrepancies in genetic and biochemical abnormalities

artículo científico publicado en 2017

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

Various aspects of pathogenesis, clinical course and treatment of myocarditis. (II)

artículo científico publicado en 1987

What do tachycardiomyopathy belong to?: reply

[Cardiac amyloidosis--an update]

scientific article published on 01 July 2004

[Cardiovascular complications of influenza]

artículo científico publicado en 2003

[Cardiovascular magnetic resonance in the diagnosis of myocarditis]

artículo científico publicado en 2010

[Classification of the cardiomyopathies]

scientific article published on 01 May 2008

[Echocardiographic evaluation of left atrial function in dilated cardiomyopathy with restricted and non-restricted Doppler transmitral flow]

artículo científico publicado en 2002

[Endomyocardial biopsy in children and adolescents]

artículo científico publicado en 1989

[Endomyocardial disease]

artículo científico publicado en 2009

[Familial dilated cardiomyopathy with autosomal mode of inheritance. Case report]

scientific article published on 01 December 1993

[Frequency of DRB1* and DQB1* alleles in Polish patients with dilated cardiomyopathy]

artículo científico publicado en 2002

[Laminopathies--interdisciplinary problem]

scientific article published on 01 March 2008

[Myocardial microabscesses detected by endomyocardial biopsy in a patient with dilated cardiomyopathy and celiac disease: a case report]

artículo científico publicado en 2006

[Peripartum cardiomyopathy - description of the condition and case presentation]

artículo científico publicado en 2009

[RF ablation of longstanding persistent atrial fibrillation in patient with familial dilated cardiomyopathy]

artículo científico publicado en 2008

[Reversible dilated cardiomyopathy in a patient with acute, advanced heart failure and intense endothelial inflammatory reaction in endomyocardial biopsy--a case report]

artículo científico publicado en 2006

[Various aspects of the pathogenesis, clinical course and treatment of myocarditis. II]

artículo científico publicado en 1987

Lista de obras de Zofia Bilińska

A Novel DSP Truncating Variant in a Family with Episodic Myocardial Injury in the Course of Arrhythmogenic Cardiomyopathy-A Possible Role of a Low Penetrance NLRP3 Variant

A Recurrent Exertional Syncope and Sudden Cardiac Arrest in a Young Athlete with Known Pathogenic p.Arg420Gln Variant in the RYR2 Gene

A combination of quinidine/mexiletine reduces arrhythmia in dilated cardiomyopathy in two patients with R814W SCN5A mutation

A different background of arrhythmia in siblings with a positive family history of sudden death at young age

A fatal outcome of thoracic aortic aneurysm in a male patient with bicuspid aortic valve

A new c.1621 C>G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype–phenotype correlation

A new missense mutation, p.Arg719Leu, of the beta-myosin heavy chain gene in a patient with familial hypertrophic cardiomyopathy

A novel HCN4 variant related to familial sinus bradycardia, left ventricular noncompaction and thoracic aortic aneurysm

A novel truncating variant in the LAMP2 gene in a young woman with hypertrophic cardiomyopathy and variable clinical course in the family

A study in Polish patients with cardiomyopathy emphasizes pathogenicity of phospholamban (PLN) mutations at amino acid position 9 and low penetrance of heterozygous null PLN mutations

Acoustic quantification assessment of left atrial area and function in patients with dilated nonischaemic cardiomyopathy with and without restriction in Doppler study

Active lymphocytic myocarditis treated with murine OKT3 monoclonal antibody in a patient presenting with intractable ventricular tachycardia.

Adrenergic beta receptor blockaders in congestive heart failure: potential mechanisms of their action

Analysis of De Novo Mutations in Sporadic Cardiomyopathies Emphasizes Their Clinical Relevance and Points to Novel Candidate Genes

Antibody response to influenza vaccine in coronary artery disease: a substudy of the FLUCAD study

Assessment of the inflammatory process by endomyocardial biopsy in patients with dilated cardiomyopathy based on pathological and immunohistochemical methods.

Atypical forms of hypertrophic cardiomyopathy

Autophagy in transition from hypertrophic cardiomyopathy to heart failure

Autosomal recessive, familial, isolated dilated cardiomyopathy due to compound desmoplakin gene mutations

Baseline clinical characteristics and midterm prognosis of STE-ACS and NSTE-ACS patients with normal coronary arteries.

Brain natriuretic peptide plasma levels in ischemic and nonischemic advanced heart failure.

Cardiac amyloidosis diagnosed by endomyocardial biopsy. Clinical, histopathological, immunohistochemical and ultrastructural studies

Cardiovascular complication of cocaine abuse

Classification of the cardiomyopathies: a position statement from the European Society Of Cardiology Working Group on Myocardial and Pericardial Diseases

Clinical Applications for Next Generation Sequencing in Cardiology

Clinical Features and Natural History of PRKAG2 Variant Cardiac Glycogenosis

Clinical Phenotypes and Prognosis of Dilated Cardiomyopathy Caused by Truncating Variants in the TTN Gene

Coincidence of Andersen-Tawil syndrome and Marfan syndrome: A case report

Coronary computed tomographic angiography for prediction of procedural and intermediate outcome of bypass grafting to left anterior descending artery occlusion with failed visualization on conventional angiography.

Cumulative incidence of coronary lesions with vulnerable characteristics in patients with stable angina pectoris: an intravascular ultrasound and angiographic study

Determinants of prognosis in nonischemic dilated cardiomyopathy

Dilated Cardiomyopathy Due to BLC2-Associated Athanogene 3 (BAG3) Mutations

Dilated cardiomyopathy caused by LMNA mutations. Clinical and morphological studies

Dilated cardiomyopathy in children and adolescents. Diagnostic problems, clinical course and prognosis

Dilated cardiomyopathy in children: clinical course and prognosis

Dilated cardiomyopathy in the postgenomic era

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

Dilated cardiomyopathy: clinical problems evaluated on the basis of our data

Does p.Q247X in TRIM63 cause human hypertrophic cardiomyopathy?

ESC EORP Cardiomyopathy Registry: real-life practice of genetic counselling and testing in adult cardiomyopathy patients

Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy.

Familial dilated cardiomyopathy: evidence for clinical and immunogenetic heterogeneity

Familial thoracic aortic aneurysms and dissections (FTAAD)

Genetic and ultrastructural studies in dilated cardiomyopathy patients: a large deletion in the lamin A/C gene is associated with cardiomyocyte nuclear envelope disruption

Genetic counselling and testing in cardiomyopathies: a position statement of the European Society of Cardiology Working Group on Myocardial and Pericardial Diseases

Genetic muscle disorder mimicking atrial arrhythmias with conduction defects requiring pacemaker implantation

Genome-wide association analysis in dilated cardiomyopathy reveals two new players in systolic heart failure on chromosomes 3p25.1 and 22q11.23

Homozygous truncating mutation in NRAP gene identified by whole exome sequencing in a patient with dilated cardiomyopathy.

Hypertrophic cardiomyopathy--a new look at the significance of hypertrophy

Impact of cardiac magnetic resonance on the diagnosis of hypertrophic cardiomyopathy - a 10-year experience with over 1000 patients

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

In vivo and in vitro examination of the functional significances of novel lamin gene mutations in heart failure patients

Increased frequency of organ-specific cardiac antibodies in healthy relatives of patients with dilated cardiomyopathy: evidence for autoimmunity in Polish families

Influenza vaccination in secondary prevention from coronary ischaemic events in coronary artery disease: FLUCAD study

Intrafamilial variability of cardiovascular abnormalities in relation to p.R460H TGFBR2 mutation

LMNA mutations in Polish patients with dilated cardiomyopathy: prevalence, clinical characteristics, and in vitro studies

Lamin A/C mutations in dilated cardiomyopathy

Lamin missense mutations-the spectrum of phenotype variability is increasing

Late results of immunosuppressive therapy in patients with heart failure and biopsy proven myocarditis

Left ventricular enlargement is common in relatives of patients with dilated cardiomyopathy

Level of angiotensin II and aldosterone in plasma is often elevated in patients with heart failure treated with converting enzyme inhibitors--preliminary results

Myocarditis: diagnostic problems

New therapeutic goals--new drugs in heart failure treatment

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

Novel truncating desmoplakin mutation as a potential cause of sudden cardiac death in a family.

Obliteration of cardiomyocyte nuclear architecture in a patient with LMNA gene mutation.

Organ-specific cardiac autoantibodies in dilated cardiomyopathy. Frequency and clinical correlates in Polish patients.

Plasma concentrations of N-terminal atrial natriuretic peptide are raised in asymptomatic relatives of dilated cardiomyopathy patients with left ventricular enlargement

Platelet reactivity on aspirin, clopidogrel and abciximab in patients with acute coronary syndromes and reduced estimated glomerular filtration rate.

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

Prognostic value of the electrocardiogram in dilated cardiomyopathy

Protein Kinase C Alpha Cellular Distribution, Activity, and Proximity with Lamin A/C in Striated Muscle Laminopathies

Quantification of mitral regurgitation in patients with hypertrophic cardiomyopathy using aortic and pulmonary flow data: impacts of left ventricular outflow tract obstruction and different left ventricular segmentation methods.

Rapid and effective response of the R222Q SCN5A to quinidine treatment in a patient with Purkinje-related ventricular arrhythmia and familial dilated cardiomyopathy: a case report.

Recurrent ventricular fibrillation during a febrile illness as the first manifestation of Brugada syndrome--a case report

Restrictive cardiomyopathy due to novel desmin gene mutation

Severe Course of Peripartum Cardiomyopathy and Subsequent Recovery in a Patient with a Novel TTN Gene-Truncating Mutation

Significance of dyslipidaemia in patients with heart failure of unexplained aetiology.

Specific contribution of lamin A and lamin C in the development of laminopathies.