Lista de obras - L Varga - Dominio Público Uruguay

"Nuts and Bolts" of Laboratory Evaluation of Angioedema

artículo científico publicado en 2016

A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymes

artículo científico publicado en 2014

A novel assay to quantitate MASP-2/ficolin-3 complexes in serum

scientific article published on 08 November 2012

A novel prophylaxis with C1-inhibitor concentrate in hereditary angioedema during erythema marginatum.

artículo científico publicado en 2017

A systematic analysis of the complement pathways in patients with neuromyelitis optica indicates alteration but no activation during remission.

artículo científico publicado en 2013

Acquired angioedema associated with chronic hepatitis C

scientific article published on 01 April 1999

Acquired angioedema associated with primary antiphospholipid syndrome in a patient with antithrombin III deficiency

artículo científico publicado en 2008

Activation of the ficolin-lectin pathway during attacks of hereditary angioedema

artículo científico publicado en 2014

Acute abdominal attack of hereditary angioneurotic oedema associated with ultrasound abnormalities suggestive of acute hepatitis

scientific article published on 01 January 2002

Adverse effects of danazol prophylaxis on the lipid profiles of patients with hereditary angioedema.

artículo científico publicado en 2005

Alternative complement pathway activation during invasive coronary procedures in acute myocardial infarction and stable angina pectoris

artículo científico publicado en 2016

Angiooedema Due to Acquired Deficiency of C1-Esterase Inhibitor Associated with Leucocytoclastic Vasculitis ⬇️

artículo científico publicado el 1 de agosto de 2001

Anti-cholesterol antibody levels in hereditary angioedema.

artículo científico publicado en 2007

Antibodies against human heat-shock protein (hsp) 60 and mycobacterial hsp65 differ in their antigen specificity and complement-activating ability

artículo científico publicado en 1999

Are these patients indeed resistant to treatment with C1 inhibitor concentrate?

scientific article published on 17 October 2011

Assessment of inhibitory antibodies in patients with hereditary angioedema treated with plasma-derived C1 inhibitor.

artículo científico

Association between early onset and organ manifestations of systemic lupus erythematosus (SLE) and a down-regulating promoter polymorphism in the MBL2 gene

article

Association of Low Ficolin-Lectin Pathway Parameters with Cardiac Syndrome X.

artículo científico publicado en 2016

Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?

artículo científico publicado en 2011

Association of celiac disease and hereditary angioneurotic edema

scientific article published on 01 October 2002

Association of high serum concentration of the third component of complement (C3) with pre-existing severe coronary artery disease and new vascular events in women

artículo científico publicado en 2004

Atrial natriuretic peptide as a novel biomarker of hereditary angioedema

artículo científico publicado en 2016

Bacteriuria increases the risk of edematous attacks in hereditary angioedema with C1-inhibitor deficiency.

artículo científico publicado en 2016

Baseline level of functional C1-inhibitor correlates with disease severity scores in hereditary angioedema

scientific article published on 27 November 2009

C1 and C4 abnormalities in chronic lymphocytic leukaemia and their significance

artículo científico publicado en 1987

C1 inhibitor: quantification and purification

artículo científico publicado en 2014

C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patients

scientific article published on 05 June 2006

C1-inhibitor autoantibodies in SLE

artículo científico publicado en 2010

C1r-C1s-C1inhibitor (C1rs-C1inh) complex measurements in tears of patients before and after penetrating keratoplasty

scientific article published on 01 February 2002

Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema.

artículo científico publicado en 2004

Clinical management of hereditary angio-oedema in children.

artículo científico publicado en 2002

Coincidence of hereditary angioedema (HAE) with Crohn's disease

artículo científico publicado en 1999

Comparative study of the complement-activating and specific IgE-binding properties of ragweed pollen allergen

scientific article published on 01 April 1997

Complement activation in the nasal mucosa following nasal ragweed-allergen challenge

scientific article published on 01 August 2001

Complete kinetic follow-up of symptoms and complement parameters during a hereditary angioedema attack

artículo científico publicado en 2017

Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2015

Danazol therapy for hereditary angio-oedema in children

scientific article published on 01 September 1999

Dancing with Complement C4 and the RP-C4-CYP21-TNX (RCCX) Modules of the Major Histocompatibility Complex ⬇️

artículo científico publicado el 1 de enero de 2003

Decreased inhibition of immune precipitation by sera with the C2 B allotype

scientific article published on 01 April 1991

Deep venous thrombosis associated with acquired angioedema type II in a patient heterozygous for the mutation of factor V Leiden: effective treatment and follow-up for four years

artículo científico publicado en 2006

Depressed activation of the lectin pathway of complement in hereditary angioedema

Early complement activation follows eversion carotid endarterectomy and correlates with the time of clamping of the carotid artery.

artículo científico publicado en 2008

Elevated C1rC1sC1inh levels independently predict atherosclerotic coronary heart disease

artículo científico publicado en 2012

Endothelial cell activation during edematous attacks of hereditary angioedema types I and II

artículo científico publicado en 2014

Eradication of Helicobacter pylori and improvement of hereditary angioneurotic oedema

artículo científico publicado en 2001

Erythema marginatum preceding an acute oedematous attack of hereditary angioneurotic oedema

artículo científico publicado en 2001

Esophageal leiomyoma incidentally recognized during an acute attack of hereditary angioneurotic edema

scientific article published on 01 May 2001

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

artículo científico publicado en 2015

First report of icatibant treatment in a pregnant patient with hereditary angioedema

artículo científico publicado en 2016

Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema

artículo científico publicado en 2014

Functional analysis of the mannose-binding lectin complement pathway in normal pregnancy and preeclampsia.

artículo científico publicado en 2010

Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema.

artículo científico publicado en 2008

Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy.

artículo científico publicado en 2007

Hereditary angioedema: molecular and clinical differences among European populations.

artículo científico publicado en 2014

High levels of acute phase proteins and soluble 70 kDa heat shock proteins are independent and additive risk factors for mortality in colorectal cancer

artículo científico publicado en 2010

High normal serum levels of C3 and C1 inhibitor, two acute-phase proteins belonging to the complement system, occur more frequently in patients with Crohn's disease than ulcerative colitis.

artículo científico publicado en 2003

Home treatment of attacks with conestat alfa in hereditary angioedema due to C1-inhibitor deficiency.

artículo científico publicado en 2014

Home treatment of hereditary angioedema with icatibant administered by health care professionals

artículo científico publicado en 2011

Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema

artículo científico publicado en 2018

Immunological alterations in anti-HTLV-III negative haemophiliacs and homosexual men in Hungary.

artículo científico publicado en 1985

In vitro complement activation by ragweed allergen extract in the sera of ragweed allergic and non-allergic persons

scientific article published on 01 November 1995

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

scientific article published on 09 August 2016

Lack of increased prevalence of immunoregulatory disorders in hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2011

Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations

artículo científico publicado en 2012

Long-term danazol prophylaxis does not lead to increased carotid intima-media thickness in hereditary angioedema patients.

artículo científico publicado en 2007

Long-term efficacy of danazol treatment in hereditary angioedema.

artículo científico publicado en 2010

Low C1-Inhibitor Levels Predict Early Restenosis After Eversion Carotid Endarterectomy

scientific article published on 04 October 2007

Management of hereditary angioedema in pediatric patients.

artículo científico publicado en 2007

Management of pregnancies in a hereditary angioedema patient after treatment with attenuated androgens since childhood

artículo científico publicado en 2014

Neutrophil activation during attacks in patients with hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2015

Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1.

artículo científico publicado en 2016

Novel duplication in the F12 gene in a patient with recurrent angioedema

artículo científico publicado en 2013

Parameters of the classical complement pathway predict disease severity in hereditary angioedema

artículo científico publicado en 2011

Prophylactic therapy in children with hereditary angioedema.

artículo científico publicado en 2012

Ragweed allergy: correlation between skin reactivity and in vitro complement activation

scientific article published on 01 December 1998

Recombinant human C1-inhibitor in the treatment of acute angioedema attacks.

artículo científico publicado en 2007

Relationship between complement components C4A and C4B diversities and two TNFA promoter polymorphisms in two healthy Caucasian populations

artículo científico publicado en 2003

Relationship between copy number of genes (C4A, C4B) encoding the fourth component of complement and the clinical course of hereditary angioedema (HAE)

article

Reply

artículo científico publicado en 2017

Risk of thromboembolism in patients with hereditary angioedema treated with plasma-derived C1-inhibitor

artículo científico publicado en 2016

Role of complement in the pathomechanism of atherosclerotic vascular diseases.

artículo científico publicado en 2009

Serum anti-cholesterol antibodies in chronic hepatitis-C patients during IFN-alpha-2b treatment.

artículo científico publicado en 2003

Short-term prophylaxis in a patient with acquired C1-INH deficiency

artículo científico publicado en 2014

Short-term prophylaxis in hereditary angioedema due to deficiency of the C1-inhibitor--a long-term survey

Streptokinase does not activate the complement system

artículo científico publicado en 2000

Strong complement activation after acute ischemic stroke is associated with unfavorable outcomes.

artículo científico publicado en 2008

Strong correlation of high EBNA-1-IgG levels with edematous attacks involving upper airway mucosa in hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2011

Studies on the interactions between C-reactive protein and complement proteins.

artículo científico publicado en 2007

Studies on the mechanisms of allergen-induced activation of the classical and lectin pathways of complement

artículo científico publicado en 2003

Successful outcome using C1-inhibitor concentrate in acute pancreatitis caused by hereditary angioedema

artículo científico publicado en 2011

Successful pregnancy outcome after treatment with C1-inhibitor concentrate in a patient with hereditary angioedema and a history of four miscarriages

artículo científico publicado en 2012

Successful prophylaxis with recombinant human C1 inhibitor in a patient with hereditary angioedema

artículo científico publicado en 2014

The Hungarian HAE experience

artículo científico publicado en 2003

The Levels of the Lectin Pathway Serine Protease MASP-1 and Its Complex Formation with C1 Inhibitor Are Linked to the Severity of Hereditary Angioedema.

artículo científico publicado en 2015

The effect of long-term danazol treatment on haematological parameters in hereditary angioedema

artículo científico publicado en 2016

The efficacy of short-term danazol prophylaxis in hereditary angioedema patients undergoing maxillofacial and dental procedures

artículo científico publicado en 1999

The influence of trigger factors on hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2014

The role of complement activation in the pathogenesis of Fuchs' dystrophy.

artículo científico publicado en 2013

The role of ficolins and MASPs in hereditary angioedema due to C1-inhibitor deficiency

artículo científico publicado en 2013

The role of the complement system in hereditary angioedema.

artículo científico publicado en 2017

The severity of clinical symptoms in ragweed-allergic patients is related to the extent of ragweed-induced complement activation in their sera

artículo científico publicado en 1997

The use of 'real-time' complement analysis to differentiate atypical haemolytic uraemic syndrome from other forms of thrombotic microangiopathies

artículo científico publicado en 2012

Thyroid hormones and complement parameters in hereditary angioedema with C1-inhibitor deficiency.

artículo científico publicado en 2016

Treatment of attacks with plasma-derived C1-inhibitor concentrate in pediatric hereditary angioedema patients

scientific article published on 11 October 2012

Treatment with C1-inhibitor concentrate does not induce IgM type anti-C1 inhibitor antibodies in patients with hereditary angioedema ⬇️

artículo científico publicado el 15 de diciembre de 2010

Ultrasonography in the diagnosis and monitoring of ascites in acute abdominal attacks of hereditary angioneurotic oedema.

artículo científico publicado en 2001

Usefulness of detection of complement activation products in evaluating SLE activity

scientific article published on 01 January 2000

rhC1INH: a new drug for the treatment of attacks in hereditary angioedema caused by C1-inhibitor deficiency.

artículo científico publicado en 2011

Lista de obras de L Varga

"Nuts and Bolts" of Laboratory Evaluation of Angioedema

A novel assay to diagnose hereditary angioedema utilizing inhibition of bradykinin-forming enzymes

A novel assay to quantitate MASP-2/ficolin-3 complexes in serum

A novel prophylaxis with C1-inhibitor concentrate in hereditary angioedema during erythema marginatum.

A systematic analysis of the complement pathways in patients with neuromyelitis optica indicates alteration but no activation during remission.

Acquired angioedema associated with chronic hepatitis C

Acquired angioedema associated with primary antiphospholipid syndrome in a patient with antithrombin III deficiency

Activation of the ficolin-lectin pathway during attacks of hereditary angioedema

Acute abdominal attack of hereditary angioneurotic oedema associated with ultrasound abnormalities suggestive of acute hepatitis

Adverse effects of danazol prophylaxis on the lipid profiles of patients with hereditary angioedema.

Alternative complement pathway activation during invasive coronary procedures in acute myocardial infarction and stable angina pectoris

Angiooedema Due to Acquired Deficiency of C1-Esterase Inhibitor Associated with Leucocytoclastic Vasculitis ⬇️

Anti-cholesterol antibody levels in hereditary angioedema.

Antibodies against human heat-shock protein (hsp) 60 and mycobacterial hsp65 differ in their antigen specificity and complement-activating ability

Are these patients indeed resistant to treatment with C1 inhibitor concentrate?

Assessment of inhibitory antibodies in patients with hereditary angioedema treated with plasma-derived C1 inhibitor.

Association between early onset and organ manifestations of systemic lupus erythematosus (SLE) and a down-regulating promoter polymorphism in the MBL2 gene

Association of Low Ficolin-Lectin Pathway Parameters with Cardiac Syndrome X.

Association of celiac disease and hereditary angioedema due to C1-inhibitor deficiency. Screening patients with hereditary angioedema for celiac disease: is it worth the effort?

Association of celiac disease and hereditary angioneurotic edema

Association of high serum concentration of the third component of complement (C3) with pre-existing severe coronary artery disease and new vascular events in women

Atrial natriuretic peptide as a novel biomarker of hereditary angioedema

Bacteriuria increases the risk of edematous attacks in hereditary angioedema with C1-inhibitor deficiency.

Baseline level of functional C1-inhibitor correlates with disease severity scores in hereditary angioedema

C1 and C4 abnormalities in chronic lymphocytic leukaemia and their significance

C1 inhibitor: quantification and purification

C1-inhibitor (C1-INH) autoantibodies in hereditary angioedema. Strong correlation with the severity of disease in C1-INH concentrate naïve patients

C1-inhibitor autoantibodies in SLE

C1r-C1s-C1inhibitor (C1rs-C1inh) complex measurements in tears of patients before and after penetrating keratoplasty

Canadian 2003 International Consensus Algorithm For the Diagnosis, Therapy, and Management of Hereditary Angioedema.

Clinical management of hereditary angio-oedema in children.

Coincidence of hereditary angioedema (HAE) with Crohn's disease

Comparative study of the complement-activating and specific IgE-binding properties of ragweed pollen allergen

Complement activation in the nasal mucosa following nasal ragweed-allergen challenge

Complete kinetic follow-up of symptoms and complement parameters during a hereditary angioedema attack

Comprehensive study into the activation of the plasma enzyme systems during attacks of hereditary angioedema due to C1-inhibitor deficiency

Danazol therapy for hereditary angio-oedema in children

Dancing with Complement C4 and the RP-C4-CYP21-TNX (RCCX) Modules of the Major Histocompatibility Complex ⬇️

Decreased inhibition of immune precipitation by sera with the C2 B allotype

Deep venous thrombosis associated with acquired angioedema type II in a patient heterozygous for the mutation of factor V Leiden: effective treatment and follow-up for four years

Depressed activation of the lectin pathway of complement in hereditary angioedema

Early complement activation follows eversion carotid endarterectomy and correlates with the time of clamping of the carotid artery.

Elevated C1rC1sC1inh levels independently predict atherosclerotic coronary heart disease

Endothelial cell activation during edematous attacks of hereditary angioedema types I and II

Eradication of Helicobacter pylori and improvement of hereditary angioneurotic oedema

Erythema marginatum preceding an acute oedematous attack of hereditary angioneurotic oedema

Esophageal leiomyoma incidentally recognized during an acute attack of hereditary angioneurotic edema

F12-46C/T polymorphism as modifier of the clinical phenotype of hereditary angioedema

First report of icatibant treatment in a pregnant patient with hereditary angioedema

Frequency of the virilising effects of attenuated androgens reported by women with hereditary angioedema

Functional analysis of the mannose-binding lectin complement pathway in normal pregnancy and preeclampsia.

Hereditary angiodema: a current state-of-the-art review, VII: Canadian Hungarian 2007 International Consensus Algorithm for the Diagnosis, Therapy, and Management of Hereditary Angioedema.

Hereditary angioedema: a decade of human C1-inhibitor concentrate therapy.

Hereditary angioedema: molecular and clinical differences among European populations.

High levels of acute phase proteins and soluble 70 kDa heat shock proteins are independent and additive risk factors for mortality in colorectal cancer

High normal serum levels of C3 and C1 inhibitor, two acute-phase proteins belonging to the complement system, occur more frequently in patients with Crohn's disease than ulcerative colitis.

Home treatment of attacks with conestat alfa in hereditary angioedema due to C1-inhibitor deficiency.

Home treatment of hereditary angioedema with icatibant administered by health care professionals

Idiopathic Nonhistaminergic Acquired Angioedema Versus Hereditary Angioedema

Immunological alterations in anti-HTLV-III negative haemophiliacs and homosexual men in Hungary.

In vitro complement activation by ragweed allergen extract in the sera of ragweed allergic and non-allergic persons

International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency.

Lack of increased prevalence of immunoregulatory disorders in hereditary angioedema due to C1-inhibitor deficiency

Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations

Long-term danazol prophylaxis does not lead to increased carotid intima-media thickness in hereditary angioedema patients.

Long-term efficacy of danazol treatment in hereditary angioedema.

Low C1-Inhibitor Levels Predict Early Restenosis After Eversion Carotid Endarterectomy

Management of hereditary angioedema in pediatric patients.

Management of pregnancies in a hereditary angioedema patient after treatment with attenuated androgens since childhood

Neutrophil activation during attacks in patients with hereditary angioedema due to C1-inhibitor deficiency

Novel Vasoregulatory Aspects of Hereditary Angioedema: the Role of Arginine Vasopressin, Adrenomedullin and Endothelin-1.

Novel duplication in the F12 gene in a patient with recurrent angioedema

Parameters of the classical complement pathway predict disease severity in hereditary angioedema

Prophylactic therapy in children with hereditary angioedema.

Ragweed allergy: correlation between skin reactivity and in vitro complement activation

Recombinant human C1-inhibitor in the treatment of acute angioedema attacks.

Relationship between complement components C4A and C4B diversities and two TNFA promoter polymorphisms in two healthy Caucasian populations

Relationship between copy number of genes (C4A, C4B) encoding the fourth component of complement and the clinical course of hereditary angioedema (HAE)

Reply