Lista de obras - Marco Cicardi - Dominio Público Uruguay

A cluster of mutations within a short triplet repeat in the C1 inhibitor gene.

artículo científico publicado en 1994

A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy

artículo científico publicado en 2015

A simple endocrinological cause of a complex cardiovascular picture.

artículo científico publicado en 2010

A transcriptomics study of hereditary angioedema attacks

scientific article published on 04 May 2018

A young man with cough, fever and epigastric pain.

artículo científico publicado en 2014

Acquired C1 esterase inhibitor deficiency

Acquired C1-inhibitor deficiency and lymphoproliferative disorders: a tight relationship

artículo científico

Acquired C1-inhibitor deficiency associated with antiidiotypic antibody to monoclonal immunoglobulins

scientific article published on 01 February 1985

Acquired deficiency of the inhibitor of the first complement component: presentation, diagnosis, course, and conventional management.

artículo científico publicado en 2006

Activation of blood coagulation in chronic urticaria: pathophysiological and clinical implications. [corrected]

artículo científico publicado en 2010

Activation of complement and kinin systems after thrombolytic therapy in patients with acute myocardial infarction. A comparison between streptokinase and recombinant tissue-type plasminogen activator

artículo científico publicado en 1994

Activation of the contact system and fibrinolysis in autoimmune acquired angioedema: A rationale for prophylactic use of tranexamic acid

artículo científico publicado en 1994

Alterations of coagulation and fibrinolysis in patients with angioedema due to C1-inhibitor deficiency

scientific article published on 01 March 2012

An open-label study to evaluate the long-term safety and efficacy of lanadelumab for prevention of attacks in hereditary angioedema: design of the HELP study extension

artículo científico publicado en 2017

Angioedema Due to Bradykinin Dysregulation

artículo científico publicado en 2018

Angioedema Phenotypes: Disease Expression and Classification.

artículo científico publicado en 2016

Angioedema associated with angiotensin-converting enzyme inhibitor use: outcome after switching to a different treatment

artículo científico publicado en 2004

Angioedema due to C1 inhibitor deficiency in 2010.

scientific article published on 22 May 2010

Angioedema due to acquired C1-inhibitor deficiency: a bridging condition between autoimmunity and lymphoproliferation

artículo científico publicado en 2008

Angioedema due to angiotensin-converting enzyme inhibitors

artículo científico publicado en 1999

Angiotensin-converting enzyme inhibitor-related angioedema: how to deal with it.

artículo científico publicado en 2006

Autoimmune C1 inhibitor deficiency: Report of eight patients

artículo científico publicado en 1993

Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.

artículo científico publicado en 1983

Bradykinin and the pathophysiology of angioedema

artículo científico publicado en 2003

C1 INH concentrate in the therapy of hereditary angioedema

scientific article published on 01 February 1983

C1 esterase inhibitor concentrates and attenuated androgens - Authors' reply

artículo científico publicado en 2018

C1 inhibitor function and anti-C1 inhibitor autoantibodies in patients with HIV type 1 infection

scientific article published on 01 January 1999

C1 inhibitor gene expression in patients with hereditary angioedema: quantitative evaluation by means of real-time RT-PCR

artículo científico publicado en 2004

C1-inhibitor deficiency and angioedema.

artículo científico publicado en 2001

C1-inhibitor deficiency and angioedema: molecular mechanisms and clinical progress

scientific article published on 21 January 2009

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

artículo científico publicado en 2004

Catabolism of C1 inhibitor influences the response to replacement therapy in hereditary angioedema.

artículo científico publicado en 2016

Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group

artículo científico publicado en 2014

Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema.

artículo científico publicado en 2017

Clinical and pathological findings of a fatal systemic capillary leak syndrome (Clarkson disease): a case report

artículo científico publicado en 2015

Clinical impact of peripheral attacks in hereditary angioedema patients.

artículo científico publicado en 2012

Complement and contact system activation in acute congestive heart failure patients.

artículo científico

Consumption of C4b-binding protein (C4BP) during in vivo activation of the classical complement pathway

artículo científico publicado en 1999

Content validity of visual analog scales to assess symptom severity of acute angioedema attacks in adults with hereditary angioedema: an interview study

artículo científico publicado en 2012

Contraindications to the use of ace inhibitors in patients with C1 esterase inhibitor deficiency

artículo científico publicado en 1991

Costs and effects of on-demand treatment of hereditary angioedema in Italy: a prospective cohort study of 167 patients

scientific article published on 30 July 2018

Current treatment options for hereditary angioedema due to C1 inhibitor deficiency

artículo científico publicado en 2015

Danazol and stanozolol in long-term prophylactic treatment of hereditary angioedema

artículo científico publicado en 1980

Diagnosing angioedema.

artículo científico publicado en 2013

Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency

artículo científico publicado en 2017

Disease expression in women with hereditary angioedema.

artículo científico publicado en 2008

Does acquired angioedema increase the risk of surgery with cardiopulmonary bypass?

artículo científico publicado en 2000

Ecallantide for the treatment of acute attacks in hereditary angioedema

artículo científico publicado en 2010

Ecallantide for treatment of acute attacks of acquired C1 esterase inhibitor deficiency.

artículo científico publicado en 2013

Effect of Lanadelumab Compared With Placebo on Prevention of Hereditary Angioedema Attacks: A Randomized Clinical Trial

artículo científico publicado en 2018

Effect of treatment with 17 alpha-alkylated androgens on C4 conversion products in hereditary angioedema studied by crossed immunoelectrophoresis.

artículo científico publicado en 1982

Effects of radiographic contrast media

artículo científico publicado en 1997

Efficacy and safety of recombinant human C1-inhibitor for the treatment of attacks of hereditary angioedema: European open-label extension study.

artículo científico publicado en 2012

Efficacy of on-demand treatment in reducing morbidity in patients with hereditary angioedema due to C1 inhibitor deficiency.

artículo científico publicado en 2015

Elevated plasma levels of vascular permeability factors in C1 inhibitor-deficient hereditary angioedema

artículo científico publicado en 2016

Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: a multicenter, prospective study.

artículo científico publicado en 2018

Established and new treatments for hereditary angioedema: An update.

artículo científico publicado en 2007

Exposure-Response Model of Subcutaneous C1-Inhibitor Concentrate to Estimate the Risk of Attacks in Patients With Hereditary Angioedema.

artículo científico publicado en 2018

Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema

scientific article published on 01 December 2000

Guidance for diagnosis and treatment of acute angioedema in the emergency department: consensus statement by a panel of Italian experts.

artículo científico

Helicobacter pylori Infection as a Triggering Factor of Attacks in Patients with Hereditary Angioedema

scientific article published on 01 June 2007

Hepatic function and fibrinolysis in patients with hereditary angioedema undergoing long-term treatment with tranexamic acid.

artículo científico publicado en 1978

Hereditary and acquired complement component 1 esterase inhibitor deficiency: a review for the hematologist

artículo científico publicado en 2012

Hereditary angio-oedema

artículo científico publicado en 2012

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

artículo científico publicado en 1996

Hereditary angioedema: Assessing the hypothesis for underlying autonomic dysfunction

artículo científico publicado en 2017

Hereditary angioedema: an appraisal of 104 cases

artículo científico publicado en 1982

High prevalence of splenic marginal zone lymphoma among patients with acquired C1 inhibitor deficiency

artículo científico publicado en 2016

High rate of hepatitis B viral breakthrough in elderly non-Hodgkin lymphomas patients treated with Rituximab based chemotherapy.

artículo científico publicado en 2016

High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiency

artículo científico publicado en 2014

How do we treat patients with hereditary angioedema

artículo científico publicado en 2003

Icatibant treatment for acquired C1‐inhibitor deficiency: a real‐world observational study ⬇️

artículo científico publicado el 12 de junio de 2012

Idiopathic capillary leak syndrome: Evidence of CD8-positive lymphocytes surrounding damaged endothelial cells☆, ☆☆, ★

article

Idiopathic nonhistaminergic angioedema

artículo científico publicado en 1999

In vivo study of the complement system during infusion of radiographic contrast media

artículo científico publicado en 1986

Increased expression of C1-inhibitor mRNA in patients with hereditary angioedema treated with Danazol.

artículo científico publicado en 2003

Infusion of C1-inhibitor plasma concentrate prevents hyperamylasemia induced by endoscopic sphincterotomy

artículo científico publicado en 1995

Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight

artículo científico publicado en 2018

Intermittent therapy with danazol in hereditary angioedema

artículo científico publicado en 1978

International consensus and practical guidelines on the gynecologic and obstetric management of female patients with hereditary angioedema caused by C1 inhibitor deficiency ⬇️

artículo científico publicado el 24 de diciembre de 2011

Local bradykinin generation in hereditary angioedema

artículo científico publicado en 1999

Long-Term Outcomes with Subcutaneous C1-Inhibitor Replacement Therapy for Prevention of Hereditary Angioedema Attacks

artículo científico publicado en 2019

Long-term follow-up of 111 patients with angiotensin-converting enzyme inhibitor-related angioedema.

artículo científico publicado en 2011

Long-term prophylaxis in hereditary angio-oedema: a systematic review.

artículo científico

Lung ultrasonography for the assessment of rapid extravascular water variation: evidence from hemodialysis patients

artículo científico publicado en 2011

Lymphoproliferative disease and acquired C1 inhibitor deficiency

scientific article published on 01 May 2007

Mechanisms of C1-inhibitor deficiency.

artículo científico publicado en 2002

Molecular basis for the deficiency of complement 1 inhibitor in type I hereditary angioneurotic edema.

artículo científico publicado en 1987

Morphologic evaluation of the liver in hereditary angioedema patients on long-term treatment with androgen derivatives

artículo científico publicado en 1983

Mutation of the angiopoietin-1 gene (ANGPT1) associates with a new type of hereditary angioedema.

artículo científico publicado en 2017

Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: functional and structural correlates.

artículo científico publicado en 2008

Natural history and clinical impact of cryoglobulins in chronic hepatitis C: 10-year prospective study of 343 patients.

artículo científico publicado en 2007

New topics in bradykinin research.

artículo científico

Novel pathogenic mechanism and therapeutic approaches to angioedema associated with C1 inhibitor deficiency

artículo científico publicado en 2009

Novelties in the Diagnosis and Treatment of Angioedema

artículo científico publicado en 2016

Ongoing contact activation in patients with hereditary angioedema

artículo científico publicado en 2013

Oral Plasma Kallikrein Inhibitor for Prophylaxis in Hereditary Angioedema

article

Paroxysmal Permeability Disorders: Development of a Microfluidic Device to Assess Endothelial Barrier Function

artículo científico publicado en 2019

Pathophysiology of Hereditary Angioedema

artículo científico publicado en 2014

Phase II study results of a replacement therapy for hereditary angioedema with subcutaneous C1-inhibitor concentrate

artículo científico publicado en 2015

Plasma biomarkers of acute attacks in patients with angioedema due to C1-inhibitor deficiency

scientific article published on 04 December 2008

Plasma bradykinin in angio-oedema.

artículo científico publicado en 1998

Plasma levels of C1- inhibitor complexes and cleaved C1- inhibitor in patients with hereditary angioneurotic edema.

artículo científico publicado en 1990

Plasmin is a natural trigger for bradykinin production in patients with hereditary angioedema with factor XII mutations.

artículo científico publicado en 2016

Population pharmacokinetics of subcutaneous C1-inhibitor for prevention of attacks in patients with hereditary angioedema

artículo científico publicado en 2018

Presentation, diagnosis and treatment of angioedema without wheals: a retrospective analysis of a cohort of 1058 patients.

artículo científico publicado en 2014

Prevalence and risk factors for the presence of serum cryoglobulins in patients with chronic hepatitis C

artículo científico publicado en 2000

Prevention of hereditary angioedema attacks with a subcutaneous C1 inhibitor

artículo científico publicado en 2017

Profile of infective endocarditis observed from 2003 - 2010 in a single center in Italy

artículo científico publicado en 2013

Rapid detection by fluorescent multiplex PCR of exon deletions and duplications in the C1 inhibitor gene of hereditary angioedema patients

artículo científico publicado en 2001

Recent advances in the use of C1 inhibitor as a therapeutic agent.

artículo científico publicado en 2003

Recombinant human C1 esterase inhibitor (Conestat alfa) for prophylaxis to prevent attacks in adult and adolescent patients with hereditary angioedema

scientific article published on 13 September 2018

Recombinant human C1 esterase inhibitor for acute hereditary angioedema attacks with upper airway involvement.

artículo científico publicado en 2017

Recombinant human C1 esterase inhibitor for prophylaxis of hereditary angio-oedema: a phase 2, multicentre, randomised, double-blind, placebo-controlled crossover trial

artículo científico publicado en 2017

Recombinant human C1-inhibitor for the treatment of acute angioedema attacks in patients with hereditary angioedema.

artículo científico publicado en 2010

Recombinant replacement therapy for hereditary angioedema due to C1 inhibitor deficiency

artículo científico publicado en 2015

Recurrent Retroperitoneal Angioedema

artículo científico publicado en 2018

Reduction in transmission of hepatitis C after the introduction of a heat-treatment step in the production of C1-inhibitor concentrate.

artículo científico publicado en 1995

Relevance of lymphoproliferative disorders and of anti-C1 inhibitor autoantibodies in acquired angio-oedema

artículo científico publicado en 1996

Replacement therapy in hereditary and acquired angioedema

artículo científico publicado en 1992

Replacement therapy with C1 esterase inhibitors for hereditary angioedema.

artículo científico publicado en 2010

Reply

artículo científico publicado en 2017

Research on complement: old issues revisited and a novel sphere of influence.

artículo científico publicado en 2003

Review of recent guidelines and consensus statements on hereditary angioedema therapy with focus on self-administration.

artículo científico

Secreted Phospholipases A2 in Hereditary Angioedema With C1-Inhibitor Deficiency

scientific article published on 23 July 2018

Side effects of long-term prophylaxis with attenuated androgens in hereditary angioedema: comparison of treated and untreated patients

artículo científico publicado en 1997

Splenic marginal zone lymphomas in acquired C1-inhibitor deficiency: clinical and molecular characterization

artículo científico publicado en 2018

Standard care impact on angioedema because of hereditary C1 inhibitor deficiency: a 21-month prospective study in a cohort of 103 patients

scientific article published on 29 October 2010

Successful resolution of bowel obstruction in a patient with hereditary angioedema

artículo científico publicado en 2008

Swelling isn't swell

artículo científico publicado en 2004

Target levels of functional C1-inhibitor in hereditary angioedema.

artículo científico

The Role of Failing Autonomic Nervous System on Life-Threatening Idiopathic Systemic Capillary Leak Syndrome.

artículo científico publicado en 2018

The acquired deficiency of C1-inhibitor: lymphoproliferation and angioedema.

artículo científico publicado en 2010

The metabolism of C1 inhibitor and C1q in patients with acquired C1-inhibitor deficiency

artículo científico publicado en 1986

The role of genetics in the current diagnostic workup of idiopathic non-histaminergic angioedema

artículo científico publicado en 2018

The safety of treatments for angioedema with hereditary C1 inhibitor deficiency.

artículo científico

The systemic capillary leak syndrome: appearance of interleukin-2-receptor-positive cells during attacks

artículo científico publicado en 1990

Therapeutic management of hereditary angioedema due to C1 inhibitor deficiency.

artículo científico

Treatment effect of switching from intravenous to subcutaneous C1-inhibitor for prevention of hereditary angioedema attacks: COMPACT subgroup findings

scientific article published on 17 January 2019

Treatment of acquired angioedema with icatibant: a case report

artículo científico publicado en 2010

Use of subcutaneous-C1 INH for acute therapy and prophylaxis of a child with HAE

artículo científico publicado en 2015

[Angioedema and the role of bradykinins: new treatments and implications in patients with heart failure]

artículo científico publicado en 2016

Lista de obras de Marco Cicardi

A cluster of mutations within a short triplet repeat in the C1 inhibitor gene.

A nationwide survey of hereditary angioedema due to C1 inhibitor deficiency in Italy

A simple endocrinological cause of a complex cardiovascular picture.

A transcriptomics study of hereditary angioedema attacks

A young man with cough, fever and epigastric pain.

Acquired C1 esterase inhibitor deficiency

Acquired C1-inhibitor deficiency and lymphoproliferative disorders: a tight relationship

Acquired C1-inhibitor deficiency associated with antiidiotypic antibody to monoclonal immunoglobulins

Acquired deficiency of the inhibitor of the first complement component: presentation, diagnosis, course, and conventional management.

Activation of blood coagulation in chronic urticaria: pathophysiological and clinical implications. [corrected]

Activation of complement and kinin systems after thrombolytic therapy in patients with acute myocardial infarction. A comparison between streptokinase and recombinant tissue-type plasminogen activator

Activation of the contact system and fibrinolysis in autoimmune acquired angioedema: A rationale for prophylactic use of tranexamic acid

Alterations of coagulation and fibrinolysis in patients with angioedema due to C1-inhibitor deficiency

An open-label study to evaluate the long-term safety and efficacy of lanadelumab for prevention of attacks in hereditary angioedema: design of the HELP study extension

Angioedema Due to Bradykinin Dysregulation

Angioedema Phenotypes: Disease Expression and Classification.

Angioedema associated with angiotensin-converting enzyme inhibitor use: outcome after switching to a different treatment

Angioedema due to C1 inhibitor deficiency in 2010.

Angioedema due to acquired C1-inhibitor deficiency: a bridging condition between autoimmunity and lymphoproliferation

Angioedema due to angiotensin-converting enzyme inhibitors

Angiotensin-converting enzyme inhibitor-related angioedema: how to deal with it.

Autoimmune C1 inhibitor deficiency: Report of eight patients

Behavior in vivo of normal and dysfunctional C1 inhibitor in normal subjects and patients with hereditary angioneurotic edema.

Bradykinin and the pathophysiology of angioedema

C1 INH concentrate in the therapy of hereditary angioedema

C1 esterase inhibitor concentrates and attenuated androgens - Authors' reply

C1 inhibitor function and anti-C1 inhibitor autoantibodies in patients with HIV type 1 infection

C1 inhibitor gene expression in patients with hereditary angioedema: quantitative evaluation by means of real-time RT-PCR

C1-inhibitor deficiency and angioedema.

C1-inhibitor deficiency and angioedema: molecular mechanisms and clinical progress

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

Catabolism of C1 inhibitor influences the response to replacement therapy in hereditary angioedema.

Classification, diagnosis, and approach to treatment for angioedema: consensus report from the Hereditary Angioedema International Working Group

Cleaved kininogen as a biomarker for bradykinin release in hereditary angioedema.

Clinical and pathological findings of a fatal systemic capillary leak syndrome (Clarkson disease): a case report

Clinical impact of peripheral attacks in hereditary angioedema patients.

Complement and contact system activation in acute congestive heart failure patients.

Consumption of C4b-binding protein (C4BP) during in vivo activation of the classical complement pathway

Content validity of visual analog scales to assess symptom severity of acute angioedema attacks in adults with hereditary angioedema: an interview study

Contraindications to the use of ace inhibitors in patients with C1 esterase inhibitor deficiency

Costs and effects of on-demand treatment of hereditary angioedema in Italy: a prospective cohort study of 167 patients

Current treatment options for hereditary angioedema due to C1 inhibitor deficiency

Danazol and stanozolol in long-term prophylactic treatment of hereditary angioedema

Diagnosing angioedema.

Diagnosis, Course, and Management of Angioedema in Patients With Acquired C1-Inhibitor Deficiency

Disease expression in women with hereditary angioedema.

Does acquired angioedema increase the risk of surgery with cardiopulmonary bypass?

Ecallantide for the treatment of acute attacks in hereditary angioedema

Ecallantide for treatment of acute attacks of acquired C1 esterase inhibitor deficiency.

Effect of Lanadelumab Compared With Placebo on Prevention of Hereditary Angioedema Attacks: A Randomized Clinical Trial

Effect of treatment with 17 alpha-alkylated androgens on C4 conversion products in hereditary angioedema studied by crossed immunoelectrophoresis.

Effects of radiographic contrast media

Efficacy and safety of recombinant human C1-inhibitor for the treatment of attacks of hereditary angioedema: European open-label extension study.

Efficacy of on-demand treatment in reducing morbidity in patients with hereditary angioedema due to C1 inhibitor deficiency.

Elevated plasma levels of vascular permeability factors in C1 inhibitor-deficient hereditary angioedema

Emotional processes and stress in children affected by hereditary angioedema with C1-inhibitor deficiency: a multicenter, prospective study.

Established and new treatments for hereditary angioedema: An update.

Exposure-Response Model of Subcutaneous C1-Inhibitor Concentrate to Estimate the Risk of Attacks in Patients With Hereditary Angioedema.

Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema

Guidance for diagnosis and treatment of acute angioedema in the emergency department: consensus statement by a panel of Italian experts.

Helicobacter pylori Infection as a Triggering Factor of Attacks in Patients with Hereditary Angioedema

Hepatic function and fibrinolysis in patients with hereditary angioedema undergoing long-term treatment with tranexamic acid.

Hereditary and acquired complement component 1 esterase inhibitor deficiency: a review for the hematologist

Hereditary angio-oedema

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

Hereditary angioedema: Assessing the hypothesis for underlying autonomic dysfunction

Hereditary angioedema: an appraisal of 104 cases

High prevalence of splenic marginal zone lymphoma among patients with acquired C1 inhibitor deficiency

High rate of hepatitis B viral breakthrough in elderly non-Hodgkin lymphomas patients treated with Rituximab based chemotherapy.

High-molecular-weight kininogen cleavage correlates with disease states in the bradykinin-mediated angioedema due to hereditary C1-inhibitor deficiency

How do we treat patients with hereditary angioedema

Icatibant treatment for acquired C1‐inhibitor deficiency: a real‐world observational study ⬇️

Idiopathic capillary leak syndrome: Evidence of CD8-positive lymphocytes surrounding damaged endothelial cells☆, ☆☆, ★

Idiopathic nonhistaminergic angioedema

In vivo study of the complement system during infusion of radiographic contrast media

Increased expression of C1-inhibitor mRNA in patients with hereditary angioedema treated with Danazol.

Infusion of C1-inhibitor plasma concentrate prevents hyperamylasemia induced by endoscopic sphincterotomy

Intermittent C1-Inhibitor Deficiency Associated with Recessive Inheritance: Functional and Structural Insight