List of works - Karim Wahbi

Abnormal sodium current properties contribute to cardiac electrical and contractile dysfunction in a mouse model of myotonic dystrophy type 1.

scientific article published on 10 December 2014

Acute coronary syndrome in human immunodeficiency virus-infected patients: characteristics and 1 year prognosis

scientific article published on 21 October 2010

Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry

scientific article published on June 2017

Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcome.

scientific article published on 10 February 2016

Atrio-ventricular block requiring pacemaker in patients with late onset Pompe disease

scientific article published on 24 April 2014

Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution

scientific article published on 22 December 2014

Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvement

article

Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.

scientific article

CNS disease triggering Takotsubo stress cardiomyopathy

scientific article published on 26 August 2014

CNS-disease affecting the heart: brain-heart disorders

scientific article published on 8 July 2014

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.

scientific article published on 12 September 2016

Cardiac findings in congenital muscular dystrophies.

scientific article published on 02 August 2010

Cardiac implantable electronic devices in tracheotomized muscular dystrophy patients: Safety and risks

scientific article published on 06 August 2016

Cardiac involvement in laminopathies.

scientific article published on 11 November 2015

Cardiac involvement in systemic sclerosis assessed by tissue-doppler echocardiography during routine care: A controlled study of 100 consecutive patients

scientific article published on 01 June 2008

Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNA

scientific article published on 01 February 2010

Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care.

scientific article published on 12 December 2016

Cardiomyopathy in neurological disorders ⬇️

scientific article published on February 22, 2013

Coding region of the sorbin gene in different species.

scientific article published in December 2001

Combination of copeptin and high-sensitivity cardiac troponin T assay in unstable angina and non-ST-segment elevation myocardial infarction: a pilot study

scientific article published on 22 December 2010

Consensus statement on standard of care for congenital muscular dystrophies

scientific article

Cross-sectional retrospective study of muscle function in patients with glycogen storage disease type III.

scientific article published on 28 June 2016

Delayed cardiomyopathy in dystrophin deficient mdx mice relies on intrinsic glutathione resource.

scientific article

Development and Validation of a New Scoring System to Predict Survival in Patients With Myotonic Dystrophy Type 1.

scientific article published on 5 February 2018

Dilated cardiomyopathy in patients with mutations in anoctamin 5

scientific article published on 03 October 2012

Genotype and other determinants of respiratory function in myotonic dystrophy type 1.

scientific article published on 26 December 2017

High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.

scientific article

High diagnostic performance of a high-sensitivity cardiac troponin T assay in patients with suspected acute coronary syndrome

scientific article published on 20 October 2010

High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation.

scientific article published on 12 December 2012

How to diagnose an acute coronary syndrome in 2015?

scientific article published on March 2015

Hyperckemia and myalgia are common presentations of anoctamin-5-related myopathy in French patients

scientific article published on 10 February 2017

In B-cell chronic lymphocytic leukemias, 7q21 translocations lead to overexpression of the CDK6 gene

scientific article published on 01 August 2003

Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1.

scientific article published in March 2017

Influence of age and renal function on high-sensitivity cardiac troponin T diagnostic accuracy for the diagnosis of acute myocardial infarction.

scientific article

Involvement of a human endogenous retroviral sequence (THE-7) in a t(7;14)(q21;q32) chromosomal translocation associated with a B cell chronic lymphocytic leukemia.

scientific article published in August 1997

Lamin and the heart

scientific article published on 25 November 2017

Left bundle branch block in Duchenne muscular dystrophy: Prevalence, genetic relationship and prognosis.

scientific article published on 5 January 2018

Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control study.

scientific article published on 29 May 2009

Left ventricular non-compaction in a patient with myotonic dystrophy type 2.

scientific article

Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa.

scientific article published on 30 August 2017

Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseases

scientific article published on 29 July 2015

Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy.

scientific article

Low rates of immediate coronary angiography among young adults resuscitated from sudden cardiac arrest

scientific article published on 16 December 2019

Meta-analysis of Renin-Angiotensin-aldosterone blockade for heart failure in presence of preserved left ventricular function.

scientific article published on 30 December 2010

Mid-regional pro atrial natriuretic peptide allows the accurate identification of patients with atrial fibrillation of short time of onset: a pilot study

scientific article published on 17 August 2011

Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy

scientific article published on 19 June 2011

Mitochondrial disease: learning from Charlie's lesson, trying to cure, trying much more to care

scientific article published on 27 June 2018

Mutation in lamin A/C sensitizes the myocardium to exercise-induced mechanical stress but has no effect on skeletal muscles in mouse.

scientific article published on 26 May 2016

Myocardial dysfunction in rheumatoid arthritis: a controlled tissue-Doppler echocardiography study

scientific article published on 01 September 2007

Myofibrillar myopathies: State of the art, present and future challenges

scientific article published on 02 September 2015

N-Terminal-proBrain natriuretic peptide measurement at presentation to identify patients with recent onset of atrial fibrillation

scientific article published on 09 November 2011

N-terminal pro-brain natriuretic peptide in systemic sclerosis: a new cornerstone of cardiovascular assessment?

scientific article published on 03 December 2008

Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2D.

scientific article

Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic study

scientific article published on 28 December 2012

Non Random Distribution of DMD Deletion Breakpoints and Implication of Double Strand Breaks Repair and Replication Error Repair Mechanisms.

scientific article published in May 2016

Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats

scientific article published on 07 August 2018

Performance of glycogen phosphorylase isoenzyme BB is weak in the detection of patients with non-ST-elevation acute coronary syndrome

scientific article published on 28 July 2011

Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up

scientific article published on September 2007

Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1

scientific article

Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.

scientific article published on 21 November 2016

Prediction of pulmonary hypertension related to systemic sclerosis by an index based on simple clinical observations.

scientific article

Proceedings of Réanimation 2017, the French Intensive Care Society International Congress

scientific article published on 10 January 2017

Reduced inotropic reserve is predictive of further degradation in left ventricular ejection fraction in patients with Duchenne muscular dystrophy

scientific article published in February 2015

Risk for Complications after Pacemaker or Cardioverter Defibrillator Implantations in Patients with Myotonic Dystrophy Type 1.

scientific article published on 6 June 2017

Selection of BCR/ABL-negative stem cells from marrow or blood of patients with chronic myeloid leukemia

scientific article published on 01 July 1999

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.

scientific article published on 11 April 2016

Two new cases of mitochondrial myopathy with exercise intolerance, hyperlactatemia and cardiomyopathy, caused by recessive SLC25A4 mutations

scientific article published on 17 August 2017

[Arrhythmia follow-up of children and adolescents with neuromuscular diseases]

scientific article published on 01 May 2007

[Cardiac involvement in dystrophinopathies]

scientific article published on 01 December 2015

[Early detection of myocardial disease in young patients with Becker's muscular dystrophy asymptomatic from the cardiac point of view: value of myocardial doppler tissue imaging]

scientific article published on 01 March 2007

List of works by Karim Wahbi

Abnormal sodium current properties contribute to cardiac electrical and contractile dysfunction in a mouse model of myotonic dystrophy type 1.

Acute coronary syndrome in human immunodeficiency virus-infected patients: characteristics and 1 year prognosis

Association Between Mutation Size and Cardiac Involvement in Myotonic Dystrophy Type 1: An Analysis of the DM1-Heart Registry

Atrial flutter in myotonic dystrophy type 1: Patient characteristics and clinical outcome.

Atrio-ventricular block requiring pacemaker in patients with late onset Pompe disease

Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolution

Blood glutathione decrease in subjects carrying lamin A/C gene mutations is an early marker of cardiac involvement

Brugada syndrome and abnormal splicing of SCN5A in myotonic dystrophy type 1.

CNS disease triggering Takotsubo stress cardiomyopathy

CNS-disease affecting the heart: brain-heart disorders

Cardiac arrhythmia and late-onset muscle weakness caused by a myofibrillar myopathy with unusual histopathological features due to a novel missense mutation in FLNC.

Cardiac findings in congenital muscular dystrophies.

Cardiac implantable electronic devices in tracheotomized muscular dystrophy patients: Safety and risks

Cardiac involvement in laminopathies.

Cardiac involvement in systemic sclerosis assessed by tissue-doppler echocardiography during routine care: A controlled study of 100 consecutive patients

Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNA

Cardiac manifestations of congenital LMNA-related muscular dystrophy in children: three case reports and recommendations for care.

Cardiomyopathy in neurological disorders ⬇️

Coding region of the sorbin gene in different species.

Combination of copeptin and high-sensitivity cardiac troponin T assay in unstable angina and non-ST-segment elevation myocardial infarction: a pilot study

Consensus statement on standard of care for congenital muscular dystrophies

Cross-sectional retrospective study of muscle function in patients with glycogen storage disease type III.

Delayed cardiomyopathy in dystrophin deficient mdx mice relies on intrinsic glutathione resource.

Development and Validation of a New Scoring System to Predict Survival in Patients With Myotonic Dystrophy Type 1.

Dilated cardiomyopathy in patients with mutations in anoctamin 5

Genotype and other determinants of respiratory function in myotonic dystrophy type 1.

High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal study.

High diagnostic performance of a high-sensitivity cardiac troponin T assay in patients with suspected acute coronary syndrome

High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation.

How to diagnose an acute coronary syndrome in 2015?

Hyperckemia and myalgia are common presentations of anoctamin-5-related myopathy in French patients

In B-cell chronic lymphocytic leukemias, 7q21 translocations lead to overexpression of the CDK6 gene

Incidence and predictors of sudden death, major conduction defects and sustained ventricular tachyarrhythmias in 1388 patients with myotonic dystrophy type 1.

Influence of age and renal function on high-sensitivity cardiac troponin T diagnostic accuracy for the diagnosis of acute myocardial infarction.

Involvement of a human endogenous retroviral sequence (THE-7) in a t(7;14)(q21;q32) chromosomal translocation associated with a B cell chronic lymphocytic leukemia.

Lamin and the heart

Left bundle branch block in Duchenne muscular dystrophy: Prevalence, genetic relationship and prognosis.

Left ventricular dysfunction and cardiac arrhythmias are frequent in type 2 myotonic dystrophy: a case control study.

Left ventricular non-compaction in a patient with myotonic dystrophy type 2.

Long term longitudinal study of muscle function in patients with glycogen storage disease type IIIa.

Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseases

Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy.

Low rates of immediate coronary angiography among young adults resuscitated from sudden cardiac arrest

Meta-analysis of Renin-Angiotensin-aldosterone blockade for heart failure in presence of preserved left ventricular function.

Mid-regional pro atrial natriuretic peptide allows the accurate identification of patients with atrial fibrillation of short time of onset: a pilot study

Misregulation of miR-1 processing is associated with heart defects in myotonic dystrophy

Mitochondrial disease: learning from Charlie's lesson, trying to cure, trying much more to care

Mutation in lamin A/C sensitizes the myocardium to exercise-induced mechanical stress but has no effect on skeletal muscles in mouse.

Myocardial dysfunction in rheumatoid arthritis: a controlled tissue-Doppler echocardiography study

Myofibrillar myopathies: State of the art, present and future challenges

N-Terminal-proBrain natriuretic peptide measurement at presentation to identify patients with recent onset of atrial fibrillation

N-terminal pro-brain natriuretic peptide in systemic sclerosis: a new cornerstone of cardiovascular assessment?

Natural History of Cardiac and Respiratory Involvement, Prognosis and Predictive Factors for Long-Term Survival in Adult Patients with Limb Girdle Muscular Dystrophies Type 2C and 2D.

Neutral lipid storage disease with myopathy: a whole-body nuclear MRI and metabolic study

Non Random Distribution of DMD Deletion Breakpoints and Implication of Double Strand Breaks Repair and Replication Error Repair Mechanisms.

Non invasive mechanical ventilation in DM1: The strong correlation between lung function, neurological-cognitive function and CTG repeats

Performance of glycogen phosphorylase isoenzyme BB is weak in the detection of patients with non-ST-elevation acute coronary syndrome

Perindopril preventive treatment on mortality in Duchenne muscular dystrophy: 10 years' follow-up

Polyglucosan body myopathy caused by defective ubiquitin ligase RBCK1

Prediction of long-term prognosis by heteroplasmy levels of the m.3243A>G mutation in patients with the mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes syndrome.

Prediction of pulmonary hypertension related to systemic sclerosis by an index based on simple clinical observations.

Proceedings of Réanimation 2017, the French Intensive Care Society International Congress

Reduced inotropic reserve is predictive of further degradation in left ventricular ejection fraction in patients with Duchenne muscular dystrophy

Risk for Complications after Pacemaker or Cardioverter Defibrillator Implantations in Patients with Myotonic Dystrophy Type 1.

Selection of BCR/ABL-negative stem cells from marrow or blood of patients with chronic myeloid leukemia

Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy.

Two new cases of mitochondrial myopathy with exercise intolerance, hyperlactatemia and cardiomyopathy, caused by recessive SLC25A4 mutations

[Arrhythmia follow-up of children and adolescents with neuromuscular diseases]

[Cardiac involvement in dystrophinopathies]

[Early detection of myocardial disease in young patients with Becker's muscular dystrophy asymptomatic from the cardiac point of view: value of myocardial doppler tissue imaging]