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Unmet Cardiac Clinical Needs in Adult Mucopolysaccharidoses

Frontiers in cardiovascular medicine, 2022-06, Vol.9, p.907175-907175

2022

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Editorial: Cardiac issues in adults with mucopolysaccharidosis

Frontiers in cardiovascular medicine, 2022-08, Vol.9, p.1016386-1016386

2022

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Timing is everything: Clinical courses of Hunter syndrome associated with age at initiation of therapy in a sibling pair

Molecular genetics and metabolism reports, 2022-03, Vol.30, p.100845-100845, Article 100845

2022

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The Carotid Intima-Media Thickness and Arterial Stiffness of Pediatric Mucopolysaccharidosis Patients Are Increased Compared to Both Pediatric and Adult Controls

International journal of molecular sciences, 2017-03, Vol.18 (3), p.637-637

2017

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Mechanical circulatory support in patients with heart failure secondary to transposition of the great arteries

The Journal of heart and lung transplantation, 2010-11, Vol.29 (11), p.1302-1305

2010

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Successful rapid staged hybrid approach for obstructed total anomalous pulmonary venous connection

Journal of cardiac surgery, 2022-12, Vol.37 (12), p.5501-5504

2022

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Duration of high-dose aspirin therapy does not affect long-term coronary artery outcomes in Kawasaki disease

Pediatric research, 2018-06, Vol.83 (6), p.1136-1145

2018

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Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management

Journal of inherited metabolic disease, 2011-12, Vol.34 (6), p.1183-1197

2011

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Anaesthesia and airway management in mucopolysaccharidosis

Journal of inherited metabolic disease, 2013-03, Vol.36 (2), p.211-219

2013

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Mortality after hematopoietic stem cell transplantation for severe mucopolysaccharidosis type I: the 30-year University of Minnesota experience

Journal of inherited metabolic disease, 2017-03, Vol.40 (2), p.271-280

2017

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Enhancing efficacy of stem cell transplantation to the heart with a PEGylated fibrin biomatrix

Tissue engineering. Part A, 2008-06, Vol.14 (6), p.1025-1036

2008

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Cardiac Findings After Enzyme Replacement Therapy for Mucopolysaccharidosis Type I

The American journal of cardiology, 2006-08, Vol.98 (3), p.416-418

2006

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Tele-Pediatric Intensive Care for Critically Ill Children in Syria

Telemedicine journal and e-health, 2018-08, Vol.24 (8), p.621-623

2018

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Unique medical issues in adult patients with mucopolysaccharidoses

European journal of internal medicine, 2016-10, Vol.34, p.2-10

2016

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Angiotensin receptor blockade mediated amelioration of mucopolysaccharidosis type I cardiac and craniofacial pathology

Journal of inherited metabolic disease, 2017-03, Vol.40 (2), p.281-289

2017

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Endothelial function in children and adolescents with mucopolysaccharidosis

Journal of inherited metabolic disease, 2013-03, Vol.36 (2), p.221-225

2013

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Carotid intima–media thickness is increased in patients with treated mucopolysaccharidosis types I and II, and correlates with arterial stiffness

Molecular genetics and metabolism, 2014-02, Vol.111 (2), p.128-132

2014

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Recommendations for the management of MPS IVA: systematic evidence- and consensus-based guidance

Orphanet journal of rare diseases, 2019-06, Vol.14 (1), p.137-137, Article 137

2019

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SARS-CoV-2 Variants and Multisystem Inflammatory Syndrome in Children

The New England journal of medicine, 2023-04, Vol.388 (17), p.1624-1626

2023

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Recommendations for the management of MPS VI: systematic evidence- and consensus-based guidance

Orphanet journal of rare diseases, 2019-05, Vol.14 (1), p.118-118, Article 118

2019

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Usefulness of bone marrow transplantation in the Hurler syndrome

The American journal of cardiology, 2003-10, Vol.92 (7), p.882-886

2003

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Medium-Term Complications Associated With Coronary Artery Aneurysms After Kawasaki Disease: A Study From the International Kawasaki Disease Registry

Journal of the American Heart Association, 2020-08, Vol.9 (15), p.e016440-e016440

2020

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Kawasaki Disease in the Time of COVID-19 and MIS-C: The International Kawasaki Disease Registry

Canadian journal of cardiology, 2024-01, Vol.40 (1), p.58-72

2024

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Variation in Pharmacologic Management of Patients with Kawasaki Disease with Coronary Artery Aneurysms

The Journal of pediatrics, 2022-01, Vol.240, p.164-170.e1

2022

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Unmet Cardiac Clinical Needs in Adult Mucopolysaccharidoses

Editorial: Cardiac issues in adults with mucopolysaccharidosis

Timing is everything: Clinical courses of Hunter syndrome associated with age at initiation of therapy in a sibling pair

The Carotid Intima-Media Thickness and Arterial Stiffness of Pediatric Mucopolysaccharidosis Patients Are Increased Compared to Both Pediatric and Adult Controls

Mechanical circulatory support in patients with heart failure secondary to transposition of the great arteries

Successful rapid staged hybrid approach for obstructed total anomalous pulmonary venous connection

Duration of high-dose aspirin therapy does not affect long-term coronary artery outcomes in Kawasaki disease

Cardiac disease in patients with mucopolysaccharidosis: presentation, diagnosis and management

Anaesthesia and airway management in mucopolysaccharidosis

Mortality after hematopoietic stem cell transplantation for severe mucopolysaccharidosis type I: the 30-year University of Minnesota experience

Enhancing efficacy of stem cell transplantation to the heart with a PEGylated fibrin biomatrix

Cardiac Findings After Enzyme Replacement Therapy for Mucopolysaccharidosis Type I

Tele-Pediatric Intensive Care for Critically Ill Children in Syria

Unique medical issues in adult patients with mucopolysaccharidoses

Angiotensin receptor blockade mediated amelioration of mucopolysaccharidosis type I cardiac and craniofacial pathology

Endothelial function in children and adolescents with mucopolysaccharidosis

Carotid intima–media thickness is increased in patients with treated mucopolysaccharidosis types I and II, and correlates with arterial stiffness

Recommendations for the management of MPS IVA: systematic evidence- and consensus-based guidance

SARS-CoV-2 Variants and Multisystem Inflammatory Syndrome in Children

Recommendations for the management of MPS VI: systematic evidence- and consensus-based guidance

Usefulness of bone marrow transplantation in the Hurler syndrome

Medium-Term Complications Associated With Coronary Artery Aneurysms After Kawasaki Disease: A Study From the International Kawasaki Disease Registry

Kawasaki Disease in the Time of COVID-19 and MIS-C: The International Kawasaki Disease Registry

Variation in Pharmacologic Management of Patients with Kawasaki Disease with Coronary Artery Aneurysms

Cardiac Biomarkers Aid in Differentiation of Kawasaki Disease from Multisystem Inflammatory Syndrome in Children Associated with COVID-19

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