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Multidisciplinary management of Hunter syndrome

Pediatrics (Evanston), 2009-12, Vol.124 (6), p.e1228-e1239

2009

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Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy

Journal of inherited metabolic disease, 2013-03, Vol.36 (2), p.385-394

2013

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The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapy

Clinical genetics, 2004-04, Vol.65 (4), p.299-307

2004

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Normal values of M mode echocardiographic measurements of more than 2000 healthy infants and children in central Europe

British heart journal, 2000-06, Vol.83 (6), p.667-672

2000

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Fabry disease in children and response to enzyme replacement therapy: results from the Fabry Outcome Survey

Clinical genetics, 2012-05, Vol.81 (5), p.485-490

2012

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Safety of agalsidase alfa in patients with Fabry disease under 7 years

Acta Paediatrica, 2011-04, Vol.100 (4), p.605-611

2011

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Association between polymorphisms of endothelial nitric oxide synthase gene (NOS3) and left posterior wall thickness (LPWT) of the heart in Fabry disease

Journal of inherited metabolic disease, 2008-12, Vol.31 (Suppl 2), p.349-356

2008

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Electrocardiographic signs of hypertrophy in Fabry disease-associated hypertrophic cardiomyopathy

Acta Paediatrica, 2002-11, Vol.91 (s439), p.21-27

2002

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Transcatheter closure of secundum atrial septal defects with the atrial septal defect occlusion system (ASDOS): initial experience in children

Heart (British Cardiac Society), 1996-01, Vol.75 (1), p.83-88

1996

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Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature

Genetics in medicine, 2010-11, Vol.12 (11), p.668-679

2010

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Cardio- Renal Outcomes With Long- Term Agalsidase Alfa Enzyme Replacement Therapy: A 10- Year Fabry Outcome Survey (FOS) Analysis

Drug design, development and therapy, 2019-01, Vol.13, p.3705-3715

2019

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Cardiac manifestations of Anderson–Fabry disease in heterozygous females

Journal of the American College of Cardiology, 2002-11, Vol.40 (9), p.1668-1674

2002

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Acute aortic dissection after balloon angioplasty of a recoarctation and treatment by stenting and distal membrane fenestration in a child

Heart (British Cardiac Society), 2011-10, Vol.97 (20), p.1699-1700

2011

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Anderson–Fabry disease: Clinical manifestations of disease in female heterozygotes

Journal of inherited metabolic disease, 2001-11, Vol.24 (7), p.715-724

2001

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The effect of idursulfase on growth in patients with Hunter syndrome: Data from the Hunter Outcome Survey (HOS)

Molecular genetics and metabolism, 2013-05, Vol.109 (1), p.41-48

2013

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Modified hemi-Fontan operation and subsequent nonsurgical Fontan completion

The Journal of thoracic and cardiovascular surgery, 1995-09, Vol.110 (3), p.865-867

1995

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Complete atrioventricular septal defect associated with tetralogy of Fallot. Favourable outcome of transatrial transpulmonary repair

Journal of cardiovascular surgery, 2000-02, Vol.41 (1), p.17

2000

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The heart in Anderson Fabry disease

Clinical research in cardiology, 2002-10, Vol.91 (10), p.786-795

2002

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Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome Survey

International journal of clinical practice (Esher), 2006-09, Vol.60 (9), p.1053-1059

2006

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Low-energy epicardial pacing in children: the benefit of autocapture

The Annals of thoracic surgery, 1999-10, Vol.68 (4), p.1380-1383

1999

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Fabry disease: focus on cardiac manifestations and molecular mechanisms

Herz, 2002-11, Vol.27 (7), p.699-702

2002

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Reduced inotropic support after aprotinin therapy during pediatric cardiac operations

The Annals of thoracic surgery, 1999, Vol.67 (1), p.173-176

1999

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Biodegradation of tungsten embolisation coils used in children

Pediatric radiology, 2002-12, Vol.32 (12), p.839-843

2002

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Sense and nonsense of exposure prophylaxis in communal club installations for children and adolescents -- a contribution to the implementation of the German Defence Against Infection law from a point of view of preventive paediatrics

Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)), 2002-12, Vol.64 (12), p.669

2002

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Clinical performance of the native pulmonary valve in the systemic circulation

The Journal of heart valve disease, 1998-11, Vol.7 (6), p.620

1998

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Multidisciplinary management of Hunter syndrome

Enzyme replacement therapy for mucopolysaccharidosis VI: long-term cardiac effects of galsulfase (Naglazyme®) therapy

The Mainz Severity Score Index: a new instrument for quantifying the Anderson-Fabry disease phenotype, and the response of patients to enzyme replacement therapy

Normal values of M mode echocardiographic measurements of more than 2000 healthy infants and children in central Europe

Fabry disease in children and response to enzyme replacement therapy: results from the Fabry Outcome Survey

Safety of agalsidase alfa in patients with Fabry disease under 7 years

Association between polymorphisms of endothelial nitric oxide synthase gene (NOS3) and left posterior wall thickness (LPWT) of the heart in Fabry disease

Electrocardiographic signs of hypertrophy in Fabry disease-associated hypertrophic cardiomyopathy

Transcatheter closure of secundum atrial septal defects with the atrial septal defect occlusion system (ASDOS): initial experience in children

Effects of enzyme replacement therapy in Fabry disease—A comprehensive review of the medical literature

Cardio- Renal Outcomes With Long- Term Agalsidase Alfa Enzyme Replacement Therapy: A 10- Year Fabry Outcome Survey (FOS) Analysis

Cardiac manifestations of Anderson–Fabry disease in heterozygous females

Acute aortic dissection after balloon angioplasty of a recoarctation and treatment by stenting and distal membrane fenestration in a child

Anderson–Fabry disease: Clinical manifestations of disease in female heterozygotes

The effect of idursulfase on growth in patients with Hunter syndrome: Data from the Hunter Outcome Survey (HOS)

Modified hemi-Fontan operation and subsequent nonsurgical Fontan completion

Complete atrioventricular septal defect associated with tetralogy of Fallot. Favourable outcome of transatrial transpulmonary repair

The heart in Anderson Fabry disease

Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome Survey

Low-energy epicardial pacing in children: the benefit of autocapture

Fabry disease: focus on cardiac manifestations and molecular mechanisms

Reduced inotropic support after aprotinin therapy during pediatric cardiac operations

Biodegradation of tungsten embolisation coils used in children

Sense and nonsense of exposure prophylaxis in communal club installations for children and adolescents -- a contribution to the implementation of the German Defence Against Infection law from a point of view of preventive paediatrics

Clinical performance of the native pulmonary valve in the systemic circulation

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