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Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium

Clinical pharmacology and therapeutics, 2017-03, Vol.101 (3), p.341-358

2017

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Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey

European journal of clinical investigation, 2004-03, Vol.34 (3), p.236-242

2004

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Natural course of Fabry disease: changing pattern of causes of death in FOS – Fabry Outcome Survey

Journal of medical genetics, 2009-08, Vol.46 (8), p.548-552

2009

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Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data

The Lancet (British edition), 2009-12, Vol.374 (9706), p.1986-1996

2009

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Fabry disease: overall effects of agalsidase alfa treatment

European journal of clinical investigation, 2004-12, Vol.34 (12), p.838-844

2004

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Low‐Turnover Bone Disease in Hypercalcemic Hyperparathyroidism After Kidney Transplantation

American journal of transplantation, 2007-11, Vol.7 (11), p.2515-2521

2007

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Hearing loss in Fabry disease: data from the Fabry Outcome Survey

European journal of clinical investigation, 2006-09, Vol.36 (9), p.654-662

2006

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Agalsidase alpha and hearing in Fabry disease: data from the Fabry Outcome Survey

European journal of clinical investigation, 2006-09, Vol.36 (9), p.663-667

2006

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Clinical manifestations of Fabry disease in children : Data from the Fabry Outcome Survey

Acta pædiatrica (Oslo), 2006, Vol.95 (1), p.86-92

2006

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Classification of chronic kidney disease by estimated glomerular filtration rate

European journal of clinical investigation, 2008-04, Vol.38 (4), p.253-259

2008

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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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Intravenous iron therapy: well-tolerated, yet not harmless

European journal of clinical investigation, 2005-12, Vol.35 (s3), p.46-51

2005

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The expanding clinical spectrum of Anderson–Fabry disease: a challenge to diagnosis in the novel era of enzyme replacement therapy

Journal of internal medicine, 2004-06, Vol.255 (6), p.629-636

2004

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CORRIGENDUM: Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium

Clinical pharmacology and therapeutics, 2017-07, Vol.102 (1), p.152-152

2017

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Anaemia after renal transplantation

European journal of clinical investigation, 2005-12, Vol.35 (s3), p.89-94

2005

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Central venous catheter pinch-off and fracture: recognition, prevention and management

Bone marrow transplantation (Basingstoke), 2003-05, Vol.31 (10), p.927-930

2003

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P0871 : Real life experience with interferon/ribavirin-free antiviral treatment in renal transplant recipients and endstage renal disease-patients on dialysis infected with hepatitis C virus

Journal of hepatology, 2015-04, Vol.62, p.S667-S667

2015

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Thrombotic microangiopathy : Relevant new aspects for intensive care physicians

Medizinische Klinik, Intensivmedizin und Notfallmedizin, 2016-06, Vol.111 (5), p.434

2016

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An inosine 5′-monophosphate dehydrogenase 2 single-nucleotide polymorphism impairs the effect of mycophenolic acid

The pharmacogenomics journal, 2010-02, Vol.10 (1), p.70-76

2010

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High prevalence of subclinical hypothyroidism in patients with Anderson–Fabry disease

Journal of inherited metabolic disease, 2005-01, Vol.28 (5), p.715-722

2005

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Hormonal profile and fertility in patients with Anderson-Fabry disease

International journal of clinical practice (Esher), 2005-09, Vol.59 (9), p.1025-1028

2005

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Patterns of co-occurrence of three single nucleotide polymorphisms of the 5,10-methylenetetrahydrofolate reductase gene in kidney transplant recipients

European journal of clinical investigation, 2004-09, Vol.34 (9), p.613-618

2004

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Low clinical penetrance of homozygosity for HFE C282Y: implications for genetic testing?

European journal of clinical investigation, 2003-09, Vol.33 (9), p.737-739

2003

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Fabry outcome survey: need for documentation of dermatological, ophthalmologic and psychiatric affections: authors' reply

European journal of clinical investigation, 2004-07, Vol.34 (7), p.517-517

2004

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Granulocyte function in patients with L-ferritin iron-responsive element (IRE) 39C→T-positive hereditary hyperferritinaemia-cataract syndrome

European journal of clinical investigation, 2004-10, Vol.34 (10), p.701-708

2004

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Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium

Fabry disease defined: baseline clinical manifestations of 366 patients in the Fabry Outcome Survey

Natural course of Fabry disease: changing pattern of causes of death in FOS – Fabry Outcome Survey

Enzyme replacement therapy with agalsidase alfa in patients with Fabry's disease: an analysis of registry data

Fabry disease: overall effects of agalsidase alfa treatment

Low‐Turnover Bone Disease in Hypercalcemic Hyperparathyroidism After Kidney Transplantation

Hearing loss in Fabry disease: data from the Fabry Outcome Survey

Agalsidase alpha and hearing in Fabry disease: data from the Fabry Outcome Survey

Clinical manifestations of Fabry disease in children : Data from the Fabry Outcome Survey

Classification of chronic kidney disease by estimated glomerular filtration rate

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

Intravenous iron therapy: well-tolerated, yet not harmless

The expanding clinical spectrum of Anderson–Fabry disease: a challenge to diagnosis in the novel era of enzyme replacement therapy

CORRIGENDUM: Implementing Pharmacogenomics in Europe: Design and Implementation Strategy of the Ubiquitous Pharmacogenomics Consortium

Anaemia after renal transplantation

Central venous catheter pinch-off and fracture: recognition, prevention and management

P0871 : Real life experience with interferon/ribavirin-free antiviral treatment in renal transplant recipients and endstage renal disease-patients on dialysis infected with hepatitis C virus

Thrombotic microangiopathy : Relevant new aspects for intensive care physicians

An inosine 5′-monophosphate dehydrogenase 2 single-nucleotide polymorphism impairs the effect of mycophenolic acid

High prevalence of subclinical hypothyroidism in patients with Anderson–Fabry disease

Hormonal profile and fertility in patients with Anderson-Fabry disease

Patterns of co-occurrence of three single nucleotide polymorphisms of the 5,10-methylenetetrahydrofolate reductase gene in kidney transplant recipients

Low clinical penetrance of homozygosity for HFE C282Y: implications for genetic testing?

Fabry outcome survey: need for documentation of dermatological, ophthalmologic and psychiatric affections: authors' reply

Granulocyte function in patients with L-ferritin iron-responsive element (IRE) 39C→T-positive hereditary hyperferritinaemia-cataract syndrome

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