Christiaan S. van Woerden

Primary hyperoxaluria Type 1: indications for screening and guidance for diagnosis and treatment

Pierre Cochat, Sally A. Hulton, Cécile Acquaviva et al. · Nephrology Dialysis Transplantation · 2012 · 330 citations · Full text

Primary hyperoxaluria type 1 in The Netherlands: prevalence and outcome

Christiaan S. van Woerden · Nephrology Dialysis Transplantation · 2003 · 178 citations · Full text

Clinical implications of mutation analysis in primary hyperoxaluria type 1

Christiaan S. van Woerden, Jaap W. Groothoff, Frits A. Wijburg et al. · Kidney International · 2004 · 131 citations · Full text

Primary Hyperoxaluria, Genetic Disorder, Genetics +5

Data from a large European study indicate that the outcome of primary hyperoxaluria type 1 correlates with the AGXT mutation type

Giorgia Mandrile, Christiaan S. van Woerden, Paola Berchialla et al. · Kidney International · 2014 · 130 citations · Full text

Large European Study, Allelic Variant, Primary Hyperoxaluria +13

Carrier frequency of the V377I (1129G>A) MVK mutation, associated with Hyper-IgD and periodic fever syndrome, in the Netherlands

Sander M. Houten, Christiaan S. van Woerden, Frits A. Wijburg et al. · European Journal of Human Genetics · 2003 · 99 citations · Full text

Carrier Frequency, Periodic Fever Syndrome, Autoimmune Disease +12