P.F. Ippel

Spinocerebellar ataxias in the Netherlands

Bart P.C. van de Warrenburg, Richard J. Sinke, Corien C. Verschuuren‐Bemelmans et al. · Neurology · 2002 · 254 citations · Full text

Life Sciences, Genetics, Neurology +17

Cardiac involvement in carriers of Duchenne and Becker muscular dystrophy

Edo M Hoogerwaard, Poll A. van der Wouw, Arthur A.M. Wilde et al. · Neuromuscular Disorders · 1999 · 181 citations

Medicine, Cardiology, Cardiovascular Genetics +13

WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations

Katrin Friedrich, Lin Lee, Dru F. Leistritz et al. · Human Genetics · 2010 · 101 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

S. M. Schade van Westrum, Edo M Hoogerwaard, Lukas Dekker et al. · Neurology · 2011 · 70 citations

Medicine, Cardiology, Clinical Sciences +15

Clinical and genetic analysis of a four-generation family with a distinct autosomal dominant cerebellar ataxia

Helenius J. Schelhaas, P.F. Ippel, G. Hageman et al. · Journal of Neurology · 2001 · 64 citations

Life Sciences, Genetics, Molecular Genetics +13