R.R. Frants

Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 p16Leiden

Hans F. A. Vasen, Nelleke A. Gruis, R.R. Frants et al. · International Journal of Cancer · 2000 · 311 citations

Life Sciences, Genetics, Oncology +17

CDKN2 explains part of the clinical phenotype in Dutch familial atypical multiple-mole melanoma (FAMMM) syndrome families

Nelleke A. Gruis, Lodewijk A. Sandkuijl, Pieter A. van der Velden et al. · Melanoma Research · 1995 · 112 citations

Life Sciences, Genetics, Molecular Genetics +17

First Mutation in the Voltage-Gated Na _v 1.1 Subunit Gene <i>SCN1A</i> with Co-Occurring Familial Hemiplegic Migraine and Epilepsy

M‐J Castro, AH Stam, Carolina Lemos et al. · Cephalalgia · 2008 · 90 citations · Full text

Life Sciences, Genetics, Neurology +17

Familial Hemiplegic Migraine: A Clinical Comparison of Families Linked and Unlinked to Chromosome 19

GM Terwindt, R.A. Ophoff, J. Haan et al. · Cephalalgia · 1996 · 74 citations

Life Sciences, Genetics, Neurology +13

Is Familial Hemiplegic Migraine a Hereditary form of Basilar Migraine?

J. Haan, GM Terwindt, RA Ophoff et al. · Cephalalgia · 1995 · 71 citations

Life Sciences, Neurology, Neuroscience +16