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The Journal of Headache and Pain|December 30, 2017
Experts' opinion about the primary headache diagnostic criteria of the ICHD-3rd edition beta in children and adolescentsAynur Özge, Noemi Faedda, Ishaq Abu-Arafeh, et al.Movement Disorders : Official Journal of the Movement Disorder Society|October 18, 2006
New syndromic form of benign hereditary chorea is associated with a deletion of TITF-1 and PAX-9 contiguous genesDavid Devos, Isabelle Vuillaume, Alix de Becdelievre, et al.American Journal of Medical Genetics. Part A|March 27, 2014
Further delineation of eye manifestations in homozygous 15q13.3 microdeletions including TRPM1: a differential diagnosis of ceroid lipofuscinosisAlice Masurel-Paulet, Isabelle Drumare, Muriel Holder, et al.Neurology|October 15, 2021
Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic StudyFlorence Riant, Caroline Roos, Agathe Roubertie, et al.Nature|September 2, 2011
Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locusSébastien Jacquemont, Alexandre Reymond, Flore Zufferey, et al.Pageof 3