A citation-based method for searching scientific literature

Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
Times Cited: 128



Florence Riant, Emmanuel Roze, Cecile Barbance, Aurélie Méneret, Lucie Guyant-Maréchal, Christian Lucas, Pascal Sabouraud, Agnes Trébuchon, Christel Depienne, Elisabeth Tournier-Lasserve. Neurology 2012
Times Cited: 76




List of shared articles



Times cited

The Spectrum of PRRT2-Associated Disorders: Update on Clinical Features and Pathophysiology.
Annamaria Landolfi, Paolo Barone, Roberto Erro. Front Neurol 2021
0

Paroxysmal Movement Disorders.
Susan Harvey, Mary D King, Kathleen M Gorman. Front Neurol 2021
0

PRRT2 variants and effectiveness of various antiepileptic drugs in self-limited familial infantile epilepsy.
Qianlei Zhao, Ying Hu, Zhenwei Liu, Shiyu Fang, Feixia Zheng, Xiaoyu Wang, Feng Li, Xiucui Li, Zhongdong Lin. Seizure 2021
0

Genetics of migraine.
A Ducros. Rev Neurol (Paris) 2021
1

Familial hemiplegic migraine with a PRRT2 mutation: Phenotypic variations and carbamazepine efficacy.
Sato Suzuki-Muromoto, Rika Kosaki, Kenjiro Kosaki, Masaya Kubota. Brain Dev 2020
6

Diagnostic and therapeutic aspects of hemiplegic migraine.
Vincenzo Di Stefano, Marianna Gabriella Rispoli, Noemi Pellegrino, Alessandro Graziosi, Eleonora Rotondo, Christian Napoli, Daniela Pietrobon, Filippo Brighina, Pasquale Parisi. J Neurol Neurosurg Psychiatry 2020
20

Clinical spectrum and genotype-phenotype correlations in PRRT2 Italian patients.
Ganna Balagura, Antonella Riva, Francesca Marchese, Michele Iacomino, Francesca Madia, Thea Giacomini, Maria Margherita Mancardi, Elisabetta Amadori, Maria Stella Vari, Vincenzo Salpietro,[...]. Eur J Paediatr Neurol 2020
4

Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants.
Heidi G Sutherland, Neven Maksemous, Cassie L Albury, Omar Ibrahim, Robert A Smith, Rod A Lea, Larisa M Haupt, Bronwyn Jenkins, Benjamin Tsang, Lyn R Griffiths. Cells 2020
3

The Phenotypic Spectrum of PRRT2-Associated Paroxysmal Neurologic Disorders in Childhood.
Jan Henje Döring, Afshin Saffari, Thomas Bast, Knut Brockmann, Laura Ehrhardt, Walid Fazeli, Wibke G Janzarik, Gerhard Kluger, Hiltrud Muhle, Rikke S Møller,[...]. Biomedicines 2020
5

Advances in genetics of migraine.
Heidi G Sutherland, Cassie L Albury, Lyn R Griffiths. J Headache Pain 2019
38


Clinical spectrum of hemiplegic migraine and chances of finding a pathogenic mutation.
Nadine Pelzer, Joost Haan, Anine H Stam, Lisanne S Vijfhuizen, Stephany C Koelewijn, Amber Smagge, Boukje de Vries, Michel D Ferrari, Arn M J M van den Maagdenberg, Gisela M Terwindt. Neurology 2018
27