A citation-based method for searching scientific literature

Darius Ebrahimi-Fakhari, Afshin Saffari, Ana Westenberger, Christine Klein. Brain 2015
Times Cited: 130



Alice R Gardiner, Kailash P Bhatia, Maria Stamelou, Russell C Dale, Manju A Kurian, Susanne A Schneider, G M Wali, Tim Counihan, Anthony H Schapira, Sian D Spacey, Enza-Maria Valente, Laura Silveira-Moriyama, Hélio A G Teive, Salmo Raskin, Josemir W Sander, Andrew Lees, Tom Warner, Dimitri M Kullmann, Nicholas W Wood, Michael Hanna, Henry Houlden. Neurology 2012
Times Cited: 111




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 Genetic Movement Disorders and Epilepsy.
Claudio M de Gusmão, Lucas Garcia, Mohamad A Mikati, Samantha Su, Laura Silveira-Moriyama. Front Neurol 2021
2

Age-dependent neurological phenotypes in a mouse model of PRRT2-related diseases.
Fay Aj, McMahon T, Im C, Bair-Marshall C, Niesner Kj, Li H, Nelson A, Voglmaier Sm, Fu Y-H, Ptáček Lj. Neurogenetics 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



Treatment of Paroxysmal Dyskinesia.
Anna Latorre, Kailash P Bhatia. Neurol Clin 2020
8


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

Paroxysmal and cognitive phenotypes in Prrt2 mutant mice.
Louise Robertson, Travis Featherby, Stuart Howell, James Hughes, Paul Thomas. Genes Brain Behav 2019
2

Current therapies and therapeutic decision making for childhood-onset movement disorders.
Shekeeb S Mohammad, Simon P Paget, Russell C Dale. Mov Disord 2019
6

PRRT2 missense mutations cluster near C-terminus and frequently lead to protein mislocalization.
Meng-Han Tsai, Fang-Shin Nian, Mei-Hsin Hsu, Wei-Szu Liu, Yo-Tsen Liu, Chen Liu, Po-Hsi Lin, Daw-Yang Hwang, Yao-Chung Chuang, Jin-Wu Tsai. Epilepsia 2019
6

Paroxysmal movement disorders - practical update on diagnosis and management.
Claudio M De Gusmao, Laura Silveira-Moriyama. Expert Rev Neurother 2019
5


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