A citation-based method for searching scientific literature

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



Rianne van Vliet, Guido Breedveld, Johanneke de Rijk-van Andel, Eva Brilstra, Nienke Verbeek, Corien Verschuuren-Bemelmans, Maartje Boon, Johnny Samijn, Karin Diderich, Ingrid van de Laar, Ben Oostra, Vincenzo Bonifati, Anneke Maat-Kievit. Neurology 2012
Times Cited: 54




List of shared articles



Times cited

Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China.
Li Cao, Xiaojun Huang, Ning Wang, Zhiying Wu, Cheng Zhang, Weihong Gu, Shuyan Cong, Jianhua Ma, Ling Wei, Yanchun Deng,[...]. Transl Neurodegener 2021
0

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

Novel PRRT2 gene variants identified in paroxysmal kinesigenic dyskinesia and benign familial infantile epilepsy in Chinese families.
Jialinzi He, Haiyun Tang, Chaorong Liu, Langzi Tan, Wenbiao Xiao, Bo Xiao, Hongyu Long, Lili Long. Exp Ther Med 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

The Genotype and Phenotype of Proline-Rich Transmembrane Protein 2 Associated Disorders in Chinese Children.
Han-Yu Luo, Ling-Ling Xie, Si-Qi Hong, Xiu-Juan Li, Mei Li, Yue Hu, Jian-Nan Ma, Peng Wu, Min Zhong, Min Cheng,[...]. Front Pediatr 2021
0

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

Functional study and pathogenicity classification of PRRT2 missense variants in PRRT2-related disorders.
Shao-Yun Zhao, Li-Xi Li, Yu-Lan Chen, Yi-Jun Chen, Gong-Lu Liu, Hai-Lin Dong, Dian-Fu Chen, Hong-Fu Li, Zhi-Ying Wu. CNS Neurosci Ther 2020
4

The clinical and genetic spectrum in infants with (an) unprovoked cluster(s) of focal seizures.
Aalt van Roest, Anouk Van de Vel, Damien Lederer, Berten Ceulemans. Eur J Paediatr Neurol 2020
2

Clinical and Genetic Overview of Paroxysmal Movement Disorders and Episodic Ataxias.
Giacomo Garone, Alessandro Capuano, Lorena Travaglini, Federica Graziola, Fabrizia Stregapede, Ginevra Zanni, Federico Vigevano, Enrico Bertini, Francesco Nicita. Int J Mol Sci 2020
13

PRRT2-related phenotypes in patients with a 16p11.2 deletion.
Danique R M Vlaskamp, Petra M C Callenbach, Patrick Rump, Lucia A A Giannini, Eva H Brilstra, Trijnie Dijkhuizen, Yvonne J Vos, Anne-Marie F van der Kevie-Kersemaekers, Jeroen Knijnenburg, Nicole de Leeuw,[...]. Eur J Med Genet 2019
7

[An adult female with proline-rich transmembrane protein 2 related paroxysmal disorders manifesting paroxysmal kinesigenic choreoathetosis and epileptic seizures].
Yasuto Tanabe, Takumi Taira, Akihiro Shimotake, Takeshi Inoue, Tomonari Awaya, Takeo Kato, Akira Kuzuya, Akio Ikeda, Ryosuke Takahashi. Rinsho Shinkeigaku 2019
2

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

PRRT2 mutations in Japanese patients with benign infantile epilepsy and paroxysmal kinesigenic dyskinesia.
Akihisa Okumura, Keiko Shimojima, Hirokazu Kurahashi, Shingo Numoto, Shino Shimada, Atsushi Ishii, Iori Ohmori, Satoru Takahashi, Tomonari Awaya, Tetsuo Kubota,[...]. Seizure 2019
8

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

Inherited and Acquired Choreas.
Claudio M de Gusmao, Jeff L Waugh. Semin Pediatr Neurol 2018
5