A citation-based method for searching scientific literature

O Zhuchenko, J Bailey, P Bonnen, T Ashizawa, D W Stockton, C Amos, W B Dobyns, S H Subramony, H Y Zoghbi, C C Lee. Nat Genet 1997
Times Cited: 978



J Jen, G W Kim, R W Baloh. Neurology 2004
Times Cited: 150




List of shared articles



Times cited

The electrophysiological footprint of CACNA1A disorders.
Elisabetta Indelicato, Iris Unterberger, Wolfgang Nachbauer, Andreas Eigentler, Matthias Amprosi, Fiona Zeiner, Edda Haberlandt, Manuela Kaml, Elke Gizewski, Sylvia Boesch. J Neurol 2021
2

Paroxysmal Genetic Movement Disorders and Epilepsy.
Claudio M de Gusmão, Lucas Garcia, Mohamad A Mikati, Samantha Su, Laura Silveira-Moriyama. Front Neurol 2021
0


Targeting Alternative Splicing as a Potential Therapy for Episodic Ataxia Type 2.
Fanny Jaudon, Simona Baldassari, Ilaria Musante, Agnes Thalhammer, Federico Zara, Lorenzo A Cingolani. Biomedicines 2020
1

Two distinct phenotypes, hemiplegic migraine and episodic Ataxia type 2, caused by a novel common CACNA1A variant.
Rosaria Nardello, Giorgia Plicato, Giuseppe Donato Mangano, Elena Gennaro, Salvatore Mangano, Filippo Brighina, Vincenzo Raieli, Antonina Fontana. BMC Neurol 2020
3

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
8

Spinocerebellar ataxia: an update.
Roisin Sullivan, Wai Yan Yau, Emer O'Connor, Henry Houlden. J Neurol 2019
33

Advances in genetics of migraine.
Heidi G Sutherland, Cassie L Albury, Lyn R Griffiths. J Headache Pain 2019
23

The neuropsychiatric phenotype in CACNA1A mutations: a retrospective single center study and review of the literature.
E Indelicato, W Nachbauer, E Karner, A Eigentler, M Wagner, I Unterberger, W Poewe, M Delazer, S Boesch. Eur J Neurol 2019
12

Paroxysmal movement disorders - practical update on diagnosis and management.
Claudio M De Gusmao, Laura Silveira-Moriyama. Expert Rev Neurother 2019
3

Episodic ataxias.
Joanna C Jen, Jijun Wan. Handb Clin Neurol 2018
3

Novel missense variant of CACNA1A gene in a Slovak family with episodic ataxia type 2.
Andrea Petrovicova, Miroslav Brozman, Egon Kurca, Tibor Gobo, Jana Dluha, Klaudia Kalmarova, Vladimir Nosal, Martina Hikkelova, Adriana Krajciova, Tatiana Burjanivova,[...]. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub 2017
5