A citation-based method for searching scientific literature

Paola Giunti, Elide Mantuano, Marina Frontali. Int J Mol Sci 2020
Times Cited: 1







List of co-cited articles
articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


CaV2.1 channelopathies.
Daniela Pietrobon. Pflugers Arch 2010
134
100

Episodic ataxia and channelopathies.
N Gordon. Brain Dev 1998
28
100

Variable K(+) channel subunit dysfunction in inherited mutations of KCNA1.
Ruth Rea, Alexander Spauschus, Louise H Eunson, Michael G Hanna, Dimitri M Kullmann. J Physiol 2002
48
100

Clinical spectrum of episodic ataxia type 2.
J Jen, G W Kim, R W Baloh. Neurology 2004
175
100


Loss-of-function EA2 mutations are associated with impaired neuromuscular transmission.
J Jen, J Wan, M Graves, H Yu, A F Mock, C J Coulin, G Kim, Q Yue, D M Papazian, R W Baloh. Neurology 2001
98
100

Episodic ataxia type-1 mutations in the Kv1.1 potassium channel display distinct folding and intracellular trafficking properties.
L N Manganas, S Akhtar, D E Antonucci, C R Campomanes, J O Dolly, J S Trimmer. J Biol Chem 2001
51
100

Ultrastructural localization of Shaker-related potassium channel subunits and synapse-associated protein 90 to septate-like junctions in rat cerebellar Pinceaux.
G Laube, J Röper, J C Pitt, S Sewing, U Kistner, C C Garner, O Pongs, R W Veh. Brain Res Mol Brain Res 1996
103
100



A wide spectrum of clinical, neurophysiological and neuroradiological abnormalities in a family with a novel CACNA1A mutation.
Romina Romaniello, Claudio Zucca, Alessandra Tonelli, Sara Bonato, Cinzia Baschirotto, Nicoletta Zanotta, Roberta Epifanio, Andrea Righini, Nereo Bresolin, Maria T Bassi,[...]. J Neurol Neurosurg Psychiatry 2010
34
100

High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2.
C Denier, A Ducros, K Vahedi, A Joutel, P Thierry, A Ritz, G Castelnovo, T Deonna, P Gérard, J L Devoize,[...]. Neurology 1999
144
100

Clinical neurophysiology of the episodic ataxias: insights into ion channel dysfunction in vivo.
Susan E Tomlinson, Michael G Hanna, Dimitri M Kullmann, S Veronica Tan, David Burke. Clin Neurophysiol 2009
27
100

FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9.
Julie Piarroux, Florence Riant, Véronique Humbertclaude, Ganaelle Remerand, Jessica Hadjadj, Franck Rejou, Christine Coubes, Lucile Pinson, Pierre Meyer, Agathe Roubertie. Ann Clin Transl Neurol 2020
12
100

A novel KCNA1 mutation identified in an Italian family affected by episodic ataxia type 1.
P Imbrici, F Gualandi, M C D'Adamo, M Taddei Masieri, P Cudia, D De Grandis, R Mannucci, I Nicoletti, S J Tucker, A Ferlini,[...]. Neuroscience 2008
29
100

Kv1.1 knock-in ataxic mice exhibit spontaneous myokymic activity exacerbated by fatigue, ischemia and low temperature.
Orazio Brunetti, Paola Imbrici, Fabio Massimo Botti, Vito Enrico Pettorossi, Maria Cristina D'Adamo, Mario Valentino, Christian Zammit, Marina Mora, Sara Gibertini, Giuseppe Di Giovanni,[...]. Neurobiol Dis 2012
26
100


Clinical manifestations of episodic ataxia type 5.
Miguel González Sánchez, Silvia Izquierdo, Sara Álvarez, Rosa Eva Bautista Alonso, José Berciano, José Gazulla. Neurol Clin Pract 2019
2
100


Reduced ACh release at neuromuscular synapses of heterozygous leaner Ca(v)2.1-mutant mice.
Simon Kaja, Rob C G Van De Ven, Rune R Frants, Michel D Ferrari, Arn M J M Van Den Maagdenberg, Jaap J Plomp. Synapse 2008
10
100

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.
J L Steckley, G C Ebers, M Z Cader, R S McLachlan. Neurology 2001
47
100

Therapy of episodic ataxias: case report and review of the literature.
Daniele Orsucci, Laura Maria Raglione, Monica Mazzoni, Marco Vista. Drugs Context 2019
4
100

7
100

A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions.
Paola Imbrici, Concetta Altamura, Francesca Gualandi, Giuseppe Felice Mangiatordi, Marcella Neri, Giovanni De Maria, Alessandra Ferlini, Alessandro Padovani, Maria Cristina D'Adamo, Orazio Nicolotti,[...]. Mol Cell Neurosci 2017
13
100


Novel mutation in KCNA1 causes episodic ataxia with paroxysmal dyspnea.
Steven J Shook, Hafsa Mamsa, Joanna C Jen, Robert W Baloh, Lan Zhou. Muscle Nerve 2008
25
100


Expanding the phenotype of potassium channelopathy: severe neuromyotonia and skeletal deformities without prominent Episodic Ataxia.
M Kinali, H Jungbluth, L H Eunson, C A Sewry, A Y Manzur, E Mercuri, M G Hanna, F Muntoni. Neuromuscul Disord 2004
41
100

Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons.
H Wang, D D Kunkel, T M Martin, P A Schwartzkroin, B L Tempel. Nature 1993
520
100

Axonal ion channels from bench to bedside: a translational neuroscience perspective.
Arun V Krishnan, Cindy S-Y Lin, Susanna B Park, Matthew C Kiernan. Prog Neurobiol 2009
127
100

The neuronal channelopathies.
Dimitri M Kullmann. Brain 2002
99
100

Kcna1-mutant rats dominantly display myokymia, neuromyotonia and spontaneous epileptic seizures.
Saeko Ishida, Yu Sakamoto, Takeshi Nishio, Stéphanie Baulac, Mitsuru Kuwamura, Yukihiro Ohno, Akiko Takizawa, Shuji Kaneko, Tadao Serikawa, Tomoji Mashimo. Brain Res 2012
26
100

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability.
L H Eunson, R Rea, S M Zuberi, S Youroukos, C P Panayiotopoulos, R Liguori, P Avoni, R C McWilliam, J B Stephenson, M G Hanna,[...]. Ann Neurol 2000
169
100


Episodic ataxia type 2 showing ictal hyperhidrosis with hypothermia and interictal chronic diarrhea due to a novel CACNA1A mutation.
D I Zafeiriou, F Lehmann-Horn, E Vargiami, E Teflioudi, A Ververi, K Jurkat-Rott. Eur J Paediatr Neurol 2009
11
100

Kv1.1 Channelopathies: Pathophysiological Mechanisms and Therapeutic Approaches.
Maria Cristina D'Adamo, Antonella Liantonio, Jean-Francois Rolland, Mauro Pessia, Paola Imbrici. Int J Mol Sci 2020
11
100

A novel de novo pathogenic mutation in the CACNA1A gene.
Shinsuke Fujioka, Sruti Rayaprolu, Christina Sundal, Daniel F Broderick, William A Langley, John Shoffner, Lauren C Hyams, Rosa Rademakers, Neill R Graff-Radford, William Tatum,[...]. Mov Disord 2012
2
100

A novel mutation in CACNA1A gene in a Saudi female with episodic ataxia type 2 with no response to acetazolamide or 4-aminopyridine.
Hussein Algahtani, Bader Shirah, Raghad Algahtani, Mohammad H Al-Qahtani, Angham Abdulrahman Abdulkareem, Muhammad Imran Naseer. Intractable Rare Dis Res 2019
3
100

In vivo impact of presynaptic calcium channel dysfunction on motor axons in episodic ataxia type 2.
Susan E Tomlinson, S Veronica Tan, David Burke, Robyn W Labrum, Andrea Haworth, Vaneesha S Gibbons, Mary G Sweeney, Robert C Griggs, Dimitri M Kullmann, Hugh Bostock,[...]. Brain 2016
8
100

Recent progress on the molecular organization of myelinated axons.
Steven S Scherer, Edgardo J Arroyo. J Peripher Nerv Syst 2002
118
100

A mouse model of episodic ataxia type-1.
Paco S Herson, Michael Virk, Nathan R Rustay, Chris T Bond, John C Crabbe, John P Adelman, James Maylie. Nat Neurosci 2003
98
100

Kv1.1 deletion augments the afferent hypoxic chemosensory pathway and respiration.
David D Kline, Maria C F Buniel, Patricia Glazebrook, Ying-Jie Peng, Angelina Ramirez-Navarro, Nanduri R Prabhakar, Diana L Kunze. J Neurosci 2005
27
100


Episodic ataxia type 1 without episodic ataxia: the diagnostic utility of nerve excitability studies in individuals with KCNA1 mutations.
S Veronica Tan, Elizabeth Wraige, Karine Lascelles, Hugh Bostock. Dev Med Child Neurol 2013
9
100

The neurological update: therapies for cerebellar ataxias in 2020.
J Gandini, Mario Manto, T Bremova-Ertl, K Feil, M Strupp. J Neurol 2020
8
100



Zebrafish as a Model System for the Study of Severe CaV2.1 (α1A) Channelopathies.
Sidharth Tyagi, Angeles B Ribera, Roger A Bannister. Front Mol Neurosci 2020
4
100

Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2.
R A Maselli, J Wan, V Dunne, M Graves, R W Baloh, R L Wollmann, J Jen. Neurology 2003
30
100

Characterization of the Kv1.1 I262T and S342I mutations associated with episodic ataxia 1 with distinct phenotypes.
Jing Zhu, Rami Alsaber, Jian Zhao, Eugenia Ribeiro-Hurley, William B Thornhill. Arch Biochem Biophys 2012
15
100


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.