A citation-based method for searching scientific literature

Valentina Pelliccia, Silvia Ferranti, Rosa Mostardini, Salvatore Grosso. Neurol Sci 2020
Times Cited: 1







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



Times Cited
  Times     Co-cited
Similarity


Progressive GAA expansions in dorsal root ganglia of Friedreich's ataxia patients.
Irene De Biase, Astrid Rasmussen, Dan Endres, Sahar Al-Mahdawi, Antonella Monticelli, Sergio Cocozza, Mark Pook, Sanjay I Bidichandani. Ann Neurol 2007
74
100

G130V, a common FRDA point mutation, appears to have arisen from a common founder.
M B Delatycki, M Knight, M Koenig, M Cossée, R Williamson, S M Forrest. Hum Genet 1999
27
100

15-White Dots APP-Coo-Test: a reliable touch-screen application for assessing upper limb movement impairment in patients with cerebellar ataxias.
Giuseppe Arcuria, Christian Marcotulli, Claudio Galasso, Francesco Pierelli, Carlo Casali. J Neurol 2019
4
100

Friedreich's ataxia: point mutations and clinical presentation of compound heterozygotes.
M Cossée, A Dürr, M Schmitt, N Dahl, P Trouillas, P Allinson, M Kostrzewa, A Nivelon-Chevallier, K H Gustavson, A Kohlschütter,[...]. Ann Neurol 1999
244
100

Mapping of the second Friedreich's ataxia (FRDA2) locus to chromosome 9p23-p11: evidence for further locus heterogeneity.
K Christodoulou, F Deymeer, P Serdaroğlu, C Ozdemir, M Poda, D M Georgiou, P Ioannou, M Tsingis, E Zamba, L T Middleton. Neurogenetics 2001
22
100

Monitoring progression in Friedreich ataxia (FRDA): the use of clinical scales.
Katrin Bürk, Stefanie R Schulz, Jörg B Schulz. J Neurochem 2013
34
100

A wearable proprioceptive stabilizer for rehabilitation of limb and gait ataxia in hereditary cerebellar ataxias: a pilot open-labeled study.
Luca Leonardi, Maria Gabriella Aceto, Christian Marcotulli, Giuseppe Arcuria, Mariano Serrao, Francesco Pierelli, Paolo Paone, Alessandro Filla, Alessandro Roca, Carlo Casali. Neurol Sci 2017
15
100

Interpreting change scores of tests and measures used in physical therapy.
Stephen M Haley, Maria A Fragala-Pinkham. Phys Ther 2006
424
100



Gait pattern in inherited cerebellar ataxias.
Mariano Serrao, Francesco Pierelli, Alberto Ranavolo, Francesco Draicchio, Carmela Conte, Romildo Don, Roberto Di Fabio, Margherita LeRose, Luca Padua, Giorgio Sandrini,[...]. Cerebellum 2012
76
100

Adult norms for a commercially available Nine Hole Peg Test for finger dexterity.
Kimatha Oxford Grice, Kimberly A Vogel, Viet Le, Ana Mitchell, Sonia Muniz, Mary Ann Vollmer. Am J Occup Ther 2003
296
100

Radial diffusivity in the cerebellar peduncles correlates with clinical severity in Friedreich ataxia.
Christian Clemm von Hohenberg, Michael F Schocke, Marlene C Wigand, Wolfgang Nachbauer, Charles R G Guttmann, Marek Kubicki, Martha E Shenton, Sylvia Boesch, Karl Egger. Neurol Sci 2013
24
100

Friedreich ataxia: molecular mechanisms, redox considerations, and therapeutic opportunities.
Renata Santos, Sophie Lefevre, Dominika Sliwa, Alexandra Seguin, Jean-Michel Camadro, Emmanuel Lesuisse. Antioxid Redox Signal 2010
117
100

Friedreich's ataxia: clinical heterogeneity in two sisters.
M Armani, M Zortea, E Pastorello, S Lombardi, S Tonello, L Zuliani, M T Rigoni, C P Trevisan. Neurol Sci 2006
2
100

SCA Functional Index: a useful compound performance measure for spinocerebellar ataxia.
T Schmitz-Hübsch, P Giunti, D A Stephenson, C Globas, L Baliko, F Saccà, C Mariotti, M Rakowicz, S Szymanski, J Infante,[...]. Neurology 2008
79
100


Comparison of three clinical rating scales in Friedreich ataxia (FRDA).
Katrin Bürk, Ulrike Mälzig, Stefanie Wolf, Suzette Heck, Konstantinos Dimitriadis, Tanja Schmitz-Hübsch, Sascha Hering, Tobias M Lindig, Verena Haug, Dagmar Timmann,[...]. Mov Disord 2009
83
100


Clinical and genetic study of Friedreich ataxia in an Australian population.
M B Delatycki, D B Paris, R J Gardner, G A Nicholson, N Nassif, E Storey, J C MacMillan, V Collins, R Williamson, S M Forrest. Am J Med Genet 1999
94
100

Deferiprone in Friedreich ataxia: a 6-month randomized controlled trial.
Massimo Pandolfo, Javier Arpa, Martin B Delatycki, Kim Hanh Le Quan Sang, Caterina Mariotti, Arnold Munnich, Irene Sanz-Gallego, Geneieve Tai, Mark A Tarnopolsky, Franco Taroni,[...]. Ann Neurol 2014
68
100

Friedreich ataxia in carriers of unstable borderline GAA triplet-repeat alleles.
Rajesh Sharma, Irene De Biase, Mariluz Gómez, Martin B Delatycki, Tetsuo Ashizawa, Sanjay I Bidichandani. Ann Neurol 2004
32
100

Scale for the assessment and rating of ataxia: development of a new clinical scale.
T Schmitz-Hübsch, S Tezenas du Montcel, L Baliko, J Berciano, S Boesch, C Depondt, P Giunti, C Globas, J Infante, J-S Kang,[...]. Neurology 2006
907
100

GIFT-1, a phase IIa clinical trial to test the safety and efficacy of IFNγ administration in FRDA patients.
Christian Marcotulli, Silvia Fortuni, Gaetano Arcuri, Barbara Tomassini, Luca Leonardi, Francesco Pierelli, Roberto Testi, Carlo Casali. Neurol Sci 2016
11
100

How does performance of the Friedreich Ataxia Functional Composite compare to rating scales?
Geneieve Tai, Eppie M Yiu, Martin B Delatycki, Louise A Corben. J Neurol 2017
7
100

The multiple sclerosis functional composite: different practice effects in the three test components.
Alessandra Solari, Davide Radice, Letizia Manneschi, Luisa Motti, Enrico Montanari. J Neurol Sci 2005
74
100

Somatic instability of the expanded GAA repeats in Friedreich's ataxia.
Ashlee Long, Jill S Napierala, Urszula Polak, Lauren Hauser, Arnulf H Koeppen, David R Lynch, Marek Napierala. PLoS One 2017
26
100

A comparison of three measures of upper limb function in Friedreich ataxia.
L A Corben, G Tai, C Wilson, V Collins, A J Churchyard, M B Delatycki. J Neurol 2010
19
100

The GAA triplet-repeat sequence in Friedreich ataxia shows a high level of somatic instability in vivo, with a significant predilection for large contractions.
Rajesh Sharma, Saeeda Bhatti, Mariluz Gomez, Rhonda M Clark, Cynthia Murray, Tetsuo Ashizawa, Sanjay I Bidichandani. Hum Mol Genet 2002
51
100

Association between trinucleotide CAG repeats of the DNA polymerase gene (POLG) with age of onset of Iranian Friedreich's ataxia patients.
Mohammad Mehdi Heidari, Massoud Houshmand, Saman Hosseinkhani, Shahriar Nafissi, Barbara Scheiber-Mojdehkar, Mehri Khatami. Neurol Sci 2008
7
100

Ataxia rating scales--psychometric profiles, natural history and their application in clinical trials.
Jonas Alex Morales Saute, Karina Carvalho Donis, Carmen Serrano-Munuera, David Genis, Luís Torres Ramirez, Pilar Mazzetti, Luis Velázquez Pérez, Pilar Latorre, Jorge Sequeiros, Antoni Matilla-Dueñas,[...]. Cerebellum 2012
71
100

Long-term effect of epoetin alfa on clinical and biochemical markers in friedreich ataxia.
Francesco Saccà, Giorgia Puorro, Angela Marsili, Antonella Antenora, Chiara Pane, Carlo Casali, Christian Marcotulli, Giovanni Defazio, Daniele Liuzzi, Chiara Tatillo,[...]. Mov Disord 2016
17
100

The relationship between trinucleotide (GAA) repeat length and clinical features in Friedreich ataxia.
A Filla, G De Michele, F Cavalcanti, L Pianese, A Monticelli, G Campanella, S Cocozza. Am J Hum Genet 1996
376
100

Clinical features of Friedreich's ataxia: classical and atypical phenotypes.
Michael H Parkinson, Sylvia Boesch, Wolfgang Nachbauer, Caterina Mariotti, Paola Giunti. J Neurochem 2013
115
100

Autosomal recessive ataxias: 20 types, and counting.
Emília Katiane Embiruçu, Marcília Lima Martyn, David Schlesinger, Fernando Kok. Arq Neuropsiquiatr 2009
24
100

Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion.
V Campuzano, L Montermini, M D Moltò, L Pianese, M Cossée, F Cavalcanti, E Monros, F Rodius, F Duclos, A Monticelli,[...]. Science 1996
100

Responsiveness of different rating instruments in spinocerebellar ataxia patients.
T Schmitz-Hübsch, R Fimmers, M Rakowicz, R Rola, E Zdzienicka, R Fancellu, C Mariotti, C Linnemann, L Schöls, D Timmann,[...]. Neurology 2010
89
100

Open-label pilot study of oral methylprednisolone for the treatment of patients with friedreich ataxia.
Maya Patel, Kimberly Schadt, Ashley McCormick, Charles Isaacs, Yi Na Dong, David R Lynch. Muscle Nerve 2019
3
100

Absence of aprataxin gene mutations in a Greek cohort with sporadic early onset ataxia and normal GAA triplets in frataxin gene.
C Daiou, K Christodoulou, G Xiromerisiou, M Panas, E Dardiotis, A Kladi, M Speletas, G Ntaios, A Papadimitriou, A Germenis,[...]. Neurol Sci 2010
4
100

Oxidative stress and protease dysfunction in the yeast model of Friedreich ataxia.
Anne-Laure Bulteau, Andrew Dancis, Monique Gareil, Jean-Jacques Montagne, Jean-Michel Camadro, Emmanuel Lesuisse. Free Radic Biol Med 2007
69
100

Composite cerebellar functional severity score: validation of a quantitative score of cerebellar impairment.
Sophie Tezenas du Montcel, Perrine Charles, Pascale Ribai, Cyril Goizet, Alice Le Bayon, Pierre Labauge, Lucie Guyant-Maréchal, Sylvie Forlani, Celine Jauffret, Nadia Vandenberghe,[...]. Brain 2008
55
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.