A citation-based method for searching scientific literature

B W Soong, R S Liu. J Neurol Neurosurg Psychiatry 1998
Times Cited: 39







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



Times Cited
  Times     Co-cited
Similarity


Autosomal dominant cerebellar ataxia type I. MRI-based volumetry of posterior fossa structures and basal ganglia in spinocerebellar ataxia types 1, 2 and 3.
T Klockgether, M Skalej, D Wedekind, A R Luft, D Welte, J B Schulz, M Abele, K Bürk, F Laccone, A Brice,[...]. Brain 1998
132
33

Characteristic magnetic resonance imaging findings in Machado-Joseph disease.
Y Murata, S Yamaguchi, H Kawakami, Y Imon, H Maruyama, T Sakai, T Kazuta, T Ohtake, M Nishimura, T Saida,[...]. Arch Neurol 1998
98
33

Dopamine transporter positron emission tomography in spinocerebellar ataxias type 1, 2, 3, and 6.
Ullrich Wüllner, Michael Reimold, Michael Abele, Katrin Bürk, Martina Minnerop, Bernd-Michael Dohmen, Hans-Juergen Machulla, Roland Bares, Thomas Klockgether. Arch Neurol 2005
70
33

Positron emission tomography (PET) in Machado-Joseph disease.
T Taniwaki, T Sakai, T Kobayashi, Y Kuwabara, M Otsuka, Y Ichiya, K Masuda, I Goto. J Neurol Sci 1997
43
30

CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.
Y Kawaguchi, T Okamoto, M Taniwaki, M Aizawa, M Inoue, S Katayama, H Kawakami, S Nakamura, M Nishimura, I Akiguchi. Nat Genet 1994
30


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
990
28


Brain single-photon emission computed tomography and magnetic resonance imaging in Machado-Joseph disease.
E C Etchebehere, F Cendes, I Lopes-Cendes, J A Pereira, M C Lima, C R Sansana, C A Silva, M F Camargo, A O Santos, C D Ramos,[...]. Arch Neurol 2001
35
28

Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis.
Ludger Schöls, Peter Bauer, Thorsten Schmidt, Thorsten Schulte, Olaf Riess. Lancet Neurol 2004
667
25

Metabolic characterization of spinocerebellar ataxia type 6.
B Soong , R Liu , L Wu , Y Lu , H Lee. Arch Neurol 2001
28
32

Visualization, quantification and correlation of brain atrophy with clinical symptoms in spinocerebellar ataxia types 1, 3 and 6.
Jörg B Schulz, Johannes Borkert, Stefanie Wolf, Tanja Schmitz-Hübsch, Maryla Rakowicz, Caterina Mariotti, Ludger Schöls, Dagmar Timmann, Bart van de Warrenburg, Alexandra Dürr,[...]. Neuroimage 2010
113
23

Biological and clinical characteristics of individuals at risk for spinocerebellar ataxia types 1, 2, 3, and 6 in the longitudinal RISCA study: analysis of baseline data.
Heike Jacobi, Kathrin Reetz, Sophie Tezenas du Montcel, Peter Bauer, Caterina Mariotti, Lorenzo Nanetti, Maria Rakowicz, Anna Sulek, Alexandra Durr, Perrine Charles,[...]. Lancet Neurol 2013
113
23

Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.
Kathrin Reetz, Ana S Costa, Shahram Mirzazade, Anna Lehmann, Agnes Juzek, Maria Rakowicz, Romana Boguslawska, Ludger Schöls, Christoph Linnemann, Caterina Mariotti,[...]. Brain 2013
86
23

Decreased dopamine transporter binding in Machado-Joseph disease.
T C Yen, C S Lu, K Y Tzen, S P Wey, Y H Chou, Y H Weng, P F Kao, G Ting. J Nucl Med 2000
51
20

Reduced striatal [123 I]FP-CIT binding in SCA2 patients without parkinsonism.
Andrea Varrone, Elena Salvatore, Giuseppe De Michele, Paolo Barone, Valeria Sansone, Maria Teresa Pellecchia, Imma Castaldo, Giovanni Coppola, Arturo Brunetti, Marco Salvatore,[...]. Ann Neurol 2004
48
20

PET and MRI reveal early evidence of neurodegeneration in spinocerebellar ataxia type 17.
Kathrin Brockmann, Matthias Reimold, Christoph Globas, Till Karsten Hauser, Uwe Walter, Hans-Jürgen Machulla, Arndt Rolfs, Ludger Schöls. J Nucl Med 2012
31
25

A multimodal evaluation of microstructural white matter damage in spinocerebellar ataxia type 3.
Rachel P Guimarães, Anelyssa D'Abreu, Clarissa L Yasuda, Marcondes C França, Beatriz H B Silva, Fabio A M Cappabianco, Felipe P G Bergo, Iscia T Lopes-Cendes, Fernando Cendes. Mov Disord 2013
53
20


Autosomal dominant cerebellar ataxia type I clinical features and MRI in families with SCA1, SCA2 and SCA3.
K Bürk, M Abele, M Fetter, J Dichgans, M Skalej, F Laccone, O Didierjean, A Brice, T Klockgether. Brain 1996
178
17

Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions.
S Gilman, A A Sima, L Junck, K J Kluin, R A Koeppe, M E Lohman, R Little. Ann Neurol 1996
113
17


Brainstem neurodegeneration correlates with clinical dysfunction in SCA1 but not in SCA2. A quantitative volumetric, diffusion and proton spectroscopy MR study.
L Guerrini, F Lolli, A Ginestroni, G Belli, R Della Nave, C Tessa, S Foresti, M Cosottini, S Piacentini, F Salvi,[...]. Brain 2004
78
17

Dissociation of grey and white matter reduction in spinocerebellar ataxia type 3 and 6: a voxel-based morphometry study.
Carsten Lukas, Ludger Schöls, Barbara Bellenberg, Udo Rüb, Horst Przuntek, Gebhard Schmid, Odo Köster, Boris Suchan. Neurosci Lett 2006
56
17


Axonal dysfunction in the deep white matter in Machado-Joseph disease.
Anelyssa D'Abreu, Marcondes França, Simone Appenzeller, Iscia Lopes-Cendes, Fernando Cendes. J Neuroimaging 2009
27
25

Neocortical atrophy in Machado-Joseph disease: a longitudinal neuroimaging study.
Anelyssa D'Abreu, Marcondes C França, Clarissa L Yasuda, Bruno A G Campos, Iscia Lopes-Cendes, Fernando Cendes. J Neuroimaging 2012
56
17

Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features.
A Dürr, G Stevanin, G Cancel, C Duyckaerts, N Abbas, O Didierjean, H Chneiweiss, A Benomar, O Lyon-Caen, J Julien,[...]. Ann Neurol 1996
344
15

Proton magnetic resonance spectroscopy in an Italian family with spinocerebellar ataxia type 1.
M Mascalchi, M Tosetti, R Plasmati, M C Bianchi, C Tessa, F Salvi, M Frontali, F Valzania, C Bartolozzi, C A Tassinari. Ann Neurol 1998
58
15


Spinocerebellar ataxia type 6: gaze-evoked and vertical nystagmus, Purkinje cell degeneration, and variable age of onset.
C M Gomez, R M Thompson, J T Gammack, S L Perlman, W B Dobyns, C L Truwit, D S Zee, H B Clark, J H Anderson. Ann Neurol 1997
206
15


SCA-2 presenting as parkinsonism in an Alberta family: clinical, genetic, and PET findings.
S Furtado, M Farrer, Y Tsuboi, M L Klimek, R de la Fuente-Fernández, J Hussey, P Lockhart, D B Calne, O Suchowersky, A J Stoessl,[...]. Neurology 2002
67
15

Executive and emotional dysfunction in Machado-Joseph disease.
Tricia M Zawacki, Janet Grace, Joseph H Friedman, Lewis Sudarsky. Mov Disord 2002
56
15

Abnormalities of dopaminergic neurotransmission in SCA2: a combined 123I-betaCIT and 123I-IBZM SPECT study.
Sylvia M Boesch, Eveline Donnemiller, Jörg Müller, Klaus Seppi, Helga Weirich-Schwaiger, Werner Poewe, Gregor K Wenning. Mov Disord 2004
35
17

Quantitative assessment of cerebral blood flow in genetically confirmed spinocerebellar ataxia type 6.
Kie Honjo, Tomohiko Ohshita, Hideshi Kawakami, Hiromitsu Naka, Yukari Imon, Hirofumi Maruyama, Yasuyo Mimori, Masayasu Matsumoto. Arch Neurol 2004
21
28

Cognitive impairments in Machado-Joseph disease.
Yoshinari Kawai, Akinori Takeda, Yuji Abe, Yukihiko Washimi, Fumiaki Tanaka, Gen Sobue. Arch Neurol 2004
59
15

PET study of brain acetylcholinesterase in cerebellar degenerative disorders.
Shigeki Hirano, Hitoshi Shinotoh, Kimihito Arai, Akiyo Aotsuka, Fumihiko Yasuno, Noriko Tanaka, Tsuneyoshi Ota, Koichi Sato, Kiyoshi Fukushi, Shuji Tanada,[...]. Mov Disord 2008
21
28

SCA3: neurological features, pathogenesis and animal models.
Olaf Riess, Udo Rüb, Annalisa Pastore, Peter Bauer, Ludger Schöls. Cerebellum 2008
152
15

Gray matter volume deficits in spinocerebellar ataxia: an optimized voxel based morphometric study.
Gaurav Goel, Pramod Kumar Pal, Shivashankar Ravishankar, Ganesan Venkatasubramanian, Peruvumba N Jayakumar, Nithin Krishna, Meera Purushottam, Jitender Saini, Mohammed Faruq, Mitali Mukherji,[...]. Parkinsonism Relat Disord 2011
44
15


White matter damage is related to ataxia severity in SCA3.
J-S Kang, J C Klein, S Baudrexel, R Deichmann, D Nolte, R Hilker. J Neurol 2014
32
18

Spinocerebellar ataxia type 6. Molecular and clinical features of 35 Japanese patients including one homozygous for the CAG repeat expansion.
R Matsumura, N Futamura, Y Fujimoto, S Yanagimoto, H Horikawa, A Suzumura, T Takayanagi. Neurology 1997
130
12

Intranuclear inclusions of expanded polyglutamine protein in spinocerebellar ataxia type 3.
H L Paulson, M K Perez, Y Trottier, J Q Trojanowski, S H Subramony, S S Das, P Vig, J L Mandel, K H Fischbeck, R N Pittman. Neuron 1997
666
12

Spinocerebellar ataxia type 6: genotype and phenotype in German kindreds.
L Schöls, R Krüger, G Amoiridis, H Przuntek, J T Epplen, O Riess. J Neurol Neurosurg Psychiatry 1998
126
12

Clinical features and natural history of spinocerebellar ataxia type 1.
H Sasaki, T Fukazawa, T Yanagihara, T Hamada, K Shima, A Matsumoto, K Hashimoto, N Ito, A Wakisaka, K Tashiro. Acta Neurol Scand 1996
50
12

Cerebral glucose hypermetabolism in Friedreich's ataxia detected with positron emission tomography.
S Gilman, L Junck, D S Markel, R A Koeppe, K J Kluin. Ann Neurol 1990
33
15

Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel.
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
12

Progressive atrophy of cerebellum and brainstem as a function of age and the size of the expanded CAG repeats in the MJD1 gene in Machado-Joseph disease.
O Onodera, J Idezuka, S Igarashi, Y Takiyama, K Endo, H Takano, M Oyake, H Tanaka, T Inuzuka, T Hayashi,[...]. Ann Neurol 1998
51
12

Fluorodopa and raclopride PET analysis of patients with Machado-Joseph disease.
H Shinotoh, B Thiessen, B J Snow, S Hashimoto, P MacLeod, I Silveira, G A Rouleau, M Schulzer, D B Calne. Neurology 1997
19
26


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.