A citation-based method for searching scientific literature

R H Walker, H H Jung, C Dobson-Stone, L Rampoldi, A Sano, F Tison, A Danek. Neurology 2007
Times Cited: 67







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



Times Cited
  Times     Co-cited
Similarity


Chorein detection for the diagnosis of chorea-acanthocytosis.
Carol Dobson-Stone, Antonio Velayos-Baeza, Lea A Filippone, Sarah Westbury, Alexander Storch, Torsten Erdmann, Stephen J Wroe, Klaus L Leenders, Anthony E Lang, Maria Teresa Dotti,[...]. Ann Neurol 2004
94
35

A conserved sorting-associated protein is mutant in chorea-acanthocytosis.
L Rampoldi, C Dobson-Stone, J P Rubio, A Danek, R M Chalmers, N W Wood, C Verellen, X Ferrer, A Malandrini, G M Fabrizi,[...]. Nat Genet 2001
204
29

The gene encoding a newly discovered protein, chorein, is mutated in chorea-acanthocytosis.
S Ueno , Y Maruki, M Nakamura, Y Tomemori, K Kamae, H Tanabe, Y Yamashita, S Matsuda, S Kaneko, A Sano. Nat Genet 2001
183
29

Testing for acanthocytosis A prospective reader-blinded study in movement disorder patients.
Alexander Storch, Markus Kornhass, Johannes Schwarz. J Neurol 2005
57
31

McLeod neuroacanthocytosis: genotype and phenotype.
A Danek, J P Rubio, L Rampoldi, M Ho, C Dobson-Stone, F Tison, W A Symmans, M Oechsner, W Kalckreuth, J M Watt,[...]. Ann Neurol 2001
131
25

Neuroacanthocytosis. A clinical, haematological and pathological study of 19 cases.
R J Hardie, H W Pullon, A E Harding, J S Owen, M Pires, G L Daniels, Y Imai, V P Misra, R H King, J M Jacobs. Brain 1991
201
20

Clinical features and molecular bases of neuroacanthocytosis.
Luca Rampoldi, Adrian Danek, Anthony P Monaco. J Mol Med (Berl) 2002
109
20

Neuroacanthocytosis: new developments in a neglected group of dementing disorders.
Adrian Danek, Hans H Jung, Mariarosa A B Melone, Luca Rampoldi, Vania Broccoli, Ruth H Walker. J Neurol Sci 2005
53
24

Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis.
C Dobson-Stone, A Danek, L Rampoldi, R J Hardie, R M Chalmers, N W Wood, S Bohlega, M T Dotti, A Federico, M Shizuka,[...]. Eur J Hum Genet 2002
96
17

Neuroacanthocytosis syndromes.
Hans H Jung, Adrian Danek, Ruth H Walker. Orphanet J Rare Dis 2011
95
17

Late appearance of acanthocytes during the course of chorea-acanthocytosis.
G Sorrentino, A De Renzo, S Miniello, O Nori, V Bonavita. J Neurol Sci 1999
36
30

Tongue protrusion and feeding dystonia: a hallmark of chorea-acanthocytosis.
Benedikt Bader, Ruth H Walker, Mathias Vogel, Mario Prosiegel, Jacqueline McIntosh, Adrian Danek. Mov Disord 2010
40
27

McLeod myopathy revisited: more neurogenic and less benign.
Ekkehard Hewer, Adrian Danek, Benedikt G Schoser, Marcelo Miranda, Ross Reichard, Claudia Castiglioni, Matthias Oechsner, Hans H Goebel, Frank L Heppner, Hans H Jung. Brain 2007
37
27

Familial temporal lobe epilepsy as a presenting feature of choreoacanthocytosis.
Abdullah Al-Asmi, An C Jansen, AmanPreet Badhwar, François Dubeau, Donatella Tampieri, Chaim Shustik, Suha Mercho, Ghislaine Savard, Carol Dobson-Stone, Anthony P Monaco,[...]. Epilepsia 2005
41
24

Neuroacanthocytosis.
Adrian Danek, Ruth H Walker. Curr Opin Neurol 2005
53
16

Early clinical heterogeneity in choreoacanthocytosis.
Alexander Lossos, Carol Dobson-Stone, Anthony P Monaco, Dov Soffer, Ezra Rahamim, J P Newman, Saidi Mohiddin, Lameh Fananapazir, Israela Lerer, Eduard Linetsky,[...]. Arch Neurol 2005
28
32

Genetic, clinical, and radiographic delineation of Hallervorden-Spatz syndrome.
Susan J Hayflick, Shawn K Westaway, Barbara Levinson, Bing Zhou, Monique A Johnson, Katherine H L Ching, Jane Gitschier. N Engl J Med 2003
430
11

Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein.
M Ho, J Chelly, N Carter, A Danek, P Crocker, A P Monaco. Cell 1994
193
11

Huntington's disease--like 2 can present as chorea-acanthocytosis.
R H Walker, A Rasmussen, D Rudnicki, S E Holmes, E Alonso, T Matsuura, T Ashizawa, B Davidoff-Feldman, R L Margolis. Neurology 2003
59
13

Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromes.
Ruth H Walker, Adrian Danek, Carol Dobson-Stone, Renzo Guerrini, Hans H Jung, Anne-Louise Lafontaine, Luca Rampoldi, François Tison, Eva Andermann. Mov Disord 2006
23
34

Huntington's disease phenocopies are clinically and genetically heterogeneous.
Edward J Wild, Ese E Mudanohwo, Mary G Sweeney, Susanne A Schneider, Jon Beck, Kailash P Bhatia, Martin N Rossor, Mary B Davis, Sarah J Tabrizi. Mov Disord 2008
70
11

Characteristic head drops and axial extension in advanced chorea-acanthocytosis.
Susanne A Schneider, Anthony E Lang, Elena Moro, Benedikt Bader, Adrian Danek, Kailash P Bhatia. Mov Disord 2010
40
20

Novel pathogenic mutations and copy number variations in the VPS13A gene in patients with chorea-acanthocytosis.
Akiyuki Tomiyasu, Masayuki Nakamura, Mio Ichiba, Shuichi Ueno, Shinji Saiki, Mizuki Morimoto, Jan Kobal, Yasufumi Kageyama, Toshio Inui, Koichi Wakabayashi,[...]. Am J Med Genet B Neuropsychiatr Genet 2011
44
18

McLeod syndrome: a novel mutation, predominant psychiatric manifestations, and distinct striatal imaging findings.
H H Jung, M Hergersberg, S Kneifel, H Alkadhi, R Schiess, M Weigell-Weber, G Daniels, S Kollias, K Hess. Ann Neurol 2001
54
12

Analysis of the human VPS13 gene family.
Antonio Velayos-Baeza, Andrea Vettori, Richard R Copley, Carol Dobson-Stone, A P Monaco. Genomics 2004
141
10

Benign X-linked myopathy with acanthocytes (McLeod syndrome). Its relationship to X-linked muscular dystrophy.
M Swash, M S Schwartz, N D Carter, R Heath, M Leak, K L Rogers. Brain 1983
67
8

A new phenotype (McLeod) in the Kell blood-group system.
F H ALLEN, S M KRABBE, P A CORCORAN. Vox Sang 1961
118
8

Kell and XK immunohistochemistry in McLeod myopathy.
H H Jung, D Russo, C Redman, S Brandner. Muscle Nerve 2001
35
17

McLeod phenotype associated with a XK missense mutation without hematologic, neuromuscular, or cerebral involvement.
Hans H Jung, Martin Hergersberg, Marco Vogt, Jens Pahnke, Valerie Treyer, Benno Röthlisberger, Spyros S Kollias, David Russo, Beat M Frey. Transfusion 2003
26
23

A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2.
S E Holmes, E O'Hearn, A Rosenblatt, C Callahan, H S Hwang, R G Ingersoll-Ashworth, A Fleisher, G Stevanin, A Brice, N T Potter,[...]. Nat Genet 2001
197
8

Huntington disease phenocopy is a familial prion disease.
R C Moore, F Xiang, J Monaghan, D Han, Z Zhang, L Edström, M Anvret, S B Prusiner. Am J Hum Genet 2001
88
8

Head of the caudate nucleus is most vulnerable in chorea-acanthocytosis: a voxel-based morphometry study.
Karsten Henkel, Adrian Danek, Jordan Grafman, John Butman, Jan Kassubek. Mov Disord 2006
32
18

Severe tongue protrusion dystonia: clinical syndromes and possible treatment.
S A Schneider, A Aggarwal, M Bhatt, E Dupont, S Tisch, P Limousin, P Lee, N Quinn, K P Bhatia. Neurology 2006
86
8

Clinical and molecular genetic assessment of a chorea-acanthocytosis pedigree.
Mio Ichiba, Masayuki Nakamura, Akira Kusumoto, Emiko Mizuno, Yutaka Kurano, Mieko Matsuda, Maiko Kato, Asumi Agemura, Yuko Tomemori, Shinji Muroya,[...]. J Neurol Sci 2007
26
23

The neuropathological features of neuroacanthocytosis.
J O Rinne, S E Daniel, F Scaravilli, M Pires, A E Harding, C D Marsden. Mov Disord 1994
58
10

Improvement of severe trunk spasms by bilateral high-frequency stimulation of the motor thalamus in a patient with chorea-acanthocytosis.
Pierre Burbaud, Alain Rougier, Xavier Ferrer, Dominique Guehl, E Cuny, Pierre Arne, Ch Gross, B Bioulac. Mov Disord 2002
25
24

Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis.
Carol Dobson-Stone, Antonio Velayos-Baeza, An Jansen, Frederick Andermann, François Dubeau, Francine Robert, Anne Summers, Anthony E Lang, Sylvain Chouinard, Adrian Danek,[...]. Neurogenetics 2005
22
27


White matter abnormalities on MRI in neuroacanthocytosis.
D J Nicholl, I Sutton, M T Dotti, S G Supple, A Danek, M Lawden. J Neurol Neurosurg Psychiatry 2004
21
23

Huntington's Disease-like 2 (HDL2) in North America and Japan.
Russell L Margolis, Susan E Holmes, Adam Rosenblatt, Lisa Gourley, Elizabeth O'Hearn, Christopher A Ross, William K Seltzer, Ruth H Walker, Tetsuo Ashizawa, Astrid Rasmussen,[...]. Ann Neurol 2004
65
7

Huntington's disease-like phenotype due to trinucleotide repeat expansions in the TBP and JPH3 genes.
Giovanni Stevanin, Hiroto Fujigasaki, Anne-Sophie Lebre, Agnes Camuzat, Cecile Jeannequin, Catherine Dode, Junko Takahashi, Chankranira San, Robert Bellance, Alexis Brice,[...]. Brain 2003
116
7

Self-mutilation in chorea-acanthocytosis: Manifestation of movement disorder or psychopathology?
Ruth H Walker, Qinyue Liu, Mio Ichiba, Shinji Muroya, Masyuki Nakamura, Akira Sano, Cheryl A Kennedy, Gary Sclar. Mov Disord 2006
18
27

Development of mesial temporal lobe epilepsy in chorea-acanthocytosis.
R Scheid, B Bader, D V Ott, A Merkenschlager, A Danek. Neurology 2009
23
21

Phenotypic variation among brothers with the McLeod neuroacanthocytosis syndrome.
Ruth H Walker, Hans H Jung, François Tison, Soohee Lee, Adrian Danek. Mov Disord 2007
23
17

The Kell blood group system: Kell and XK membrane proteins.
S Lee, D Russo, C M Redman. Semin Hematol 2000
67
5

The Kell and XK proteins of the Kell blood group are not co-expressed in the central nervous system.
Audrey Clapéron, Claude Hattab, Vincent Armand, Suzanne Trottier, Olivier Bertrand, Tanja Ouimet. Brain Res 2007
19
21

Elevated serum creatine phosphokinase in subjects with McLeod syndrome.
W L Marsh, N J Marsh, A Moore, W A Symmans, C L Johnson, C M Redman. Vox Sang 1981
51
7

Huntington's disease like-2 neuropathology.
Penny E Greenstein, Jean-Paul G Vonsattel, Russell L Margolis, Jeffrey T Joseph. Mov Disord 2007
32
12


Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation.
Patrick F Chinnery, Douglas E Crompton, Daniel Birchall, Margaret J Jackson, Alan Coulthard, Anne Lombès, Niall Quinn, Adrian Wills, Nicholas Fletcher, John P Mottershead,[...]. Brain 2007
132
5


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.