A citation-based method for searching scientific literature

R D Yee, M R Farlow, D A Suzuki, K F Betelak, B Ghetti. Arch Ophthalmol 1992
Times Cited: 14







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



Times Cited
  Times     Co-cited
Similarity


Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum.
M R Farlow, R D Yee, S R Dlouhy, P M Conneally, B Azzarelli, B Ghetti. Neurology 1989
80
42


Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene.
S R Dlouhy, K Hsiao, M R Farlow, T Foroud, P M Conneally, P Johnson, S B Prusiner, M E Hodes, B Ghetti. Nat Genet 1992
171
35

Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family.
B Ghetti, F Tagliavini, C L Masters, K Beyreuther, G Giaccone, L Verga, M R Farlow, P M Conneally, S R Dlouhy, B Azzarelli. Neurology 1989
161
35

Mutant prion proteins in Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
K Hsiao, S R Dlouhy, M R Farlow, C Cass, M Da Costa, P M Conneally, M E Hodes, B Ghetti, S B Prusiner. Nat Genet 1992
214
35

Prion protein preamyloid and amyloid deposits in Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
G Giaccone, L Verga, O Bugiani, B Frangione, D Serban, S B Prusiner, M R Farlow, B Ghetti, F Tagliavini. Proc Natl Acad Sci U S A 1992
75
35

Prion protein mutation in family first reported by Gerstmann, Sträussler, and Scheinker.
H A Kretzschmar, G Honold, F Seitelberger, M Feucht, P Wessely, P Mehraein, H Budka. Lancet 1991
108
35

[Morbus Gerstmann-Sträussler-Scheinker. The Sch. family-a report of three cases (author's transl)].
F Schumm, J W Boellaard, W Schlote, M Stöhr. Arch Psychiatr Nervenkr (1970) 1981
29
28

Familial dementia with PrP-positive amyloid plaques: a variant of Gerstmann-Sträussler syndrome.
D Nochlin, S M Sumi, T D Bird, A D Snow, C M Leventhal, K Beyreuther, C L Masters. Neurology 1989
98
28


Phenotypic variability of Gerstmann-Sträussler-Scheinker disease is associated with prion protein heterogeneity.
P Piccardo, S R Dlouhy, P M Lievens, K Young, T D Bird, D Nochlin, D W Dickson, H V Vinters, T R Zimmerman, I R Mackenzie,[...]. J Neuropathol Exp Neurol 1998
159
28

Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome.
T Kitamoto, M Ohta, K Doh-ura, S Hitoshi, Y Terao, J Tateishi. Biochem Biophys Res Commun 1993
151
28

Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.
C Tranchant, K Doh-ura, J M Warter, G Steinmetz, Y Chevalier, A Hanauer, T Kitamoto, J Tateishi. J Neurol Neurosurg Psychiatry 1992
46
28

Mutations in familial Creutzfeldt-Jakob disease and Gerstmann-Sträussler-Scheinker's syndrome.
D Goldgaber, L G Goldfarb, P Brown, D M Asher, W T Brown, S Lin, J W Teener, S M Feinstone, R Rubenstein, R J Kascsak. Exp Neurol 1989
244
28

[Mutation of codon 117 of the prion gene in Gerstmann-Sträussler-Scheinker disease].
C Tranchant, K Doh-Ura, G Steinmetz, Y Chevalier, T Kitamoto, J Tateishi, J M Warter. Rev Neurol (Paris) 1991
30
28

Beta PP participates in PrP-amyloid plaques of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
O Bugiani, G Giaccone, L Verga, B Pollo, B Frangione, M R Farlow, F Tagliavini, B Ghetti. J Neuropathol Exp Neurol 1993
48
28

Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome.
K Hsiao, H F Baker, T J Crow, M Poulter, F Owen, J D Terwilliger, D Westaway, J Ott, S B Prusiner. Nature 1989
711
28

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation).
P Barbanti, G Fabbrini, M Salvatore, R Petraroli, F Cardone, B Maras, M Equestre, G Macchi, G L Lenzi, M Pocchiari. Neurology 1996
56
21

Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease.
P Brown, C J Gibbs, P Rodgers-Johnson, D M Asher, M P Sulima, A Bacote, L G Goldfarb, D C Gajdusek. Ann Neurol 1994
615
21

Gerstmann-Sträussler-Scheinker's disease. Electron-microscopic observations on a brain biopsy.
W Schlote, J W Boellaard, F Schumm, M Stöhr. Acta Neuropathol 1980
42
21

Abnormal eye movements in Creutzfeldt-Jakob disease.
M P Grant, M Cohen, R B Petersen, G M Halmagyi, A McDougall, R J Tusa, R J Leigh. Ann Neurol 1993
42
21

Geotropic ocular deviation with skew and absence of saccade in Creutzfelt-Jakob disease.
T Yokota, K Tsuchiya, M Yamane, M Hayashi, H Tanabe, H Tsukagoshi. J Neurol Sci 1991
8
37

Gerstmann-Sträussler-Scheinker disease with coincidental familial onset.
A J Hudson, M A Farrell, R Kalnins, J C Kaufmann. Ann Neurol 1983
31
21

Amyloid protein of Gerstmann-Sträussler-Scheinker disease (Indiana kindred) is an 11 kd fragment of prion protein with an N-terminal glycine at codon 58.
F Tagliavini, F Prelli, J Ghiso, O Bugiani, D Serban, S B Prusiner, M R Farlow, B Ghetti, B Frangione. EMBO J 1991
169
21

Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.
P Piccardo, J J Liepnieks, A William, S R Dlouhy, M R Farlow, K Young, D Nochlin, T D Bird, R R Nixon, M J Ball,[...]. Am J Pathol 2001
62
21


A new PRNP mutation (G131V) associated with Gerstmann-Sträussler-Scheinker disease.
P K Panegyres, K Toufexis, B A Kakulas, L Cernevakova, P Brown, B Ghetti, P Piccardo, S R Dlouhy. Arch Neurol 2001
56
21

Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165.
P Piccardo, B Ghetti, D W Dickson, H V Vinters, G Giaccone, O Bugiani, F Tagliavini, K Young, S R Dlouhy, C Seiler. J Neuropathol Exp Neurol 1995
29
21

Gerstmann-Sträussler-Scheinker disease and the Indiana kindred.
B Ghetti, S R Dlouhy, G Giaccone, O Bugiani, B Frangione, M R Farlow, F Tagliavini. Brain Pathol 1995
108
21

A68 is a component of paired helical filaments of Gerstmann-Sträussler-Scheinker disease, Indiana kindred.
F Tagliavini, G Giaccone, F Prelli, L Verga, M Porro, J Q Trojanowski, M R Farlow, B Frangione, B Ghetti, O Bugiani. Brain Res 1993
38
21

Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.
G R Mallucci, T A Campbell, A Dickinson, J Beck, M Holt, G Plant, K W de Pauw, R N Hakin, C E Clarke, S Howell,[...]. Brain 1999
55
21

A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis.
T Kitamoto, N Amano, Y Terao, Y Nakazato, T Isshiki, T Mizutani, J Tateishi. Ann Neurol 1993
88
21

Gerstmann-Sträussler syndrome--a variant type: amyloid plaques and Alzheimer's neurofibrillary tangles in cerebral cortex.
N Amano, S Yagishita, S Yokoi, Y Itoh, J Kinoshita, T Mizutani, T Matsuishi. Acta Neuropathol 1992
36
21

Familial Gerstmann-Sträussler-Scheinker disease with neurofibrillary tangles.
B Ghetti, F Tagliavini, G Giaccone, O Bugiani, B Frangione, M R Farlow, S R Dlouhy. Mol Neurobiol 1994
56
21

An amber mutation of prion protein in Gerstmann-Sträussler syndrome with mutant PrP plaques.
T Kitamoto, R Iizuka, J Tateishi. Biochem Biophys Res Commun 1993
168
21

Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndrome.
P Brown, L G Goldfarb, W T Brown, D Goldgaber, R Rubenstein, R J Kascsak, D C Guiroy, P Piccardo, J W Boellaard, D C Gajdusek. Neurology 1991
46
21

The original Gerstmann-Sträussler-Scheinker family of Austria: divergent clinicopathological phenotypes but constant PrP genotype.
J A Hainfellner, S Brantner-Inthaler, L Cervenáková, P Brown, T Kitamoto, J Tateishi, H Diringer, P P Liberski, H Regele, M Feucht. Brain Pathol 1995
103
21


[An autopsy case of Gerstmann-Sträusser-Scheinker's disease with spastic paraplegia as its principal feature].
Y Nakazato, R Ohno, T Negishi, K Hamaguchi, E Arai. Rinsho Shinkeigaku 1991
12
25

A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease.
M Yamada, Y Itoh, H Fujigasaki, S Naruse, K Kaneko, T Kitamoto, J Tateishi, E Otomo, M Hayakawa, J Tanaka. Neurology 1993
43
21

Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele.
F Tagliavini, F Prelli, M Porro, G Rossi, G Giaccone, M R Farlow, S R Dlouhy, B Ghetti, O Bugiani, B Frangione. Cell 1994
127
21


Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism.
L G Goldfarb, R B Petersen, M Tabaton, P Brown, A C LeBlanc, P Montagna, P Cortelli, J Julien, C Vital, W W Pendelbury. Science 1992
546
21

AN ATAXIC FORM OF SUBACUTE PRESENILE POLIOENCEPHALOPATHY (CREUTZFELDT-JAKOB DISEASE).
B BROWNELL, D R OPPENHEIMER. J Neurol Neurosurg Psychiatry 1965
132
14

The ataxic (cerebellar) form of Creutzfeldt-Jakob disease.
K Jellinger, W D Heiss, E Deisenhammer. J Neurol 1974
36
14


New variant Creutzfeldt-Jakob disease: psychiatric features.
M Zeidler, E C Johnstone, R W Bamber, C M Dickens, C J Fisher, A F Francis, R Goldbeck, R Higgo, E C Johnson-Sabine, G J Lodge,[...]. Lancet 1997
126
14



New variant of Creutzfeldt-Jakob disease in a 26-year-old French man.
G Chazot, E Broussolle, C l Lapras, T Blättler, A Aguzzi, N Kopp. Lancet 1996
183
14


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.