Information Technology Reference
In-Depth Information
Tabl e 7. 5
Strong negative
factor loading in factor one
suggesting a unique specialty.
These articles Pathfinder
networks are used, but not in
any way similar to a typical
publication in the Pathfinder
specialty
Publication
F1
McCain KW, 1995, J Am Soc Inform Sci, v46, p306
0.619
Bush V, 1945, Atlantic Monthly, v176, p101
0.631
Kamada T, 1989, Inform Process Lett, v31, p7
0.651
Chen CM, 1996, Hum-Comput Interact, v11, p125
0.652
Conklin J, 1987, IEEE Comput, v20, p17
0.657
Braam RR, 1991, J Am Soc Inform Sci, v42, p233
0.661
Marshall C, 1994, P Echt 94 Ed Sept, p13
0.661
Dillon A, 1996, Int J Hum-Comput St, v45, p619
0.664
Green SJ, 1998, P 7 Int World Wid We
0.664
Benyon D, 1997, P Hum Comp Int Inter, p39
0.664
0.666
Campagnoni FR, 1989, Acm T Inform Syst, v7, p271
McCain KW, 1990, J Am Soc Inform Sci, v41, p433
0.667
White HD, 1981, J Am Soc Inform Sci, v32, p163
0.668
Hemmje M, 1994, P 17 Ann Int Acm Sig, p249
0.670
White HD, 1997, Annu Rev Inform Sci, v32, p99
0.672
Small H, 1973, J Am Soc Inform Sci, v24, p265
0.673
Chen C, 1997, New Rev Hypermedia M, v3, p67
0.675
Vicente KJ, 1988, Int J Man Mach Stud, v29, p647
0.680
Deerwester S, 1990, J Am Soc Inform Sci, v41, p391
0.680
Small H, 1999, J Am Soc Inform Sci, v50, p799
0.682
Chen C, 1998, P 9 Acm C Hyp Hyp Hy, p77
0.684
Chalmers M, 1992, P 15 Ann Int Acm Sig, p330
0.688
Chen CM, 1998, J Visual Lang Comput, v9, p267
0.693
Chen CM, 1998, Interact Comput, v10, p107
0.695
Salton G, 1983, Intro Modern Informa
0.697
White HD, 1998, J Am Soc Inform Sci, v49, p327
0.724
Small H, 1997, Scientometrics, v38, p275
0.724
Hetzler B, 1998, P 5 Int Isko C Struc
0.724
Small H, 1994, Scientometrics, v30, p229
0.724
Chen HC, 1998, J Am Soc Inform Sci, v49, p582
0.727
Fox KL, 1999, J Am Soc Inform Sci, v50, p616
0.736
Chen CM, 1999, Inform Process Manag, v35, p401
0.743
neurologists. It is the principal form of a number of human TSE diseases. In humans,
the prion-based disease is related to CJD, Kuru (transmitted by cannibalism),
Gerstmann-Straussler-Scheinker Disease (GSS), and Fatal Familial Insomnia (FFI).
Creutzfeldt-Jakob Disease (CJD) is an illness usually found in people aged over
55. It was first identified by two German neurologists in 1920 and has no known
cause. Patients die about 6 months after diagnosis. It is the principal form of
a number of human Transmissible Spongiform Encephalopathy (TSE) diseases.
New variant CJD (vCJD) is an unrecognized variant of CJD discovered by the
National CJD Surveillance Unit in Edinburgh. vCJD is characterized clinically by
a progressive neuropsychiatric disorder. Neuropathology shows marked spongiform
change throughout the brain. The media reported a growing concern in the general
public that BSE may have passed from cattle to humans.
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