REFERENCES - RESEARCH FRONT: 2
| Times Cited | Reference | Title |
| 15 |
GOATE A, 1991, NATURE, V349, P704 |
null |
| 15 |
BROWN P, 1986, ANN NEUROL, V20, P597 |
null |
| 13 |
PRUSINER SB, 1982, SCIENCE, V216, P136 |
null |
| 12 |
PARCHI P, 1999, ANN NEUROL, V46, P224 |
null |
| 12 |
PRUSINER SB, 1991, SCIENCE, V252, P1515 |
null |
| 11 |
HSICH G, 1996, NEW ENGL J MED, V335, P924 |
null |
| 11 |
ZERR I, 1998, ANN NEUROL, V43, P32 |
null |
| 11 |
MEDORI R, 1992, NEW ENGL J MED, V326, P444 |
FATAL FAMILIAL INSOMNIA, A PRION DISEASE WITH A MUTATION AT CODON-178 OF THE PRION PROTEIN GENE |
| 11 |
MASTERS CL, 1979, ANN NEUROL, V5, P177 |
null |
| 10 |
COLLINGE J, 1994, NATURE, V370, P295 |
null |
| 10 |
MASTERS CL, 1978, BRAIN, V101, P333 |
null |
| 9 |
SHERRINGTON R, 1995, NATURE, V375, P754 |
null |
| 9 |
DEARMOND SJ, 1987, NEUROLOGY, V37, P1271 |
null |
| 9 |
HSIAO K, 1989, NATURE, V338, P342 |
null |
| 9 |
GOLDFARB LG, 1992, SCIENCE, V258, P806 |
null |
| 9 |
BROWN P, 1994, ANN NEUROL, V35, P513 |
null |
| 9 |
COLLINGE J, 1990, LANCET, V336, P7 |
null |
| 9 |
WELLS GAH, 1987, VET REC, V121, P419 |
null |
| 9 |
LEVYLAHAD E, 1995, SCIENCE, V269, P973 |
null |
| 8 |
MASTERS CL, 1981, BRAIN, V104, P559 |
null |
| 7 |
PRUSINER SB, 1993, ARCH NEUROL-CHICAGO, V50, P1129 |
null |
| 7 |
WILL RG, 1996, LANCET, V347, P921 |
null |
| 7 |
BUDKA H, 1995, BRAIN PATHOL, V5, P459 |
null |
| 7 |
WILL RG, 1984, J NEUROL NEUROSUR PS, V47, P134 |
null |
| 7 |
WINDL O, 1996, HUM GENET, V98, P259 |
null |
| 7 |
HUTTON M, 1998, NATURE, V393, P702 |
null |
| 7 |
OWEN F, 1989, LANCET, V1, P51 |
null |
| 7 |
PRUSINER SB, 1997, SCIENCE, V278, P245 |
null |
| 6 |
LASZLO L, 1992, J PATHOL, V166, P333 |
null |
| 6 |
ZAHN R, 2000, P NATL ACAD SCI USA, V97, P145 |
NMR solution structure of the human prion protein |
| 6 |
MANETTO V, 1992, NEUROLOGY, V42, P312 |
null |
| 6 |
BELL JE, 1993, BR MED B, V49, P738 |
null |
| 6 |
COLLINGE J, 1991, LANCET, V337, P1441 |
null |
| 6 |
RICHARDSON EP, 1995, BRAIN PATHOL, V5, P33 |
null |
| 6 |
COLLINGE J, 1992, BRAIN, V115, P687 |
INHERITED PRION DISEASE WITH 144 BASE PAIR GENE INSERTION .2. CLINICAL AND PATHOLOGICAL FEATURES |