-
1
-
-
0028156770
-
Summary of the proceedings of the first international workshop on CADASIL, Paris, May 19-21, 1993
-
Bousser, M. G., and Tournier-Lasserve, E. (1994). Summary of the proceedings of the first international workshop on CADASIL, Paris, May 19-21, 1993. Stroke 25: 704-707.
-
(1994)
Stroke
, vol.25
, pp. 704-707
-
-
Bousser, M.G.1
Tournier-Lasserve, E.2
-
2
-
-
0012688996
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): Main clinical findings in five families
-
Chabriat, H., Tournier-Lasserve, E., and Nibbio, A. (1994). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): Main clinical findings in five families. Stroke 25: 258.
-
(1994)
Stroke
, vol.25
, pp. 258
-
-
Chabriat, H.1
Tournier-Lasserve, E.2
Nibbio, A.3
-
3
-
-
0027366195
-
Faster sequential genetic linkage computations
-
Cottingham, R. W., Idury, R. M., and Schaffer, A. A. (1993). Faster sequential genetic linkage computations. Am. J. Hum. Genet. 53: 252-263.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 252-263
-
-
Cottingham, R.W.1
Idury, R.M.2
Schaffer, A.A.3
-
4
-
-
0016681496
-
Familial hemiplegic migraine
-
Glista, G. G., Mellinger, J. F., and Rooke, E. D. (1975). Familial hemiplegic migraine. Mayo Clin. Proc. 50: 307-311.
-
(1975)
Mayo Clin. Proc.
, vol.50
, pp. 307-311
-
-
Glista, G.G.1
Mellinger, J.F.2
Rooke, E.D.3
-
5
-
-
0028231090
-
The 1993-1994 Généthon human linkage map
-
Gyapay, G., Morisette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-1994 Généthon human linkage map. Nature Genet. 7: 246-339.
-
(1994)
Nature Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morisette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
6
-
-
0027306090
-
A gene for familial hemiplegic maps to chromosome 19
-
Joutel, A., Bousser, M. G., Biousse, V., Labauge, P., Chabriat, H., Nibbio, A., Maciazek, J., Meyer, B., Bach, M. A., Weissenbach, J., Lathrop, G. M., and Tournier-Lasserve, E. (1993). A gene for familial hemiplegic maps to chromosome 19. Nature Genet. 5: 40-45.
-
(1993)
Nature Genet.
, vol.5
, pp. 40-45
-
-
Joutel, A.1
Bousser, M.G.2
Biousse, V.3
Labauge, P.4
Chabriat, H.5
Nibbio, A.6
Maciazek, J.7
Meyer, B.8
Bach, M.A.9
Weissenbach, J.10
Lathrop, G.M.11
Tournier-Lasserve, E.12
-
7
-
-
0342499587
-
Strategies for multilocus analysis in humans
-
Lathrop, G. M., Lalouel, J. M., Julier, C., and Ott, J. (1984). Strategies for multilocus analysis in humans. Proc. Natl. Acad. Sci. USA 81: 3443-3446.
-
(1984)
Proc. Natl. Acad. Sci. USA
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
8
-
-
0023275907
-
Mendelian etiologies of stroke
-
Natowitz, M., and Kelley, R. I. (1987). Mendelian etiologies of stroke. Ann. Neurol. 22: 175-192.
-
(1987)
Ann. Neurol.
, vol.22
, pp. 175-192
-
-
Natowitz, M.1
Kelley, R.I.2
-
9
-
-
0028943944
-
Cerebral autosomal dominant arteriopathy with infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large italian family
-
Sabbadini, G., Francia, A., Calandriello, L., Di Biasi, C., Trasimeni, G., Gualdi, G. F., Palladini, G., Manfredi, M., and Frontali, M. (1995). Cerebral autosomal dominant arteriopathy with infarcts and leucoencephalopathy (CADASIL). Clinical, neuroimaging, pathological and genetic study of a large Italian family. Brain 118: 207-215.
-
(1995)
Brain
, vol.118
, pp. 207-215
-
-
Sabbadini, G.1
Francia, A.2
Calandriello, L.3
Di Biasi, C.4
Trasimeni, G.5
Gualdi, G.F.6
Palladini, G.7
Manfredi, M.8
Frontali, M.9
-
10
-
-
0028986010
-
Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: Evidence of probable locus heterogeneity
-
St. Clair, D., Bolt, J., Morris, S., and Doyle, D. (1995). Hereditary multi-infarct dementia unlinked to chromosome 19q12 in a large Scottish pedigree: Evidence of probable locus heterogeneity. J. Med. Genet. 32: 57-60.
-
(1995)
J. Med. Genet.
, vol.32
, pp. 57-60
-
-
St Clair, D.1
Bolt, J.2
Morris, S.3
Doyle, D.4
-
11
-
-
0027479304
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12
-
Tournier-Lasserve, E., Joutel, A., Melki, J., Weissenbach, J., Lathrop, G. M., Chabriat, H., Mas, J. L., Cabanis, E. A., Baudrimont, M., Maciazek, J., Bach, M.-A., and Bousser, M.-G. (1993). Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nature Genet. 3: 256-259.
-
(1993)
Nature Genet.
, vol.3
, pp. 256-259
-
-
Tournier-Lasserve, E.1
Joutel, A.2
Melki, J.3
Weissenbach, J.4
Lathrop, G.M.5
Chabriat, H.6
Mas, J.L.7
Cabanis, E.A.8
Baudrimont, M.9
Maciazek, J.10
Bach, M.-A.11
Bousser, M.-G.12
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