-
1
-
-
0023731159
-
Familial Alzheimer's disease in American descendants of the Volga Germans: Probable genetic founder effect
-
Bird, T.D., Lampe, T.H., Nemens, E.J., Miner, G.W., Sumi, S.M. and Schellenberg, G.D. (1988) Familial Alzheimer's disease in American descendants of the Volga Germans: probable genetic founder effect. Ann. Neurol., 23: 25-31.
-
(1988)
Ann. Neurol.
, vol.23
, pp. 25-31
-
-
Bird, T.D.1
Lampe, T.H.2
Nemens, E.J.3
Miner, G.W.4
Sumi, S.M.5
Schellenberg, G.D.6
-
2
-
-
0029119112
-
Familial non-specific dementia maps to chromosome 3
-
Brown, J., Ashworth, A., Gydesen, S., Sorensen, A., Rossor, M., Hardy, J. and Collinge, J. (1995) Familial non-specific dementia maps to chromosome 3. Hum. Mol. Genet., 4: 1625-1628.
-
(1995)
Hum. Mol. Genet.
, vol.4
, pp. 1625-1628
-
-
Brown, J.1
Ashworth, A.2
Gydesen, S.3
Sorensen, A.4
Rossor, M.5
Hardy, J.6
Collinge, J.7
-
3
-
-
0028816454
-
A large pedigree with early-onset Alzheimer's disease: Clinical, neuropathologic, and genetic characterization
-
Campion, D., Brice, A., Hannequin, D., Tardieu, S., Dubois, B., Calenda, A., Brun, E., Penet, C., Tayot, J., Martinez, M., Bellis, M., Mallet, J., Agid, Y, and Clerget-Darpoux, F. (1995) A large pedigree with early-onset Alzheimer's disease: clinical, neuropathologic, and genetic characterization. Neurology, 45: 80-85.
-
(1995)
Neurology
, vol.45
, pp. 80-85
-
-
Campion, D.1
Brice, A.2
Hannequin, D.3
Tardieu, S.4
Dubois, B.5
Calenda, A.6
Brun, E.7
Penet, C.8
Tayot, J.9
Martinez, M.10
Bellis, M.11
Mallet, J.12
Agid, Y.13
Clerget-Darpoux, F.14
-
4
-
-
0028901768
-
Binswanger's disease-revisited
-
Caplan, L.R. (1995) Binswanger's disease-revisited. Neurology, 45: 626-633.
-
(1995)
Neurology
, vol.45
, pp. 626-633
-
-
Caplan, L.R.1
-
5
-
-
0029089247
-
Clinical spectrum of CADASIL: A study of 7 families
-
Chabriat, H., Vahedi, K., Iba-Zizen, M.T., Joutel, A., Nibbio, A., Nagy, T.G., Krebs, M.O., Julien, J., Dubois, B., Ducrocq, X., Levasseur, M., Homeyer, P., Mas, J.L., Lyon-Caen, O., Tournier Lasserve, E. and Bousser, M.G. (1995) Clinical spectrum of CADASIL: a study of 7 families. Lancet, 346: 934-939.
-
(1995)
Lancet
, vol.346
, pp. 934-939
-
-
Chabriat, H.1
Vahedi, K.2
Iba-Zizen, M.T.3
Joutel, A.4
Nibbio, A.5
Nagy, T.G.6
Krebs, M.O.7
Julien, J.8
Dubois, B.9
Ducrocq, X.10
Levasseur, M.11
Homeyer, P.12
Mas, J.L.13
Lyon-Caen, O.14
Tournier Lasserve, E.15
Bousser, M.G.16
-
7
-
-
0024487020
-
Fabry disease: Molecular genetics of the inherited nephropathy
-
Desnick, R.J., Astrin, K.H. and Bishop, D.F. (1989) Fabry disease: molecular genetics of the inherited nephropathy. Adv. Nephrol. Necker Hosp., 18: 113-127.
-
(1989)
Adv. Nephrol. Necker Hosp.
, vol.18
, pp. 113-127
-
-
Desnick, R.J.1
Astrin, K.H.2
Bishop, D.F.3
-
8
-
-
0029655609
-
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval
-
Ducros, A., Nagy, T., Alamowitch, S., Nibbio, A., Joutel, A., Vahedi, K., Chabriat, H., Iba-Zizen, M.T., Julien, J., Davous, P., Goas, J.Y., Lyon-Caen, O., Dubois, B., Ducrocq, X., Salsa, F., Ragno, M., Burkhard, P., Bassetti, C., Hutchinson, M., Vérin, M., Viader, F., Chapon, F., Levasseur, M., Mas, J.L., Delrieu, O., Maciazek, J., Prieur, M., Mohrenweiser, H., Bach, J.F., Bousser, M.G. and Tournier-Lasserve, E. (1996) Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, genetic homogeneity, and mapping of the locus within a 2-cM interval. Am. J. Hum. Genet., 58: 171-181.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 171-181
-
-
Ducros, A.1
Nagy, T.2
Alamowitch, S.3
Nibbio, A.4
Joutel, A.5
Vahedi, K.6
Chabriat, H.7
Iba-Zizen, M.T.8
Julien, J.9
Davous, P.10
Goas, J.Y.11
Lyon-Caen, O.12
Dubois, B.13
Ducrocq, X.14
Salsa, F.15
Ragno, M.16
Burkhard, P.17
Bassetti, C.18
Hutchinson, M.19
Vérin, M.20
Viader, F.21
Chapon, F.22
Levasseur, M.23
Mas, J.L.24
Delrieu, O.25
Maciazek, J.26
Prieur, M.27
Mohrenweiser, H.28
Bach, J.F.29
Bousser, M.G.30
Tournier-Lasserve, E.31
more..
-
9
-
-
0028905614
-
Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension
-
Fukutake, T. and Hirayama, K. (1995) Familial young-adult-onset arteriosclerotic leukoencephalopathy with alopecia and lumbago without arterial hypertension. Eur. Neurol., 35: 69-79.
-
(1995)
Eur. Neurol.
, vol.35
, pp. 69-79
-
-
Fukutake, T.1
Hirayama, K.2
-
10
-
-
0028008517
-
Small arterial granular degeneration in familial Binswanger's syndrome
-
Gutiérrez-Molina, M., Caminero Rodríguez, A., Martínez García, C., Arpa Gutiérrez, J., Morales Bastos, C. and Amer, G. (1994) Small arterial granular degeneration in familial Binswanger's syndrome. Acta Neuropathol., 87: 98-105.
-
(1994)
Acta Neuropathol.
, vol.87
, pp. 98-105
-
-
Gutiérrez-Molina, M.1
Caminero Rodríguez, A.2
Martínez García, C.3
Arpa Gutiérrez, J.4
Morales Bastos, C.5
Amer, G.6
-
11
-
-
0028231090
-
The 1993-1994 Généthon human genetic linkage map
-
Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M. and Weissenbach, J. (1994) The 1993-1994 Généthon human genetic linkage map. Nature Genet., 7: 246-339.
-
(1994)
Nature Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, 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
-
12
-
-
0025048011
-
Hereditary cerebral haemorrhage with amyloidosis, Duch type
-
Hann, J., Roos, R.A.C., Algra, P.R., Lanser, J.B.K., Bots, G.T.A.M, and Vegter-van der Vlis, M. (1990) Hereditary cerebral haemorrhage with amyloidosis, Duch type. Brain, 113: 1251-1267.
-
(1990)
Brain
, vol.113
, pp. 1251-1267
-
-
Hann, J.1
Roos, R.A.C.2
Algra, P.R.3
Lanser, J.B.K.4
Bots, G.T.A.M.5
Vegter-Van Der Vlis, M.6
-
13
-
-
0026795527
-
MELAS: An original case and clinical criteria for diagnosis
-
Hirano, M., Ricci, E., Koenigsberger, M.R., Defendini, R., Pavlakis, S.G., DeVivo, D.C., DiMauro, S. and Rowland, L.P. (1992) MELAS: an original case and clinical criteria for diagnosis. Neuromuscul. Disord., 2: 125-135.
-
(1992)
Neuromuscul. Disord.
, vol.2
, pp. 125-135
-
-
Hirano, M.1
Ricci, E.2
Koenigsberger, M.R.3
Defendini, R.4
Pavlakis, S.G.5
DeVivo, D.C.6
DiMauro, S.7
Rowland, L.P.8
-
14
-
-
0028785253
-
Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL)
-
Hutchinson, M., O'Riordan, J., Javed, M., Quin, E., Macerlaine, D., Willcox, T., Parfrey, N., Nagy, T.G. and Tournier-Lasserve, E. (1995) Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Ann. Neurol., 38: 817-824.
-
(1995)
Ann. Neurol.
, vol.38
, pp. 817-824
-
-
Hutchinson, M.1
O'Riordan, J.2
Javed, M.3
Quin, E.4
Macerlaine, D.5
Willcox, T.6
Parfrey, N.7
Nagy, T.G.8
Tournier-Lasserve, E.9
-
15
-
-
0025341975
-
Dementia lacking distinctive histologic features: A common non-Alzheimer degenerative dementia
-
Knopman, D.S., Mastri, A.R., Frey II, W.H., Sung, J.H. and Rustan, T (1990) Dementia lacking distinctive histologic features: a common non-Alzheimer degenerative dementia. Neurology, 40: 251-256.
-
(1990)
Neurology
, vol.40
, pp. 251-256
-
-
Knopman, D.S.1
Mastri, A.R.2
Frey W.H. II3
Sung, J.H.4
Rustan, T.5
-
16
-
-
0027971051
-
Phenotype of chromosome 14-linked familial Alzheimer's disease in a large kindred
-
Lampe, T.H., Bird, T.D., Nochlin, D., Nemens, E., Risse, S.C., Sumi, S.M., Koerker, R., Leaird, B., Wier, M. and Raskind, M.A. (1994) Phenotype of chromosome 14-linked familial Alzheimer's disease in a large kindred. Ann. Neurol., 36: 368-378.
-
(1994)
Ann. Neurol.
, vol.36
, pp. 368-378
-
-
Lampe, T.H.1
Bird, T.D.2
Nochlin, D.3
Nemens, E.4
Risse, S.C.5
Sumi, S.M.6
Koerker, R.7
Leaird, B.8
Wier, M.9
Raskind, M.A.10
-
17
-
-
0021344005
-
Easy calculations of lod scores and genetic risks on small computers
-
Lathrop, G.M. and Lalouel, J.M. (1984) Easy calculations of lod scores and genetic risks on small computers. Am. J. Hum. Genet. 36: 460-465.
-
(1984)
Am. J. Hum. Genet.
, vol.36
, pp. 460-465
-
-
Lathrop, G.M.1
Lalouel, J.M.2
-
18
-
-
0021850103
-
Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
-
Lathrop, G.M., Lalouel, J.M., Julien, C. and Ott, J. (1985) Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am. J. Hum. Genet., 37: 482-498.
-
(1985)
Am. J. Hum. Genet.
, vol.37
, pp. 482-498
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julien, C.3
Ott, J.4
-
19
-
-
0029150716
-
A familial Alzheimer's disease locus on chromosome 1
-
Levy-Lahad, E., Wijsman, E.M., Nemens, E., Anderson, L., Goddard, K.A.B., Weber, J.L., Bird, T.D. and Schellenberg, G.D. (1995) A familial Alzheimer's disease locus on chromosome 1. Science, 269: 970-973.
-
(1995)
Science
, vol.269
, pp. 970-973
-
-
Levy-Lahad, E.1
Wijsman, E.M.2
Nemens, E.3
Anderson, L.4
Goddard, K.A.B.5
Weber, J.L.6
Bird, T.D.7
Schellenberg, G.D.8
-
20
-
-
0029939676
-
Homocysteine and vascular disease
-
McCully, K.S. (1996) Homocysteine and vascular disease. Nature Med., 2: 386-389.
-
(1996)
Nature Med.
, vol.2
, pp. 386-389
-
-
McCully, K.S.1
-
21
-
-
0027356278
-
Familial parkinsonism and dementia with 'ballooned neurons'
-
Mizutani, T., Inose, T., Nakajima, S. and Gambetti, P. (1993) Familial parkinsonism and dementia with 'ballooned neurons'. Adv. Neurol., 60: 613-617.
-
(1993)
Adv. Neurol.
, vol.60
, pp. 613-617
-
-
Mizutani, T.1
Inose, T.2
Nakajima, S.3
Gambetti, P.4
-
22
-
-
0029035113
-
Familial mitochondrial encephalomyopathy with deaf-mutism, ophthalmoplegia and leukodystrophy
-
Nakagawa, M., Kaminishi, Y., Isashiki, Y., Yamada, H., Higuchi, I., Uchida, Y. and Osame, M. (1995) Familial mitochondrial encephalomyopathy with deaf-mutism, ophthalmoplegia and leukodystrophy. Acta Neurol. Scand., 92: 102-108.
-
(1995)
Acta Neurol. Scand.
, vol.92
, pp. 102-108
-
-
Nakagawa, M.1
Kaminishi, Y.2
Isashiki, Y.3
Yamada, H.4
Higuchi, I.5
Uchida, Y.6
Osame, M.7
-
24
-
-
0029101491
-
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
-
Rogaev, E.I., Sherrington, R., Rogaeva, E.A., Levesque, G., Ikeda, M., Liang, Y., Chi, H., Lin, C., Holman, K., Tsuda, T., Mar, L., Sorbi, S., Nacmias, B., Piacentini, S., Amaducci, L., Chumakov, I., Cohen, D., Lannfelt, L., Fraser, P.E., Rommens, J.M. and St. George-Hyslop, P.H. (1995) Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature, 376: 775-778.
-
(1995)
Nature
, vol.376
, pp. 775-778
-
-
Rogaev, E.I.1
Sherrington, R.2
Rogaeva, E.A.3
Levesque, G.4
Ikeda, M.5
Liang, Y.6
Chi, H.7
Lin, C.8
Holman, K.9
Tsuda, T.10
Mar, L.11
Sorbi, S.12
Nacmias, B.13
Piacentini, S.14
Amaducci, L.15
Chumakov, I.16
Cohen, D.17
Lannfelt, L.18
Fraser, P.E.19
Rommens, J.M.20
St. George-Hyslop, P.H.21
more..
-
25
-
-
0028113875
-
Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL
-
Ruchoux, M.-M., Chabriat, H., Bousser, M.-G., Baudrimont, M. and Tournier-Lasserve, E. (1994) Presence of ultrastructural arterial lesions in muscle and skin vessels of patients with CADASIL. Stroke, 25: 2291-2292.
-
(1994)
Stroke
, vol.25
, pp. 2291-2292
-
-
Ruchoux, M.-M.1
Chabriat, H.2
Bousser, M.-G.3
Baudrimont, M.4
Tournier-Lasserve, E.5
-
26
-
-
0028943944
-
Cerebral autosomal dominant arteriopathy with subcortical infarctions and leukoencephalopathy (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 subcortical infarctions and leukoencephalopathy (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
-
27
-
-
0029004341
-
Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease
-
Sherrington, R., Rogaev, E.I., Liang, Y., Rogaeva, E.A., Levesque, G., Ikeda, M., Chi, H., Lin, C., Li, G., Holman, K., Tsuda, T., Mar, L., Foncin, J.-F., Bruni, A.C., Montesi, M.P., Sorbi, S., Rainero, I., Pinessi, L., Nee, L., Chumakov, I., Pollen, D., Brookes, A., Sanseau, P., Polinsky, R.J., Wasco, W., Da Silva, H.A.R., Haines, J.L., Pericak-Vance, M.A., Tanzi, R.E., Roses, A.D., Fraser, P.E., Rommens, J.M. and St. George-Hyslop, P.H. (1995) Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature, 375: 754-760.
-
(1995)
Nature
, vol.375
, pp. 754-760
-
-
Sherrington, R.1
Rogaev, E.I.2
Liang, Y.3
Rogaeva, E.A.4
Levesque, G.5
Ikeda, M.6
Chi, H.7
Lin, C.8
Li, G.9
Holman, K.10
Tsuda, T.11
Mar, L.12
Foncin, J.-F.13
Bruni, A.C.14
Montesi, M.P.15
Sorbi, S.16
Rainero, I.17
Pinessi, L.18
Nee, L.19
Chumakov, I.20
Pollen, D.21
Brookes, A.22
Sanseau, P.23
Polinsky, R.J.24
Wasco, W.25
Da Silva, H.A.R.26
Haines, J.L.27
Pericak-Vance, M.A.28
Tanzi, R.E.29
Roses, A.D.30
Fraser, P.E.31
Rommens, J.M.32
St. George-Hyslop, P.H.33
more..
-
28
-
-
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
-
29
-
-
0027174318
-
Presenile-onset cerebral adrenoleukodystrophy presenting as Balint's syndrome and dementia
-
Uyama, E., Iwagoe, H., Maeda, J., Nakamura, M., Terasaki, T. and Ando, M. (1993) Presenile-onset cerebral adrenoleukodystrophy presenting as Balint's syndrome and dementia. Neurology, 43: 1249-1251.
-
(1993)
Neurology
, vol.43
, pp. 1249-1251
-
-
Uyama, E.1
Iwagoe, H.2
Maeda, J.3
Nakamura, M.4
Terasaki, T.5
Ando, M.6
-
30
-
-
0028858163
-
New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: Migraine as the prominent clinical feature
-
Vérin, M., Rolland, Y., Landgraf, F., Chabriat, H., Bompais, B., Michel, A., Vahedi, K., Martinet, J.P., Tournier-Lasserve, E., Lemaitre, M.H. and Edan, G. (1995) New phenotype of the cerebral autosomal dominant arteriopathy mapped to chromosome 19: migraine as the prominent clinical feature. J. Neurol. Neurosurg. Psychiatry, 59: 579-585.
-
(1995)
J. Neurol. Neurosurg. Psychiatry
, vol.59
, pp. 579-585
-
-
Vérin, M.1
Rolland, Y.2
Landgraf, F.3
Chabriat, H.4
Bompais, B.5
Michel, A.6
Vahedi, K.7
Martinet, J.P.8
Tournier-Lasserve, E.9
Lemaitre, M.H.10
Edan, G.11
-
31
-
-
0025801744
-
Apolipoprotein E genotyping by one-stage PCR
-
Wenham, P.R., Price, W.H. and Blundell, G. (1991) Apolipoprotein E genotyping by one-stage PCR. Lancet, 337: 1158-1159.
-
(1991)
Lancet
, vol.337
, pp. 1158-1159
-
-
Wenham, P.R.1
Price, W.H.2
Blundell, G.3
-
32
-
-
0027976226
-
The microvascular changes in cases of hereditary multi-infarct disease of the brain
-
Zhang, W.W., Ma, K.C., Andersen, O., Sourander, P., Tollesson, P.O. and Olsson, Y. (1994) The microvascular changes in cases of hereditary multi-infarct disease of the brain. Acta Neuropathol., 87: 317-324.
-
(1994)
Acta Neuropathol.
, vol.87
, pp. 317-324
-
-
Zhang, W.W.1
Ma, K.C.2
Andersen, O.3
Sourander, P.4
Tollesson, P.O.5
Olsson, Y.6
|