-
1
-
-
0027514354
-
Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment
-
7678184
-
HP Adams Jr BH Bendixen LJ Kappelle, et al. 1993 Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment Stroke 24 35 41 7678184
-
(1993)
Stroke
, vol.24
, pp. 35-41
-
-
Adams Jr, H.P.1
Bendixen, B.H.2
Kappelle, L.J.3
-
2
-
-
0030791665
-
Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes
-
DOI 10.1093/brain/120.10.1713
-
PF Chinnery N Howell RN Lightowlers, et al. 1997 Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes Brain 120 1713 1721 10.1093/brain/120.10.1713 9365365 (Pubitemid 27443048)
-
(1997)
Brain
, vol.120
, Issue.10
, pp. 1713-1721
-
-
Chinnery, P.F.1
Howell, N.2
Lightowlers, R.N.3
Turnbull, D.M.4
-
3
-
-
0026681490
-
MELAS: Clinical features, biochemistry, and molecular genetics
-
10.1002/ana.410310408 1:STN:280:DyaK383msVOjsw%3D%3D 1586140
-
E Ciafaloni E Ricci S Shanske, et al. 1992 MELAS: clinical features, biochemistry, and molecular genetics Ann Neurol 31 391 398 10.1002/ana.410310408 1:STN:280:DyaK383msVOjsw%3D%3D 1586140
-
(1992)
Ann Neurol
, vol.31
, pp. 391-398
-
-
Ciafaloni, E.1
Ricci, E.2
Shanske, S.3
-
4
-
-
39749121457
-
POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection
-
DOI 10.1093/brain/awn007
-
BA Engelsen C Tzoulis B Karlsen, et al. 2008 POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection Brain 131 818 828 10.1093/brain/awn007 18238797 (Pubitemid 351294723)
-
(2008)
Brain
, vol.131
, Issue.3
, pp. 818-828
-
-
Engelsen, B.A.1
Tzoulis, C.2
Karlsen, B.3
Lillebo, A.4
Laegreid, L.M.5
Aasly, J.6
Zeviani, M.7
Bindoff, L.A.8
-
5
-
-
0034852149
-
Improving the reliability of stroke subgroup classification using the Trial of ORG 10172 in Acute Stroke Treatment (TOAST) criteria
-
1:STN:280:DC%2BD3MvpsFymuw%3D%3D 11340215
-
LB Goldstein MR Jones DB Matchar, et al. 2001 Improving the reliability of stroke subgroup classification using the Trial of ORG 10172 in Acute Stroke Treatment (TOAST) criteria Stroke 32 1091 1098 1:STN:280:DC%2BD3MvpsFymuw%3D%3D 11340215
-
(2001)
Stroke
, vol.32
, pp. 1091-1098
-
-
Goldstein, L.B.1
Jones, M.R.2
Matchar, D.B.3
-
6
-
-
0029072327
-
Clinical features of MELAS and mitochondrial DNA mutations
-
10.1002/mus.880181422
-
Y Goto 1995 Clinical features of MELAS and mitochondrial DNA mutations Muscle Nerve 18 S107 S112 10.1002/mus.880181422
-
(1995)
Muscle Nerve
, vol.18
-
-
Goto, Y.1
-
7
-
-
0025666322
-
A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
-
10.1038/348651a0 1:CAS:528:DyaK3MXls1Kqsw%3D%3D 2102678
-
Y Goto I Nonaka S Horai 1990 A mutation in the tRNA(Leu)(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies Nature 348 651 653 10.1038/348651a0 1:CAS:528:DyaK3MXls1Kqsw%3D%3D 2102678
-
(1990)
Nature
, vol.348
, pp. 651-653
-
-
Goto, Y.1
Nonaka, I.2
Horai, S.3
-
9
-
-
26444476117
-
Pathogenesis of stroke-like episodes in MELAS: Analysis of neurovascular cellular mechanisms
-
DOI 10.2174/1567202052773544
-
T Iizuka S Sakai 2005 Pathogenesis of stroke-like episodes in MELAS: analysis of neurovascular cellular mechanisms Curr Neurovasc Res 2 29 45 10.2174/1567202052773544 1:CAS:528:DC%2BD2MXitFyktrs%3D 16181098 (Pubitemid 41419944)
-
(2005)
Current Neurovascular Research
, vol.2
, Issue.1
, pp. 29-45
-
-
Iizuka, T.1
Sakai, F.2
-
10
-
-
0035779379
-
Human population genetics: Lessons from Finland
-
DOI 10.1146/annurev.genom.2.1.103
-
J Kere 2001 Human population genetics: lessons from Finland Annu Rev Genomics Hum Genet 2 103 128 10.1146/annurev.genom.2.1.103 1:CAS:528: DC%2BD3MXos1antLY%3D 11701645 (Pubitemid 35265002)
-
(2001)
Annual Review of Genomics and Human Genetics
, vol.2
, pp. 103-128
-
-
Kere, J.1
-
11
-
-
0030874726
-
Epidemiology and etiology of ischemic stroke in young adults aged 18 to 44 years in northern Sweden
-
1:STN:280:DyaK2svkvVKrtQ%3D%3D 9303012
-
B Kristensen J Malm B Carlberg, et al. 1997 Epidemiology and etiology of ischemic stroke in young adults aged 18 to 44 years in northern Sweden Stroke 28 1702 1709 1:STN:280:DyaK2svkvVKrtQ%3D%3D 9303012
-
(1997)
Stroke
, vol.28
, pp. 1702-1709
-
-
Kristensen, B.1
Malm, J.2
Carlberg, B.3
-
12
-
-
33748115079
-
Regional differences among the Finns: A Y-chromosomal perspective
-
10.1016/j.gene.2006.03.004 1:CAS:528:DC%2BD28XmsVGmurk%3D 16644145
-
T Lappalainen S Koivumäki E Salmela, et al. 2006 Regional differences among the Finns: a Y-chromosomal perspective Gene 376 207 215 10.1016/j.gene.2006.03.004 1:CAS:528:DC%2BD28XmsVGmurk%3D 16644145
-
(2006)
Gene
, vol.376
, pp. 207-215
-
-
Lappalainen, T.1
Koivumäki, S.2
Salmela, E.3
-
13
-
-
0032497128
-
Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine
-
DOI 10.1016/S0140-6736(05)79190-X
-
K Majamaa S Finnilä J Turkka, et al. 1998 Mitochondrial DNA haplogroup U as a risk factor for occipital stroke in migraine Lancet 352 455 456 10.1016/S0140-6736(05)79190-X 1:CAS:528:DyaK1cXlsleqt70%3D 9708761 (Pubitemid 28362800)
-
(1998)
Lancet
, vol.352
, Issue.9126
, pp. 455-456
-
-
Majamaa, K.1
Finnila, S.2
Turkka, J.3
Hassinen, I.E.4
-
14
-
-
0032231623
-
Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: Prevalence of the mutation in an adult population
-
DOI 10.1086/301959
-
K Majamaa JS Moilanen S Uimonen, et al. 1998 Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population Am J Hum Genet 63 447 454 10.1086/301959 1:CAS:528:DyaK1cXlslWrtbY%3D 9683591 (Pubitemid 30418626)
-
(1998)
American Journal of Human Genetics
, vol.63
, Issue.2
, pp. 447-454
-
-
Majamaa, K.1
Moilanen, J.S.2
Uimonen, S.3
Remes, A.M.4
Salmela, P.I.5
Karppa, M.6
Majamaa-Voltti, K.A.M.7
Rusanen, H.8
Sorri, M.9
Peuhkurinen, K.J.10
Hassinen, I.E.11
-
15
-
-
0030686478
-
The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct
-
1:STN:280:DyaK1c%2FjvFWrtA%3D%3D 9371917
-
K Majamaa J Turkka M Kärppä, et al. 1997 The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct Neurology 49 1331 1334 1:STN:280:DyaK1c%2FjvFWrtA%3D%3D 9371917
-
(1997)
Neurology
, vol.49
, pp. 1331-1334
-
-
Majamaa, K.1
Turkka, J.2
Kärppä, M.3
-
16
-
-
0023889006
-
MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission
-
1:STN:280:DyaL1c3gt1ChtA%3D%3D 3362373
-
P Montagna R Gallassi R Medori, et al. 1988 MELAS syndrome: characteristic migrainous and epileptic features and maternal transmission Neurology 38 751 754 1:STN:280:DyaL1c3gt1ChtA%3D%3D 3362373
-
(1988)
Neurology
, vol.38
, pp. 751-754
-
-
Montagna, P.1
Gallassi, R.2
Medori, R.3
-
17
-
-
0842265185
-
Etiology of and risk factors for cerebral infarction in young adults in western Norway: A population-based case-control study
-
DOI 10.1046/j.1351-5101.2003.00700.x
-
H Naess HI Nyland L Thomassen, et al. 2004 Etiology of and risk factors for cerebral infarction in young adults in western Norway: a population-based case-control study Eur J Neurol 11 25 30 10.1046/j.1351-5101.2003.00700.x 1:STN:280:DC%2BD3snhtVCrsg%3D%3D 14692884 (Pubitemid 38174918)
-
(2004)
European Journal of Neurology
, vol.11
, Issue.1
, pp. 25-30
-
-
Naess, H.1
Nyland, H.I.2
Thomassen, L.3
Aarseth, J.4
Myhr, K.-M.5
-
18
-
-
33847671417
-
Mitochondrial haplogroup A is a genetic risk factor for atherothrombotic cerebral infarction in Japanese females
-
DOI 10.1016/j.mito.2006.11.002, PII S1567724906002194, Mitochondria and Life
-
Y Nishigaki Y Yamada N Fuku, et al. 2007 Mitochondrial haplogroup A is a genetic risk factor for atherothrombotic cerebral infarction in Japanese females Mitochondrion 7 72 79 10.1016/j.mito.2006.11.002 1:CAS:528:DC%2BD2sXisl2rtro%3D 17257906 (Pubitemid 46351955)
-
(2007)
Mitochondrion
, vol.7
, Issue.1-2
, pp. 72-79
-
-
Nishigaki, Y.1
Yamada, Y.2
Fuku, N.3
Matsuo, H.4
Segawa, T.5
Watanabe, S.6
Kato, K.7
Yokoi, K.8
Yamaguchi, S.9
Nozawa, Y.10
Tanaka, M.11
-
19
-
-
0037605876
-
Finnish Disease Heritage I: Characteristics, causes, background
-
R Norio 2003 Finnish Disease Heritage I: characteristics, causes, background Hum Genet 112 441 456 12627295 (Pubitemid 36869044)
-
(2003)
Human Genetics
, vol.112
, Issue.5-6
, pp. 441-456
-
-
Norio, R.1
-
20
-
-
0037605877
-
Finnish Disease Heritage II: Population prehistory and genetic roots of Finns
-
12627296
-
R Norio 2003 Finnish Disease Heritage II: population prehistory and genetic roots of Finns Hum Genet 112 457 469 12627296
-
(2003)
Hum Genet
, vol.112
, pp. 457-469
-
-
Norio, R.1
-
21
-
-
0021143782
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
-
10.1002/ana.410160409 1:STN:280:DyaL2M%2FksFequg%3D%3D 6093682
-
SG Pavlakis PC Phillips S DiMauro, et al. 1984 Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome Ann Neurol 16 481 488 10.1002/ana.410160409 1:STN:280: DyaL2M%2FksFequg%3D%3D 6093682
-
(1984)
Ann Neurol
, vol.16
, pp. 481-488
-
-
Pavlakis, S.G.1
Phillips, P.C.2
Dimauro, S.3
-
22
-
-
0034574603
-
Use of population isolates for mapping complex traits
-
10.1038/35042049 1:CAS:528:DC%2BD3MXisVCgs78%3D 11252747
-
L Peltonen A Palotie K Lange 2000 Use of population isolates for mapping complex traits Nat Rev Genet 1 182 190 10.1038/35042049 1:CAS:528: DC%2BD3MXisVCgs78%3D 11252747
-
(2000)
Nat Rev Genet
, vol.1
, pp. 182-190
-
-
Peltonen, L.1
Palotie, A.2
Lange, K.3
-
23
-
-
0023148111
-
Clinical features and mechanism of occipital infarction
-
DOI 10.1002/ana.410210311
-
MS Pessin PS Lathi MB Cohen, et al. 1987 Clinical features and mechanism of occipital infarction Ann Neurol 21 290 299 10.1002/ana.410210311 1:STN:280:DyaL2s3mvFCitg%3D%3D 3606035 (Pubitemid 17035286)
-
(1987)
Annals of Neurology
, vol.21
, Issue.3
, pp. 290-299
-
-
Pessin, M.S.1
Lathi, E.S.2
Cohen, M.B.3
-
24
-
-
55849116691
-
Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in northern Europe
-
10.1317/journal.pone.0003519 10.1371/journal.pone.0003519 18949038
-
E Salmela T Lappalainen I Fransson, et al. 2008 Genome-wide analysis of single nucleotide polymorphisms uncovers population structure in northern Europe PloS ONE 3 10 e3519 10.1317/journal.pone.0003519 10.1371/journal.pone.0003519 18949038
-
(2008)
PloS ONE
, vol.3
, Issue.10
, pp. 3519
-
-
Salmela, E.1
Lappalainen, T.2
Fransson, I.3
-
25
-
-
0037208858
-
The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction
-
12471464
-
K Tanji J Gamez C Cervera, et al. 2003 The A8344G mutation in mitochondrial DNA associated with stroke-like episodes and gastrointestinal dysfunction Acta Neuropathol 105 69 75 12471464
-
(2003)
Acta Neuropathol
, vol.105
, pp. 69-75
-
-
Tanji, K.1
Gamez, J.2
Cervera, C.3
-
26
-
-
0030468182
-
Classification of European mtDNAs from an analysis of three European populations
-
1:CAS:528:DyaK2sXkslymug%3D%3D 8978068
-
A Torroni K Huoponen P Francalacci, et al. 1996 Classification of European mtDNAs from an analysis of three European populations Genetics 144 1835 1850 1:CAS:528:DyaK2sXkslymug%3D%3D 8978068
-
(1996)
Genetics
, vol.144
, pp. 1835-1850
-
-
Torroni, A.1
Huoponen, K.2
Francalacci, P.3
-
27
-
-
0027182910
-
Migraine and risk of ischaemic stroke: A case-control study
-
10.1136/bmj.307.6899.289 1:STN:280:DyaK3szosF2jug%3D%3D 8374374
-
C Tzourio S Iglesias JB Hubert, et al. 1993 Migraine and risk of ischaemic stroke: a case-control study BMJ 307 289 292 10.1136/bmj.307.6899.289 1:STN:280:DyaK3szosF2jug%3D%3D 8374374
-
(1993)
BMJ
, vol.307
, pp. 289-292
-
-
Tzourio, C.1
Iglesias, S.2
Hubert, J.B.3
-
28
-
-
0028959691
-
Case-control study of migraine and risk of ischaemic stroke in young women
-
1:STN:280:DyaK2M3islSntw%3D%3D 7711619
-
C Tzourio A Tehindrazanarivelo S Iglésias, et al. 1995 Case-control study of migraine and risk of ischaemic stroke in young women BMJ 310 830 833 1:STN:280:DyaK2M3islSntw%3D%3D 7711619
-
(1995)
BMJ
, vol.310
, pp. 830-833
-
-
Tzourio, C.1
Tehindrazanarivelo, A.2
Iglésias, S.3
-
29
-
-
0025924416
-
Rapid detection of the A-G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF)
-
1:CAS:528:DyaK3MXksVens7Y%3D 1899320
-
M Zeviani P Amati N Bresolin, et al. 1991 Rapid detection of the A-G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF) Am J Hum Genet 48 203 211 1:CAS:528:DyaK3MXksVens7Y%3D 1899320
-
(1991)
Am J Hum Genet
, vol.48
, pp. 203-211
-
-
Zeviani, M.1
Amati, P.2
Bresolin, N.3
|