-
1
-
-
0023783589
-
Incidence of stroke in young adults in Florence, Italy
-
Nencini P, Inzitari D, Baruffi MC, et al. Incidence of stroke in young adults in Florence, Italy. Stroke 1988;19:977-981.
-
(1988)
Stroke
, vol.19
, pp. 977-981
-
-
Nencini, P.1
Inzitari, D.2
Baruffi, M.C.3
-
2
-
-
0027462907
-
A prospective study of cerebral ischemia in the young. Analysis of pathogenic determinants
-
Carolei A, Marini C, Ferranti E, et al. A prospective study of cerebral ischemia in the young. Analysis of pathogenic determinants. Stroke 1993;24:362-367.
-
(1993)
Stroke
, vol.24
, pp. 362-367
-
-
Carolei, A.1
Marini, C.2
Ferranti, E.3
-
3
-
-
0028362471
-
Prognosis of young adults with ischemic stroke. A long-term follow-up study assessing recurrent vascular events and functional outcome in the Iowa Registry of Stroke in Young Adults
-
Rappelle LJ, Adams HP Jr, Heffner ML, et al. Prognosis of young adults with ischemic stroke. A long-term follow-up study assessing recurrent vascular events and functional outcome in the Iowa Registry of Stroke in Young Adults. Stroke 1994;25:1360-1365.
-
(1994)
Stroke
, vol.25
, pp. 1360-1365
-
-
Rappelle, L.J.1
Adams H.P., Jr.2
Heffner, M.L.3
-
4
-
-
0028942933
-
Ischemic stroke in young adults. Experience in 329 patients enrolled in the Iowa Registry of Stroke in Young Adults
-
Adams HP Jr, Rappelle LJ, Biller J, et al. Ischemic stroke in young adults. Experience in 329 patients enrolled in the Iowa Registry of Stroke in Young Adults. Arch Neurol 1995;52:491-495.
-
(1995)
Arch Neurol
, vol.52
, pp. 491-495
-
-
Adams H.P., Jr.1
Rappelle, L.J.2
Biller, J.3
-
5
-
-
0023748709
-
The Lausanne Stroke Registry: Analysis of 1000 consecutive patients with first stroke
-
Bogousslavsky J, van Melle G, Regli F. The Lausanne Stroke Registry: analysis of 1000 consecutive patients with first stroke. Stroke 1988;19:1083-1092.
-
(1988)
Stroke
, vol.19
, pp. 1083-1092
-
-
Bogousslavsky, J.1
Van Melle, G.2
Regli, F.3
-
6
-
-
0027249378
-
The etiology of posterior circulation infarcts: A prospective study using magnetic resonance imaging and magnetic resonance angiography
-
Bogousslavsky J, Regli F, Maeder P, Meuli R, Nader J. The etiology of posterior circulation infarcts: a prospective study using magnetic resonance imaging and magnetic resonance angiography. Neurology 1993;43:1528-1533.
-
(1993)
Neurology
, vol.43
, pp. 1528-1533
-
-
Bogousslavsky, J.1
Regli, F.2
Maeder, P.3
Meuli, R.4
Nader, J.5
-
7
-
-
0023179362
-
Ischemic stroke in adults younger than 30 years of age
-
Bogousslavsky J, Regli F. Ischemic stroke in adults younger than 30 years of age. Arch Neurol 1987;44:479-482.
-
(1987)
Arch Neurol
, vol.44
, pp. 479-482
-
-
Bogousslavsky, J.1
Regli, F.2
-
8
-
-
0023148111
-
Clinical features and mechanism of occipital infarction
-
Pessin MS, Lathi ES, Cohen MB, et al. Clinical features and mechanism of occipital infarction. Ann Neurol 1987;21:290-299.
-
(1987)
Ann Neurol
, vol.21
, pp. 290-299
-
-
Pessin, M.S.1
Lathi, E.S.2
Cohen, M.B.3
-
9
-
-
0026681490
-
MELAS: Clinical features, biochemistry, and molecular genetics
-
Ciafaloni E, Ricci E, Shanske S, et al. MELAS: clinical features, biochemistry, and molecular genetics. Ann Neurol 1992; 31:391-398.
-
(1992)
Ann Neurol
, vol.31
, pp. 391-398
-
-
Ciafaloni, E.1
Ricci, E.2
Shanske, S.3
-
10
-
-
0026708671
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): A correlative study of the clinical features and mitochondrial DNA mutation
-
Goto Y, Horai S, Matsuoka T, et al. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation. Neurology 1992;42:545-550.
-
(1992)
Neurology
, vol.42
, pp. 545-550
-
-
Goto, Y.1
Horai, S.2
Matsuoka, T.3
-
11
-
-
0028227936
-
Mitochondrial encephalomyopathies: Clinical and molecular analysis
-
Schon EA, Hirano M, DiMauro S. Mitochondrial encephalomyopathies: clinical and molecular analysis. J Bioenerg Biomembr 1994;26:291-299.
-
(1994)
J Bioenerg Biomembr
, vol.26
, pp. 291-299
-
-
Schon, E.A.1
Hirano, M.2
DiMauro, S.3
-
12
-
-
0002560834
-
Mitochondrial myopathies: Clinical features, investigation, treatment and genetic councelling
-
Schapira AHV, DiMauro S, eds. Oxford: Butterworth-Heinemann
-
Hammans SR, Morgan-Hughes JA. Mitochondrial myopathies: clinical features, investigation, treatment and genetic councelling. In: Schapira AHV, DiMauro S, eds. Mitochondrial disorders in neurology. Oxford: Butterworth-Heinemann, 1994:49-74.
-
(1994)
Mitochondrial Disorders in Neurology
, pp. 49-74
-
-
Hammans, S.R.1
Morgan-Hughes, J.A.2
-
13
-
-
0027510301
-
Cerebral blood flow in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
-
Ooiwa Y, Uematsu Y, Terada T, et al. Cerebral blood flow in mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Stroke 1993;24:304-309.
-
(1993)
Stroke
, vol.24
, pp. 304-309
-
-
Ooiwa, Y.1
Uematsu, Y.2
Terada, T.3
-
15
-
-
0028817051
-
MELAS syndrome: Imaging and proton MR spectroscopic findings
-
Castillo M, Kwock L, Green C. MELAS syndrome: imaging and proton MR spectroscopic findings. AJNR Am J Neuroradiol 1995;16:233-239.
-
(1995)
AJNR Am J Neuroradiol
, vol.16
, pp. 233-239
-
-
Castillo, M.1
Kwock, L.2
Green, C.3
-
17
-
-
0027228506
-
Mitochondrial disorders: Analysis of their clinical and imaging characteristics
-
Barkovich AJ, Good WV, Koch TK, Berg BO. Mitochondrial disorders: analysis of their clinical and imaging characteristics. AJNR Am J Neuroradiol 1993;14:1119-1137.
-
(1993)
AJNR Am J Neuroradiol
, vol.14
, pp. 1119-1137
-
-
Barkovich, A.J.1
Good, W.V.2
Koch, T.K.3
Berg, B.O.4
-
18
-
-
0025534162
-
Leu(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)
-
Leu(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes). Biochem Biophys Res Commun 1990;173:816-822.
-
(1990)
Biochem Biophys Res Commun
, vol.173
, pp. 816-822
-
-
Kobayashi, Y.1
Momoi, M.Y.2
Tominaga, K.3
-
19
-
-
0027365494
-
Lys intergenic 9-bp deletion and other mtDNA markers clearly reveal that the Tharus (South Nepal) have Oriental affinities
-
Lys intergenic 9-bp deletion and other mtDNA markers clearly reveal that the Tharus (South Nepal) have Oriental affinities. Am J Hum Genet 1993;53:609-618.
-
(1993)
Am J Hum Genet
, vol.53
, pp. 609-618
-
-
Passarino, G.1
Semino, O.2
Modiano, G.3
Santachiara-Benerecetti, A.S.4
-
20
-
-
0024242545
-
Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
-
Wallace DC, Singh G, Lott MT, et al. Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. Science 1988;242:1427-1430.
-
(1988)
Science
, vol.242
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
-
21
-
-
0027514354
-
Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial
-
Adams HP Jr, Bendixen BH, Kappelle LJ, et al. Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. Stroke 1993;24:25-41.
-
(1993)
Stroke
, vol.24
, pp. 25-41
-
-
Adams H.P., Jr.1
Bendixen, B.H.2
Kappelle, L.J.3
-
22
-
-
0028107258
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): Current concepts
-
Hirano M, Pavlakis SG. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): current concepts. J Child Neurol 1994;9:4-13.
-
(1994)
J Child Neurol
, vol.9
, pp. 4-13
-
-
Hirano, M.1
Pavlakis, S.G.2
-
23
-
-
0028218473
-
Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy
-
Houshmand M, Larsson NG, Holme E, et al. Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy. Biochim Biophys Acta 1994; 1226:49-55.
-
(1994)
Biochim Biophys Acta
, vol.1226
, pp. 49-55
-
-
Houshmand, M.1
Larsson, N.G.2
Holme, E.3
-
24
-
-
0024343409
-
Vascular involvement in mitochondrial myopathy
-
Sakuta R, Nonaka I. Vascular involvement in mitochondrial myopathy. Ann Neurol 1989;25:594-601.
-
(1989)
Ann Neurol
, vol.25
, pp. 594-601
-
-
Sakuta, R.1
Nonaka, I.2
-
25
-
-
0027452892
-
Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency
-
Muller-Höcker J, Hubner G, Bise K, et al. Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency. Arch Pathol Lab Med 1993;117:202-210.
-
(1993)
Arch Pathol Lab Med
, vol.117
, pp. 202-210
-
-
Muller-Höcker, J.1
Hubner, G.2
Bise, K.3
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