-
1
-
-
0028942933
-
Ischemic stroke in young adults: Experience in 329 patients enrolled in the Iowa Registry of stroke in young adults
-
Adams HP Jr., Kappelle 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 Jr., H.P.1
Kappelle, L.J.2
Biller, J.3
-
2
-
-
0030874726
-
Epidemiology and etiology of ischemic stroke in young adults aged 18 to 44 years in northern Sweden
-
Kristensen B, Malm J, Carlberg B, et al. Epidemiology and etiology of ischemic stroke in young adults aged 18 to 44 years in northern Sweden. Stroke 1997;28:1702-1709.
-
(1997)
Stroke
, vol.28
, pp. 1702-1709
-
-
Kristensen, B.1
Malm, J.2
Carlberg, B.3
-
3
-
-
0036901467
-
Stroke in the young in the northern Manhattan stroke study
-
Jacobs BS, Boden-Albala B, Lin IF, Sacco RL. Stroke in the young in the northern Manhattan stroke study. Stroke 2002;33:2789-2793.
-
(2002)
Stroke
, vol.33
, pp. 2789-2793
-
-
Jacobs, B.S.1
Boden-Albala, B.2
Lin, I.F.3
Sacco, R.L.4
-
4
-
-
0037243718
-
Ischaemic stroke in young people: A prospective and long-term follow-up study
-
Musolino R, La Spina P, Granata A, et al. Ischaemic stroke in young people: a prospective and long-term follow-up study. Cerebrovasc Dis 2003;15:121-128.
-
(2003)
Cerebrovasc Dis
, vol.15
, pp. 121-128
-
-
Musolino, R.1
La Spina, P.2
Granata, A.3
-
5
-
-
2342477751
-
-
Siqueira JI Neto, Santos AC, Fabio SR, Sakamoto AC. Cerebral infarction in patients aged 15 to 40 years. Stroke 1996;27:2016-2019.
-
Siqueira JI Neto, Santos AC, Fabio SR, Sakamoto AC. Cerebral infarction in patients aged 15 to 40 years. Stroke 1996;27:2016-2019.
-
-
-
-
7
-
-
0021143782
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome
-
Pavlakis SG, Philips PC, Dimauro S, De Vivo DC, Rowland LP. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: a distinctive clinical syndrome. Ann Neurol 1984;16:481-488.
-
(1984)
Ann Neurol
, vol.16
, pp. 481-488
-
-
Pavlakis, S.G.1
Philips, P.C.2
Dimauro, S.3
De Vivo, D.C.4
Rowland, L.P.5
-
8
-
-
0034005475
-
Mitochondrial myopathy diagnosis
-
Shoffner JM. Mitochondrial myopathy diagnosis. Neurol Clin 2000;18:105-123.
-
(2000)
Neurol Clin
, vol.18
, pp. 105-123
-
-
Shoffner, J.M.1
-
9
-
-
0023410065
-
MELAS (mitochondrial encephalopathy, lactic acidosis and stroke-like episodes): Relato de um caso
-
Werneck LC, Abdalla H, Lohr A. MELAS (mitochondrial encephalopathy, lactic acidosis and stroke-like episodes): relato de um caso. Arq Neuropsiquiatr 1987;45:288-294.
-
(1987)
Arq Neuropsiquiatr
, vol.45
, pp. 288-294
-
-
Werneck, L.C.1
Abdalla, H.2
Lohr, A.3
-
10
-
-
0034676760
-
Increased risk of stroke in patients with the A12308G polymorphism in mitochondria
-
Pulkes Y, Seeney MG, Hanna MG. Increased risk of stroke in patients with the A12308G polymorphism in mitochondria. Lancet 2000:356:2068-2069.
-
(2000)
Lancet
, vol.356
, pp. 2068-2069
-
-
Pulkes, Y.1
Seeney, M.G.2
Hanna, M.G.3
-
11
-
-
0242494492
-
Slowly progressive spread of the stroke-like lesion in MELAS
-
Iizuka T, Sakai F, Kan S, Suzuki N. Slowly progressive spread of the stroke-like lesion in MELAS. Neurology 2003:61:1238-1244.
-
(2003)
Neurology
, vol.61
, pp. 1238-1244
-
-
Iizuka, T.1
Sakai, F.2
Kan, S.3
Suzuki, N.4
-
12
-
-
0028109362
-
-
Marie SKN, Goto Y, Passos-Bueno MR, et al. A Caucasian family with the 3271 mutation in mitochondrial DNA. Biochem Med Biol 1994;52:136-139.
-
Marie SKN, Goto Y, Passos-Bueno MR, et al. A Caucasian family with the 3271 mutation in mitochondrial DNA. Biochem Med Biol 1994;52:136-139.
-
-
-
-
13
-
-
0027514354
-
Classification of subtype of acute ischemic stroke: Definitions for use in a multicenter clinical trial
-
Adams HP, Bendixen BH, Kappelle J, et al. Classification of subtype of acute ischemic stroke: definitions for use in a multicenter clinical trial. Stroke 1993;24:35-41.
-
(1993)
Stroke
, vol.24
, pp. 35-41
-
-
Adams, H.P.1
Bendixen, B.H.2
Kappelle, J.3
-
14
-
-
0029961518
-
Arterial territories of the human brain: Brainstem and cerebellum
-
Tatu L, Moulin T, Bogousslavsky J, Duvernoy H. Arterial territories of the human brain: brainstem and cerebellum. Neurology 1996;47:1125-1135.
-
(1996)
Neurology
, vol.47
, pp. 1125-1135
-
-
Tatu, L.1
Moulin, T.2
Bogousslavsky, J.3
Duvernoy, H.4
-
15
-
-
0031747954
-
Arterial territories of the human brain: Cerebral hemispheres
-
Tatu L, Moulin T, Bogousslavsky J, Duvernoy H. Arterial territories of the human brain: cerebral hemispheres. Neurology 1998;50:1699-1708.
-
(1998)
Neurology
, vol.50
, pp. 1699-1708
-
-
Tatu, L.1
Moulin, T.2
Bogousslavsky, J.3
Duvernoy, H.4
-
16
-
-
34547644016
-
-
Dubowitz V. Histological and histochemical stains and reactions. In Dubowitz V, Sewry CA, Fitzsimons RB (Eds). Muscle biopsy: a practical approach. London, Bailure-Tindall; 1985:19-40.
-
Dubowitz V. Histological and histochemical stains and reactions. In Dubowitz V, Sewry CA, Fitzsimons RB (Eds). Muscle biopsy: a practical approach. London, Bailure-Tindall; 1985:19-40.
-
-
-
-
17
-
-
22944465152
-
-
The International Classification of Headache Disorders, 2.Ed
-
The International Classification of Headache Disorders, 2.Ed. Cephalalgia 2004;24(Suppl 1):24-36.
-
(2004)
Cephalalgia
, vol.24
, Issue.SUPPL. 1
, pp. 24-36
-
-
-
18
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polensky HE. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 1988;16:1215.
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polensky, H.E.3
-
19
-
-
0030686478
-
The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct
-
Majamaa K, Turkka J, Karppa M, Winqvist S, Hassinen I. The common MELAS mutation A3243G in mitochondrial DNA among young patients with an occipital brain infarct. Neurology 1997;49:1331-1334.
-
(1997)
Neurology
, vol.49
, pp. 1331-1334
-
-
Majamaa, K.1
Turkka, J.2
Karppa, M.3
Winqvist, S.4
Hassinen, I.5
-
20
-
-
0033931918
-
Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritance
-
Di Gennaro G, Buzzi MG, Ciccarelli O, et al. Assessing the relative incidence of mitochondrial DNA A3243G in migraine without aura with maternal inheritance. Headache 2000;40:568-571.
-
(2000)
Headache
, vol.40
, pp. 568-571
-
-
Di Gennaro, G.1
Buzzi, M.G.2
Ciccarelli, O.3
-
21
-
-
3142672016
-
Study of mitochondrial DNA mutations in patients with migraine with prolonged aura
-
Rozen TD, Shanske S, Otaegui D, et al. Study of mitochondrial DNA mutations in patients with migraine with prolonged aura. Headache 2004;44:674-677.
-
(2004)
Headache
, vol.44
, pp. 674-677
-
-
Rozen, T.D.1
Shanske, S.2
Otaegui, D.3
-
22
-
-
28144463235
-
Case 36-2005: A 61-year-old woman with seizure, disturbed gait, and altered mental status
-
Dickerson BC, Holtzman D, Grant E, Tian D. Case 36-2005: a 61-year-old woman with seizure, disturbed gait, and altered mental status. NEJM 2005;353:2271-2280.
-
(2005)
NEJM
, vol.353
, pp. 2271-2280
-
-
Dickerson, B.C.1
Holtzman, D.2
Grant, E.3
Tian, D.4
-
23
-
-
0034870693
-
Retrospective study of a large population of patients affected with mitochondrial disorders: Clinical, morphological and molecular genetic evaluation
-
Sciacco M, Prelle A, Comi GP, et al. Retrospective study of a large population of patients affected with mitochondrial disorders: clinical, morphological and molecular genetic evaluation. J Neurol 2001;248:778-788.
-
(2001)
J Neurol
, vol.248
, pp. 778-788
-
-
Sciacco, M.1
Prelle, A.2
Comi, G.P.3
-
24
-
-
0027163613
-
Ophalmologic manifestations in MELAS syndrome
-
Fang W, Huang CC, Lee CC, Chieng SY, Pang CY, Wei YH. Ophalmologic manifestations in MELAS syndrome. Arch Neurol 1993;50:977-980.
-
(1993)
Arch Neurol
, vol.50
, pp. 977-980
-
-
Fang, W.1
Huang, C.C.2
Lee, C.C.3
Chieng, S.Y.4
Pang, C.Y.5
Wei, Y.H.6
-
25
-
-
0026906885
-
Mutation in mitochondrial tRNA leu (UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
-
Van den Ouweland JMW, Lemkes HHPJ, Ruitenbeek LA, et al. Mutation in mitochondrial tRNA leu (UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness. Nature Genetics 1992;1:368-371.
-
(1992)
Nature Genetics
, vol.1
, pp. 368-371
-
-
Van den Ouweland, J.M.W.1
Lemkes, H.H.P.J.2
Ruitenbeek, L.A.3
-
26
-
-
0029804924
-
Monozygotic twins with MELAS-like syndrome lacking ragged red fibers and lactic acidaemia
-
Melberg A, Akerlund P, RAininko R, et al. Monozygotic twins with MELAS-like syndrome lacking ragged red fibers and lactic acidaemia. Acta Neurol Scand 1996;94:233.
-
(1996)
Acta Neurol Scand
, vol.94
, pp. 233
-
-
Melberg, A.1
Akerlund, P.2
RAininko, R.3
-
27
-
-
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
-
28
-
-
0023270881
-
Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy
-
Ohama E, Ohara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T. Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy Acta Neuropathol 1987;74:226-233.
-
(1987)
Acta Neuropathol
, vol.74
, pp. 226-233
-
-
Ohama, E.1
Ohara, S.2
Ikuta, F.3
Tanaka, K.4
Nishizawa, M.5
Miyatake, T.6
-
29
-
-
11144355448
-
Cerebral lactic acidosis correlates with neurological impairment in MELAS
-
Kaufmann P, Shungu DC, Sano MC, et al. Cerebral lactic acidosis correlates with neurological impairment in MELAS. Neurology 2004;62:1297-1302.
-
(2004)
Neurology
, vol.62
, pp. 1297-1302
-
-
Kaufmann, P.1
Shungu, D.C.2
Sano, M.C.3
-
30
-
-
0035109913
-
Diffusion-weighted imaging in a case of mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes
-
Yonemura K, Hasegawa Y, Kimura K, Minematsu K, Yamagushi T. Diffusion-weighted imaging in a case of mitochondrial myopathy, encephalopathy, lactic acidosis and strokelike episodes. AJNR 2001;22:269-272.
-
(2001)
AJNR
, vol.22
, pp. 269-272
-
-
Yonemura, K.1
Hasegawa, Y.2
Kimura, K.3
Minematsu, K.4
Yamagushi, T.5
-
31
-
-
4644269393
-
Varying loads of the mitochondrial DNA A3243G mutation in different tissues: Implications for diagnosis
-
Shanske S, Pancrudo J, Kaufmann P, et al. Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosis. Am J Med Genet 2004;130:134-137.
-
(2004)
Am J Med Genet
, vol.130
, pp. 134-137
-
-
Shanske, S.1
Pancrudo, J.2
Kaufmann, P.3
-
32
-
-
0031416014
-
Anesthetic considerations in patients presenting with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome
-
Thompson VA, Wahr JA. Anesthetic considerations in patients presenting with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome. Anesth Analg 1997;85:1404-1406.
-
(1997)
Anesth Analg
, vol.85
, pp. 1404-1406
-
-
Thompson, V.A.1
Wahr, J.A.2
-
33
-
-
13844321746
-
L-arginine improves the symptoms of strokelike episodes in MELAS
-
Koga Y, Akita Y, Nishioka J, et al. L-arginine improves the symptoms of strokelike episodes in MELAS. Neurology 2005;64:710-712.
-
(2005)
Neurology
, vol.64
, pp. 710-712
-
-
Koga, Y.1
Akita, Y.2
Nishioka, J.3
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