-
1
-
-
34248586627
-
MELAS associated with mutations in the POLG1 gene
-
DOI 10.1212/01.wnl.0000261929.92478.3e, PII 0000611420070515000018
-
Deschauer M, Tennant S, Rokicka A, He L, Kraya T, Turnbull DM, et al. MELAS associated with mutations in the POLG1 gene. Neurology 2007; 68: 1741-2. (Pubitemid 46763266)
-
(2007)
Neurology
, vol.68
, Issue.20
, pp. 1741-1742
-
-
Deschauer, M.1
Tennant, S.2
Rokicka, A.3
He, L.4
Kraya, T.5
Turnbull, D.M.6
Zierz, S.7
Taylor, R.W.8
-
2
-
-
77949878549
-
Drugs interfering with mitochondrial disorders
-
Finsterer J, Segall L. Drugs interfering with mitochondrial disorders. Drug Chem Toxicol 2010; 33: 138-51.
-
(2010)
Drug Chem Toxicol
, vol.33
, pp. 138-151
-
-
Finsterer, J.1
Segall, L.2
-
3
-
-
34250833548
-
Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation
-
DOI 10.1111/j.1600-0404.2007.00836.x
-
Finsterer J. Genetic, pathogenetic, and phenotypic implications of the mitochondrial A3243G tRNALeu(UUR) mutation. Acta Neurol Scand 2007; 116: 1-14. (Pubitemid 46976273)
-
(2007)
Acta Neurologica Scandinavica
, vol.116
, Issue.1
, pp. 1-14
-
-
Finsterer, J.1
-
4
-
-
0242494492
-
Slowly progressive spread of the stroke-like lesions in MELAS
-
Iizuka T, Sakai F, Kan S, Suzuki N. Slowly progressive spread of the stroke-like lesions in MELAS. Neurology 2003; 61: 1238-44. (Pubitemid 37377544)
-
(2003)
Neurology
, vol.61
, Issue.9
, pp. 1238-1244
-
-
Iizuka, T.1
Sakai, F.2
Kan, S.3
Suzuki, N.4
-
5
-
-
0037167550
-
Neuronal hyperexcitability in stroke-like episodes of MELAS syndrome
-
Iizuka T, Sakai F, Suzuki N, Hata T, Tsukahara S, Fukuda M, et al. Neuronal hyperexcitability in stroke-like episodes of MELAS syndrome. Neurology 2002; 59: 816-24.
-
(2002)
Neurology
, vol.59
, pp. 816-824
-
-
Iizuka, T.1
Sakai, F.2
Suzuki, N.3
Hata, T.4
Tsukahara, S.5
Fukuda, M.6
-
6
-
-
59149103919
-
Different neuroradiological findings during two stroke-like-episodes in a patient with a congenital disorder of glycosylation type Ia
-
Ishikawa N, Tajima G, Ono H, Kobayashi M. Different neuroradiological findings during two stroke-like-episodes in a patient with a congenital disorder of glycosylation type Ia. Brain Dev 2009; 31: 240-3.
-
(2009)
Brain Dev
, vol.31
, pp. 240-243
-
-
Ishikawa, N.1
Tajima, G.2
Ono, H.3
Kobayashi, M.4
-
7
-
-
45849142222
-
Serial brain imaging analysis of stroke-like-episodes in MELAS
-
Ito H, Mori K, Harada M, Minato M, Naito E, Takeuchi M, et al. Serial brain imaging analysis of stroke-like-episodes in MELAS. Brain Dev 2008; 30: 483-8.
-
(2008)
Brain Dev
, vol.30
, pp. 483-488
-
-
Ito, H.1
Mori, K.2
Harada, M.3
Minato, M.4
Naito, E.5
Takeuchi, M.6
-
8
-
-
4444325550
-
Beneficial effect of L-arginine for stroke-like episode in MELAS
-
DOI 10.1016/j.braindev.2004.01.006, PII S0387760404000403
-
Kubota M, Sakakihara Y, Mori M, Yamagata T, Momoi-Yoshida M. Beneficial effect of L-arginine for stroke-like episode in MELAS. Brain Dev 2004; 26: 481-3. (Pubitemid 39209388)
-
(2004)
Brain and Development
, vol.26
, Issue.7
, pp. 481-483
-
-
Kubota, M.1
Sakakihara, Y.2
Mori, M.3
Yamagata, T.4
Momoi-Yoshida, M.5
-
9
-
-
33847632882
-
Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA
-
DOI 10.1007/s11011-006-9039-9
-
Lin CM, Thajeb P. Valproic acid aggravates epilepsy due to MELAS in a patient with an A3243G mutation of mitochondrial DNA. Metab Brain Dis 2007; 22: 105-9. (Pubitemid 46354826)
-
(2007)
Metabolic Brain Disease
, vol.22
, Issue.1
, pp. 105-109
-
-
Lin, C.-M.1
Thajeb, P.2
-
10
-
-
0033809548
-
Serial diffusion-weighted imaging in MELAS
-
Ohshita T, Oka M, Imon Y, Watanabe C, Katayama S, Yamaguchi S, et al. Serial diffusion-weighted imaging in MELAS. Neuroradiology 2000; 42: 651-6.
-
(2000)
Neuroradiology
, vol.42
, pp. 651-656
-
-
Ohshita, T.1
Oka, M.2
Imon, Y.3
Watanabe, C.4
Katayama, S.5
Yamaguchi, S.6
-
11
-
-
74949124717
-
Inherited metabolic disorders and stroke part 1: Fabry disease and mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
-
Testai FD, Gorelick PB. Inherited metabolic disorders and stroke part 1: Fabry disease and mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Arch Neurol 2010; 67: 19-24.
-
(2010)
Arch Neurol
, vol.67
, pp. 19-24
-
-
Testai, F.D.1
Gorelick, P.B.2
-
12
-
-
0034924390
-
Carnitine-responsive carnitine insufficiency in a case of mtDNA 8993T>C mutation associated Leigh syndrome
-
DOI 10.1023/A:1010537527291
-
Toth G, Morava E, Bene J, Selhorst JJ, Overmars H, Vreken P, et al. Carnitine-responsive carnitine insufficiency in a case of mtDNA 8993T>C mutation associated Leigh syndrome. J Inherit Metab Dis 2001; 24: 421-2. (Pubitemid 32677529)
-
(2001)
Journal of Inherited Metabolic Disease
, vol.24
, Issue.3
, pp. 421-422
-
-
Toth, G.1
Morava, E.2
Bene, J.3
Selhorst, J.J.M.4
Overmars, H.5
Vreken, P.6
Molnar, J.7
Farkas, V.8
Melegh, B.9
-
13
-
-
60549093363
-
Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like-episodes
-
Tzoulis C, Bindoff LA. Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like-episodes. Stroke 2009; 40: e15-7.
-
(2009)
Stroke
, vol.40
-
-
Tzoulis, C.1
Bindoff, L.A.2
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