-
1
-
-
0035933047
-
Epileptic phenotypes associated with mitochondrial disorders
-
Canafoglia L., Franceschetti S., Antozzi C., et al. Epileptic phenotypes associated with mitochondrial disorders. Neurology 2001, 56:1340-1346.
-
(2001)
Neurology
, vol.56
, pp. 1340-1346
-
-
Canafoglia, L.1
Franceschetti, S.2
Antozzi, C.3
-
2
-
-
38449111685
-
Genetics of epilepsy
-
Charria-Ortiz G.A. Genetics of epilepsy. Medicina 2007, 67:601-613.
-
(2007)
Medicina
, vol.67
, pp. 601-613
-
-
Charria-Ortiz, G.A.1
-
3
-
-
34249788681
-
Gene expression, genetics, and genomics in epilepsy: Some answers, more questions
-
Crino P.B. Gene expression, genetics, and genomics in epilepsy: Some answers, more questions. Epilepsia 2007, 48(Suppl 2):42-50.
-
(2007)
Epilepsia
, vol.48
, pp. 42-50
-
-
Crino, P.B.1
-
4
-
-
34247170462
-
FXYD1 is a MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice
-
Deng V., Matagne V., Banine F., et al. FXYD1 is a MeCP2 target gene overexpressed in the brains of Rett syndrome patients and Mecp2-null mice. Human Molecular Genetics 2007, 16:640-650.
-
(2007)
Human Molecular Genetics
, vol.16
, pp. 640-650
-
-
Deng, V.1
Matagne, V.2
Banine, F.3
-
6
-
-
33748377123
-
Central nervous system manifestations of mitochondrial disorders
-
Finsterer J. Central nervous system manifestations of mitochondrial disorders. Acta Neurologica Scandinavica 2006, 114:217-238.
-
(2006)
Acta Neurologica Scandinavica
, vol.114
, pp. 217-238
-
-
Finsterer, J.1
-
7
-
-
33751422108
-
Mitochondrial dysfunction and ultrastructural damage in the hippocampus of pilocarpine-induced epileptic rat
-
Gao J., Chi Z.F., Liu X.W., et al. Mitochondrial dysfunction and ultrastructural damage in the hippocampus of pilocarpine-induced epileptic rat. Neuroscience Letters 2007, 411:152-157.
-
(2007)
Neuroscience Letters
, vol.411
, pp. 152-157
-
-
Gao, J.1
Chi, Z.F.2
Liu, X.W.3
-
8
-
-
33747594579
-
Genetic malformations of cortical development
-
Guerrini R., Marini C. Genetic malformations of cortical development. Experimental Brain Research 2006, 173:322-333.
-
(2006)
Experimental Brain Research
, vol.173
, pp. 322-333
-
-
Guerrini, R.1
Marini, C.2
-
10
-
-
33745713884
-
Phenotypic spectrum associated with mutations of mitochondrial polymerase gamma gene
-
Horvath R., Hudson G., Ferrari G., et al. Phenotypic spectrum associated with mutations of mitochondrial polymerase gamma gene. Brain 2006, 129:1674-1684.
-
(2006)
Brain
, vol.129
, pp. 1674-1684
-
-
Horvath, R.1
Hudson, G.2
Ferrari, G.3
-
11
-
-
33749001168
-
Mitochondrial DNA polymerase-gamma and human disease
-
Hudson G., Chinnery P.F. Mitochondrial DNA polymerase-gamma and human disease. Human Molecular Genetics 2006, 15:R244-R252.
-
(2006)
Human Molecular Genetics
, vol.15
, pp. R244-R252
-
-
Hudson, G.1
Chinnery, P.F.2
-
12
-
-
35848970048
-
Preliminary explorations of the role of mitochondrial proteins in refractory epilepsy: Some findings from comparative proteomics
-
Jiang W., Du B., Chi Z., et al. Preliminary explorations of the role of mitochondrial proteins in refractory epilepsy: Some findings from comparative proteomics. Journal of Neuroscience Research 2007, 85:3160-3170.
-
(2007)
Journal of Neuroscience Research
, vol.85
, pp. 3160-3170
-
-
Jiang, W.1
Du, B.2
Chi, Z.3
-
13
-
-
16444368606
-
Gene expression profiling: A new tool for pediatric neurology? editorial review
-
Johnston M.V. Gene expression profiling: A new tool for pediatric neurology? editorial review. Current Opinion in Neurology 2005, 18:89-90.
-
(2005)
Current Opinion in Neurology
, vol.18
, pp. 89-90
-
-
Johnston, M.V.1
-
14
-
-
42049090387
-
Epigenetics in congenital diseases and pervasive developmental disorders
-
Kubota T. Epigenetics in congenital diseases and pervasive developmental disorders. Environmental Health and Preventive Medicine 2008, 13:3-7.
-
(2008)
Environmental Health and Preventive Medicine
, vol.13
, pp. 3-7
-
-
Kubota, T.1
-
15
-
-
0036221686
-
The role of mitochondria in epileptogenesis
-
Kunz W.S. The role of mitochondria in epileptogenesis. Current Opinion in Neurology 2002, 15:179-184.
-
(2002)
Current Opinion in Neurology
, vol.15
, pp. 179-184
-
-
Kunz, W.S.1
-
17
-
-
33644802338
-
Analysis of genetically complex epilepsies
-
Ottman R. Analysis of genetically complex epilepsies. Epilepsia 2005, 46(Suppl 10):7-14.
-
(2005)
Epilepsia
, vol.46
, pp. 7-14
-
-
Ottman, R.1
-
18
-
-
46349088952
-
Diseases caused by defects of mitochondrial carriers: A review
-
Palmieri, F (2008) Diseases caused by defects of mitochondrial carriers: A review. Biochimica Biophysica et Acta 1777: 564-578.
-
(2008)
Biochimica Biophysica et Acta
, vol.1777
, pp. 564-578
-
-
Palmieri, F.1
-
19
-
-
8544253949
-
Mitochondrial dysfunction and oxidative stress: Cause and consequence of epileptic seizures
-
Patel M. Mitochondrial dysfunction and oxidative stress: Cause and consequence of epileptic seizures. Free Radical Biology and Medicine 2004, 37:1951-1962.
-
(2004)
Free Radical Biology and Medicine
, vol.37
, pp. 1951-1962
-
-
Patel, M.1
-
20
-
-
85069849094
-
An epileptic disease with genomic imprinting disorder: Angelman syndrome
-
Saitoh S. An epileptic disease with genomic imprinting disorder: Angelman syndrome. Neuroscience Research 2007, 58(Suppl 1):S7.
-
(2007)
Neuroscience Research
, vol.58
, pp. S7
-
-
Saitoh, S.1
-
21
-
-
10744230894
-
Gene expression profile analysis of cortical dysplasia by cDNA arrays
-
Seung-Ki K., Wang K., Hong S.J., et al. Gene expression profile analysis of cortical dysplasia by cDNA arrays. Epilepsy Research 2003, 56:175-183.
-
(2003)
Epilepsy Research
, vol.56
, pp. 175-183
-
-
Seung-Ki, K.1
Wang, K.2
Hong, S.J.3
-
22
-
-
0035019225
-
Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders
-
Sternberg D., Chatzoglou E., Laforet P., et al. Mitochondrial DNA transfer RNA gene sequence variations in patients with mitochondrial disorders. Brain 2001, 124:984-994.
-
(2001)
Brain
, vol.124
, pp. 984-994
-
-
Sternberg, D.1
Chatzoglou, E.2
Laforet, P.3
-
23
-
-
33646360581
-
Relation of pregnancy and neonatal factors to subsequent development of childhood epilepsy: A population-based cohort study
-
Whitehead E., Dodds L., Joseph K.S., et al. Relation of pregnancy and neonatal factors to subsequent development of childhood epilepsy: A population-based cohort study. Pediatrics 2006, 117:1298-1306.
-
(2006)
Pediatrics
, vol.117
, pp. 1298-1306
-
-
Whitehead, E.1
Dodds, L.2
Joseph, K.S.3
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