-
1
-
-
77957957247
-
The mitochondrial proteome and human disease
-
doi:10.146/anurev-genom-082509-141720 PubMed
-
Calvo SE, Mootha VK. The mitochondrial proteome and human disease. Annu Rev Genomics Hum Genet. 2010;11(1):25-44. doi:10.146/anurev-genom-082509-141720 PubMed
-
(2010)
Annu Rev Genomics Hum Genet
, vol.11
, Issue.1
, pp. 25-44
-
-
Calvo, S.E.1
Mootha, V.K.2
-
2
-
-
0037972522
-
Mitochondrial respiratory-chain diseases
-
DOI 10.1056/NEJMra022567
-
DiMauro S, Schon EA. Mitochondrial respiratory-chain diseases. N Engl J Med. 2003;348(26):2656-2668. doi:10.1056/NEJMra02567 PubMed (Pubitemid 36741594)
-
(2003)
New England Journal of Medicine
, vol.348
, Issue.26
, pp. 2656-2668
-
-
DiMauro, S.1
Schon, E.A.2
-
3
-
-
0004235298
-
-
American Psychiatric Association. Fourth Edition, Text Revision. Washington, DC: American Psychiatric Association
-
American Psychiatric Association. Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition, Text Revision. Washington, DC: American Psychiatric Association; 2000.
-
(2000)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
4
-
-
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(4884):1427-1430. doi:10.126/science.3201231 PubMed (Pubitemid 19008070)
-
(1988)
Science
, vol.242
, Issue.4884
, pp. 1427-1430
-
-
Wallace, D.C.1
Singh, G.2
Lott, M.T.3
Hodge, J.A.4
Schurr, G.T.5
Lezza, A.M.S.6
Elsas II, L.J.7
Nikoskelainen, E.K.8
-
5
-
-
0033862962
-
The epidemiology of pathogenic mitochondrial DNA mutations
-
DOI 10.1002/1531-8249(200008)48:2<188::AID-ANA8>3.0.CO;2-P
-
Chinnery PF, Johnson MA, Wardell TM, et al. The epidemiology of pathogenic mitochondrial DNA mutations. Ann Neurol. 2000;48(2): 188-193. doi:10.102/1531-8249(208)48:2〈18:AID-ANA8〉3.0.CO;2-PubMed (Pubitemid 30617037)
-
(2000)
Annals of Neurology
, vol.48
, Issue.2
, pp. 188-193
-
-
Chinnery, P.F.1
Johnson, M.A.2
Wardell, T.M.3
Singh-Kler, R.4
Hayes, C.5
Brown, D.T.6
Taylor, R.W.7
Bindoff, L.A.8
Turnbull, D.M.9
-
6
-
-
39049156470
-
Prevalence of mitochondrial DNA disease in adults
-
DOI 10.1002/ana.21217
-
Schaefer AM, McFarland R, Blakely EL, et al. Prevalence of mitochondrial DNA disease in adults. Ann Neurol. 2008;63(1):35-39. doi:10.102/ana.21217 PubMed (Pubitemid 351240549)
-
(2008)
Annals of Neurology
, vol.63
, Issue.1
, pp. 35-39
-
-
Schaefer, A.M.1
McFarland, R.2
Blakely, E.L.3
He, L.4
Whittaker, R.G.5
Taylor, R.W.6
Chinnery, P.F.7
Turnbull, D.M.8
-
7
-
-
79952959359
-
Mitochondrial dysfunction and pathology in bipolar disorder and schizophrenia
-
doi:10.1016/j.ijdevneu.2010.08.07 PubMed
-
Clay HB, Sillivan S, Konradi C. Mitochondrial dysfunction and pathology in bipolar disorder and schizophrenia. Int J Dev Neurosci. 2011;29(3):311-324. doi:10.1016/j.ijdevneu.2010.08.07 PubMed
-
(2011)
Int J Dev Neurosci
, vol.29
, Issue.3
, pp. 311-324
-
-
Clay, H.B.1
Sillivan, S.2
Konradi, C.3
-
8
-
-
34447132960
-
Psychiatric comorbidity in 36 adults with mitochondrial cytopathies
-
Fattal O, Link J, Quinn K, et al. Psychiatric comorbidity in 36 adults with mitochondrial cytopathies. CNS Spectr. 2007;12(6):429-438. PubMed (Pubitemid 47035289)
-
(2007)
CNS Spectrums
, vol.12
, Issue.6
, pp. 429-438
-
-
Fattal, O.1
Link, J.2
Quinn, K.3
Cohen, B.H.4
Franco, K.5
-
9
-
-
23944518354
-
Risperidone-induced psychosis and depression in a child with a mitochondrial disorder
-
DOI 10.1089/cap.2005.15.520
-
Ahn MS, Sims KB, Frazier JA. Risperidone-induced psychosis and depression in a child with a mitochondrial disorder. J Child Adolesc Psychopharmacol. 2005;15(3):520-525. doi:10.1089/cap.205.15.520 PubMed (Pubitemid 41192836)
-
(2005)
Journal of Child and Adolescent Psychopharmacology
, vol.15
, Issue.3
, pp. 520-525
-
-
Ahn, M.S.1
Sims, K.B.2
Frazier, J.A.3
-
10
-
-
0033837482
-
Psychosis and progressing dementia: Presenting features of a mitochondriopathy
-
Amemiya S, Hamamoto M, Goto Y, et al. Psychosis and progressing dementia: presenting features of a mitochondriopathy. Neurology. 2000;55(4):600-601. PubMed (Pubitemid 30647271)
-
(2000)
Neurology
, vol.55
, Issue.4
, pp. 600-601
-
-
Amemiya, S.1
Hamamoto, M.2
Goto, Y.3
Komaki, H.4
Nishino, I.5
Nonaka, I.6
Katayama, Y.7
-
11
-
-
22844444188
-
Deep white matter pathologic features in watershed regions: A novel pattern of central nervous system involvement in MELAS
-
DOI 10.1001/archneur.62.7.1154
-
Apostolova LG, White M, Moore SA, et al. Deep white matter pathologic features in watershed regions: a novel pattern of central nervous system involvement in MELAS. Arch Neurol. 2005;62(7):1154-1156. doi:10.101/archneur.62. 7.154 PubMed (Pubitemid 41043741)
-
(2005)
Archives of Neurology
, vol.62
, Issue.7
, pp. 1154-1156
-
-
Apostolova, L.G.1
White, M.2
Moore, S.A.3
Davis, P.H.4
-
12
-
-
0027055141
-
An autopsy case of mitochondrial encephalomyopathy (MELAS) with special reference to extra-neuromuscular abnormalities
-
Ban S, Mori N, Saito K, et al. An autopsy case of mitochondrial encephalomyopathy (MELAS) with special reference to extraneuromuscular abnormalities. Acta Pathol Jpn. 1992;42(11):818-825. PubMed (Pubitemid 23020393)
-
(1992)
Acta Pathologica Japonica
, vol.42
, Issue.11
, pp. 818-825
-
-
Ban, S.1
Mori, N.2
Saito, K.3
Mizukami, K.4
Suzuki, T.5
Shiraishi, H.6
-
13
-
-
0029938221
-
MELAS: Clinical and pathologic correlations with MRI, xenon/CT, and MR spectroscopy
-
Clark JM, Marks MP, Adalsteinsson E, et al. MELAS: Clinical and pathologic correlations with MRI, xenon/CT, and MR spectroscopy. Neurology. 1996;46(1):223-227. PubMed (Pubitemid 26156134)
-
(1996)
Neurology
, vol.46
, Issue.1
, pp. 223-227
-
-
Clark, J.M.1
Marks, M.P.2
Adalsteinsson, E.3
Spielman, D.M.4
Shuster, D.5
Horoupian, D.6
Albers, G.W.7
-
14
-
-
0035198238
-
Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C>T mutation
-
DOI 10.1023/A:1012719211505
-
Campos Y, García A, Eiris J, et al. Mitochondrial myopathy, cardiomyopathy and psychiatric illness in a Spanish family harbouring the mtDNA 3303C > T mutation. J Inherit Metab Dis. 2001;24(6):685-687. doi:10.1023/A:101271921505 PubMed (Pubitemid 33130091)
-
(2001)
Journal of Inherited Metabolic Disease
, vol.24
, Issue.6
, pp. 685-687
-
-
Campos, Y.1
Garcia, A.2
Eiris, J.3
Fuster, M.4
Rubio, J.C.5
Martin, M.A.6
Del, H.P.7
Pintos, E.8
Castro-Gago, M.9
Arenas, J.10
-
15
-
-
0024822523
-
Kearns-Sayre syndrome: Mitochondrial encephalomyopathy caused by deficiency of the respiratory chain
-
PubMed
-
Desnuelle C, Pellissier JF, Serratrice G, et al. [Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain]. Rev Neurol (Paris). 1989;145(12):842-850. PubMed
-
(1989)
Rev Neurol (Paris)
, vol.145
, Issue.12
, pp. 842-850
-
-
Desnuelle, C.1
Pellissier, J.F.2
Serratrice, G.3
-
16
-
-
0345505275
-
Alterations of rCBF and mitochondrial dysfunction in major depressive disorder: A case report
-
doi:10.1034/j.160-047.203.0218.x PubMed
-
Gardner A, Pagani M, Wibom R, et al. Alterations of rCBF and mitochondrial dysfunction in major depressive disorder: a case report. Acta Psychiatr Scand. 2003;107(3):233-239. doi:10.1034/j.160-047.203.0218.x PubMed
-
(2003)
Acta Psychiatr Scand
, vol.107
, Issue.3
, pp. 233-239
-
-
Gardner, A.1
Pagani, M.2
Wibom, R.3
-
17
-
-
0030717547
-
Psychiatric symptoms in a patient with diabetes mellitus associated with point mutation in mitochondrial DNA
-
DOI 10.1016/S0006-3223(97)00351-X, PII S000632239700351X
-
Inagaki T, Ishino H, Seno H, et al. Psychiatric symptoms in a patient with diabetes mellitus associated with point mutation in mitochondrial DNA. Biol Psychiatry. 1997;42(11):1067-1069. doi:10.1016/S06-323(97)0351-X PubMed (Pubitemid 27496437)
-
(1997)
Biological Psychiatry
, vol.42
, Issue.11
, pp. 1067-1069
-
-
Inagaki, T.1
Ishino, H.2
Seno, H.3
Ohguni, S.4
Tanaka, J.5
Kato, Y.6
-
18
-
-
0035960570
-
A mutation in mt tRNALeu(UUR) causing a neuropsychiatric syndrome with depression and cataract
-
Jaksch M, Lochmuller H, Schmitt F, et al. A mutation in mt tRNALeu(UUR) causing a neuropsychiatric syndrome with depression and cataract. Neurology. 2001;57(10):1930-1931. PubMed (Pubitemid 33096717)
-
(2001)
Neurology
, vol.57
, Issue.10
, pp. 1930-1931
-
-
Jaksch, M.1
Lochmuller, H.2
Schmitt, F.3
Volpel, B.4
Obermaier-Kusser, B.5
Horvath, R.6
-
19
-
-
9444264677
-
Alzheimer-type pathology in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
-
DOI 10.1007/s004010050524
-
Kaido M, Fujimura H, Soga F, et al. Alzheimer-type pathology in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). Acta Neuropathol. 1996;92(3):312-318. doi:10.107/s0401050524 PubMed (Pubitemid 26278964)
-
(1996)
Acta Neuropathologica
, vol.92
, Issue.3
, pp. 312-318
-
-
Kaido, M.1
Fujimura, H.2
Soga, F.3
Toyooka, K.4
Yoshikawa, H.5
Nishimura, T.6
Higashi, T.7
Inui, K.8
Imanishi, H.9
Yorifuji, S.10
Yanagihara, T.11
-
20
-
-
0036653405
-
Psychiatric symptoms in a patient with the clinical features of MELAS
-
Kiejna A, DiMauro S, Adamowski T, et al. Psychiatric symptoms in a patient with the clinical features of MELAS. Med Sci Monit. 2002;8(7):CS66-CS72. PubMed (Pubitemid 34826780)
-
(2002)
Medical Science Monitor
, vol.8
, Issue.7
-
-
Kiejna, A.1
DiMauro, S.2
Adamowski, T.3
Rymaszewska, J.4
Leszek, J.5
Pachalska, M.6
-
21
-
-
1642512286
-
Persistent organic personality change as rare psychiatric manifestation of MELAS syndrome
-
PubMed doi:10.107/s0415-03-0260-8
-
Köller H, Kornischka J, Neuen-Jacob E, et al. Persistent organic personality change as rare psychiatric manifestation of MELAS syndrome. J Neurol. 2003;250(12):1501-1502. PubMed doi:10.107/s0415-03-0260-8
-
(2003)
J Neurol
, vol.250
, Issue.12
, pp. 1501-1502
-
-
Köller, H.1
Kornischka, J.2
Neuen-Jacob, E.3
-
22
-
-
68149108296
-
Psychiatric comorbidity and impact on health service utilization in a community sample of patients with epilepsy
-
doi:10.1/j.1528-167.209.02165.x PubMed
-
Lacey CJ, Salzberg MR, Roberts H, et al. Psychiatric comorbidity and impact on health service utilization in a community sample of patients with epilepsy. Epilepsia. 2009;50(8):1991-1994. doi:10.1/j.1528-167.209.02165.x PubMed
-
(2009)
Epilepsia
, vol.50
, Issue.8
, pp. 1991-1994
-
-
Lacey, C.J.1
Salzberg, M.R.2
Roberts, H.3
-
23
-
-
0030869026
-
Mental disorders in diabetic patients with mitochondrial transfer RNA(Leu (UUR)) mutation at position 3243
-
DOI 10.1016/S0006-3223(97)00280-1, PII S0006322397002801
-
Miyaoka H, Suzuki Y, Taniyama M, et al. Mental disorders in diabetic patients with mitochondrial transfer RNA(Leu) (UUR) mutation at position 3243. Biol Psychiatry. 1997;42(6):524-526. doi:10.1016/S06-323(97)0280-1 PubMed (Pubitemid 27394622)
-
(1997)
Biological Psychiatry
, vol.42
, Issue.6
, pp. 524-526
-
-
Miyaoka, H.1
Suzuki, Y.2
Taniyama, M.3
Miyaoka, Y.4
Shishikura, K.5
Kamijima, K.6
Atsumi, Y.7
Matsuoka, K.8
-
24
-
-
0026566806
-
Central nervous system changes in mitochondrial encephalomyopathy: Light and electron microscopic study
-
doi:10.107/BF0713541 PubMed
-
Mizukami K, Sasaki M, Suzuki T, et al. Central nervous system changes in mitochondrial encephalomyopathy: light and electron microscopic study. Acta Neuropathol. 1992;83(4):449-452. doi:10.107/BF0713541 PubMed
-
(1992)
Acta Neuropathol
, vol.83
, Issue.4
, pp. 449-452
-
-
Mizukami, K.1
Sasaki, M.2
Suzuki, T.3
-
25
-
-
0028118798
-
Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder
-
Nørby S, Lestienne P, Nelson I, et al. Juvenile Kearns-Sayre syndrome initially misdiagnosed as a psychosomatic disorder. J Med Genet. 1994;31(1):45-50. doi:10.136/jmg.31.1.45 PubMed (Pubitemid 24037946)
-
(1994)
Journal of Medical Genetics
, vol.31
, Issue.1
, pp. 45-50
-
-
Norby, S.1
Lestienne, P.2
Nelson, I.3
Nielsen, I.-M.4
Schmalbruch, H.5
Sjo, O.6
Warburg, M.7
-
26
-
-
0031158099
-
Diabetes mellitus associated with mitochondrial myopathy and schizophrenia: A possible link between diabetes mellitus and schizophrenia
-
doi:10.102/(SICI)1096-9136(19706)14:6<503:AID-DIA394>3.0.CO;2-1 PubMed
-
Odawara M, Isaka M, Tada K, et al. Diabetes mellitus associated with mitochondrial myopathy and schizophrenia: a possible link between diabetes mellitus and schizophrenia. Diabet Med. 1997;14(6):503. doi:10.102/(SICI)1096- 9136(19706)14:6<503:AID-DIA394>3.0.CO;2-1 PubMed
-
(1997)
Diabet Med
, vol.14
, Issue.6
, pp. 503
-
-
Odawara, M.1
Isaka, M.2
Tada, K.3
-
27
-
-
0030907493
-
Depressive disorder due to mitochondrial transfer RNA(Leu(UUR)) mutation
-
DOI 10.1016/S0006-3223(97)00005-X, PII S000632239700005X
-
Onishi H, Kawanishi C, Iwasawa T, et al. Depressive disorder due to mitochondrial transfer RNALeu(UUR) mutation. Biol Psychiatry. 1997;41(11):1137-1139. doi:10.1016/S06-323(97)05-X PubMed (Pubitemid 27240008)
-
(1997)
Biological Psychiatry
, vol.41
, Issue.11
, pp. 1137-1139
-
-
Onishi, H.1
Kawanishi, C.2
Iwasawa, T.3
Osaka, H.4
Hanihara, T.5
Inoue, K.6
Yamada, Y.7
Kosaka, K.8
-
28
-
-
0031744223
-
Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: An autopsy report
-
Prayson RA, Wang N. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS) syndrome: an autopsy report. Arch Pathol Lab Med. 1998;122(11):978-981. PubMed (Pubitemid 28521044)
-
(1998)
Archives of Pathology and Laboratory Medicine
, vol.122
, Issue.11
, pp. 978-981
-
-
Prayson, R.A.1
Wang, N.2
-
29
-
-
0025908312
-
Therapeutic effect of sodium dichloroacetate on visual and auditory hallucinations in a patient with MELAS
-
doi:10.105/s-208-1071436 PubMed
-
Saijo T, Naito E, Ito M, et al. Therapeutic effect of sodium dichloroacetate on visual and auditory hallucinations in a patient with MELAS. Neuropediatrics. 1991;22(3):166-167. doi:10.105/s-208-1071436 PubMed
-
(1991)
Neuropediatrics
, vol.22
, Issue.3
, pp. 166-167
-
-
Saijo, T.1
Naito, E.2
Ito, M.3
-
30
-
-
0036837742
-
MELAS: A neuropsychological and radiological follow-up study. Mitochondrial encephalomyopathy, lactic acidosis and stroke
-
doi:10.1034/j.160-0404.202.01089.x PubMed
-
Sartor H, Loose R, Tucha O, et al. MELAS: a neuropsychological and radiological follow-up study. Mitochondrial encephalomyopathy, lactic acidosis and stroke. Acta Neurol Scand. 2002;106(5):309-313. doi:10.1034/j.160-0404.202. 01089.x PubMed
-
(2002)
Acta Neurol Scand
, vol.106
, Issue.5
, pp. 309-313
-
-
Sartor, H.1
Loose, R.2
Tucha, O.3
-
31
-
-
0027268334
-
MELAS point mutation with unusual clinical presentation
-
DOI 10.1016/0960-8966(93)90058-R
-
Shanske AL, Shanske S, Silvestri G, et al. MELAS point mutation with unusual clinical presentation. Neuromuscul Disord. 1993;3(3):191-193. doi:10.1016/0960-896(93)9058-R PubMed (Pubitemid 23250402)
-
(1993)
Neuromuscular Disorders
, vol.3
, Issue.3
, pp. 191-193
-
-
Shanske, A.L.1
Shanske, S.2
Silvestri, G.3
Tanji, K.4
Wertheim, D.5
Lipper, S.6
-
32
-
-
0033623674
-
Coenzyme Q10 improves psychiatric symptoms in adult-onset mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: A case report
-
doi:10.1080/048670286 PubMed
-
Shinkai T, Nakashima M, Ohmori O, et al. Coenzyme Q10 improves psychiatric symptoms in adult-onset mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes: a case report. Aust N Z J Psychiatry. 2000;34(6):1034-1035. doi:10.1080/048670286 PubMed
-
(2000)
Aust N Z J Psychiatry
, vol.34
, Issue.6
, pp. 1034-1035
-
-
Shinkai, T.1
Nakashima, M.2
Ohmori, O.3
-
33
-
-
0035851315
-
mtDNA disease in the primary care setting
-
Spellberg B, Carroll RM, Robinson E, et al. mtDNA disease in the primary care setting. Arch Intern Med. 2001;161(20):2497-2500. doi:10.101/archinte.161. 20.2497 PubMed (Pubitemid 33043124)
-
(2001)
Archives of Internal Medicine
, vol.161
, Issue.20
, pp. 2497-2500
-
-
Spellberg, B.1
Carroll, R.M.2
Robinson, E.3
Brass, E.4
-
34
-
-
0025262101
-
Manic-depressive psychosis in a patient with mitochondrial myopathy - A case report
-
Stewart JB, Naylor GJ. Manic-depressive psychosis in a patient with mitochondrial myopathy - a case report. Med Sci Res. 1990;18:265-266. (Pubitemid 20157040)
-
(1990)
Medical Science Research
, vol.18
, Issue.7
, pp. 265-266
-
-
Stewart, J.B.1
Naylor, G.J.2
-
35
-
-
0026637067
-
Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia
-
doi:10.172/JCI15856 PubMed
-
Suomalainen A, Majander A, Haltia M, et al. Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegia. J Clin Invest. 1992;90(1):61-66. doi:10.172/JCI15856 PubMed
-
(1992)
J Clin Invest
, vol.90
, Issue.1
, pp. 61-66
-
-
Suomalainen, A.1
Majander, A.2
Haltia, M.3
-
36
-
-
85047675867
-
Psychiatric disturbance in mitochondrial encephalomyopathy
-
doi:10.136/jnp.52.7.920-a PubMed
-
Suzuki T, Koizumi J, Shiraishi H, et al. Psychiatric disturbance in mitochondrial encephalomyopathy. J Neurol Neurosurg Psychiatry. 1989;52(7):920-922. doi:10.136/jnp.52.7.920-a PubMed
-
(1989)
J Neurol Neurosurg Psychiatry
, vol.52
, Issue.7
, pp. 920-922
-
-
Suzuki, T.1
Koizumi, J.2
Shiraishi, H.3
-
37
-
-
0025237072
-
Mitochondrial encephalomyopathy (MELAS) with mental disorder. CT, MRI and SPECT findings
-
Suzuki T, Koizumi J, Shiraishi H, et al. Mitochondrial encephalomyopathy (MELAS) with mental disorder: CT, MRI and SPECT findings. Neuroradiology. 1990;32(1):74-76. doi:10.107/BF0593949 PubMed (Pubitemid 20084615)
-
(1990)
Neuroradiology
, vol.32
, Issue.1
, pp. 74-76
-
-
Suzuki, T.1
Koizumi, J.2
Shiraishi, H.3
Ishikawa, N.4
Ofuku, K.5
Sasaki, M.6
Hori, T.7
Ohkoshi, N.8
Anno, I.9
-
38
-
-
0027427537
-
Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) gene
-
PubMed
-
Sweeney MG, Bundey S, Brockington M, et al. Mitochondrial myopathy associated with sudden death in young adults and a novel mutation in the mitochondrial DNA leucine transfer RNA(UUR) gene. Q J Med. 1993;86(11):709-713. PubMed
-
(1993)
Q J Med
, vol.86
, Issue.11
, pp. 709-713
-
-
Sweeney, M.G.1
Bundey, S.2
Brockington, M.3
-
39
-
-
0031948744
-
Psychiatric symptoms in MELAS; A case report [7]
-
Thomeer EC, Verhoeven WM, van de Vlasakker CJ, et al. Psychiatric symptoms in MELAS; a case report. J Neurol Neurosurg Psychiatry. 1998;64(5):692-693. doi:10.136/jnp.64.5.692 PubMed (Pubitemid 28204172)
-
(1998)
Journal of Neurology Neurosurgery and Psychiatry
, vol.64
, Issue.5
, pp. 692-693
-
-
Thomeer, E.C.1
Verhoeven, W.M.A.2
Van De, V.C.J.W.3
Klompenhouwer, J.L.4
-
40
-
-
0026347397
-
A case of mitochondrial encephalomyopathy with schizophrenic psychosis, dementia and neuroleptic malignant syndrome
-
PubMed
-
Yamazaki M, Igarashi H, Hamamoto M, et al. [A case of mitochondrial encephalomyopathy with schizophrenic psychosis, dementia and neuroleptic malignant syndrome]. Rinsho Shinkeigaku. 1991;31(11):1219-1223. PubMed
-
(1991)
Rinsho Shinkeigaku
, vol.31
, Issue.11
, pp. 1219-1223
-
-
Yamazaki, M.1
Igarashi, H.2
Hamamoto, M.3
-
41
-
-
33750957959
-
Mania as a first presentation in mitochondrial myopathy [3]
-
DOI 10.1111/j.1440-1819.2006.01599.x
-
Grover S, Padhy SK, Das CP, et al. Mania as a first presentation in mitochondrial myopathy. Psychiatry Clin Neurosci. 2006;60(6):774-775. doi:10.1/j.140-1819.206.0159.x PubMed (Pubitemid 44736608)
-
(2006)
Psychiatry and Clinical Neurosciences
, vol.60
, Issue.6
, pp. 774-775
-
-
Grover, S.1
Padhy, S.K.2
Das, C.P.3
Vasishta, R.K.4
Sharan, P.5
Chakrabarti, S.6
-
42
-
-
77952938719
-
Rare autosomal dominant POLG1 mutation in a family with metabolic strokes, posterior column spinal degeneration, and multi-endocrine disease
-
doi:10.17/08307380934313 PubMed
-
Hopkins SE, Somoza A, Gilbert DL. Rare autosomal dominant POLG1 mutation in a family with metabolic strokes, posterior column spinal degeneration, and multi-endocrine disease. J Child Neurol. 2010;25(6):752-756. doi:10.17/08307380934313 PubMed
-
(2010)
J Child Neurol
, vol.25
, Issue.6
, pp. 752-756
-
-
Hopkins, S.E.1
Somoza, A.2
Gilbert, D.L.3
-
43
-
-
59649114327
-
Major depression in adolescent children consecutively diagnosed with mitochondrial disorder
-
doi:10.1016/j.jad.208.06.023 PubMed
-
Koene S, Kozicz TL, Rodenburg RJ, et al. Major depression in adolescent children consecutively diagnosed with mitochondrial disorder. J Affect Disord. 2009;114(1-3):327-332. doi:10.1016/j.jad.208.06.023 PubMed
-
(2009)
J Affect Disord
, vol.114
, Issue.1-3
, pp. 327-332
-
-
Koene, S.1
Kozicz, T.L.2
Rodenburg, R.J.3
-
44
-
-
77953588757
-
POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype
-
doi:10.186/1471-237-10-29 PubMed
-
Komulainen T, Hinttala R, Kärppä M, et al. POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype. BMC Neurol. 2010;10(1):29. doi:10.186/1471-237-10-29 PubMed
-
(2010)
BMC Neurol
, vol.10
, Issue.1
, pp. 29
-
-
Komulainen, T.1
Hinttala, R.2
Kärppä, M.3
-
45
-
-
37349031029
-
Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: Report of a family
-
DOI 10.1016/j.jad.2007.05.016, PII S016503270700208X
-
Mancuso M, Ricci G, Choub A, et al. Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a family. J Affect Disord. 2008;106(1-2):173-177. doi:10.1016/j.jad.207.05.016 PubMed (Pubitemid 350309660)
-
(2008)
Journal of Affective Disorders
, vol.106
, Issue.1-2
, pp. 173-177
-
-
Mancuso, M.1
Ricci, G.2
Choub, A.3
Filosto, M.4
DiMauro, S.5
Davidzon, G.6
Tessa, A.7
Santorelli, F.M.8
Murri, L.9
Siciliano, G.10
-
46
-
-
0035949746
-
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family
-
Rantamäki M, Krahe R, Paetau A, et al. Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family. Neurology. 2001;57(6):1043-1049. PubMed (Pubitemid 32880201)
-
(2001)
Neurology
, vol.57
, Issue.6
, pp. 1043-1049
-
-
Rantamaki, M.1
Krahe, R.2
Paetau, A.3
Cormand, B.4
Mononen, I.5
Udd, B.6
-
47
-
-
0037306425
-
Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene
-
DOI 10.1016/S0960-8966(02)00221-3
-
Siciliano G, Tessa A, Petrini S, et al. Autosomal dominant external ophthalmoplegia and bipolar affective disorder associated with a mutation in the ANT1 gene. Neuromuscul Disord. 2003;13(2):162-165. doi:10.1016/S0960-896(02) 021-3 PubMed (Pubitemid 36140012)
-
(2003)
Neuromuscular Disorders
, vol.13
, Issue.2
, pp. 162-165
-
-
Siciliano, G.1
Tessa, A.2
Petrini, S.3
Mancuso, M.4
Bruno, C.5
Grieco, G.S.6
Malandrini, A.7
DeFlorio, L.8
Martini, B.9
Federico, A.10
Nappi, G.11
Santorelli, F.M.12
Murri, L.13
-
48
-
-
80053635007
-
Recurrent major depression, ataxia, and cardiomyopathy: Association with a novel POLG mutation?
-
doi:10.2147/NDT.S20153 PubMed
-
Verhoeven WM, Egger JI, Kremer BP, et al. Recurrent major depression, ataxia, and cardiomyopathy: association with a novel POLG mutation? Neuropsychiatr Dis Treat. 2011;7:293-296. doi:10.2147/NDT.S20153 PubMed
-
(2011)
Neuropsychiatr Dis Treat
, vol.7
, pp. 293-296
-
-
Verhoeven, W.M.1
Egger, J.I.2
Kremer, B.P.3
-
49
-
-
78149475340
-
Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidity
-
doi:10.101/archneurol.2010.283 PubMed
-
Young TM, Blakely EL, Swalwell H, et al. Mitochondrial transfer RNA(Phe) mutation associated with a progressive neurodegenerative disorder characterized by psychiatric disturbance, dementia, and akinesia-rigidity. Arch Neurol. 2010;67(11):1399-1402. doi:10.101/archneurol.2010.283 PubMed
-
(2010)
Arch Neurol
, vol.67
, Issue.11
, pp. 1399-1402
-
-
Young, T.M.1
Blakely, E.L.2
Swalwell, H.3
-
50
-
-
77956233741
-
The use of neuroimaging in the diagnosis of mitochondrial disease
-
doi:10.102/dr.103 PubMed
-
Friedman SD, Shaw DW, Ishak G, et al. The use of neuroimaging in the diagnosis of mitochondrial disease. Dev Disabil Res Rev. 2010;16(2):129-135. doi:10.102/dr.103 PubMed
-
(2010)
Dev Disabil Res Rev
, vol.16
, Issue.2
, pp. 129-135
-
-
Friedman, S.D.1
Shaw, D.W.2
Ishak, G.3
-
51
-
-
18544378181
-
Brain magnetic resonance imaging findings in patients with mitochondrial cytopathies
-
DOI 10.1001/archneur.62.5.737
-
Barragán-Campos HM, Vallée JN, Lô D, et al. Brain magnetic resonance imaging findings in patients with mitochondrial cytopathies. Arch Neurol. 2005;62(5):737-742. doi:10.101/archneur.62.5.737 PubMed (Pubitemid 40656088)
-
(2005)
Archives of Neurology
, vol.62
, Issue.5
, pp. 737-742
-
-
Barragan-Campos, H.M.1
Vallee, J.-N.2
Lo, D.3
Barrera-Ramirez, C.F.4
Argote-Greene, M.5
Sanchez-Guerrero, J.6
Estanol, B.7
Guillevin, R.8
Chiras, J.9
-
52
-
-
58149328514
-
Batteries not included: Diagnosis and management of mitochondrial disease
-
doi:10.1/j.1365-2796.208.0206.x PubMed
-
McFarland R, Turnbull DM. Batteries not included: diagnosis and management of mitochondrial disease. J Intern Med. 2009;265(2):210-228. doi:10.1/j.1365-2796.208.0206.x PubMed
-
(2009)
J Intern Med
, vol.265
, Issue.2
, pp. 210-228
-
-
McFarland, R.1
Turnbull, D.M.2
-
53
-
-
28844465125
-
Mitochondrial myopathies: Diagnosis, exercise intolerance, and treatment options
-
DOI 10.1249/01.mss.0000177341.89478.06
-
Tarnopolsky MA, Raha S. Mitochondrial myopathies: diagnosis, exercise intolerance, and treatment options. Med Sci Sports Exerc. 2005;37(12):2086-2093. doi:10.1249/01.ms.017341.89478.06 PubMed (Pubitemid 41780735)
-
(2005)
Medicine and Science in Sports and Exercise
, vol.37
, Issue.12
, pp. 2086-2093
-
-
Tarnopolsky, M.A.1
Raha, S.2
-
54
-
-
65549158070
-
Metabolic myopathies: Update 2009
-
doi:10.1097/CND.0b013e3181903126 PubMed
-
van Adel BA, Tarnopolsky MA. Metabolic myopathies: update 2009. J Clin Neuromuscul Dis. 2009;10(3):97-121. doi:10.1097/CND.0b013e3181903126 PubMed
-
(2009)
J Clin Neuromuscul Dis
, vol.10
, Issue.3
, pp. 97-121
-
-
Van Adel, B.A.1
Tarnopolsky, M.A.2
-
55
-
-
51249120293
-
The mitochondrial cocktail: Rationale for combined nutraceutical therapy in mitochondrial cytopathies
-
doi:10.1016/j.adr.208.05.01 PubMed
-
Tarnopolsky MA. The mitochondrial cocktail: rationale for combined nutraceutical therapy in mitochondrial cytopathies. Adv Drug Deliv Rev. 2008;60(13-14):1561-1567. doi:10.1016/j.adr.208.05.01 PubMed
-
(2008)
Adv Drug Deliv Rev
, vol.60
, Issue.13-14
, pp. 1561-1567
-
-
Tarnopolsky, M.A.1
-
56
-
-
33847000236
-
Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders
-
doi:10.102/mus.2068 PubMed
-
Rodriguez MC, MacDonald JR, Mahoney DJ, et al. Beneficial effects of creatine, CoQ10, and lipoic acid in mitochondrial disorders. Muscle Nerve. 2007;35(2):235-242. doi:10.102/mus.2068 PubMed
-
(2007)
Muscle Nerve
, vol.35
, Issue.2
, pp. 235-242
-
-
Rodriguez, M.C.1
MacDonald, J.R.2
Mahoney, D.J.3
-
57
-
-
78149325680
-
A randomized trial of coenzyme Q10 in mitochondrial disorders
-
doi:10.102/mus.21758 PubMed
-
Glover EI, Martin J, Maher A, et al. A randomized trial of coenzyme Q10 in mitochondrial disorders. Muscle Nerve. 2010;42(5):739-748. doi:10.102/mus.21758 PubMed
-
(2010)
Muscle Nerve
, vol.42
, Issue.5
, pp. 739-748
-
-
Glover, E.I.1
Martin, J.2
Maher, A.3
-
58
-
-
77949845941
-
Treating psychiatric illness in patients with mitochondrial disorders
-
letter PubMed
-
Anglin RE, Rosebush PI, Mazurek MF. Treating psychiatric illness in patients with mitochondrial disorders [letter]. Psychosomatics. 2010;51(2):179. PubMed
-
(2010)
Psychosomatics
, vol.51
, Issue.2
, pp. 179
-
-
Anglin, R.E.1
Rosebush, P.I.2
Mazurek, M.F.3
-
59
-
-
0027177218
-
Neuroleptic medications inhibit complex I of the electron transport chain
-
Burkhardt C, Kelly JP, Lim YH, et al. Neuroleptic medications inhibit complex I of the electron transport chain. Ann Neurol. 1993;33(5):512-517. doi:10.102/ana.41030516 PubMed (Pubitemid 23143036)
-
(1993)
Annals of Neurology
, vol.33
, Issue.5
, pp. 512-517
-
-
Burkhardt, C.1
Kelly, J.P.2
Lim, Y.-H.3
Filley, C.M.4
Parker Jr., W.D.5
-
60
-
-
0027267796
-
Valproate and mitochondria
-
DOI 10.1016/0006-2952(93)90404-K
-
Ponchaut S, Veitch K. Valproate and mitochondria. Biochem Pharmacol. 1993;46(2):199-204. doi:10.1016/06-2952(93)90404-K PubMed (Pubitemid 23218602)
-
(1993)
Biochemical Pharmacology
, vol.46
, Issue.2
, pp. 199-204
-
-
Ponchaut, S.1
Veitch, K.2
-
61
-
-
0033546906
-
Age and cause of death in mitochondrial diseases
-
Klopstock T, Jaksch M, Gasser T. Age and cause of death in mitochondrial diseases. Neurology. 1999;53(4):855-857. PubMed (Pubitemid 29448313)
-
(1999)
Neurology
, vol.53
, Issue.4
, pp. 855-857
-
-
Klopstock, T.1
Jaksch, M.2
Gasser, T.3
|