178 related articles for article (PubMed ID: 17588675)
1. Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a family.
Mancuso M; Ricci G; Choub A; Filosto M; DiMauro S; Davidzon G; Tessa A; Santorelli FM; Murri L; Siciliano G
J Affect Disord; 2008 Feb; 106(1-2):173-7. PubMed ID: 17588675
[TBL] [Abstract][Full Text] [Related]
2. Mitochondrial encephalomyopathy with autosomal dominant inheritance: a clinical and genetic entity of mitochondrial diseases.
Kawai H; Akaike M; Yokoi K; Nishida Y; Kunishige M; Mine H; Saito S
Muscle Nerve; 1995 Jul; 18(7):753-60. PubMed ID: 7783765
[TBL] [Abstract][Full Text] [Related]
3. Mitochondrial DNA 3243A>G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia.
Munakata K; Iwamoto K; Bundo M; Kato T
Biol Psychiatry; 2005 Mar; 57(5):525-32. PubMed ID: 15737668
[TBL] [Abstract][Full Text] [Related]
4. Quantitative analysis of the 4977-bp common deletion of mitochondrial DNA in postmortem frontal cortex from patients with bipolar disorder and schizophrenia.
Fuke S; Kametani M; Kato T
Neurosci Lett; 2008 Jul; 439(2):173-7. PubMed ID: 18514404
[TBL] [Abstract][Full Text] [Related]
5. An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
Zeviani M; Servidei S; Gellera C; Bertini E; DiMauro S; DiDonato S
Nature; 1989 May; 339(6222):309-11. PubMed ID: 2725645
[TBL] [Abstract][Full Text] [Related]
6. [Acute presentation of leukodystrophy due to mitochondrial cytopathology and multiple deletions of mitochondrial DNA].
Rábano JA; Playan A; Guirado F; Montoya J; Baldellou A; López-Pisón J
Rev Neurol; 1998 Dec; 27(160):1005-7. PubMed ID: 9951025
[TBL] [Abstract][Full Text] [Related]
7. [Application of long PCR method to detection of mitochondrial DNA deletions in mitochondrial encephalomyopathies].
Yamamoto M; Shimokawa M; Hamada K
Nihon Rinsho; 1997 Dec; 55(12):3282-5. PubMed ID: 9436451
[TBL] [Abstract][Full Text] [Related]
8. Deficient hippocampal neuron expression of proteasome, ubiquitin, and mitochondrial genes in multiple schizophrenia cohorts.
Altar CA; Jurata LW; Charles V; Lemire A; Liu P; Bukhman Y; Young TA; Bullard J; Yokoe H; Webster MJ; Knable MB; Brockman JA
Biol Psychiatry; 2005 Jul; 58(2):85-96. PubMed ID: 16038679
[TBL] [Abstract][Full Text] [Related]
9. Fear of harm, a possible phenotype of pediatric bipolar disorder: a dimensional approach to diagnosis for genotyping psychiatric syndromes.
Papolos D; Mattis S; Golshan S; Molay F
J Affect Disord; 2009 Nov; 118(1-3):28-38. PubMed ID: 19631388
[TBL] [Abstract][Full Text] [Related]
10. The other, forgotten genome: mitochondrial DNA and mental disorders.
Kato T
Mol Psychiatry; 2001 Nov; 6(6):625-33. PubMed ID: 11673790
[TBL] [Abstract][Full Text] [Related]
11. Difficulty identifying spinocerebellar ataxia 17 from preceding psychiatric symptoms.
Ohi K; Hashimoto R; Sugai F; Yasuda Y; Tagami S; Takamura H; Morihara T; Okochi M; Tanaka T; Kudo T; Sakoda S; Takeda M
Psychiatry Clin Neurosci; 2008 Oct; 62(5):625. PubMed ID: 18950389
[No Abstract] [Full Text] [Related]
12. Increased levels of a mitochondrial DNA deletion in the brain of patients with bipolar disorder.
Kato T; Stine OC; McMahon FJ; Crowe RR
Biol Psychiatry; 1997 Nov; 42(10):871-5. PubMed ID: 9359971
[TBL] [Abstract][Full Text] [Related]
13. Altered cerebral glucose metabolism in a family with clinical features resembling mitochondrial neurogastrointestinal encephalomyopathy syndrome in association with multiple mitochondrial DNA deletions.
Lehnhardt FG; Horvath R; Ullrich R; Kracht L; Sobesky J; Möller-Hartmann W; Jacobs AH; Haupt WF
Arch Neurol; 2008 Mar; 65(3):407-11. PubMed ID: 18332256
[TBL] [Abstract][Full Text] [Related]
14. Sequence and functional analyses of mtDNA in a maternally inherited family with bipolar disorder and depression.
Munakata K; Fujii K; Nanko S; Kunugi H; Kato T
Mutat Res; 2007 Apr; 617(1-2):119-24. PubMed ID: 17320116
[TBL] [Abstract][Full Text] [Related]
15. Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogeneses.
Carrozzo R; Hirano M; Fromenty B; Casali C; Santorelli FM; Bonilla E; DiMauro S; Schon EA; Miranda AF
Neurology; 1998 Jan; 50(1):99-106. PubMed ID: 9443465
[TBL] [Abstract][Full Text] [Related]
16. A novel polymerase gamma mutation in a family with ophthalmoplegia, neuropathy, and Parkinsonism.
Mancuso M; Filosto M; Oh SJ; DiMauro S
Arch Neurol; 2004 Nov; 61(11):1777-9. PubMed ID: 15534189
[TBL] [Abstract][Full Text] [Related]
17. Mitochondrial DNA 3644T-->C mutation associated with bipolar disorder.
Munakata K; Tanaka M; Mori K; Washizuka S; Yoneda M; Tajima O; Akiyama T; Nanko S; Kunugi H; Tadokoro K; Ozaki N; Inada T; Sakamoto K; Fukunaga T; Iijima Y; Iwata N; Tatsumi M; Yamada K; Yoshikawa T; Kato T
Genomics; 2004 Dec; 84(6):1041-50. PubMed ID: 15533721
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial neurogastrointestinal encephalomyopathy mimicking anorexia nervosa.
Feddersen B; DE LA Fontaine L; Sass JO; Lutz J; Abicht A; Klopstock T; Verma IC; Meisenzahl E; Pogarell O
Am J Psychiatry; 2009 Apr; 166(4):494-5. PubMed ID: 19339372
[No Abstract] [Full Text] [Related]
19. Epidemiology of pediatric mitochondrial respiratory chain disorders in northwest Spain.
Castro-Gago M; Blanco-Barca MO; Campos-González Y; Arenas-Barbero J; Pintos-Martínez E; Eirís-Puñal J
Pediatr Neurol; 2006 Mar; 34(3):204-11. PubMed ID: 16504790
[TBL] [Abstract][Full Text] [Related]
20. Quantitative analysis of mitochondrial DNA deletions in the brains of patients with bipolar disorder and schizophrenia.
Kakiuchi C; Ishiwata M; Kametani M; Nelson C; Iwamoto K; Kato T
Int J Neuropsychopharmacol; 2005 Dec; 8(4):515-22. PubMed ID: 16202181
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
