Kearns-Sayre syndrome : oncocytic transformation of choroid plexus epitheliumTANJI, Kurenai; SCHON, Eric A; DIMAURO, Salvatore et al.Journal of the neurological sciences. 2000, Vol 178, Num 1, pp 29-36, issn 0022-510XArticle

Mitochondrial abnormalities in muscle and other aging cells: Classification, causes, and effectsDIMAURO, Salvatore; TANJI, Kurenai; BONILLA, Eduardo et al.Muscle & nerve. 2002, Vol 26, Num 5, pp 597-607, issn 0148-639X, 11 p.Article

Unexpected Vascular Enrichment of SC01 over SC02 in Mammalian Tissues: Implications for Human Mitochondrial DiseaseBROSEL, Sonja; HUA YANG; TANJI, Kurenai et al.The American journal of pathology. 2010, Vol 177, Num 5, pp 2541-2548, issn 0002-9440, 8 p.Article

MERRF AND KEARNS―SAYRE OVERLAP SYNDROME DUE TO THE MITOCHONDRIAL DNA M.3291T>C MUTATIONEMMANUELE, Valentina; SILVERS, David S; SOTIRIOU, Evangelia et al.Muscle & nerve. 2011, Vol 44, Num 3, pp 448-451, issn 0148-639X, 4 p.Article

The transformation of pediatric gliomatosis cerebri to cerebellar glioblastoma multiforme presenting as supraand infratentorial acute disseminated encephalomyelitis: Case reportSENATUS, Patrick B; MCCLELLAND, Shearwood III; TANJI, Kurenai et al.Journal of neurosurgery. 2005, Vol 102, Num 1, pp 72-77, issn 0022-3085, 6 p., SUPArticle

Mitochondrial DNA dysfunction in oncocytic hepatocytesTANJI, Kurenai; BHAGAT, Govind; VU, Tuan H et al.Liver international. 2003, Vol 23, Num 5, pp 397-403, issn 1478-3223, 7 p.Article

Multicystic encephalomalacia after first-trimester intrauterine fetal death in monochorionic twinsWEISS, Joshua L; CLEARY-GOLDMAN, Jane; TANJI, Kurenai et al.American journal of obstetrics and gynecology. 2004, Vol 190, Num 2, pp 563-565, issn 0002-9378, 3 p.Article

Adefovir nephrotoxicity : Possible role of mitochondrial DNA depletionTANJI, Nozomu; TANJI, Kurenai; KAMBHAM, Neeraja et al.Human pathology. 2001, Vol 32, Num 7, pp 734-740, issn 0046-8177Article

Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA^Ile mutationEMMANUELE, Valentina; SOTIRIOU, Evangelia; SHIRAZI, Maryam et al.Journal of the neurological sciences. 2011, Vol 303, Num 1-2, pp 39-42, issn 0022-510X, 4 p.Article

Slowly progressive encephalopathy with hearing loss due to a mutation in the mtDNA tRNA^Leu(CUN) geneCOKU, Jorida; SHANSKE, Sara; MEHRAZIN, Mahsa et al.Journal of the neurological sciences. 2010, Vol 290, Num 1-2, pp 166-168, issn 0022-510X, 3 p.Article

A novel tRNA^Val mitochondrial DNA mutation causing MELASTANJI, Kurenai; KAUFMANN, Petra; KHANDJI, Alexander et al.Journal of the neurological sciences. 2008, Vol 270, Num 1-2, pp 23-27, issn 0022-510X, 5 p.Article

Amyotrophic Lateral Sclerosis With Ragged-Red FibersHIRANO, Michio; ANGELINI, Corrado; MONTAGNA, Pasquale et al.Archives of neurology (Chicago). 2008, Vol 65, Num 3, pp 403-406, issn 0003-9942, 4 p.Article

A novel ND3 mitochondrial DNA mutation in three korean children with basal ganglia lesions and complex i deficiencyJONG HEE CHAE; JIN SOOK LEE; KI JOONG KIM et al.Pediatric research. 2007, Vol 61, Num 5, pp 622-624, issn 0031-3998, 3 p., 1Article

MPVI7 Mutations Causing Adult-Onset Multisystemic Disorder With Multiple Mitochondrial DNA DeletionsGARONE, Caterina; RUBIO, Juan Carlos; CALVO, Sarah E et al.Archives of neurology (Chicago). 2012, Vol 69, Num 12, pp 1648-1651, issn 0003-9942, 4 p.Article

Decreased hippocampal expression of calbindin D_28K and cognitive impairment in MELASEMMANUELE, Valentina; GARCIA-CAZORLA, Angels; TANJI, Kurenai et al.Journal of the neurological sciences. 2012, Vol 317, Num 1-2, pp 29-34, issn 0022-510X, 6 p.Article

Loss of Myelin-Associated Glycoprotein in Kearns-Sayre SyndromeLAX, Nichola Z; CAMPBELL, Graham R; JAROS, Evelyn et al.Archives of neurology (Chicago). 2012, Vol 69, Num 4, pp 490-499, issn 0003-9942, 10 p.Article

X-Linked Dominant Scapuloperoneal Myopathy Is Due to a Mutation in the Gene Encoding Four-and-a-Half-LIM Protein 1QUINZII, Catarina M; VU, Tuan H; BLAKE, David M et al.American journal of human genetics. 2008, Vol 82, Num 1, pp 208-213, issn 0002-9297, 6 p.Article

The G13513A Mutation in the ND5 Gene of Mitochondrial DNA as a Common Cause of MELAS or Leigh Syndrome : Evidence From 12 CasesSHANSKE, Sara; COKU, Jorida; JIESHENG LU et al.Archives of neurology (Chicago). 2008, Vol 65, Num 3, pp 368-372, issn 0003-9942, 5 p.Article

Clinicopathological review: Cord compression secondary to a lesion of the cervical spine in an 11-year-old girl. CommentaryO'TOOLE, John E; CONNOLLY, E. Sander; KHANDJI, Alexander G et al.Neurosurgery. 2004, Vol 54, Num 4, pp 934-938, issn 0148-396X, 5 p.Article

Navajo neurohepatopathy: a mitochondrial DNA depletion syndrome?VU, Tuan H; TANJI, Kurenai; HOLVE, Stephen A et al.Hepatology (Baltimore, Md.). 2001, Vol 34, Num 1, pp 116-120, issn 0270-9139Article

Deoxynucleoside stress exacerbates the phenotype of a mouse model of mitochondrial neurogastrointestinal encephalopathyGARCIA-DIAZ, Beatriz; GARONE, Caterina; BARCA, Emanuele et al.Brain. 2014, Vol 137, pp 1337-1349, issn 0006-8950, 13 p., 5Article

Unbalanced deoxynucleotide pools cause mitochondrial DNA instability in thymidine phosphorylase-deficient miceLOPEZ, Luis C; AKMAN, Hasan O; TANJI, Kurenai et al.Human molecular genetics (Print). 2009, Vol 18, Num 4, pp 714-722, issn 0964-6906, 9 p.Article

Clinical features and genetics of myoclonic epilepsy with ragged red fibersDIMAURO, Salvatore; HIRANO, Michio; KAUFMANN, Petra et al.Advances in neurology. 2002, Vol 89, pp 217-229, issn 0091-3952, 13 p.Conference Paper

Navajo neurohepatopathy is caused by a mutation in the MPV17 geneKARADIMAS, Charalampos L; VU, Tuan H; BONILLA, Eduardo et al.American journal of human genetics. 2006, Vol 79, Num 3, pp 544-548, issn 0002-9297, 5 p.Article

Identical mitochondrial DNA deletion in a woman with ocular myopathy and in her son with Pearson syndromeSHANSKE, Sara; YINGYING TANG; SCHON, Eric A et al.American journal of human genetics. 2002, Vol 71, Num 3, pp 679-683, issn 0002-9297Article