Tanji K - Search Results

1

Multiple mitochondrial DNA deletions associated with autosomal recessive ophthalmoplegia and severe cardiomyopathy.

Bohlega S, Tanji K, Santorelli FM, Hirano M, al-Jishi A, DiMauro S. Bohlega S, et al. Among authors: tanji k. Neurology. 1996 May;46(5):1329-34. doi: 10.1212/wnl.46.5.1329. Neurology. 1996. PMID: 8628476

2

Immunolocalization of heat shock proteins in ragged-red fibers of patients with mitochondrial encephalomyopathies.

Sparaco M, Rosoklija G, Tanji K, Sciacco M, Latov N, DiMauro S, Bonilla E. Sparaco M, et al. Among authors: tanji k. Neuromuscul Disord. 1993 Jan;3(1):71-6. doi: 10.1016/0960-8966(93)90044-k. Neuromuscul Disord. 1993. PMID: 8101114

3

Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuria.

Minetti C, Tanji K, Chang HW, Medori R, Cordone G, DiMauro S, Bonilla E. Minetti C, et al. Among authors: tanji k. Eur J Pediatr. 1993 Oct;152(10):848-51. doi: 10.1007/BF02073385. Eur J Pediatr. 1993. PMID: 8223790

4

Multiple mitochondrial DNA deletions in sporadic inclusion body myositis: a study of 56 patients.

Santorelli FM, Sciacco M, Tanji K, Shanske S, Vu TH, Golzi V, Griggs RC, Mendell JR, Hays AP, Bertorini TE, Pestronk A, Bonilla E, DiMauro S. Santorelli FM, et al. Among authors: tanji k. Ann Neurol. 1996 Jun;39(6):789-95. doi: 10.1002/ana.410390615. Ann Neurol. 1996. PMID: 8651651

5

Heterogeneous clinical presentation of the mtDNA NARP/T8993G mutation.

Santorelli FM, Tanji K, Shanske S, DiMauro S. Santorelli FM, et al. Among authors: tanji k. Neurology. 1997 Jul;49(1):270-3. doi: 10.1212/wnl.49.1.270. Neurology. 1997. PMID: 9222207

6

Maternally inherited encephalopathy associated with a single-base insertion in the mitochondrial tRNATrp gene.

Santorelli FM, Tanji K, Sano M, Shanske S, El-Shahawi M, Kranz-Eble P, DiMauro S, De Vivo DC. Santorelli FM, et al. Among authors: tanji k. Ann Neurol. 1997 Aug;42(2):256-60. doi: 10.1002/ana.410420220. Ann Neurol. 1997. PMID: 9266739

7

Identification of a novel mutation in the mtDNA ND5 gene associated with MELAS.

Santorelli FM, Tanji K, Kulikova R, Shanske S, Vilarinho L, Hays AP, DiMauro S. Santorelli FM, et al. Among authors: tanji k. Biochem Biophys Res Commun. 1997 Sep 18;238(2):326-8. doi: 10.1006/bbrc.1997.7167. Biochem Biophys Res Commun. 1997. PMID: 9299505 Free article.

8

Mitochondrial disorders.

DiMauro S, Tanji K. DiMauro S, et al. Among authors: tanji k. Jpn J Hum Genet. 1997 Dec;42(4):473-87. doi: 10.1007/BF02767024. Jpn J Hum Genet. 1997. PMID: 9560947 Review.

9

Clinical manifestations of mitochondrial DNA depletion.

Vu TH, Sciacco M, Tanji K, Nichter C, Bonilla E, Chatkupt S, Maertens P, Shanske S, Mendell J, Koenigsberger MR, Sharer L, Schon EA, DiMauro S, DeVivo DC. Vu TH, et al. Among authors: tanji k. Neurology. 1998 Jun;50(6):1783-90. doi: 10.1212/wnl.50.6.1783. Neurology. 1998. PMID: 9633728

10

Study of mitochondrial DNA depletion in muscle by single-fiber polymerase chain reaction.

Sciacco M, Gasparo-Rippa P, Vu TH, Tanji K, Shanske S, Mendell JR, Schon EA, DiMauro S, Bonilla E. Sciacco M, et al. Among authors: tanji k. Muscle Nerve. 1998 Nov;21(11):1374-81. doi: 10.1002/(sici)1097-4598(199811)21:11<1374::aid-mus3>3.0.co;2-6. Muscle Nerve. 1998. PMID: 9771659

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