Tanji K - Search Results

1

Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.

Sue CM, Karadimas C, Checcarelli N, Tanji K, Papadopoulou LC, Pallotti F, Guo FL, Shanske S, Hirano M, De Vivo DC, Van Coster R, Kaplan P, Bonilla E, DiMauro S. Sue CM, et al. Among authors: tanji k. Ann Neurol. 2000 May;47(5):589-95. Ann Neurol. 2000. PMID: 10805329

2

New morphological approaches to the study of mitochondrial encephalomyopathies.

Bonilla E, Sciacco M, Tanji K, Sparaco M, Petruzzella V, Moraes CT. Bonilla E, et al. Among authors: tanji k. Brain Pathol. 1992 Apr;2(2):113-9. doi: 10.1111/j.1750-3639.1992.tb00679.x. Brain Pathol. 1992. PMID: 1341952 Review.

3

Immunologic study of vinculin in Duchenne muscular dystrophy.

Minetti C, Tanji K, Bonilla E. Minetti C, et al. Among authors: tanji k. Neurology. 1992 Sep;42(9):1751-4. doi: 10.1212/wnl.42.9.1751. Neurology. 1992. PMID: 1513465

4

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

5

Abnormalities in the expression of beta-spectrin in Duchenne muscular dystrophy.

Minetti C, Tanji K, Rippa PG, Morreale G, Cordone G, Bonilla E. Minetti C, et al. Among authors: tanji k. Neurology. 1994 Jun;44(6):1149-53. doi: 10.1212/wnl.44.6.1149. Neurology. 1994. PMID: 8208414

6

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

7

MELAS point mutation with unusual clinical presentation.

Shanske AL, Shanske S, Silvestri G, Tanji K, Wertheim D, Lipper S. Shanske AL, et al. Among authors: tanji k. Neuromuscul Disord. 1993 May;3(3):191-3. doi: 10.1016/0960-8966(93)90058-r. Neuromuscul Disord. 1993. PMID: 8400859

8

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

9

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

10

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

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