Tanji K - Search Results

1

Inclusion Body Myositis: A Case Presenting with Respiratory Failure and Autopsy Findings Leading to the Hypothesis of a Paraneoplastic Cause.

Dardis C, Antezana A, Tanji K, Maccabee PJ. Dardis C, et al. Among authors: tanji k. Am J Case Rep. 2017 Jun 23;18:700-706. doi: 10.12659/ajcr.903566. Am J Case Rep. 2017. PMID: 28642454 Free PMC article.

2

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

3

GYG1: A distal myopathy with polyglucosan bodies.

Nicolau S, Tracy JA, Pisapia DJ, Tanji K, Milone M. Nicolau S, et al. Among authors: tanji k. JIMD Rep. 2020 May 13;55(1):88-90. doi: 10.1002/jmd2.12129. eCollection 2020 Sep. JIMD Rep. 2020. PMID: 32905144 Free PMC article.

4

Congenital megaconial myopathy due to a novel defect in the choline kinase Beta gene.

Gutiérrez Ríos P, Kalra AA, Wilson JD, Tanji K, Akman HO, Area Gómez E, Schon EA, DiMauro S. Gutiérrez Ríos P, et al. Among authors: tanji k. Arch Neurol. 2012 May;69(5):657-61. doi: 10.1001/archneurol.2011.2333. Arch Neurol. 2012. PMID: 22782513 Free PMC article.

5

Identification of a novel nemaline myopathy-causing mutation in the troponin T1 (TNNT1) gene: a case outside of the old order Amish.

Marra JD, Engelstad KE, Ankala A, Tanji K, Dastgir J, De Vivo DC, Coffee B, Chiriboga CA. Marra JD, et al. Among authors: tanji k. Muscle Nerve. 2015 May;51(5):767-72. doi: 10.1002/mus.24528. Epub 2015 Feb 17. Muscle Nerve. 2015. PMID: 25430424

6

Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

Karadimas CL, Greenstein P, Sue CM, Joseph JT, Tanji K, Haller RG, Taivassalo T, Davidson MM, Shanske S, Bonilla E, DiMauro S. Karadimas CL, et al. Among authors: tanji k. Neurology. 2000 Sep 12;55(5):644-9. doi: 10.1212/wnl.55.5.644. Neurology. 2000. PMID: 10980727

7

X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1.

Quinzii CM, Vu TH, Min KC, Tanji K, Barral S, Grewal RP, Kattah A, Camaño P, Otaegui D, Kunimatsu T, Blake DM, Wilhelmsen KC, Rowland LP, Hays AP, Bonilla E, Hirano M. Quinzii CM, et al. Among authors: tanji k. Am J Hum Genet. 2008 Jan;82(1):208-13. doi: 10.1016/j.ajhg.2007.09.013. Am J Hum Genet. 2008. PMID: 18179901 Free PMC article.

8

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.

9

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

10

Gap junctions between fibroblasts in rat myotendon.

Tanji K, Shimizu T, Satou T, Hashimoto S, Bonilla E. Tanji K, et al. Arch Histol Cytol. 1995 Mar;58(1):97-102. doi: 10.1679/aohc.58.97. Arch Histol Cytol. 1995. PMID: 7612362

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