Bonilla E - Search Results

1

Loss of myelin-associated glycoprotein in kearns-sayre syndrome.

Lax NZ, Campbell GR, Reeve AK, Ohno N, Zambonin J, Blakely EL, Taylor RW, Bonilla E, Tanji K, DiMauro S, Jaros E, Lassmann H, Turnbull DM, Mahad DJ. Lax NZ, et al. Among authors: bonilla e. Arch Neurol. 2012 Apr;69(4):490-9. doi: 10.1001/archneurol.2011.2167. Arch Neurol. 2012. PMID: 22491194 Free PMC article.

2

The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 cases.

Shanske S, Coku J, Lu J, Ganesh J, Krishna S, Tanji K, Bonilla E, Naini AB, Hirano M, DiMauro S. Shanske S, et al. Among authors: bonilla e. Arch Neurol. 2008 Mar;65(3):368-72. doi: 10.1001/archneurol.2007.67. Arch Neurol. 2008. PMID: 18332249

3

Deletions of mitochondrial DNA in Kearns-Sayre syndrome.

Zeviani M, Moraes CT, DiMauro S, Nakase H, Bonilla E, Schon EA, Rowland LP. Zeviani M, et al. Among authors: bonilla e. Neurology. 1988 Sep;38(9):1339-46. doi: 10.1212/wnl.38.9.1339. Neurology. 1988. PMID: 3412580

4

Kearns-Sayre syndrome: unusual pattern of expression of subunits of the respiratory chain in the cerebellar system.

Tanji K, Vu TH, Schon EA, DiMauro S, Bonilla E. Tanji K, et al. Among authors: bonilla e. Ann Neurol. 1999 Mar;45(3):377-83. doi: 10.1002/1531-8249(199903)45:3<377::aid-ana14>3.0.co;2-m. Ann Neurol. 1999. PMID: 10072053

5

Disconnection of cerebellar Purkinje cells in Kearns-Sayre syndrome.

Tanji K, DiMauro S, Bonilla E. Tanji K, et al. Among authors: bonilla e. J Neurol Sci. 1999 Jun 15;166(1):64-70. doi: 10.1016/s0022-510x(99)00114-8. J Neurol Sci. 1999. PMID: 10465502 Free article.

6

Kearns-sayre syndrome: oncocytic transformation of choroid plexus epithelium.

Tanji K, Schon EA, DiMauro S, Bonilla E. Tanji K, et al. Among authors: bonilla e. J Neurol Sci. 2000 Sep 1;178(1):29-36. doi: 10.1016/s0022-510x(00)00354-3. J Neurol Sci. 2000. PMID: 11018246 Free article.

7

Mitochondrial DNA copy number threshold in mtDNA depletion myopathy.

Durham SE, Bonilla E, Samuels DC, DiMauro S, Chinnery PF. Durham SE, et al. Among authors: bonilla e. Neurology. 2005 Aug 9;65(3):453-5. doi: 10.1212/01.wnl.0000171861.30277.88. Neurology. 2005. PMID: 16087914

8

Light microscopic methods to visualize mitochondria on tissue sections.

Tanji K, Bonilla E. Tanji K, et al. Among authors: bonilla e. Methods. 2008 Dec;46(4):274-80. doi: 10.1016/j.ymeth.2008.09.027. Epub 2008 Oct 16. Methods. 2008. PMID: 18929660 Review.

9

Complex neurologic syndrome associated with the G1606A mutation of mitochondrial DNA.

Sacconi S, Salviati L, Gooch C, Bonilla E, Shanske S, DiMauro S. Sacconi S, et al. Among authors: bonilla e. Arch Neurol. 2002 Jun;59(6):1013-5. doi: 10.1001/archneur.59.6.1013. Arch Neurol. 2002. PMID: 12056939

10

Widespread tissue distribution of mitochondrial DNA deletions in Kearns-Sayre syndrome.

Shanske S, Moraes CT, Lombes A, Miranda AF, Bonilla E, Lewis P, Whelan MA, Ellsworth CA, DiMauro S. Shanske S, et al. Among authors: bonilla e. Neurology. 1990 Jan;40(1):24-8. doi: 10.1212/wnl.40.1.24. Neurology. 1990. PMID: 2296377

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