Bove K - Search Results

1

Measurement of reduced and oxidized coenzyme Q9 and coenzyme Q10 levels in mouse tissues by HPLC with coulometric detection.

Tang PH, Miles MV, Miles L, Quinlan J, Wong B, Wenisch A, Bove K. Tang PH, et al. Among authors: bove k. Clin Chim Acta. 2004 Mar;341(1-2):173-84. doi: 10.1016/j.cccn.2003.12.002. Clin Chim Acta. 2004. PMID: 14967174

2

Systematic evaluation of muscle coenzyme Q10 content in children with mitochondrial respiratory chain enzyme deficiencies.

Miles MV, Miles L, Tang PH, Horn PS, Steele PE, DeGrauw AJ, Wong BL, Bove KE. Miles MV, et al. Mitochondrion. 2008 Mar;8(2):170-80. doi: 10.1016/j.mito.2008.01.003. Epub 2008 Feb 2. Mitochondrion. 2008. PMID: 18313367

3

Muscle coenzyme Q: a potential test for mitochondrial activity and redox status.

Miles L, Miles MV, Tang PH, Horn PS, Wong BL, DeGrauw TJ, Morehart PJ, Bove KE. Miles L, et al. Pediatr Neurol. 2005 May;32(5):318-24. doi: 10.1016/j.pediatrneurol.2005.01.009. Pediatr Neurol. 2005. PMID: 15866432

4

Ubiquinol: a potential biomarker for tissue energy requirements and oxidative stress.

Miles L, Miles MV, Tang PH, Horn PS, Quinlan JG, Wong B, Wenisch A, Bove KE. Miles L, et al. Clin Chim Acta. 2005 Oct;360(1-2):87-96. doi: 10.1016/j.cccn.2005.04.009. Clin Chim Acta. 2005. PMID: 15935338

5

Importance of muscle light microscopic mitochondrial subsarcolemmal aggregates in the diagnosis of respiratory chain deficiency.

Miles L, Miles MV, Horn PS, Degrauw TJ, Wong BL, Bove KE. Miles L, et al. Hum Pathol. 2012 Aug;43(8):1249-57. doi: 10.1016/j.humpath.2011.09.016. Epub 2012 Jan 25. Hum Pathol. 2012. PMID: 22277918

6

Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods.

Miles L, Wong BL, Dinopoulos A, Morehart PJ, Hofmann IA, Bove KE. Miles L, et al. Hum Pathol. 2006 Feb;37(2):173-84. doi: 10.1016/j.humpath.2005.10.008. Epub 2005 Dec 20. Hum Pathol. 2006. PMID: 16426917

7

Non-lethal congenital hypotonia due to glycogen storage disease type IV.

Burrow TA, Hopkin RJ, Bove KE, Miles L, Wong BL, Choudhary A, Bali D, Li SC, Chen YT. Burrow TA, et al. Am J Med Genet A. 2006 Apr 15;140(8):878-82. doi: 10.1002/ajmg.a.31166. Am J Med Genet A. 2006. PMID: 16528737

8

False negative histochemical reaction for myophosphorylase activity in fulminant sepsis due to methicillin resistant Staphylococcus aureus.

Cristina Pacheco M, Miles L, Bove KE. Cristina Pacheco M, et al. Neuromuscul Disord. 2007 Dec;17(11-12):983-5. doi: 10.1016/j.nmd.2007.07.008. Epub 2007 Aug 24. Neuromuscul Disord. 2007. PMID: 17719780

9

Hepatocyte glycogen accumulation in patients undergoing dietary management of urea cycle defects mimics storage disease.

Miles L, Heubi JE, Bove KE. Miles L, et al. J Pediatr Gastroenterol Nutr. 2005 Apr;40(4):471-6. doi: 10.1097/01.mpg.0000157200.33486.ce. J Pediatr Gastroenterol Nutr. 2005. PMID: 15795597

10

Megalencephalic leukoencephalopathy with subcortical cysts: a third confirmed case with literature review.

Miles L, DeGrauw TJ, Dinopoulos A, Cecil KM, van der Knaap MS, Bove KE. Miles L, et al. Pediatr Dev Pathol. 2009 May-Jun;12(3):180-6. doi: 10.2350/08-06-0481.1. Pediatr Dev Pathol. 2009. PMID: 18821826

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

299 results

Search Page

Filters