Chan AK - Search Results

1

Homozygous TRAP1 sequence variant in a child with Leigh syndrome and normal kidneys.

Skinner SJ, Doonanco KR, Boles RG, Chan AK. Skinner SJ, et al. Among authors: chan ak. Kidney Int. 2014 Oct;86(4):860. doi: 10.1038/ki.2014.208. Kidney Int. 2014. PMID: 25265962 Free article. No abstract available.

2

Atypical presentations of leigh syndrome: a case series and review.

Huntsman RJ, Sinclair DB, Bhargava R, Chan A. Huntsman RJ, et al. Pediatr Neurol. 2005 May;32(5):334-40. doi: 10.1016/j.pediatrneurol.2004.12.009. Pediatr Neurol. 2005. PMID: 15866434 Review.

3

Mitochondrial DNA related cardiomyopathies.

Mohammed S, Bahitham W, Chan A, Chiu B, Bamforth F, Sergi C. Mohammed S, et al. Front Biosci (Elite Ed). 2012 Jan 1;4(5):1706-16. doi: 10.2741/491. Front Biosci (Elite Ed). 2012. PMID: 22201986 Free article. Review.

4

Pulmonary interstitial glycogenosis associated with pulmonary hypertension and hypertrophic cardiomyopathy.

Alkhorayyef A, Ryerson L, Chan A, Phillipos E, Lacson A, Adatia I. Alkhorayyef A, et al. Pediatr Cardiol. 2013 Feb;34(2):462-6. doi: 10.1007/s00246-012-0311-y. Epub 2012 Mar 28. Pediatr Cardiol. 2013. PMID: 22453840

5

Mitochondrial DNA depletion syndrome-an unusual reason for interstage attrition after the modified stage 1 Norwood operation.

Cave D, Ross DB, Bahitham W, Chan A, Sergi C, Adatia I. Cave D, et al. Congenit Heart Dis. 2013 Jan-Feb;8(1):E20-3. doi: 10.1111/j.1747-0803.2011.00569.x. Epub 2011 Oct 20. Congenit Heart Dis. 2013. PMID: 22011012

6

Reversible posterior leukoencephalopathy syndrome in a child with cerebral X-linked adrenoleukodystrophy treated with cyclosporine after bone marrow transplantation.

Chan AK, Bhargava R, Desai S, Joffe A. Chan AK, et al. J Inherit Metab Dis. 2003;26(6):527-36. doi: 10.1023/a:1025943829843. J Inherit Metab Dis. 2003. PMID: 14605498

7

Systolic and diastolic function assessment in fabry disease patients using speckle-tracking imaging and comparison with conventional echocardiographic measurements.

Shanks M, Thompson RB, Paterson ID, Putko B, Khan A, Chan A, Becher H, Oudit GY. Shanks M, et al. J Am Soc Echocardiogr. 2013 Dec;26(12):1407-14. doi: 10.1016/j.echo.2013.09.005. Epub 2013 Oct 11. J Am Soc Echocardiogr. 2013. PMID: 24125876

8

T₁ mapping with cardiovascular MRI is highly sensitive for Fabry disease independent of hypertrophy and sex.

Thompson RB, Chow K, Khan A, Chan A, Shanks M, Paterson I, Oudit GY. Thompson RB, et al. Circ Cardiovasc Imaging. 2013 Sep;6(5):637-45. doi: 10.1161/CIRCIMAGING.113.000482. Epub 2013 Aug 6. Circ Cardiovasc Imaging. 2013. PMID: 23922004

9

Case study for the evaluation of current treatment recommendations of guanidinoacetate methyltransferase deficiency: ineffectiveness of sodium benzoate.

Mercimek-Mahmutoglu S, Salomons GS, Chan A. Mercimek-Mahmutoglu S, et al. Pediatr Neurol. 2014 Jul;51(1):133-7. doi: 10.1016/j.pediatrneurol.2014.02.011. Epub 2014 Feb 21. Pediatr Neurol. 2014. PMID: 24766785

10

Liver failure in mitochondrial DNA depletion syndrome: the importance of serial neuroimaging in liver transplantation evaluation.

deBruyn JC, Chan AK, Bhargava R, Idikio H, Huynh HQ. deBruyn JC, et al. Among authors: chan ak. J Pediatr Gastroenterol Nutr. 2007 Aug;45(2):252-6. doi: 10.1097/MPG.0b013e318048838f. J Pediatr Gastroenterol Nutr. 2007. PMID: 17667724 No abstract available.

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