Chan A - Search Results

1

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. Among authors: chan a. 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

2

Influenza B acute necrotizing encephalopathy: a case report and literature review.

Sazgar M, Robinson JL, Chan AK, Sinclair DB. Sazgar M, et al. Pediatr Neurol. 2003 May;28(5):396-9. doi: 10.1016/s0887-8994(03)00008-0. Pediatr Neurol. 2003. PMID: 12878304 Review.

3

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

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

4

Treatment outcome of twenty-two patients with guanidinoacetate methyltransferase deficiency: An international retrospective cohort study.

Khaikin Y, Sidky S, Abdenur J, Anastasi A, Ballhausen D, Buoni S, Chan A, Cheillan D, Dorison N, Goldenberg A, Goldstein J, Hofstede FC, Jacquemont ML, Koeberl DD, Lion-Francois L, Lund AM, Mention K, Mundy H, O'Rourke D, Pitelet G, Raspall-Chaure M, Tassini M, Billette de Villemeur T, Williams M, Salomons GS, Mercimek-Andrews S. Khaikin Y, et al. Among authors: chan a. Eur J Paediatr Neurol. 2018 May;22(3):369-379. doi: 10.1016/j.ejpn.2018.02.007. Epub 2018 Feb 16. Eur J Paediatr Neurol. 2018. PMID: 29506905

5

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. 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.

6

Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (HHH) presenting with acute fulminant hepatic failure.

Mhanni AA, Chan A, Collison M, Seifert B, Lehotay DC, Sokoro A, Huynh HQ, Greenberg CR. Mhanni AA, et al. Among authors: chan a. J Pediatr Gastroenterol Nutr. 2008 Mar;46(3):312-5. doi: 10.1097/MPG.0b013e318145a8e5. J Pediatr Gastroenterol Nutr. 2008. PMID: 18376250

7

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. Among authors: chan a. Pediatr Cardiol. 2013 Feb;34(2):462-6. doi: 10.1007/s00246-012-0311-y. Epub 2012 Mar 28. Pediatr Cardiol. 2013. PMID: 22453840

8

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

9

Subcutaneous fat necrosis of the newborn and lactic acidosis.

Isaiah JH, Chan AK. Isaiah JH, et al. Pediatr Dermatol. 2007 Jul-Aug;24(4):435-6. doi: 10.1111/j.1525-1470.2007.00474.x. Pediatr Dermatol. 2007. PMID: 17845182

10

Outcomes of mitochondrial long chain fatty acid oxidation and carnitine defects from a single center metabolic genetics clinic.

Ambrose A, Sheehan M, Bahl S, Athey T, Ghai-Jain S, Chan A, Mercimek-Andrews S. Ambrose A, et al. Among authors: chan a. Orphanet J Rare Dis. 2022 Sep 15;17(1):360. doi: 10.1186/s13023-022-02512-5. Orphanet J Rare Dis. 2022. PMID: 36109795 Free PMC article. Review.

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