Feigenbaum A - Search Results

1

Solid organ transplantation in primary mitochondrial disease: Proceed with caution.

Parikh S, Karaa A, Goldstein A, Ng YS, Gorman G, Feigenbaum A, Christodoulou J, Haas R, Tarnopolsky M, Cohen BK, Dimmock D, Feyma T, Koenig MK, Mundy H, Niyazov D, Saneto RP, Wainwright MS, Wusthoff C, McFarland R, Scaglia F. Parikh S, et al. Among authors: feigenbaum a. Mol Genet Metab. 2016 Jul;118(3):178-184. doi: 10.1016/j.ymgme.2016.04.009. Epub 2016 Apr 20. Mol Genet Metab. 2016. PMID: 27312126

2

New DGK gene mutations in the hepatocerebral form of mitochondrial DNA depletion syndrome.

Mancuso M, Ferraris S, Pancrudo J, Feigenbaum A, Raiman J, Christodoulou J, Thorburn DR, DiMauro S. Mancuso M, et al. Among authors: feigenbaum a. Arch Neurol. 2005 May;62(5):745-7. doi: 10.1001/archneur.62.5.745. Arch Neurol. 2005. PMID: 15883261

3

Molecular bases of hearing loss in multi-systemic mitochondrial cytopathy.

Scaglia F, Hsu CH, Kwon H, Bai RK, Perng CL, Chang HM, Dai P, Smith EO, Whiteman DA, Feigenbaum A, Gropman A, Wong LJ. Scaglia F, et al. Among authors: feigenbaum a. Genet Med. 2006 Oct;8(10):641-52. doi: 10.1097/01.gim.0000237781.10594.d1. Genet Med. 2006. PMID: 17079881 Free article.

4

Abnormal neurological features predict poor survival and should preclude liver transplantation in patients with deoxyguanosine kinase deficiency.

Dimmock DP, Dunn JK, Feigenbaum A, Rupar A, Horvath R, Freisinger P, Mousson de Camaret B, Wong LJ, Scaglia F. Dimmock DP, et al. Among authors: feigenbaum a. Liver Transpl. 2008 Oct;14(10):1480-5. doi: 10.1002/lt.21556. Liver Transpl. 2008. PMID: 18825706 Free article.

5

The role of molecular testing and enzyme analysis in the management of hypomorphic citrullinemia.

Dimmock DP, Trapane P, Feigenbaum A, Keegan CE, Cederbaum S, Gibson J, Gambello MJ, Vaux K, Ward P, Rice GM, Wolff JA, O'Brien WE, Fang P. Dimmock DP, et al. Among authors: feigenbaum a. Am J Med Genet A. 2008 Nov 15;146A(22):2885-90. doi: 10.1002/ajmg.a.32527. Am J Med Genet A. 2008. PMID: 18925679 Free PMC article.

6

Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia.

Dimmock D, Trapane P, Feigenbaum A, Keegan CE, Cederbaum S, Gibson J, Gambello MJ, Vaux K, Ward P, Rice GM, Wolff JA, O'Brien WE, Fang P. Dimmock D, et al. Among authors: feigenbaum a. Hum Genet. 2009 Aug;126(2):341. Hum Genet. 2009. PMID: 19694025 No abstract available.

7

Novel human pathological mutations. Gene symbol: ASS1. Disease: Citrullinaemia.

Dimmock D, Trapane P, Feigenbaum A, Keegan CE, Cederbaum S, Gibson J, Gambello MJ, Vaux K, Ward P, Rice GM, Wolff JA, O'Brien WE, Fang P. Dimmock D, et al. Among authors: feigenbaum a. Hum Genet. 2009 Aug;126(2):342. Hum Genet. 2009. PMID: 19694026 No abstract available.

8

MELAS syndrome, cardiomyopathy, rhabdomyolysis, and autism associated with the A3260G mitochondrial DNA mutation.

Connolly BS, Feigenbaum AS, Robinson BH, Dipchand AI, Simon DK, Tarnopolsky MA. Connolly BS, et al. Among authors: feigenbaum as. Biochem Biophys Res Commun. 2010 Nov 12;402(2):443-7. doi: 10.1016/j.bbrc.2010.10.060. Epub 2010 Oct 20. Biochem Biophys Res Commun. 2010. PMID: 20965148

9

Long-term developmental progression in infants and young children taking sapropterin for phenylketonuria: a two-year analysis of safety and efficacy.

Longo N, Siriwardena K, Feigenbaum A, Dimmock D, Burton BK, Stockler S, Waisbren S, Lang W, Jurecki E, Zhang C, Prasad S. Longo N, et al. Among authors: feigenbaum a. Genet Med. 2015 May;17(5):365-73. doi: 10.1038/gim.2014.109. Epub 2014 Sep 18. Genet Med. 2015. PMID: 25232857 Free article. Clinical Trial.

10

The natural history of glycogen storage disease types VI and IX: Long-term outcome from the largest metabolic center in Canada.

Roscher A, Patel J, Hewson S, Nagy L, Feigenbaum A, Kronick J, Raiman J, Schulze A, Siriwardena K, Mercimek-Mahmutoglu S. Roscher A, et al. Among authors: feigenbaum a. Mol Genet Metab. 2014 Nov;113(3):171-6. doi: 10.1016/j.ymgme.2014.09.005. Epub 2014 Sep 21. Mol Genet Metab. 2014. PMID: 25266922

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