Pancrudo J - Search Results

1

Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma.

Filosto M, Mancuso M, Nishigaki Y, Pancrudo J, Harati Y, Gooch C, Mankodi A, Bayne L, Bonilla E, Shanske S, Hirano M, DiMauro S. Filosto M, et al. Among authors: pancrudo j. Arch Neurol. 2003 Sep;60(9):1279-84. doi: 10.1001/archneur.60.9.1279. Arch Neurol. 2003. PMID: 12975295

2

Clinical and genetic features in two families with MELAS and the T3271C mutation in mitochondrial DNA.

Tay SK, Shanske S, Crowe C, Shanske A, Schafer I, Pancrudo J, Lu J, Bonilla E, DiMauro S. Tay SK, et al. Among authors: pancrudo j. J Child Neurol. 2005 Feb;20(2):142-6. doi: 10.1177/08830738050200022301. J Child Neurol. 2005. PMID: 15794182

3

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: pancrudo j. Arch Neurol. 2005 May;62(5):745-7. doi: 10.1001/archneur.62.5.745. Arch Neurol. 2005. PMID: 15883261

4

Varying loads of the mitochondrial DNA A3243G mutation in different tissues: implications for diagnosis.

Shanske S, Pancrudo J, Kaufmann P, Engelstad K, Jhung S, Lu J, Naini A, DiMauro S, De Vivo DC. Shanske S, et al. Among authors: pancrudo j. Am J Med Genet A. 2004 Oct 1;130A(2):134-7. doi: 10.1002/ajmg.a.30220. Am J Med Genet A. 2004. PMID: 15372523

5

Mitochondrial myopathy associated with a novel mutation in mtDNA.

Pancrudo J, Shanske S, Coku J, Lu J, Mardach R, Akman O, Krishna S, Bonilla E, DiMauro S. Pancrudo J, et al. Neuromuscul Disord. 2007 Aug;17(8):651-4. doi: 10.1016/j.nmd.2007.04.005. Epub 2007 Jun 27. Neuromuscul Disord. 2007. PMID: 17588757 Free PMC article.

6

Mitochondrial encephalomyopathy due to a novel mutation in the tRNAGlu of mitochondrial DNA.

Pancrudo J, Shanske S, Bonilla E, Daras M, Akman HO, Krishna S, Malkin E, DiMauro S. Pancrudo J, et al. J Child Neurol. 2007 Jul;22(7):858-62. doi: 10.1177/0883073807304199. J Child Neurol. 2007. PMID: 17715279

7

A 14-year-old male with asymptomatic proteinuria and hearing loss.

Nasr SH, Corey H, Shanske S, Pancrudo J, Kaufmann P, Markowitz GS, DiMauro S, D'Agati VD. Nasr SH, et al. Among authors: pancrudo j. Am J Kidney Dis. 2003 Jan;41(1):259-64. doi: 10.1053/ajkd.2003.50068. Am J Kidney Dis. 2003. PMID: 12500247 No abstract available.

8

Infantile cardiomyopathy caused by the T14709C mutation in the mitochondrial tRNA glutamic acid gene.

Van Hove JL, Freehauf C, Miyamoto S, Vladutiu GD, Pancrudo J, Bonilla E, Lovell MA, Mierau GW, Thomas JA, Shanske S. Van Hove JL, et al. Among authors: pancrudo j. Eur J Pediatr. 2008 Jul;167(7):771-6. doi: 10.1007/s00431-007-0587-8. Epub 2007 Sep 22. Eur J Pediatr. 2008. PMID: 17891417

9

Compressive/tensile stresses and lignified cells as resistance components in joints between cladodes of Opuntia laevis (Cactaceae): responses to applied stresses.

Evans LS, Kahn-Jetter Z, Frenz C, Pancrudo J, Lagrazon K. Evans LS, et al. Among authors: pancrudo j. Environ Exp Bot. 2001 Aug;46(1):47-53. doi: 10.1016/s0098-8472(01)00085-5. Environ Exp Bot. 2001. PMID: 11378172

10

Diversity of cell lengths in terminal portions of roots: location of the proliferative cell population.

Evans LS, Lagrazon K, Pancrudo J. Evans LS, et al. Among authors: pancrudo j. Environ Exp Bot. 2001 Feb;45(1):85-94. doi: 10.1016/s0098-8472(00)00083-6. Environ Exp Bot. 2001. PMID: 11165634

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