Murdoch G - Search Results

1

Neuropathology of 22q11 deletion syndrome in an infant.

Wu P, Teot L, Murdoch G, Monaghan-Nichols AP, McFadden K. Wu P, et al. Among authors: murdoch g. Pediatr Dev Pathol. 2014 Sep-Oct;17(5):386-92. doi: 10.2350/13-11-1399-CR.1. Epub 2014 Jul 14. Pediatr Dev Pathol. 2014. PMID: 25019421

2

Janiceps conjoined twins with extreme asymmetry: case report with complete autopsy and histopathologic findings.

Kastenbaum HA, McPherson EW, Murdoch GH, Ozolek JA. Kastenbaum HA, et al. Pediatr Dev Pathol. 2009 Sep-Oct;12(5):374-82. doi: 10.2350/08-11-0555.1. Pediatr Dev Pathol. 2009. PMID: 19159129

3

Posterior reversible encephalopathy syndrome (PRES) with immune system activation, VEGF up-regulation, and cerebral amyloid angiopathy.

Kofler J, Bartynski WS, Reynolds TQ, Lieberman FS, Murdoch GH, Hamilton RL. Kofler J, et al. J Comput Assist Tomogr. 2011 Jan-Feb;35(1):39-42. doi: 10.1097/RCT.0b013e3181f31917. J Comput Assist Tomogr. 2011. PMID: 21150450

4

Identification and characterization of new long chain acyl-CoA dehydrogenases.

He M, Pei Z, Mohsen AW, Watkins P, Murdoch G, Van Veldhoven PP, Ensenauer R, Vockley J. He M, et al. Among authors: murdoch g. Mol Genet Metab. 2011 Apr;102(4):418-29. doi: 10.1016/j.ymgme.2010.12.005. Epub 2010 Dec 17. Mol Genet Metab. 2011. PMID: 21237683 Free PMC article.

5

Neuropathology in succinic semialdehyde dehydrogenase deficiency.

Knerr I, Gibson KM, Murdoch G, Salomons GS, Jakobs C, Combs S, Pearl PL. Knerr I, et al. Among authors: murdoch g. Pediatr Neurol. 2010 Apr;42(4):255-8. doi: 10.1016/j.pediatrneurol.2009.11.011. Pediatr Neurol. 2010. PMID: 20304328 Free PMC article.

6

A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.

He M, Rutledge SL, Kelly DR, Palmer CA, Murdoch G, Majumder N, Nicholls RD, Pei Z, Watkins PA, Vockley J. He M, et al. Among authors: murdoch g. Am J Hum Genet. 2007 Jul;81(1):87-103. doi: 10.1086/519219. Epub 2007 Jun 4. Am J Hum Genet. 2007. PMID: 17564966 Free PMC article.

7

Preventive immunization of aged and juvenile non-human primates to β-amyloid.

Kofler J, Lopresti B, Janssen C, Trichel AM, Masliah E, Finn OJ, Salter RD, Murdoch GH, Mathis CA, Wiley CA. Kofler J, et al. J Neuroinflammation. 2012 May 3;9:84. doi: 10.1186/1742-2094-9-84. J Neuroinflammation. 2012. PMID: 22554253 Free PMC article.

8

Paxillin and hydrogen peroxide-inducible clone 5 expression and distribution in control and Alzheimer disease hippocampi.

Caltagarone J, Hamilton RL, Murdoch G, Jing Z, DeFranco DB, Bowser R. Caltagarone J, et al. Among authors: murdoch g. J Neuropathol Exp Neurol. 2010 Apr;69(4):356-71. doi: 10.1097/NEN.0b013e3181d53d98. J Neuropathol Exp Neurol. 2010. PMID: 20448481 Free PMC article.

9

Diagnostic use of IDH1/2 mutation analysis in routine clinical testing of formalin-fixed, paraffin-embedded glioma tissues.

Horbinski C, Kofler J, Kelly LM, Murdoch GH, Nikiforova MN. Horbinski C, et al. J Neuropathol Exp Neurol. 2009 Dec;68(12):1319-25. doi: 10.1097/NEN.0b013e3181c391be. J Neuropathol Exp Neurol. 2009. PMID: 19915484

10

Akt activation is a common event in pediatric malignant gliomas and a potential adverse prognostic marker: a report from the Children's Oncology Group.

Pollack IF, Hamilton RL, Burger PC, Brat DJ, Rosenblum MK, Murdoch GH, Nikiforova MN, Holmes EJ, Zhou T, Cohen KJ, Jakacki RI; Children's Oncology Group. Pollack IF, et al. J Neurooncol. 2010 Sep;99(2):155-63. doi: 10.1007/s11060-010-0297-3. Epub 2010 Jul 4. J Neurooncol. 2010. PMID: 20607350 Free PMC article.

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