Davidzon G - Search Results

1

Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a family.

Mancuso M, Ricci G, Choub A, Filosto M, DiMauro S, Davidzon G, Tessa A, Santorelli FM, Murri L, Siciliano G. Mancuso M, et al. Among authors: davidzon g. J Affect Disord. 2008 Feb;106(1-2):173-7. doi: 10.1016/j.jad.2007.05.016. Epub 2007 Jun 22. J Affect Disord. 2008. PMID: 17588675

2

Mitochondrial DNA and disease.

Dimauro S, Davidzon G. Dimauro S, et al. Among authors: davidzon g. Ann Med. 2005;37(3):222-32. doi: 10.1080/07853890510007368. Ann Med. 2005. PMID: 16019721 Review.

3

Progressive external ophthalmoplegia and vision and hearing loss in a patient with mutations in POLG2 and OPA1.

Ferraris S, Clark S, Garelli E, Davidzon G, Moore SA, Kardon RH, Bienstock RJ, Longley MJ, Mancuso M, Gutiérrez Ríos P, Hirano M, Copeland WC, DiMauro S. Ferraris S, et al. Among authors: davidzon g. Arch Neurol. 2008 Jan;65(1):125-31. doi: 10.1001/archneurol.2007.9. Arch Neurol. 2008. PMID: 18195150 Free PMC article.

4

Early-onset familial parkinsonism due to POLG mutations.

Davidzon G, Greene P, Mancuso M, Klos KJ, Ahlskog JE, Hirano M, DiMauro S. Davidzon G, et al. Ann Neurol. 2006 May;59(5):859-62. doi: 10.1002/ana.20831. Ann Neurol. 2006. PMID: 16634032

5

Severe encephalomyopathy in a patient with homoplasmic A5814G point mutation in mitochondrial tRNACys gene.

Scuderi C, Borgione E, Musumeci S, Elia M, Castello F, Fichera M, Davidzon G, DiMauro S. Scuderi C, et al. Among authors: davidzon g. Neuromuscul Disord. 2007 Mar;17(3):258-61. doi: 10.1016/j.nmd.2006.11.006. Epub 2007 Jan 22. Neuromuscul Disord. 2007. PMID: 17241783

6

A polymorphic polymerase.

DiMauro S, Davidzon G, Hirano M. DiMauro S, et al. Among authors: davidzon g. Brain. 2006 Jul;129(Pt 7):1637-9. doi: 10.1093/brain/awl169. Brain. 2006. PMID: 16803839 Review. No abstract available.

7

POLG mutations and Alpers syndrome.

Davidzon G, Mancuso M, Ferraris S, Quinzii C, Hirano M, Peters HL, Kirby D, Thorburn DR, DiMauro S. Davidzon G, et al. Ann Neurol. 2005 Jun;57(6):921-3. doi: 10.1002/ana.20498. Ann Neurol. 2005. PMID: 15929042

8

Clinical spectrum of mitochondrial DNA depletion due to mutations in the thymidine kinase 2 gene.

Oskoui M, Davidzon G, Pascual J, Erazo R, Gurgel-Giannetti J, Krishna S, Bonilla E, De Vivo DC, Shanske S, DiMauro S. Oskoui M, et al. Among authors: davidzon g. Arch Neurol. 2006 Aug;63(8):1122-6. doi: 10.1001/archneur.63.8.1122. Arch Neurol. 2006. PMID: 16908738 Review.

9

Hereditary ferritinopathy: a novel mutation, its cellular pathology, and pathogenetic insights.

Mancuso M, Davidzon G, Kurlan RM, Tawil R, Bonilla E, Di Mauro S, Powers JM. Mancuso M, et al. Among authors: davidzon g. J Neuropathol Exp Neurol. 2005 Apr;64(4):280-94. doi: 10.1093/jnen/64.4.280. J Neuropathol Exp Neurol. 2005. PMID: 15835264

10

Neutral lipid storage disease with subclinical myopathy due to a retrotransposal insertion in the PNPLA2 gene.

Akman HO, Davidzon G, Tanji K, Macdermott EJ, Larsen L, Davidson MM, Haller RG, Szczepaniak LS, Lehman TJ, Hirano M, DiMauro S. Akman HO, et al. Among authors: davidzon g. Neuromuscul Disord. 2010 Jun;20(6):397-402. doi: 10.1016/j.nmd.2010.04.004. Epub 2010 May 14. Neuromuscul Disord. 2010. PMID: 20471263 Free PMC article.

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