Anderson G - Search Results

1

Signal transducer and activator of transcription 2 deficiency is a novel disorder of mitochondrial fission.

Shahni R, Cale CM, Anderson G, Osellame LD, Hambleton S, Jacques TS, Wedatilake Y, Taanman JW, Chan E, Qasim W, Plagnol V, Chalasani A, Duchen MR, Gilmour KC, Rahman S. Shahni R, et al. Among authors: anderson g. Brain. 2015 Oct;138(Pt 10):2834-46. doi: 10.1093/brain/awv182. Epub 2015 Jun 29. Brain. 2015. PMID: 26122121 Free PMC article.

2

Balloon cells in human cortical dysplasia and tuberous sclerosis: isolation of a pathological progenitor-like cell.

Yasin SA, Latak K, Becherini F, Ganapathi A, Miller K, Campos O, Picker SR, Bier N, Smith M, Thom M, Anderson G, Helen Cross J, Harkness W, Harding B, Jacques TS. Yasin SA, et al. Among authors: anderson g. Acta Neuropathol. 2010 Jul;120(1):85-96. doi: 10.1007/s00401-010-0677-y. Epub 2010 Mar 30. Acta Neuropathol. 2010. PMID: 20352236

3

Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRI.

Kinsler VA, Paine SM, Anderson GW, Wijesekara DS, Sebire NJ, Chong WK, Harkness W, Aylett SE, Jacques TS. Kinsler VA, et al. Acta Neuropathol. 2012 Mar;123(3):453-6. doi: 10.1007/s00401-012-0945-0. Acta Neuropathol. 2012. PMID: 22294043 Free PMC article. No abstract available.

4

Fourth ventricle rosette-forming glioneuronal tumour in children: an unusual presentation in an 8-year-old patient, discussion and review of the literature.

Thurston B, Gunny R, Anderson G, Paine S, Thompson D, Jacques T, Ternier J. Thurston B, et al. Among authors: anderson g. Childs Nerv Syst. 2013 May;29(5):839-47. doi: 10.1007/s00381-012-1993-4. Epub 2012 Dec 14. Childs Nerv Syst. 2013. PMID: 23239254 Review.

5

Nebulin (NEB) mutations in a childhood onset distal myopathy with rods and cores uncovered by next generation sequencing.

Scoto M, Cullup T, Cirak S, Yau S, Manzur AY, Feng L, Jacques TS, Anderson G, Abbs S, Sewry C, Jungbluth H, Muntoni F. Scoto M, et al. Among authors: anderson g. Eur J Hum Genet. 2013 Nov;21(11):1249-52. doi: 10.1038/ejhg.2013.31. Epub 2013 Feb 27. Eur J Hum Genet. 2013. PMID: 23443021 Free PMC article.

6

mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosis.

Yasin SA, Ali AM, Tata M, Picker SR, Anderson GW, Latimer-Bowman E, Nicholson SL, Harkness W, Cross JH, Paine SM, Jacques TS. Yasin SA, et al. Acta Neuropathol. 2013 Aug;126(2):207-18. doi: 10.1007/s00401-013-1135-4. Epub 2013 Jun 2. Acta Neuropathol. 2013. PMID: 23728790

7

The ketogenic diet component decanoic acid increases mitochondrial citrate synthase and complex I activity in neuronal cells.

Hughes SD, Kanabus M, Anderson G, Hargreaves IP, Rutherford T, O'Donnell M, Cross JH, Rahman S, Eaton S, Heales SJ. Hughes SD, et al. Among authors: anderson g. J Neurochem. 2014 May;129(3):426-33. doi: 10.1111/jnc.12646. Epub 2014 Jan 25. J Neurochem. 2014. PMID: 24383952 Free article.

8

Successful reversal of propionic acidaemia associated cardiomyopathy: evidence for low myocardial coenzyme Q10 status and secondary mitochondrial dysfunction as an underlying pathophysiological mechanism.

Baruteau J, Hargreaves I, Krywawych S, Chalasani A, Land JM, Davison JE, Kwok MK, Christov G, Karimova A, Ashworth M, Anderson G, Prunty H, Rahman S, Grünewald S. Baruteau J, et al. Among authors: anderson g. Mitochondrion. 2014 Jul;17:150-6. doi: 10.1016/j.mito.2014.07.001. Epub 2014 Jul 8. Mitochondrion. 2014. PMID: 25010387

9

Cathepsin D deficiency causes juvenile-onset ataxia and distinctive muscle pathology.

Hersheson J, Burke D, Clayton R, Anderson G, Jacques TS, Mills P, Wood NW, Gissen P, Clayton P, Fearnley J, Mole SE, Houlden H. Hersheson J, et al. Among authors: anderson g. Neurology. 2014 Nov 11;83(20):1873-5. doi: 10.1212/WNL.0000000000000981. Epub 2014 Oct 8. Neurology. 2014. PMID: 25298308 Free PMC article. No abstract available.

10

Tubular aggregates caused by serine active site containing 1 (SERAC1) mutations in a patient with a mitochondrial encephalopathy.

Wedatilake Y, Plagnol V, Anderson G, Paine SM, Clayton PT, Jacques TS, Rahman S. Wedatilake Y, et al. Among authors: anderson g. Neuropathol Appl Neurobiol. 2015 Apr;41(3):399-402. doi: 10.1111/nan.12190. Neuropathol Appl Neurobiol. 2015. PMID: 25345337 Free PMC article. No abstract available.

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