G0200335/MRC_/Medical Research Council/United Kingdom[Grants and Funding] - Search Results

Year	Number of Results
2009	4
2010	3
2011	4
2012	6
2013	1
2016	1
2017	5
2018	3
2019	1
2024	0

1

POLG-related disorders and their neurological manifestations.

Rahman S, Copeland WC. Rahman S, et al. Nat Rev Neurol. 2019 Jan;15(1):40-52. doi: 10.1038/s41582-018-0101-0. Nat Rev Neurol. 2019. PMID: 30451971 Free PMC article. Review.

2

Complex I deficiency: clinical features, biochemistry and molecular genetics.

Fassone E, Rahman S. Fassone E, et al. J Med Genet. 2012 Sep;49(9):578-90. doi: 10.1136/jmedgenet-2012-101159. J Med Genet. 2012. PMID: 22972949 Review.

3

Diagnosis and therapy in neuromuscular disorders: diagnosis and new treatments in mitochondrial diseases.

Rahman S, Hanna MG. Rahman S, et al. J Neurol Neurosurg Psychiatry. 2009 Sep;80(9):943-53. doi: 10.1136/jnnp.2008.158279. J Neurol Neurosurg Psychiatry. 2009. PMID: 19684231 Free article. Review.

4

POLG mutations and age at menopause.

Duncan AJ, Knight JA, Costello H, Conway GS, Rahman S. Duncan AJ, et al. Hum Reprod. 2012 Jul;27(7):2243-4. doi: 10.1093/humrep/des130. Epub 2012 May 2. Hum Reprod. 2012. PMID: 22552686 No abstract available.

5

Diagnosis of mitochondrial DNA depletion syndromes.

Rahman S, Poulton J. Rahman S, et al. Arch Dis Child. 2009 Jan;94(1):3-5. doi: 10.1136/adc.2008.147983. Arch Dis Child. 2009. PMID: 19103785 No abstract available.

6

Elevated cerebrospinal fluid protein in POLG-related epilepsy: Diagnostic and prognostic implications.

Hikmat O, Naess K, Engvall M, Klingenberg C, Rasmussen M, Tallaksen CME, Brodtkorb E, Fiskerstrand T, Isohanni P, Uusimaa J, Darin N, Rahman S, Bindoff LA. Hikmat O, et al. Epilepsia. 2018 Aug;59(8):1595-1602. doi: 10.1111/epi.14459. Epub 2018 Jun 19. Epilepsia. 2018. PMID: 29920680

7

Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease.

Papandreou A, Rahman S, Fratter C, Ng J, Meyer E, Carr LJ, Champion M, Clarke A, Gissen P, Hemingway C, Hussain N, Jayawant S, King MD, Lynch BJ, Mewasingh L, Patel J, Prabhakar P, Neergheen V, Pope S, Heales SJR, Poulton J, Kurian MA. Papandreou A, et al. J Inherit Metab Dis. 2018 Nov;41(6):1275-1283. doi: 10.1007/s10545-018-0227-7. Epub 2018 Aug 30. J Inherit Metab Dis. 2018. PMID: 30167885 Free PMC article.

8

The presence of anaemia negatively influences survival in patients with POLG disease.

Hikmat O, Tzoulis C, Klingenberg C, Rasmussen M, Tallaksen CME, Brodtkorb E, Fiskerstrand T, McFarland R, Rahman S, Bindoff LA. Hikmat O, et al. J Inherit Metab Dis. 2017 Nov;40(6):861-866. doi: 10.1007/s10545-017-0084-9. Epub 2017 Sep 1. J Inherit Metab Dis. 2017. PMID: 28865037

9

Kearns-Sayre syndrome caused by defective R1/p53R2 assembly.

Pitceathly RD, Fassone E, Taanman JW, Sadowski M, Fratter C, Mudanohwo EE, Woodward CE, Sweeney MG, Holton JL, Hanna MG, Rahman S. Pitceathly RD, et al. J Med Genet. 2011 Sep;48(9):610-7. doi: 10.1136/jmg.2010.088328. Epub 2011 Mar 4. J Med Genet. 2011. PMID: 21378381

10

The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations.

Hikmat O, Tzoulis C, Chong WK, Chentouf L, Klingenberg C, Fratter C, Carr LJ, Prabhakar P, Kumaraguru N, Gissen P, Cross JH, Jacques TS, Taanman JW, Bindoff LA, Rahman S. Hikmat O, et al. Genet Med. 2017 Nov;19(11):1217-1225. doi: 10.1038/gim.2017.35. Epub 2017 Apr 27. Genet Med. 2017. PMID: 28471437 Free article.

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