Hanna MG - Search Results

1

Use of whole genome sequencing to determine genetic basis of suspected mitochondrial disorders: cohort study.

Schon KR, Horvath R, Wei W, Calabrese C, Tucci A, Ibañez K, Ratnaike T, Pitceathly RDS, Bugiardini E, Quinlivan R, Hanna MG, Clement E, Ashton E, Sayer JA, Brennan P, Josifova D, Izatt L, Fratter C, Nesbitt V, Barrett T, McMullen DJ, Smith A, Deshpande C, Smithson SF, Festenstein R, Canham N, Caulfield M, Houlden H, Rahman S, Chinnery PF; Genomics England Research Consortium. Schon KR, et al. Among authors: hanna mg. BMJ. 2021 Nov 3;375:e066288. doi: 10.1136/bmj-2021-066288. BMJ. 2021. PMID: 34732400 Free PMC article. Clinical Trial.

2

MELAS: a new disease associated mitochondrial DNA mutation and evidence for further genetic heterogeneity.

Hanna MG, Nelson IP, Morgan-Hughes JA, Wood NW. Hanna MG, et al. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):512-7. doi: 10.1136/jnnp.65.4.512. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771776 Free PMC article.

3

Diagnostic utility of metabolic exercise testing in a patient with cardiovascular disease.

Elliott PM, Hanna MG, Ward SA, Chinnery PF, Turnbull DM, Wood NW, McKenna WJ. Elliott PM, et al. Among authors: hanna mg. Heart. 1999 Apr;81(4):441-3. doi: 10.1136/hrt.81.4.441. Heart. 1999. PMID: 10092577 Free PMC article.

4

Genetics and molecular pathogenesis of mitochondrial respiratory chain diseases.

Hanna MG, Nelson IP. Hanna MG, et al. Cell Mol Life Sci. 1999 May;55(5):691-706. doi: 10.1007/s000180050327. Cell Mol Life Sci. 1999. PMID: 10379358 Review.

5

Cytochrome oxidase immunohistochemistry: clues for genetic mechanisms.

Rahman S, Lake BD, Taanman JW, Hanna MG, Cooper JM, Schapira AH, Leonard JV. Rahman S, et al. Among authors: hanna mg. Brain. 2000 Mar;123 Pt 3:591-600. doi: 10.1093/brain/123.3.591. Brain. 2000. PMID: 10686181

6

Neuropathological and histochemical changes in a multiple mitochondrial DNA deletion disorder.

Cottrell DA, Ince PG, Blakely EL, Johnson MA, Chinnery PF, Hanna M, Turnbull DM. Cottrell DA, et al. J Neuropathol Exp Neurol. 2000 Jul;59(7):621-7. doi: 10.1093/jnen/59.7.621. J Neuropathol Exp Neurol. 2000. PMID: 10901234

7

Human mitochondrial DNA diseases.

Pulkes T, Hanna MG. Pulkes T, et al. Among authors: hanna mg. Adv Drug Deliv Rev. 2001 Jul 2;49(1-2):27-43. doi: 10.1016/s0169-409x(01)00124-7. Adv Drug Deliv Rev. 2001. PMID: 11377801 Review.

8

Normokalemic periodic paralysis revisited: does it exist?

Chinnery PF, Walls TJ, Hanna MG, Bates D, Fawcett PR. Chinnery PF, et al. Among authors: hanna mg. Ann Neurol. 2002 Aug;52(2):251-2. doi: 10.1002/ana.10257. Ann Neurol. 2002. PMID: 12210802

9

New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation.

Pulkes T, Liolitsa D, Eunson LH, Rose M, Nelson IP, Rahman S, Poulton J, Marchington DR, Landon DN, Debono AG, Morgan-Hughes JA, Hanna MG. Pulkes T, et al. Among authors: hanna mg. Neuromuscul Disord. 2005 May;15(5):364-71. doi: 10.1016/j.nmd.2005.01.006. Neuromuscul Disord. 2005. PMID: 15833431

10

Andersen-Tawil syndrome: new potassium channel mutations and possible phenotypic variation.

Davies NP, Imbrici P, Fialho D, Herd C, Bilsland LG, Weber A, Mueller R, Hilton-Jones D, Ealing J, Boothman BR, Giunti P, Parsons LM, Thomas M, Manzur AY, Jurkat-Rott K, Lehmann-Horn F, Chinnery PF, Rose M, Kullmann DM, Hanna MG. Davies NP, et al. Among authors: hanna mg. Neurology. 2005 Oct 11;65(7):1083-9. doi: 10.1212/01.wnl.0000178888.03767.74. Neurology. 2005. PMID: 16217063

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

592 results

Search Page