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발행년	- (예 : 2010-2015)

Public attitudes towards novel reproductive technologies: a citizens' jury on mitochondrial donation.

Academic Journal

Newson, A J; Lacey, S de; Dowling, D K; Murray, S; Sue, C M; Thorburn, D R; Gillam, L; Degeling, C; de Lacey, S

Human Reproduction. Apr2019, Vol. 34 Issue 4, p751-757. 7p. 4 Charts.

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Allogeneic hematopoietic SCT as treatment option for patients with mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): a consensus conference proposal for a standardized approach

Academic Journal

Halter, J; Schüpbach, W MM; Casali, C; Elhasid, R; Fay, K; Hammans, S; Illa, I; Kappeler, L; Krähenbühl, S; Lehmann, T; Mandel, H; Marti, R; Mattle, H; Orchard, K; Savage, D; Sue, C M; Valcarcel, D; Gratwohl, A; Hirano, M

Bone Marrow Transplantation. Mar 01, 2011 46(3):330-337

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Recurrent myoglobinuria due to a nonsense mutation in the COX I gene of mitochondrial DNA.

Academic Journal

Karadimas, C L; Greenstein, P; Sue, C M; Joseph, J T; Tanji, K; Haller, R G; Taivassalo, T; Davidson, M M; Shanske, S; Bonilla, E; DiMauro, S

Neurology; 2000 Sep 12, Vol. 55 Issue 5, p644-649, 6p

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Mitochondrial disease mimicking Charcot–Marie Tooth disease

Academic Journal

Needham, M; Duley, J; Hammond, S; Herkes, G.K.; Hirano, M; Sue, C M

JOURNAL OF NEUROLOGY, NEUROSURGERY, & PSYCHIATRY. Jan 01, 2007 78(1):99-100

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Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene.

Academic Journal

Sue CM; Tanji K; Hadjigeorgiou G; Andreu AL; Nishino I; Krishna S; Bruno C; Hirano M; Shanske S; Bonilla E; Fischel-Ghodsian N; DiMauro S; Friedman R; Sue, C M; Tanji, K; Hadjigeorgiou, G; Andreu, A L; Nishino, I; Krishna, S; Bruno, C

Neurology; 1999 Jun 10, Vol. 52 Issue 9, p1905-1908, 4p

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Neuroradiological features of six kindreds with MELAS tRNA(Leu) A2343G point mutation: implications for pathogenesis.

Academic Journal

Sue, C M; Crimmins, D S; Soo, Y S; Pamphlett, R; Presgrave, C M; Kotsimbos, N; Jean-Francois, M J; Byrne, E; Morris, J G

Journal of Neurology, Neurosurgery & Psychiatry; Aug1998, p233-240, 8p

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Mitochondrial encephalomyopathy: variable clinical expression within a single kindred.

Academic Journal

Crimmins, D; Morris, J G; Walker, G L; Sue, C M; Byrne, E; Stevens, S; Jean-Francis, B; Yiannikas, C; Pamphlett, R

Journal of Neurology, Neurosurgery & Psychiatry; Aug1993, Vol. 56 Issue 8, p900-905, 6p, 2 Black and White Photographs, 1 Diagram, 5 Charts

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Paroxysmal word deafness secondary to focal epilepsy.

Academic Journal

Fung, V S; Sue, C M; Somerville, E R

Neurology; 2000 Jan 25, Vol. 54 Issue 2, p533-534, 2p

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Mitochondrial gene mutations and diabetes mellitus.

Academic Journal

Sue, C M; Holmes-Walker, D J; Morris, J G; Boyages, S C; Crimmins, D S; Byrne, E

Lancet. 2/13/1993, Vol. 341 Issue 8842, p437-438. 2p.

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