Works matching AU Turnbull, D. M.

Results: 49

African Haplogroup L mtDNA Sequences Show Violations of Clock-like Evolution.

Published in:

Molecular Biology & Evolution, 2004, v. 21, n. 10, p. 1843, doi. 10.1093/molbev/msh184

By:

Howell, Neil;
Elson, Joanna L.;
Turnbull, D. M.;
Herrnstadt., Corinna

Publication type:

Article

Metastatic Breast Cancer Masquerading as Gastrointestinal Primary.

Published in:

American Journal of Gastroenterology (Springer Nature), 1998, v. 93, n. 1, p. 111, doi. 10.1111/j.1572-0241.1998.111_c.x

By:

Schwarz, Roderich E.;
Klimstra, David S.;
Turnbull, Alan D. M.

Publication type:

Article

Spontaneous gastroduodenal perforation in cancer patients receiving cytotoxic therapy.

Published in:

Journal of Surgical Oncology, 1989, v. 41, n. 4, p. 219, doi. 10.1002/jso.2930410405

By:

Ricci, John L.;
Turnbull, Alan D. M.

Publication type:

Article

Assessment of visual function in chronic progressive external ophthalmoplegia.

Published in:

2006

By:

Yu Wai Man, C. Y.;
Smith, T.;
Chinnery, P. F.;
Turnbull, D. M.;
Griffiths, P. G.

Publication type:

journal article

Potential compounds for the treatment of mitochondrial disease.

Published in:

British Medical Bulletin, 2015, v. 116, n. 1, p. 5, doi. 10.1093/bmb/ldv046

By:

Rai, P. K.;
Russell, O. M.;
Lightowlers, R. N.;
Turnbull, D. M.

Publication type:

Article

Adrenal insufficiency in the cancer patient: Implications for the surgeon.

Published in:

British Journal of Surgery, 1990, v. 77, n. 12, p. 1335, doi. 10.1002/bjs.1800771206

By:

Ihde, J. K.;
Turnbull, A. D. M.;
Bajorunas, D. R.

Publication type:

Article

Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.

Published in:

Diabetic Medicine, 2008, v. 25, n. 4, p. 383, doi. 10.1111/j.1464-5491.2008.02359.x

By:

Murphy, R.;
Turnbull, D. M.;
Walker, M.;
Hattersley, A. T.

Publication type:

Article

Insulin sensitivity and mitochondrial gene mutation.

Published in:

1995

By:

Walker, Mark;
Taylor, Robert W.;
Stewart, Murray W.;
Bindoff, Laurie A.;
Jackson, Margaret J.;
Alberti, George K. M. M.;
Turnbull, Douglass M.;
Kanamori, Akira;
Tanaka, Keiji;
Umezawa, Shin-chi;
Matoba, Kiyozaku;
Fujita, Yoshikuni;
Tajima, Yoshitada;
Walker, M;
Taylor, R W;
Stewart, M W;
Bindoff, L A;
Jackson, M J;
Alberti, G K;
Turnbull, D M

Publication type:

commentary

Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafness.

Published in:

1994

By:

Jackson, Margaret J.;
Bindoff, Laurence A.;
Weber, Katharina;
Wilson, Jonathan N.;
Ince, Paul;
Alberti, K. George M. M.;
Turnbull, Douglass M.;
Jackson, M J;
Bindoff, L A;
Weber, K;
Wilson, J N;
Ince, P;
Alberti, K G;
Turnbull, D M

Publication type:

journal article

HEPATIC PEROXISOMAL PROLIFERATION CAUSED BY ETHYL 2[5(4-CHLORO-PHENYL)PENTYL]OXIRAN-2- CARBOXYLATE (CPOC): A HYPOGLYCEMIC INHIBITOR OF MITOCHONDRIAL FATTY ACID OXIDATION.

Published in:

Annals of the New York Academy of Sciences, 1982, v. 386, n. 1, p. 446, doi. 10.1111/j.1749-6632.1982.tb21448.x

By:

Sherratt, H. S. A.;
Bartlett, K.;
Koundakjian, P. P.;
Turnbull, D. M.;
Osmundsen, H.;
Hoof, F. Van;
Bone, A. J.

Publication type:

Article

Mitochondrial diabetes.

Published in:

2005

By:

Walker, M.;
Taylor, R. W.;
Turnbull, D. M.

Publication type:

Other

Relationship between insulin sensitivity and insulin receptor substrate-1 mutations in non-diabetic relatives of NIDDM families.

Published in:

1996

By:

Armstrong, M;
Haldane, F;
Avery, P J;
Mitcheson, J;
Stewart, M W;
Turnbull, D M;
Walker, M

Publication type:

Journal Article

A diagnostic tattoo.

Published in:

Clinical Genetics, 2009, v. 75, n. 1, p. 37, doi. 10.1111/j.1399-0004.2008.01103.x

By:

Whittaker, R. G.;
Turnbull, D. M.

Publication type:

Article

Detection of mitochondrial DNA deletions in blood using the polymerase chain reaction: non-invasive diagnosis of mitochondrial myopathy.

Published in:

Clinical Genetics, 1991, v. 39, n. 1, p. 33, doi. 10.1111/j.1399-0004.1991.tb02982.x

By:

Poulton, J.;
Deadman, M. E.;
Turnbull, D. M.;
Lake, B.;
Gardiner, R. M.

Publication type:

Article

Systematic review of cognitive deficits in adult mitochondrial disease.

Published in:

European Journal of Neurology, 2020, v. 27, n. 1, p. 3, doi. 10.1111/ene.14068

By:

Moore, H. L.;
Blain, A. P.;
Turnbull, D. M.;
Gorman, G. S.

Publication type:

Article

Molecular pathology of MELAS and MERRF. The relationship between mutation load and clinical phenotypes.

Published in:

Brain: A Journal of Neurology, 1997, v. 120, n. 10, p. 1713, doi. 10.1093/brain/120.10.1713

By:

Chinnery, P F;
Howell, N;
Lightowlers, R N;
Turnbull, D M

Publication type:

Article

Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.

Published in:

2001

By:

Taylor, Robert W.;
Singh-Kler, Rajinder;
Hayes, Christine M.;
Smith, Philip E.M.;
Turnbull, Douglass M.;
Taylor, R W;
Singh-Kler, R;
Hayes, C M;
Smith, P E;
Turnbull, D M

Publication type:

journal article

The epidemiology of pathogenic mitochondrial DNA mutations.

Published in:

2000

By:

Chinnery, P. F.;
Johnson, M. A.;
Wardell, T. M.;
Singh-Kler, R.;
Hayes, C.;
Brown, D. T.;
Taylor, R. W.;
Bindoff, L. A.;
Turnbull, D. M.

Publication type:

journal article

Mitochondrial enzyme activity in amyotrophic lateral sclerosis: implications for the role of mitochondria in neuronal cell death.

Published in:

1999

By:

Borthwick, Gillian M.;
Johnson, Margaret A.;
Ince, Paul G.;
Shaw, Pamela J.;
Turnbull, Douglass M.;
Borthwick, G M;
Johnson, M A;
Ince, P G;
Shaw, P J;
Turnbull, D M

Publication type:

journal article

A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis.

Published in:

Annals of Neurology, 1997, v. 41, n. 3, p. 408, doi. 10.1002/ana.410410319

By:

Chinnery, P. F.;
Johnson, M. A.;
Taylor, R. W.;
Lightowlers, R. N.;
Turnbull, D. M.

Publication type:

Article

MELAS associated with a mutation in the valine transfer RNA gene of mitochondrial DNA.

Published in:

Annals of Neurology, 1996, v. 40, n. 3, p. 459, doi. 10.1002/ana.410400318

By:

Taylor, R. W.;
Chinnery, P. F.;
Haldane, F.;
Morris, A. A. M.;
Bindoff, L. A.;
Turnbull, D. M.;
Wilson, J.

Publication type:

Article

Deficiency of respiratory chain complex I is a common cause of leigh disease.

Published in:

Annals of Neurology, 1996, v. 40, n. 1, p. 25, doi. 10.1002/ana.410400107

By:

Morris, A. A. M.;
Leonard, J. V.;
Brown, G. K.;
Bidouki, S. K.;
Bindoff, L. A.;
Turnbull, D. M.;
Woodward, C. E.;
Harding, A. E.;
Lake, B. D.;
Harding, B. N.;
Farrell, M. A.;
Bell, J. E.;
Mirakhur, M.

Publication type:

Article

Absence of immunoreactive enzyme protewin in short-chain acylcoenzyme a dehydrogenase deficiency.

Published in:

Annals of Neurology, 1990, v. 28, n. 5, p. 717, doi. 10.1002/ana.410280520

By:

Farnsworth, L.;
Shepherd, I. M.;
Johnson, M. A.;
Bindoff, L. A.;
Turnbull, D. M.

Publication type:

Article

A case-comparison study of pregnant women with mitochondrial disease - what to expect?

Published in:

2019

By:

Feeney, CL;
Lim, AZ;
Fagan, E;
Blain, A;
Bright, A;
Maddison, J;
Devine, H;
Stewart, J;
Taylor, RW;
Gorman, GS;
Turnbull, DM;
Nesbitt, V;
McFarland, R;
Feeney, C L;
Lim, A Z;
Taylor, R W;
Gorman, G S;
Turnbull, D M

Publication type:

journal article

Review: Central nervous system involvement in mitochondrial disease.

Published in:

Neuropathology & Applied Neurobiology, 2017, v. 43, n. 2, p. 102, doi. 10.1111/nan.12333

By:

Lax, N. Z.;
Gorman, G. S.;
Turnbull, D. M.

Publication type:

Article

Mitochondrial DNA deletions and depletion within paraspinal muscles.

Published in:

Neuropathology & Applied Neurobiology, 2013, v. 39, n. 4, p. 377, doi. 10.1111/j.1365-2990.2012.01290.x

By:

Campbell, G. R.;
Reeve, A.;
Ziabreva, I.;
Polvikoski, T. M.;
Taylor, R. W.;
Reynolds, R.;
Turnbull, D. M.;
Mahad, D. J.

Publication type:

Article

Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions.

Published in:

2009

By:

Betts-Henderson, J.;
Jaros, E.;
Krishnan, K. J.;
Perry, R. H.;
Reeve, A. K.;
Schaefer, A. M.;
Taylor, R. W.;
Turnbull, D. M.

Publication type:

Other

Molecular neuropathology of MELAS: level of heteroplasmy in individual neurones and evidence of extensive vascular involvement.

Published in:

Neuropathology & Applied Neurobiology, 2006, v. 32, n. 4, p. 359, doi. 10.1111/j.1365-2990.2006.00731.x

By:

Betts, J.;
Jaros, E.;
Perry, R. H.;
Schaefer, A. M.;
Taylor, R. W.;
Abdel-All, Z.;
Lightowlers, R. N.;
Turnbull, D. M.

Publication type:

Article

Effects of obesity and weight loss on mitochondrial structure and function and implications for colorectal cancer risk.

Published in:

2019

By:

Breininger, S. P.;
Malcomson, F. C.;
Afshar, S.;
Turnbull, D. M.;
Greaves, L.;
Mathers, J. C.

Publication type:

journal article

Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy.

Published in:

1988

By:

Turnbull, D. M.;
Bartlett, K.;
Eyre, J. A.;
Gardner-Medwin, D.;
Johnson, M. A.;
Fisher, J.;
Watmough, N. J.

Publication type:

journal article

The investigation of mitochondrial respiratory chain disease.

Published in:

1995

By:

Morris, A A;
Jackson, M J;
Bindoff, L A;
Turnbull, D M

Publication type:

journal article

The investigation of mitochondrial respiratory chain disease.

Published in:

Journal of the Royal Society of Medicine, 1995, v. 88, n. 4, p. 217P

By:

Morris, A. A. M.;
Jackson, M. J.;
Bindoff, L. A.;
Turnbull, D. M.

Publication type:

Article

The role of cytochrome c oxidase deficient hippocampal neurones in Alzheimer's disease.

Published in:

Neuropathology & Applied Neurobiology, 2002, v. 28, n. 5, p. 390, doi. 10.1046/j.1365-2990.2002.00414.x

By:

Cottrell, D. A.;
Borthwick, G. M.;
Johnson, M. A.;
Ince, P. G.;
Turnbull, D. M.

Publication type:

Article

Accelerated ageing changes in the choroid plexus of a case with multiple mitochondrial DNA deletions.

Published in:

Neuropathology & Applied Neurobiology, 2001, v. 27, n. 3, p. 206, doi. 10.1046/j.1365-2990.2001.00315.x

By:

Cottrell, D. A.;
Ince, P. G.;
Wardell, T. M.;
Turnbull, D. M.;
Johnson, M. A.

Publication type:

Article

Hyperemesis gravidarum and first trimester sagittal sinus thrombosis.

Published in:

2008

By:

Kennelly, M. M.;
Baker, M. R.;
Birchall, D.;
Hanley, J. P.;
Turnbull, D. M.;
Loughney, A. D.

Publication type:

journal article

Pre-eclampsia and magnesium toxicity with therapeutic plasma level in a woman with m.3243A>G melas mutation.

Published in:

2008

By:

Moriarty, K. T.;
Mcfarland, R.;
Whittaker, R.;
Burch, J.;
Turnbull, H. E.;
Taylor, R. W.;
Turnbull, D. M.

Publication type:

journal article

Molecular basis for treatment of mitochondrial myopathies.

Published in:

2000

By:

Taylor, R W;
Wardell, T M;
Lightowlers, R N;
Turnbull, D M

Publication type:

journal article

Decreased insulin responsiveness of glucose uptake in cultured human skeletal muscle cells from insulin-resistant nondiabetic relatives of type 2 diabetic families.

Published in:

2000

By:

Jackson, Sandra;
Bagstaff, Stephanie M.;
Lynn, Stephen;
Yeaman, Stephen J.;
Turnbull, Douglass M.;
Walker, Mark;
Jackson, S;
Bagstaff, S M;
Lynn, S;
Yeaman, S J;
Turnbull, D M;
Walker, M

Publication type:

journal article

Mitochondrial diabetes: investigation and identification of a novel mutation.

Published in:

1998

By:

Lynn, S;
Wardell, T;
Johnson, M A;
Chinnery, P F;
Daly, M E;
Walker, M;
Turnbull, D M

Publication type:

journal article

Heteroplasmic ratio of the A3243G mitochondrial DNA mutation in single pancreatic beta cells Lynn et al.: A3243G mtDNA mutation in beta cells.

Published in:

Diabetologia, 2003, v. 46, n. 2, p. 296, doi. 10.1007/s00125-002-1018-z

By:

Lynn, S.;
Borthwick, G. M.;
Charnley, R. M.;
Walker, M.;
Turnbull, D. M.

Publication type:

Article

Intermediate expansions of a X25/frataxin gene GAA repeat and Type II diabetes: assessment using parent-offspring trios.

Published in:

Diabetologia, 2000, v. 43, n. 3, p. 384

By:

Lynn, S.;
Hattersley, A.T.;
McCarthy, M. I.;
Frayling, T. M.;
Turnbull, D. M.;
Walker, M.

Publication type:

Article

Mitochondrial disease in pregnancy: a systematic review.

Published in:

Obstetric Medicine (1753-495X), 2011, v. 4, n. 3, p. 90, doi. 10.1258/om.2011.110008

By:

Say, R. E.;
Whittaker, R. G.;
Turnbull, H. E.;
McFarland, R.;
Taylor, R. W.;
Turnbull, D. M.

Publication type:

Article

Primary adenocarcinoma of the esophagus.

Published in:

1968

By:

Turnbull, Alan D. M.;
Goodner, John T.;
Turnbull, A D;
Goodner, J T

Publication type:

journal article

Batteries not included: diagnosis and management of mitochondrial disease.

Published in:

Journal of Internal Medicine, 2009, v. 265, n. 2, p. 210, doi. 10.1111/j.1365-2796.2008.02066.x

By:

McFarland, R.;
Turnbull, D. M.

Publication type:

Article

Role of Mitochondrial DNA Mutations in Disease and Aging.

Published in:

Annals of the New York Academy of Sciences, 2000, v. 908, n. 1, p. 199, doi. 10.1111/j.1749-6632.2000.tb06647.x

By:

COTTRELL, D. A.;
BLAKELY, E. L.;
BORTHWICK, G. M.;
JOHNSON, M. A.;
TAYLOR, G. A.;
BRIERLEY, E. J.;
INCE, P. G.;
TURNBULL, D. M.

Publication type:

Article

Peptide nucleic acid and delivery to human mitochondria.

Published in:

2000

By:

Chinnery, P F;
Taylor, R W;
Diekert, K;
Lill, R;
Turnbull, D M;
Lightowlers, R N

Publication type:

Erratum

Peptide nucleic acid delivery to human mitochondria.

Published in:

Gene Therapy, 1999, v. 6, n. 12, p. 1919, doi. 10.1038/sj.gt.3301061

By:

Chinnery, P F;
Taylor, R W;
Diekert, K;
Lill, R;
Turnbull, D M;
Lightowlers, R N

Publication type:

Article

Anorexia nervosa, liquorice and hypokalaemic myopathy.

Published in:

1981

By:

Nightingale, S.;
Smith, P. E.;
Turnbull, D. M.

Publication type:

journal article

Plasma concentrations of sodium valproate: Their clinical value.

Published in:

Annals of Neurology, 1983, v. 14, n. 1, p. 38, doi. 10.1002/ana.410140107

By:

Turnbull, D. M.;
Rawlins, M. D.;
Weightman, D.;
Chadwick, D. W.

Publication type:

Article