Found: 47
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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:
- Publication type:
- 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
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- 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
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- Publication type:
- Article
A case-comparison study of pregnant women with mitochondrial disease - what to expect?
- Published in:
- 2019
- By:
- Publication type:
- journal article
Molecular basis for treatment of mitochondrial myopathies.
- Published in:
- 2000
- By:
- 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:
- Publication type:
- Article
Effects of obesity and weight loss on mitochondrial structure and function and implications for colorectal cancer risk.
- Published in:
- 2019
- By:
- Publication type:
- journal 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:
- Publication type:
- Article
The investigation of mitochondrial respiratory chain disease.
- Published in:
- 1995
- By:
- 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:
- 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
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- Publication type:
- Article
Mitochondrial diabetes.
- Published in:
- 2005
- By:
- Publication type:
- Other
Anorexia nervosa, liquorice and hypokalaemic myopathy.
- Published in:
- 1981
- By:
- Publication type:
- journal article
Primary adenocarcinoma of the esophagus.
- Published in:
- 1968
- By:
- Publication type:
- journal 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:
- 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:
- Publication type:
- 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:
- Publication type:
- Article
Relationship between insulin sensitivity and insulin receptor substrate-1 mutations in non-diabetic relatives of NIDDM families.
- Published in:
- 1996
- By:
- 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:
- 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:
- Publication type:
- Article
Alpha-synuclein pathology and Parkinsonism associated with POLG1 mutations and multiple mitochondrial DNA deletions.
- Published in:
- 2009
- By:
- 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:
- 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:
- 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:
- Publication type:
- Article
Peptide nucleic acid and delivery to human mitochondria.
- Published in:
- 2000
- By:
- 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:
- 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:
- Publication type:
- Article
Lipid storage myopathy due to glutaric aciduria type II: treatment of a potentially fatal myopathy.
- Published in:
- 1988
- By:
- Publication type:
- journal article
Insulin sensitivity and mitochondrial gene mutation.
- Published in:
- 1995
- By:
- Publication type:
- commentary
Biochemical and molecular studies of mitochondrial function in diabetes insipidus, diabetes mellitus, optic atrophy, and deafness.
- Published in:
- 1994
- By:
- 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:
- Publication type:
- Article
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:
- Publication type:
- Article
Assessment of visual function in chronic progressive external ophthalmoplegia.
- Published in:
- 2006
- By:
- Publication type:
- journal 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:
- Publication type:
- 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:
- 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:
- Publication type:
- 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:
- Publication type:
- journal article
Mitochondrial diabetes: investigation and identification of a novel mutation.
- Published in:
- 1998
- By:
- Publication type:
- journal article
Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.
- Published in:
- 2001
- By:
- Publication type:
- journal article
The epidemiology of pathogenic mitochondrial DNA mutations.
- Published in:
- 2000
- By:
- 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:
- 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:
- 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:
- 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:
- 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:
- Publication type:
- 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:
- 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:
- Publication type:
- Article