Found: 16
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Germline nuclear transfer in mice may rescue poor embryo development associated with advanced maternal age and early embryo arrest.
- Published in:
- 2020
- By:
- Publication type:
- journal article
A novel mitochondrial transfer RNA proline mutation.
- Published in:
- Journal of Inherited Metabolic Disease, 2000, v. 23, n. 8, p. 853, doi. 10.1023/A:1026729223050
- By:
- Publication type:
- Article
Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasis.
- Published in:
- 1999
- By:
- Publication type:
- journal article
A novel NDUFV1 gene mutation in complex I deficiency in consanguineous siblings with brainstem lesions and Leigh syndrome.
- Published in:
- Clinical Genetics, 2012, v. 82, n. 3, p. 264, doi. 10.1111/j.1399-0004.2011.01743.x
- By:
- Publication type:
- Article
Infantile presentation of the mitochondrial A8344G mutation.
- Published in:
- 2007
- By:
- Publication type:
- Letter
Comparative analysis of different nuclear transfer techniques to prevent the transmission of mitochondrial DNA variants.
- Published in:
- Molecular Human Reproduction, 2019, v. 25, n. 12, p. 797, doi. 10.1093/molehr/gaz062
- By:
- Publication type:
- Article
Acetazolamide for severe apnea in Pitt-Hopkins syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2012, v. 158A, n. 4, p. 932, doi. 10.1002/ajmg.a.35247
- By:
- Publication type:
- Article
Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples.
- Published in:
- Prenatal Diagnosis, 1998, v. 18, n. 10, p. 1041, doi. 10.1002/(SICI)1097-0223(1998100)18:10<1041::AID-PD407>3.0.CO;2-J
- By:
- Publication type:
- Article
Intractable ulcerative colitis of infancy in a child with mitochondrial respiratory chain disorder.
- Published in:
- 2004
- By:
- Publication type:
- journal article
Inborn oxidative phosphorylation defect as risk factor for propofol infusion syndrome.
- Published in:
- Acta Anaesthesiologica Scandinavica, 2012, v. 56, n. 4, p. 520, doi. 10.1111/j.1399-6576.2011.02628.x
- By:
- Publication type:
- Article
Butylated hydroxyanisole is more than a reactive oxygen species scavenger.
- Published in:
- 2006
- By:
- Publication type:
- Letter
Ultrastructural localization of cytochrome c in apoptosis demonstrates mitochondrial heterogeneity.
- Published in:
- Cell Death & Differentiation, 2000, v. 7, n. 4, p. 331, doi. 10.1038/sj.cdd.4400655
- By:
- Publication type:
- Article
Differential features of patients with mutations in two COX assembly genes, SURF-1 and SCO2.
- Published in:
- Annals of Neurology, 2000, v. 47, n. 5, p. 589, doi. 10.1002/1531-8249(200005)47:5<589::AID-ANA6>3.0.CO;2-D
- By:
- Publication type:
- Article
Correction to: Clinical and genetic aspects of defects in the mitochondrial iron-sulfur cluster synthesis pathway.
- Published in:
- Journal of Biological Inorganic Chemistry (JBIC), 2018, v. 23, n. 4, p. 507, doi. 10.1007/s00775-018-1564-6
- By:
- Publication type:
- Article
Clinical and genetic aspects of defects in the mitochondrial iron-sulfur cluster synthesis pathway.
- Published in:
- Journal of Biological Inorganic Chemistry (JBIC), 2018, v. 23, n. 4, p. 495, doi. 10.1007/s00775-018-1550-z
- By:
- Publication type:
- Article
Visual contribution to walking in children with Developmental Coordination Disorder.
- Published in:
- Child: Care, Health & Development, 2006, v. 32, n. 6, p. 711, doi. 10.1111/j.1365-2214.2006.00685.x
- By:
- Publication type:
- Article