Found: 7
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Homoplasmy of a mitochondrial 3697G>A mutation causes Leigh syndrome.
- Published in:
- Journal of Human Genetics, 2014, v. 59, n. 7, p. 405, doi. 10.1038/jhg.2014.41
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- Article
Change in Antidepressant Use After Initiation of ADHD Medication in Japanese Adults with Comorbid Depression: A Real-World Database Analysis.
- Published in:
- Neuropsychiatric Disease & Treatment, 2021, v. 17, p. 3097, doi. 10.2147/NDT.S325498
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- Article
Efficacy and safety of guanfacine extended‐release in Japanese adults with attention‐deficit/hyperactivity disorder: Exploratory post hoc subgroup analyses of a randomized, double‐blind, placebo‐controlled study.
- Published in:
- Neuropsychopharmacology Reports, 2021, v. 41, n. 1, p. 26, doi. 10.1002/npr2.12152
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- Article
ECHS1 Mutations Cause Combined Respiratory Chain Deficiency Resulting in Leigh Syndrome.
- Published in:
- Human Mutation, 2015, v. 36, n. 2, p. 232, doi. 10.1002/humu.22730
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- Article
Mitochondrial Complex III Deficiency Caused by a Homozygous UQCRC2 Mutation Presenting with Neonatal-Onset Recurrent Metabolic Decompensation.
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- Human Mutation, 2013, v. 34, n. 3, p. 446, doi. 10.1002/humu.22257
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- Publication type:
- Article
An exploratory study of factors associated with long-term, high-dose opioid prescription in cancer patients in Japan based on a medical claims database.
- Published in:
- Supportive Care in Cancer, 2022, v. 30, n. 8, p. 6879, doi. 10.1007/s00520-022-07121-3
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- Article
Selective Cytotoxicity of Dihydroorotate Dehydrogenase Inhibitors to Human Cancer Cells Under Hypoxia and Nutrient-Deprived Conditions.
- Published in:
- Frontiers in Pharmacology, 2018, p. 1, doi. 10.3389/fphar.2018.00997
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- Article