Found: 7
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A novel mutation of the ACADM gene (c.145C>G) associated with the common c.985A>G mutation on the other ACADM allele causes mild MCAD deficiency: a case report.
- Published in:
- 2010
- By:
- Publication type:
- Case Study
Benign paroxysmal torticollis, benign paroxysmal vertigo, and benign tonic upward gaze are not benign disorders.
- Published in:
- 2018
- By:
- Publication type:
- journal article
Topography of brain damage in metabolic hypoglycaemia is determined by age at which hypoglycaemia occurred.
- Published in:
- Developmental Medicine & Child Neurology, 2013, v. 55, n. 2, p. 162, doi. 10.1111/dmcn.12045
- By:
- Publication type:
- Article
Factors associated with treatment lag in infantile spasms Silvia Napuri et al. Treatment Lag in Infantile Spasms.
- Published in:
- Developmental Medicine & Child Neurology, 2010, v. 52, n. 12, p. 1164, doi. 10.1111/j.1469-8749.2010.03811.x
- By:
- Publication type:
- Article
Phosphatidylserine enriched with polyunsaturated n‐3 fatty acid supplementation for attention‐deficit hyperactivity disorder in children and adolescents with epilepsy: A randomized placebo‐controlled trial.
- Published in:
- Epilepsia Open, 2024, v. 9, n. 2, p. 582, doi. 10.1002/epi4.12892
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- Publication type:
- Article
ADHD in childhood epilepsy: Clinical determinants of severity and of the response to methylphenidate.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, n. 7, p. 1069, doi. 10.1111/epi.13420
- By:
- Publication type:
- Article
Epilepsy in young Tsc1<sup> +/−</sup> mice exhibits age-dependent expression that mimics that of human tuberous sclerosis complex.
- Published in:
- Epilepsia (Series 4), 2016, v. 57, n. 4, p. 648, doi. 10.1111/epi.13325
- By:
- Publication type:
- Article