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Transcriptional regulation of long-term potentiation.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 201, doi. 10.1007/s10048-016-0489-x
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- Publication type:
- Article
Acknowledgement to Referees 2015/2016.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 271, doi. 10.1007/s10048-016-0492-2
- Publication type:
- Article
A novel KCNA1 mutation in a family with episodic ataxia and malignant hyperthermia.
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- Neurogenetics, 2016, v. 17, n. 4, p. 245, doi. 10.1007/s10048-016-0486-0
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- Article
A mutation in the THG1L gene in a family with cerebellar ataxia and developmental delay.
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- Neurogenetics, 2016, v. 17, n. 4, p. 219, doi. 10.1007/s10048-016-0487-z
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- Article
Polymicrogyria and myoclonic epilepsy in autosomal recessive cutis laxa type 2A.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 251, doi. 10.1007/s10048-016-0491-3
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- Publication type:
- Article
PARP10 deficiency manifests by severe developmental delay and DNA repair defect.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 227, doi. 10.1007/s10048-016-0493-1
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- Publication type:
- Article
A customized high-resolution array-comparative genomic hybridization to explore copy number variations in Parkinson's disease.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 233, doi. 10.1007/s10048-016-0494-0
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- Publication type:
- Article
Defining the genetic basis of early onset hereditary spastic paraplegia using whole genome sequencing.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 265, doi. 10.1007/s10048-016-0495-z
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- Publication type:
- Article
New ATP8A2 gene mutations associated with a novel syndrome: encephalopathy, intellectual disability, severe hypotonia, chorea and optic atrophy.
- Published in:
- Neurogenetics, 2016, v. 17, n. 4, p. 259, doi. 10.1007/s10048-016-0496-y
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- Publication type:
- Article
Cortical gene expression: prognostic value for seizure outcome following temporal lobectomy and amygdalohippocampectomy.
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- Neurogenetics, 2016, v. 17, n. 4, p. 211, doi. 10.1007/s10048-016-0484-2
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- Article