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Your search keyword '"Pediatric Neurology and Neuromuscular Diseases Unit"' showing total 13 results

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13 results on '"Pediatric Neurology and Neuromuscular Diseases Unit"'

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1. AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

2. Rare coding variants in genes encoding GABAA receptors in genetic generalised epilepsies: an exome-based case-control study

3. Novel Compound Heterozygous Mutations inTBC1D24Cause Familial Malignant Migrating Partial Seizures of Infancy

4. Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders

5. TBC1D24 regulates neuronal migration and maturation through modulation of the ARF6-dependent pathway

6. Loss-of-function KCNH2 mutation in a family with long QT syndrome, epilepsy, and sudden death

7. Spastic paraplegia with thin corpus callosum: description of 20 new families, refinement of the SPG11 locus, candidate gene analysis and evidence of genetic heterogeneity

8. Etiological involvement of KCND1 variants in an X-linked neurodevelopmental disorder with variable expressivity.

9. Diagnostic Approach to Macrocephaly in Children.

10. Biallelic variants in HPDL cause pure and complicated hereditary spastic paraplegia.

11. RNF213 variant in a patient with Legius syndrome associated with moyamoya syndrome.

12. Genetic investigation of sudden unexpected death in epilepsy cohort by panel target resequencing.

13. Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum.

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