[Convulsions in neonatal period and infancy with rare etiology (neurogenetic disease)]. [electronic resource]
Producer: 20081231Description: 417-22 p. digitalISSN:- 0019-1442
- Amino Acid Metabolism, Inborn Errors -- complications
- Carrier Proteins -- genetics
- Cerebral Hemorrhage -- complications
- Chromosome Aberrations
- Electroencephalography
- Epilepsy, Benign Neonatal -- diagnostic imaging
- Female
- Genetic Testing
- Humans
- Hypoxia -- complications
- Infant
- Infant, Newborn
- Leigh Disease -- complications
- Male
- Membrane Proteins -- genetics
- Metabolism, Inborn Errors -- complications
- Mitochondrial Proteins -- genetics
- Molecular Chaperones
- Mutation
- Ultrasonography, Doppler
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Publication Type: Case Reports; Journal Article
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