TY  - GEN
AU  - Nagy,Andrea
AU  - Szever,Zsuzsa
AU  - Kormos,Zsuzsa
AU  - Székely,Emoke
AU  - Tóth,Edit
AU  - Smidéliusz,Lajos
AU  - Horváth,Rita
AU  - Karcagi,Vera
AU  - Schuler,Agnes
AU  - Jávorszky,Eszter
TI  - [Convulsions in neonatal period and infancy with rare etiology (neurogenetic disease)]
SN  - 0019-1442
PY  - 2008///1231
KW  - Amino Acid Metabolism, Inborn Errors
KW  - complications
KW  - Carrier Proteins
KW  - genetics
KW  - Cerebral Hemorrhage
KW  - Chromosome Aberrations
KW  - Electroencephalography
KW  - Epilepsy, Benign Neonatal
KW  - diagnostic imaging
KW  - Female
KW  - Genetic Testing
KW  - Humans
KW  - Hypoxia
KW  - Infant
KW  - Infant, Newborn
KW  - Leigh Disease
KW  - Male
KW  - Membrane Proteins
KW  - Metabolism, Inborn Errors
KW  - Mitochondrial Proteins
KW  - Molecular Chaperones
KW  - Mutation
KW  - Ultrasonography, Doppler
N1  - Publication Type: Case Reports; Journal Article
ER  -