Convulsions in neonatal period and infancy with rare etiology (neurogenetic disease);Ujszülött- ves csecsemokori görcsrohamok hatterében alló ritka neurogenetikai betegségek.

Ideggyógyászati szemle

Volumn 61, Issue 11-12, 2008, Pages 417-422

  Andrea, Nagy ^a   Zsuzsa, Szever ^a   Zsuzsa, Kormos ^a   Emoke, Székely ^a   Edit, Tóth ^a   Lajos, Smidéliusz ^a   Rita, Horváth ^a   Vera, Karcagi ^a   Agnes, Schuler ^a   Eszter, Jávorszky ^a  

^a Heim Pál Kórház Madarász Utcai Kirendeltsége   (Hungary)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; MEMBRANE PROTEIN; MITOCHONDRIAL PROTEIN; SCO2 PROTEIN, HUMAN; SURF 1 PROTEIN; SURF-1 PROTEIN; UNCLASSIFIED DRUG;

ANOXIA; ARTICLE; BENIGN CHILDHOOD EPILEPSY; BRAIN HEMORRHAGE; CASE REPORT; CHROMOSOME ABERRATION; DISORDERS OF AMINO ACID AND PROTEIN METABOLISM; DOPPLER FLOWMETRY; ECHOGRAPHY; ELECTROENCEPHALOGRAPHY; FEMALE; GENETIC SCREENING; GENETICS; HUMAN; INBORN ERROR OF METABOLISM; INFANT; LEIGH DISEASE; MALE; METABOLISM; MUTATION; NEWBORN;

AMINO ACID METABOLISM, INBORN ERRORS; ANOXIA; CARRIER PROTEINS; CEREBRAL HEMORRHAGE; CHROMOSOME ABERRATIONS; ELECTROENCEPHALOGRAPHY; EPILEPSY, BENIGN NEONATAL; FEMALE; GENETIC SCREENING; HUMANS; INFANT; INFANT, NEWBORN; LEIGH DISEASE; MALE; MEMBRANE PROTEINS; METABOLISM, INBORN ERRORS; MITOCHONDRIAL PROTEINS; MUTATION; ULTRASONOGRAPHY, DOPPLER;

EID: 58149340834     PISSN: 00191442     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)