Epileptic signs of metabolic origin;Manifestaciones epilepticas de causa metabolica

Revista de Neurologia

Volumn 28, Issue SUPPL. 1, 1999, Pages

  Herranz, J L ^a  

^a HOSPITAL UNIVERSITARIO MARQUÉS DE VALDECILLA   (Spain)

Author keywords

Children; Epilepsy; Metabolic diseases

Indexed keywords

ARTICLE; CLINICAL FEATURE; EPILEPSY; GANGLIOSIDOSIS; HUMAN; HYPERGLYCEMIA; LIPOFUSCINOSIS; MENKES SYNDROME; METABOLIC DISORDER; NIEMANN PICK DISEASE; PRESCHOOL CHILD; PYRIDOXINE DEFICIENCY; SIALIDOSIS; CEREBROSPINAL FLUID; CHILD; INBORN ERROR OF METABOLISM; INFANT; REVIEW;

CHILD; CHILD, PRESCHOOL; EPILEPSY; HUMANS; INFANT; METABOLISM, INBORN ERRORS;

EID: 0033366943     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (4)

1. Cohen BH. Metabolic and degenerative diseases associated with epilepsy. Epilepsia 1993; 34 (Suppl 3): S62-70.
2. Scriver CR, Beaudet AL, et al. The metabolic and molecular basis of inherited disease. 7 ed. New York: McGraw Hill; 1995.
3. Lyon G, Adams RD, Kolodny EH. Neurology of hereditary metabolic diseases of children. 2 ed. New York: McGraw-Hill; 1996.
4. Herranz JL, de las Cuevas I. Enfoque diagnóstico del niño con crisis mioclónicas aisladas o asociadas a otros tipos de crisis. Rev Neurol 1998; 26: 301-7.