Facomatosis que cursan con manchas acromicas, esclerosis tuberosa de Bourneville. Criterios diagnósticos y protocolo de seguimiento

Revista de Neurologia

Volumn 24, Issue 133, 1996, Pages 1056-1059

  Prats Vinas J M ^a  

^a HOSPITAL DE CRUCES   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CLINICAL PROTOCOL; EYE DISEASE; HEART DISEASE; HUMAN; KIDNEY DISEASE; PIGMENT DISORDER; REVIEW; TUBEROUS SCLEROSIS;

CLINICAL PROTOCOLS; EYE DISEASES; HEART DISEASES; HUMANS; KIDNEY DISEASES; PIGMENTATION DISORDERS; TUBEROUS SCLEROSIS;

EID: 18344418708     PISSN: 02100010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (5)

1. Jhonson WG, Gómez MR. Tuberous sclerosis and allied disorders. Ann NY Acad Seienc 1991; 615: 397.
2. Shepherd ChW, Houser OW, Gómez MR. MR findings in tuberous sclerosos complex and correlation with seizure development and mental impairment. AJNR 1995; 16: 149-155.
3. Gómez MR, Kuntz NL, Westmorland BF. Tuberous sclerosos, early onset seizures and mental subnormality: study of siscordant monozygous twins. Neurology 1982; 32: 604-611.
4. Lane VW, Samples JM. Tuberous sclerosis: case study of early seizure control and subsequent normal development. J Aut Dev Disord 1984; 14: 423-427.
5. Bebin EM, Kelly PJ, Gómez MR. Surgical treatment for epilepsy in cerebral tuberous sclerosis. Epilepsia 1993; 34: 651-657.