Association between Cowden syndrome and Lhermitte-Duclos disease: Report of two cases and review of the literature

Surgical Neurology

Volumn 61, Issue 5, 2004, Pages 447-454

  Derrey, Stéphane ^a   Proust, Francois ^a,d   Debono, Bertrand ^a   Langlois, Olivier ^a   Layet, Antoine ^b   Layet, Valérie ^e   Longy, Michel ^c   Fréger, Pierre ^a   Laquerrière, Annie ^a  

^a ROUEN UNIVERSITY HOSPITAL   (France)

^b LE HAVRE HOSPITAL   (France)

^c BORDEAUX UNIVERSITY HOSPITAL   (France)

^d HÔPITAL CHARLES NICOLLE   (France)

^e NONE

Author keywords

Cowden disease; Lhermitte Duclos disease; PTEN gene

Indexed keywords

PHOSPHATASE; PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ADULT; BRAIN SURGERY; CASE REPORT; CLINICAL EXAMINATION; CLINICAL FEATURE; COWDEN SYNDROME; DIAGNOSTIC APPROACH ROUTE; DISEASE ASSOCIATION; EXON; FEMALE; FOLLOW UP; GENE MUTATION; HISTOPATHOLOGY; HOSPITAL ADMISSION; HUMAN; HUMAN TISSUE; INTRACRANIAL HYPERTENSION; LHERMITTE DUCLOS DISEASE; MUTATIONAL ANALYSIS; NEUROPATHOLOGY; NUCLEAR MAGNETIC RESONANCE IMAGING; OUTCOMES RESEARCH; POSTOPERATIVE PERIOD; PROTEIN MOTIF; REVIEW; SURGICAL APPROACH; SURGICAL TECHNIQUE;

EID: 2142679355     PISSN: 00903019     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0090-3019(03)00576-7     Document Type: Article

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