Lhermitte-Duclos disease and Cowden disease: Clinical and genetic study in five patients with Lhermitte-Duclos disease and literature review

Acta Neurochirurgica

Volumn 146, Issue 7, 2004, Pages 679-690

  Pérez Núñez, Angel ^a   Lagares, A ^a   Benitez J ^b   Urioste, M ^b   Lobato, R D ^a   Ricoy, J R ^a   Ramos, A ^a   Gonzalez P ^a  

^a HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

^b INSTITUTO DE SALUD CARLOS III   (Spain)

Author keywords

Cerebellum; Cowden disease; Dysplasia; Gangliocytoma; Lhermitte Duclos disease; PTEN gene

Indexed keywords

PHOSPHATIDYLINOSITOL 3,4,5 TRISPHOSPHATE 3 PHOSPHATASE;

ADOLESCENT; ADULT; BRAIN DISEASE; CEREBELLUM DISEASE; CLINICAL ARTICLE; COWDEN SYNDROME; DISEASE ASSOCIATION; DYSPLASIA; FEMALE; GANGLIONEUROMA; GENE; GENE MUTATION; HISTOLOGY; HUMAN; LHERMITTE DUCLOS DISEASE; MALE; NEUROSURGERY; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; PTEN GENE; REVIEW; SCHOOL CHILD; TREATMENT OUTCOME;

ADULT; CEREBELLAR NEOPLASMS; CHILD; FEMALE; GANGLIONEUROMA; HAMARTOMA SYNDROME, MULTIPLE; HUMANS; MALE; MIDDLE AGED; PHOSPHORIC MONOESTER HYDROLASES; PTEN PHOSPHOHYDROLASE; TUMOR SUPPRESSOR PROTEINS;

EID: 18544394524     PISSN: 00016268     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Review

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