Lhermitte-Duclos-Cowden Disease
Two unrelated patients with clinical characteristics of both Lhermitte-Duclos disease and the autosomal dominant Cowden disease are reported from the Department of Neurology, University Hospital, Leiden, The Netherlands.
Saved in:
Main Author: | J Gordon Millichap (Author) |
---|---|
Format: | Book |
Published: |
Pediatric Neurology Briefs Publishers,
1991-06-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Lhermitte-Duclos disease (dysplastic gangliocytoma of the cerebellum) as a component of Cowden syndrome
by: Aparna Govindan, et al.
Published: (2012) -
Lhermitte-Duclos Disease: A Rare Lesion with Variable Presentations and Obscure Histopathology
by: Evrim ÖNDER, et al.
Published: (2018) -
Cowden Syndrome with Cortical Malformation and Epilepsy
by: J Gordon Millichap
Published: (2013) -
Cowden syndrome
by: Ravi Prakash S, et al.
Published: (2010) -
Mucocutaneous manifestations of Cowden's syndrome
by: Kundoor Vinay Kumar Reddy, et al.
Published: (2016)