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Miller, C. (2002) Cowden Disease (Multiple Hamartoma Syndrome). In: Elmets, C., Vinson, R., Libow, L., Quirk, C., James, W.W., et al., Eds., eMedicine Instant Access to the Minds of Medicine, LU, Institute for Healthcare Improvement, USA.
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has been cited by the following article:

• TITLE: Advanced Imaging Techniques in Lhermitte-Duclos Disease (LDD): A Case Report and Brief Literature Review

  AUTHORS: N. J. Delgado, A. S. Lessa, T. H. L. Carmo, G. M. Dias, E. J. A. Valadares, L. C. Campos, V. M. Vilela

  KEYWORDS: Lhermitte-Duclos Disease, Displastic Gangliocytoma, Central Nervous System, MRI

  JOURNAL NAME: Neuroscience and Medicine, Vol.8 No.1, March 28, 2017

  ABSTRACT: Lhermitte-Duclos disease (LDD), also called dysplastic gangliocytoma of the cerebellum, is a rare condition described in 1920. It represents a disorganization of cerebellar architecture with overgrowth of cerebellar ganglion cells which replace granular cells and Purkinje cells. In this report we present the case of a 62-year-old male affected by this disease, as well as literature review of the clinical, morphological and functional radiological findings.