Genetic and imaging features of cerebellar abnormalities in tuberous sclerosis complex: more insights into their pathogenesis

Author:

Manara Renzo1ORCID,Bugin Samuela2,Pelizza Maria Federica2,Sartori Stefano2,Nosadini Margherita2ORCID,Labriola Francesca3,Canevini Paola4,Vignoli Aglaia4,Toldo Irene2ORCID

Affiliation:

1. Department of Medicine and Surgery; Neuroradiology; Sezione di Neuroscienze; University of Salerno; Baronissi Italy

2. Department of Woman and Child Health; Pediatric Neurology and Neurophysiology Unit; University Hospital of Padova; Padova Italy

3. Epilepsy and Sleep Medicine Center; Neuropsychiatric Unit; ASST Santi Paolo Carlo; Milan Italy

4. Epilepsy Center; Health Sciences Department; University of Milano; Milan Italy

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Reference6 articles.

1. Cerebellar lesions are associated with TSC2 mutations in tuberous sclerosis complex: a retrospective record review study;Boronat;Dev Med Child Neurol,2017

2. Clinicopathological and immunohistochemical findings in an autopsy case of tuberous sclerosis complex;Boer;Neuropathology,2008

3. Olfactory hamartomas in tuberous sclerosis;León;J Neurol Sci,1988

4. Cerebral tuberous sclerosis: MR imaging;Nixon;Radiology,1989

5. Very small (border zone) cerebellar infarcts. Distribution, causes, mechanisms and clinical features;Amarenco;Brain,1993

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