Neuronal intranuclear (hyaline) inclusion disease and fragile X-associated tremor/ataxia syndrome: a morphological and molecular dilemma

Brain. 2017 Aug 1;140(8):e51. doi: 10.1093/brain/awx156.

Ellen Gelpi¹, Teresa Botta-Orfila^{2

3}, Laia Bodi⁴, Stefanie Marti^{2

3}, Gabor Kovacs⁵, Oriol Grau-Rivera^{1

6}, Manuel Lozano⁷, Raquel Sánchez-Valle⁶, Esteban Muñoz⁸, Francesc Valldeoriola⁸, Javier Pagonabarraga⁹, Gian-Gaetano Tartaglia^{2

3

10}, Montserrat Milà⁴

¹ Neurological Tissue Bank of the Biobanc-Hospital Clinic-IDIBAPS, Barcelona, Spain.
² Centre for Genomic Regulation (CRG), The Barcelona Institute for Science and Technology, Dr. Aiguader 88, 08003 Barcelona, Spain.
³ Universitat Pompeu Fabra (UPF), Barcelona, Spain.
⁴ Department of Genetics, Hospital Clinic de Barcelona, Barcelona, Spain.
⁵ Institute of Neurology, Medical University of Vienna, Austria.
⁶ Neurology Department, Alzheimer's disease and other Cognitive Disorders Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
⁷ Neurology Department, Hospital Germans Trias I Pujol, Badalona, Spain.
⁸ Neurology Department, Movement Disorders Unit, Hospital Clinic de Barcelona, Barcelona, Spain.
⁹ Neurology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
¹⁰ Institució Catalana de Recerca i Estudis Avançats (ICREA), Barcelona, Spain.

No abstract available

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