An update on the central nervous system manifestations of familial tumor predisposition syndromes David A. Solomon Editorial 03 February 2020 Pages: 609 - 612
An update on the central nervous system manifestations of tuberous sclerosis complex Jennifer A. Cotter Review 11 April 2019 Pages: 613 - 624
An update on the central nervous system manifestations of neurofibromatosis type 1 J. Stephen NixJaishri BlakeleyFausto J. Rodriguez Review 08 April 2019 Pages: 625 - 641
An update on the CNS manifestations of neurofibromatosis type 2 Shannon CoyRumana RashidSandro Santagata Review Open access 04 June 2019 Pages: 643 - 665
Correction to: An update on the CNS manifestations of neurofibromatosis type 2 Shannon CoyRumana RashidSandro Santagata Correction Open access 20 August 2019 Pages: 667 - 667
An update on the central nervous system manifestations of Li–Fraumeni syndrome Brent A. OrrMichael R. ClayChimene Kesserwan Review 30 August 2019 Pages: 669 - 687
An update on the central nervous system manifestations of DICER1 syndrome Leanne de KockJohn R. PriestSanda Alexandrescu Review 05 April 2019 Pages: 689 - 701
An update on the CNS manifestations of brain tumor polyposis syndromes Byungjin KimUri TaboriCynthia Hawkins Review 22 January 2020 Pages: 703 - 715
Fulminant corticobasal degeneration: a distinct variant with predominant neuronal tau aggregates Helen LingEllen GelpiTamas Revesz Original Paper Open access 16 January 2020 Pages: 717 - 734
Familial globular glial tauopathy linked to MAPT mutations: molecular neuropathology and seeding capacity of a prototypical mixed neuronal and glial tauopathy Isidro FerrerPol Andrés-BenitoJosé Antonio del Rio Original Paper Open access 06 January 2020 Pages: 735 - 771
Picalm reduction exacerbates tau pathology in a murine tauopathy model Kunie AndoRobert De DeckerJean-Pierre Brion Original Paper 10 January 2020 Pages: 773 - 789
Truncating mutations in YIF1B cause a progressive encephalopathy with various degrees of mixed movement disorder, microcephaly, and epilepsy Mohammed AlMuhaizeaRawan AlMassNamik Kaya Correspondence 31 January 2020 Pages: 791 - 794
Rare IDH1 variants are common in pediatric hemispheric diffuse astrocytomas and frequently associated with Li-Fraumeni syndrome David SumerauerLenka KrskovaMichal Zapotocky Correspondence 03 January 2020 Pages: 795 - 797