Literature DB >> 19864668

Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation.

J D Rohrer, J Beck, J D Warren, A King, S Al Sarraj, J Holton, T Revesz, J Collinge, S Mead.   

Abstract

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Year:  2009        PMID： 19864668     DOI： 10.1136/jnnp.2008.169383

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  6 in total

Review 1.  The multiple phenotypes of corticobasal syndrome and corticobasal degeneration: implications for further study.

Authors:  Bradley F Boeve
Journal:  J Mol Neurosci       Date:  2011-08-19       Impact factor: 3.444

2.  Intra-familial clinical heterogeneity due to FTLD-U with TDP-43 proteinopathy caused by a novel deletion in progranulin gene (PGRN).

Authors:  Tomasz Gabryelewicz; Mario Masellis; Mariusz Berdynski; Juan M Bilbao; Ekaterina Rogaeva; Peter St George-Hyslop; Anna Barczak; Krzysztof Czyzewski; Maria Barcikowska; Zbigniew Wszolek; Sandra E Black; Cezary Zekanowski
Journal:  J Alzheimers Dis       Date:  2010       Impact factor: 4.472

3.  Differences in Motor Features of C9orf72, MAPT, or GRN Variant Carriers With Familial Frontotemporal Lobar Degeneration.

Authors:  Philip Wade Tipton; Angela B Deutschlaender; Rodolfo Savica; Michael G Heckman; Danielle E Brushaber; Bradford C Dickerson; Ralitza H Gavrilova; Daniel H Geschwind; Nupur Ghoshal; Jonathan Graff-Radford; Neill R Graff-Radford; Murray Grossman; Ging-Yuek R Hsiung; Edward D Huey; David John Irwin; David T Jones; David S Knopman; Scott M McGinnis; Rosa Rademakers; Eliana Marisa Ramos; Leah K Forsberg; Hilary W Heuer; Chiadi Onyike; Carmela Tartaglia; Kimiko Domoto-Reilly; Erik D Roberson; Mario F Mendez; Irene Litvan; Brian S Appleby; Ian Grant; Daniel Kaufer; Adam L Boxer; Howard J Rosen; Brad F Boeve; Zbigniew K Wszolek
Journal:  Neurology       Date:  2022-07-05       Impact factor: 11.800

4.  The heritability and genetics of frontotemporal lobar degeneration.

Authors:  J D Rohrer; R Guerreiro; J Vandrovcova; J Uphill; D Reiman; J Beck; A M Isaacs; A Authier; R Ferrari; N C Fox; I R A Mackenzie; J D Warren; R de Silva; J Holton; T Revesz; J Hardy; S Mead; M N Rossor
Journal:  Neurology       Date:  2009-11-03       Impact factor: 9.910

Review 5.  Unravelling Genetic Factors Underlying Corticobasal Syndrome: A Systematic Review.

Authors:  Federica Arienti; Giulia Lazzeri; Maria Vizziello; Edoardo Monfrini; Nereo Bresolin; Maria Cristina Saetti; Marina Picillo; Giulia Franco; Alessio Di Fonzo
Journal:  Cells       Date:  2021-01-15       Impact factor: 6.600

Review 6.  Extended FTLD pedigree segregating a Belgian GRN-null mutation: neuropathological heterogeneity in one family.

Authors:  Anne Sieben; Sara Van Mossevelde; Eline Wauters; Sebastiaan Engelborghs; Julie van der Zee; Tim Van Langenhove; Patrick Santens; Marleen Praet; Paul Boon; Marijke Miatton; Sofie Van Hoecke; Mathieu Vandenbulcke; Rik Vandenberghe; Patrick Cras; Marc Cruts; Peter Paul De Deyn; Christine Van Broeckhoven; Jean-Jacques Martin
Journal:  Alzheimers Res Ther       Date:  2018-01-22       Impact factor: 6.982
  6 in total

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