Old Web
English
Sign In
Acemap
>
authorDetail
>
Inge Van Bortel
Inge Van Bortel
Pierre-and-Marie-Curie University
Exome sequencing
Pathogenesis
Mutation
Multisystem proteinopathy
Amyotrophic lateral sclerosis
2
Papers
84
Citations
0.00
KQI
Citation Trend
Filter By
Interval:
1900~2024
1900
2024
Author
Papers (2)
Sort By
Default
Most Recent
Most Early
Most Citation
No data
Journal
Conference
Others
hnRNPA2B1 and hnRNPA1 mutations are rare in patients with "multisystem proteinopathy" and frontotemporal lobar degeneration phenotypes
2014
Neurobiology of Aging
Isabelle Le Ber
Inge Van Bortel
Gaël Nicolas
Kawtar Bouya-Ahmed
Agnès Camuzat
David Wallon
Anne De Septenville
Morwena Latouche
Serena Lattante
Edor Kabashi
Ludmila Jornea
Didier Hannequin
Alexis Brice
Show All
Source
Cite
Save
Citations (49)
TREM2 mutations are rare in a French cohort of patients with frontotemporal dementia
2013
Neurobiology of Aging
Serena Lattante
Isabelle Le Ber
Agnès Camuzat
Sarah Dayan
Chloé Godard
Inge Van Bortel
Anne De Septenville
Sorana Ciura
Alexis Brice
Edor Kabashi
Show All
Source
Cite
Save
Citations (35)
1