Eva Parobkova


AuthID: R-00G-E05

Publications Awaiting Confirmation

1
TITLE: Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration  Full Text
AUTHORS: Julie van der Zee; Tim Van Langenhove; Gabor G Kovacs; Lubina Dillen; William Deschamps; Sebastiaan Engelborghs; Radoslav Matej; Mathieu Vandenbulcke; Anne Sieben; Bart Dermaut; Katrien Smets; Philip Van Damme; Celine Merlin; Annelies Laureys; Marleen Van Den Broeck; Maria Mattheijssens; Karin Peeters; Luisa Benussi; Giuliano Binetti; Roberta Ghidoni; Barbara Borroni; Alessandro Padovani; Silvana Archetti; Pau Pastor; Cristina Razquin; Sara Ortega Cubero; Isabel Hernandez; Merce Boada; Agustin Ruiz; Alexandre de Mendonca; Gabriel Miltenberger Miltenyi; Frederico Simoes do Couto; Sandro Sorbi; Benedetta Nacmias; Silvia Bagnoli; Caroline Graff; Huei Hsin Chiang; Hakan Thonberg; Robert Perneczky; Janine Diehl Schmid; Panagiotis Alexopoulos; Giovanni B Frisoni; Christian Bonvicini; Matthis Synofzik; Walter Maetzler; Jennifer Muller vom Hagen; Ludger Schoels; Tobias B Haack; Tim M Strom; Holger Prokisch; Oriol Dols Icardo; Jordi Clarimon; Alberto Lleo; Isabel Santana; Maria Rosario Almeida; Beatriz Santiago; Michael T Heneka; Frank Jessen; Alfredo Ramirez; Raquel Sanchez Valle; Albert Llado; Ellen Gelpi; Stayko Sarafov; Ivailo Tournev; Albena Jordanova; Eva Parobkova; Gian Maria Fabrizi; Silvia Testi; Eric Salmon; Thomas Stroebel; Patrick Santens; Wim Robberecht; Peter De Jonghe; Jean Jacques Martin; Patrick Cras; Rik Vandenberghe; Peter Paul De Deyn; Marc Cruts; Kristel Sleegers; Christine Van Broeckhoven; ...More
PUBLISHED: 2014, SOURCE: ACTA NEUROPATHOLOGICA, VOLUME: 128, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef

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