ProfileOfResearchers

Identificadas 144

101

TÃTULO: The central biobank and virtual biobank of BiOMarKaPD: a resource for studies on neurodegenerative diseases Full Text
AUTORES: Babette L R Reijs; Charlotte E Teunissen; Nikolai Goncharenko; Fay Betsou; Kaj Blennow; Ines Baldeiras; Frederic Brosseron; Enrica Cavedo; Tormod Fladby; Lutz Froelich; Tomasz Gabryelewicz; Hakan Gurvit; Elisabeth Kapaki; Peter Koson; Luka Kulic; Sylvain Lehmann; Piotr Lewczuk; Alberto Lleo; Walter Maetzler; Alexandre de Mendonca; Anne Marie Miller; Jose L Molinuevo; Brit Mollenhauer; Lucilla Parnetti; Uros Rot; Anja Schneider; Anja Hviid Simonsen; Fabrizio Tagliavini; Magda Tsolaki; Marcel M Verbeek; Frans R J Verhey; Marzena Zboch; Bengt Winblad; Philip Scheltens; Henrik Zetterberg; Pieter Jelle Visser; ...Mais
PUBLICAÇÃO: 2015, FONTE: FRONTIERS IN NEUROLOGY, VOLUME: 6, NÚMERO: OCT

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CrossRef: 12

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ORCID

102

TÃTULO: Rare Variants in PLD3 Do Not Affect Risk for Early-Onset Alzheimer Disease in a European Consortium Cohort. HUMAN MUTATION Full Text
AUTORES: Rita Cacace; Tobi Van den Bossche; Sebastiaan Engelborghs; Nathalie Geerts; Annelies Laureys; Lubina Dillen; Caroline Graff; Hakan Thonberg; Huei Hsin Chiang; Pau Pastor; Sara Ortega Cubero; Maria A Pastor; Janine Diehl Schmid; Panagiotis Alexopoulos; Luisa Benussi; Roberta Ghidoni; Giuliano Binetti; Benedetta Nacmias; Sandro Sorbi; Raquel Sanchez Valle; Albert Llado; Ellen Gelpi; Maria Rosario Almeida; Isabel Santana; Magda Tsolaki; Maria Koutroumani; Jordi Clarimon; Alberto Lleo; Juan Fortea; Alexandre de Mendonca; Madalena Martins; Barbara Borroni; Alessandro Padovani; Radoslav Matej; Zdenek Rohan; Mathieu Vandenbulcke; Rik Vandenberghe; Peter P De Deyn; Patrick Cras; Julie van der Zee; Kristel Sleegers; Christine Van Broeckhoven; ...Mais
PUBLICAÇÃO: 2015, FONTE: HUMAN MUTATION, VOLUME: 36, NÚMERO: 12

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103

TÃTULO: Prevalence of cerebral amyloid pathology in persons without dementia: A meta-analysis. A Meta-analysis
AUTORES: Willemijn J Jansen; Rik Ossenkoppele; Dirk L Knol; Betty M Tijms; Philip Scheltens; Frans R J Verhey; Pieter Jelle Visser; Pauline Aalten; Dag Aarsland; Daniel Alcolea; Myriam Alexander; Ina S Almdahl; Steven E Arnold; Ines Baldeiras; Henryk Barthel; Bart N M Van Berckel; Kristen Bibeau; Kaj Blennow; David J Brooks; Mark A Van Buchem; Vincent Camus; Enrica Cavedo; Kewei Chen; Gael Chetelat; Ann D Cohen; Alexander Drzezga; Sebastiaan Engelborghs; Anne M Fagan; Tormod Fladby; Adam S Fleisher; Wiesje M Van Der Flier; Lisa Ford; Stefan Forster; Juan Fortea; Nadia Foskett; Kristian S Frederiksen; Yvonne Freund Levi; Giovanni B Frisoni; Lutz Froelich; Tomasz Gabryelewicz; Kiran Dip Gill; Olymbia Gkatzima; Estrella Gomez Tortosa; Mark Forrest Gordon; Timo Grimmer; Harald Hampel; Lucrezia Hausner; Sabine Hellwig; Sanna Kaisa Herukka; Helmut Hildebrandt; Lianna Ishihara; Adrian Ivanoiu; William J Jagust; Peter Johannsen; Ramesh Kandimalla; Elisabeth Kapaki; Aleksandra Klimkowicz Mrowiec; William E Klunk; Sebastian Kohler; Norman Koglin; Johannes Kornhuber; Milica G Kramberger; Koen Van Laere; Susan M Landau; Dong Young Lee; Mony De Leon; Viviana Lisetti; Alberto Lleo; Karine Madsen; Wolfgang Maier; Jan Marcusson; Niklas Mattsson; Alexandre De Mendonca; Olga Meulenbroek; Philipp T Meyer; Mark A Mintun; Vincent Mok; Jose Luis Molinuevo; Hanne M Mollergard; John C Morris; Barbara Mroczko; Stefan Van Der Mussele; Duk L Na; Andrew Newberg; Agneta Nordberg; Arto Nordlund; Gerald P Novak; George P Paraskevas; Lucilla Parnetti; Gayan Perera; Oliver Peters; Julius Popp; Sudesh Prabhakar; Gil D Rabinovici; Inez H G B Ramakers; Lorena Rami; Catarina Resende De Oliveira; Juha O Rinne; Karen M Rodrigue; Eloy Rodriguez Rodriguez; ...Mais
PUBLICAÇÃO: 2015, FONTE: JAMA - Journal of the American Medical Association, VOLUME: 313, NÚMERO: 19

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CrossRef: 1164

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ORCID

104

TÃTULO: Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration Full Text
AUTORES: 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; ...Mais
PUBLICAÇÃO: 2014, FONTE: ACTA NEUROPATHOLOGICA, VOLUME: 128, NÚMERO: 3

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NO MEU:

ORCID

105