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Lawrence, Braden J., Urbizu, Aintzane ORCID: 0000-0001-8458-1209, Allen, Philip A., Loth, Francis, Tubbs, R. Shane, Bunck, Alexander C., Kroeger, Jan-Robert, Rocque, Brandon G., Madura, Casey, Chen, Jason A., Luciano, Mark G., Ellenbogen, Richard G., Oshinski, John N., Iskandar, Bermans J. and Martin, Bryn A.
ORCID: 0000-0003-1234-7880
(2018).
Cerebellar tonsil ectopia measurement in type I Chiari malformation patients show poor inter-operator reliability.
Fluids Barriers CNS, 15.
LONDON:
BMC.
ISSN 2045-8118
van der Lee, Sven J., Conway, Olivia J., Jansen, Iris, Carrasquillo, Minerva M., Kleineidam, Luca, van den Akker, Erik, Hernandez, Isabel, van Eijk, Kristel R., Stringa, Najada, Chen, Jason A., Zettergren, Anna, Andlauer, Till F. M., Diez-Fairen, Monica, Simon-Sanchez, Javier, Lleo, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E., Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael ORCID: 0000-0003-2589-6440, Fortea, Juan, Keogh, Michael J., Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A., Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar, Riedel-Heller, Steffi, Illan-Gala, Ignacio
ORCID: 0000-0002-5418-2052, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Then Bergh, Florian, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M., Indakoetxea, Begona, Collij, Lyduine E., Scherer, Martin, Morenas-Rodriguez, Estrella, Ironside, James W., van Berckel, Bart N. M., Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L., Pastor, Pau
ORCID: 0000-0002-7493-8777, Rodriguez Rodriguez, Eloy, Boeve, Bradley F., Petersen, Ronald C., Ferman, Tanis J., van Gerpen, Jay A., Reinders, Marcel J. T., Uitti, Ryan J., Tarraga, Lluis, Maier, Wolfgang, Dols-Icardo, Oriol
ORCID: 0000-0003-2656-8748, Kawalia, Amit, Dalmasso, Maria Carolina, Boada, Merce, Zettl, Uwe K., van Schoor, Natasja M., Beekman, Marian, Allen, Mariet, Masliah, Eliezer, de Munain, Adolfo Lopez, Pantelyat, Alexander, Wszolek, Zbigniew K., Ross, Owen A., Dickson, Dennis W., Graff-Radford, Neill R., Knopman, David, Rademakers, Rosa, Lemstra, Afina W., Pijnenburg, Yolande A. L., Scheltens, Philip, Gasser, Thomas, Chinnery, Patrick F., Hemmer, Bernhard, Huisman, Martijn A., Troncoso, Juan, Moreno, Fermin., Nohr, Ellen A., Sorensen, Thorkild I. A., Heutink, Peter, Sanchez-Juan, Pascual, Posthuma, Danielle, Clarimon, Jordi, Christensen, Kaare, Ertekin-Taner, Nilufer, Scholz, Sonja W., Ramirez, Alfredo
ORCID: 0000-0003-4991-763X, Ruiz, Agustin, Slagboom, Eline, van der Flier, Wiesje M. and Holstege, Henne
(2020).
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity (vol 138, pg 237, 2019).
Acta Neuropathol., 139 (5).
S. 959 - 963.
NEW YORK:
SPRINGER.
ISSN 1432-0533
van der Lee, Sven J., Conway, Olivia J., Jansen, Iris, Carrasquillo, Minerva M., Kleineidam, Luca, van den Akker, Erik, Hernandez, Isabel, van Eijk, Kristel R., Stringa, Najada ORCID: 0000-0001-6350-452X, Chen, Jason A., Zettergren, Anna, Andlauer, Till F. M., Diez-Fairen, Monica
ORCID: 0000-0003-1882-0309, Simon-Sanchez, Javier, Lleo, Alberto, Zetterberg, Henrik, Nygaard, Marianne, Blauwendraat, Cornelis, Savage, Jeanne E., Mengel-From, Jonas, Moreno-Grau, Sonia, Wagner, Michael
ORCID: 0000-0003-2589-6440, Fortea, Juan, Keogh, Michael J., Blennow, Kaj, Skoog, Ingmar, Friese, Manuel A.
ORCID: 0000-0001-6380-2420, Pletnikova, Olga, Zulaica, Miren, Lage, Carmen, de Rojas, Itziar
ORCID: 0000-0002-2148-381X, Riedel-Heller, Steffi, Illan-Gala, Ignacio
ORCID: 0000-0002-5418-2052, Wei, Wei, Jeune, Bernard, Orellana, Adelina, Bergh, Florian Then, Wang, Xue, Hulsman, Marc, Beker, Nina, Tesi, Niccolo, Morris, Christopher M., Indakoetxea, Begona, Collij, Lyduine E., Scherer, Martin, Morenas-Rodriguez, Estrella, Ironside, James W., van Berckel, Bart N. M., Alcolea, Daniel, Wiendl, Heinz, Strickland, Samantha L., Pastor, Pau
ORCID: 0000-0002-7493-8777, Rodriguez Rodriguez, Eloy, Boeve, Bradley F., Petersen, Ronald C., Ferman, Tanis J., van Gerpen, Jay A., Reinders, Marcel J. T., Uitti, Ryan J., Tarraga, Lluis, Maier, Wolfgang, Dols-Icardo, Oriol
ORCID: 0000-0003-2656-8748, Kawalia, Amit, Dalmasso, Maria Carolina
ORCID: 0000-0002-4901-9955, Boada, Merce, Zettl, Uwe K., van Schoor, Natasja M., Beekman, Marian, Allen, Mariet, Masliah, Eliezer, Lopez de Munain, Adolfo, Pantelyat, Alexander, Wszolek, Zbigniew K., Ross, Owen A., Dickson, Dennis W., Graff-Radford, Neill R., Knopman, David, Rademakers, Rosa, Lemstra, Afina W., Pijnenburg, Yolande A. L., Scheltens, Philip
ORCID: 0000-0002-1046-6408, Gasser, Thomas, Chinnery, Patrick F., Hemmer, Bernhard, Huisman, Martijn A., Troncoso, Juan, Moreno, Fermin, Nohr, Ellen A., Sorensen, Thorkild I. A., Heutink, Peter
ORCID: 0000-0001-5218-1737, Sanchez-Juan, Pascual, Posthuma, Danielle, Clarimon, Jordi, Christensen, Kaare
ORCID: 0000-0002-5429-5292, Ertekin-Taner, Nilufer, Scholz, Sonja W.
ORCID: 0000-0002-6623-0429, Ramirez, Alfredo
ORCID: 0000-0003-4991-763X, Ruiz, Agustin, Slagboom, Eline, van der Flier, Wiesje M. and Holstege, Henne
(2019).
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Acta Neuropathol., 138 (2).
S. 237 - 251.
NEW YORK:
SPRINGER.
ISSN 1432-0533