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| LIPAD (LRRK2/Luebeck International Parkinson's Disease) Study Protocol: Deep Phenotyping of an International Genetic Cohort. Frontiers in neurology 2021 9 12 710572. Usnich Tatiana, Vollstedt Eva-Juliane, Schell Nathalie, Skrahina Volha, Bogdanovic Xenia, Gaber Hanaa, Förster Toni M, Heuer Andreas, Koleva-Alazeh Natalia, Csoti Ilona, Basak Ayse Nazli, Ertan Sibel, Genc Gencer, Bauer Peter, Lohmann Katja, Grünewald Anne, Schymanski Emma L, Trinh Joanne, Schaake Susen, Berg Daniela, Gruber Doreen, Isaacson Stuart H, Kühn Andrea A, Mollenhauer Brit, Pedrosa David J, Reetz Kathrin, Sammler Esther M, Valente Enza Maria, Valzania Franco, Volkmann Jens, Zittel Simone, Brüggemann Norbert, Kasten Meike, Rolfs Arndt, Klein Christine, |
| PREDICT-PD: An online approach to prospectively identify risk indicators of Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society 2017 Jan . Noyce Alastair J, R'Bibo Lea, Peress Luisa, Bestwick Jonathan P, Adams-Carr Kerala L, Mencacci Niccolo E, Hawkes Christopher H, Masters Joseph M, Wood Nicholas, Hardy John, Giovannoni Gavin, Lees Andrew J, Schrag Anet |
| Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene. Movement disorders : official journal of the Movement Disorder Society 2015 Jun 30 (7): 981-6. Mirelman Anat, Alcalay Roy N, Saunders-Pullman Rachel, Yasinovsky Kira, Thaler Avner, Gurevich Tanya, Mejia-Santana Helen, Raymond Deborah, Gana-Weisz Mali, Bar-Shira Anat, Ozelius Laurie, Clark Lorraine, Orr-Urtreger Avi, Bressman Susan, Marder Karen, Giladi Nir, |
| Olfactory dysfunction in sporadic Parkinson's Disease and LRRK2 carriers. Acta neurologica Scandinavica 2014 May 129 (5): 300-6. Johansen K K, Warø B J, Aasly J |
| Nonmotor symptoms in LRRK2 G2019S associated Parkinson's disease. PloS one 2014 9 (10): e108982. Gaig Carles, Vilas Dolores, Infante Jon, Sierra María, García-Gorostiaga Inés, Buongiorno Mariateresa, Ezquerra Mario, Martí Maria José, Valldeoriola Francesc, Aguilar Miquel, Calopa Matilde, Hernandez-Vara Jorge, Tolosa Eduar |
| Cognitive performance of GBA mutation carriers with early-onset PD: the CORE-PD study. Neurology 2012 May 78 (18): 1434-40. Alcalay R N, Caccappolo E, Mejia-Santana H, Tang M -X, Rosado L, Orbe Reilly M, Ruiz D, Ross B, Verbitsky M, Kisselev S, Louis E, Comella C, Colcher A, Jennings D, Nance M, Bressman S, Scott W K, Tanner C, Mickel S, Andrews H, Waters C, Fahn S, Cote L, Frucht S, Ford B, Rezak M, Novak K, Friedman J H, Pfeiffer R, Marsh L, Hiner B, Siderowf A, Payami H, Molho E, Factor S, Ottman R, Clark L N, Marder |
| Olfactory deficits and cardiac 123I-MIBG in Parkinson's disease related to the LRRK2 R1441G and G2019S mutations. Movement disorders : official journal of the Movement Disorder Society 2011 Sep 26 (11): 2026-31. Ruiz-Martínez Javier, Gorostidi Ana, Goyenechea Estibaliz, Alzualde Ainhoa, Poza Juan José, Rodríguez Francisco, Bergareche Alberto, Moreno Fermín, López de Munain Adolfo, Martí Massó José |
| Olfactory dysfunction in LRRK2 G2019S mutation carriers. Neurology 2011 Jul 77 (4): 319-24. Saunders-Pullman R, Stanley K, Wang C, San Luciano M, Shanker V, Hunt A, Severt L, Raymond D, Ozelius L J, Lipton R B, Bressman S |
| 123I-MIBG cardiac uptake and smell identification in parkinsonian patients with LRRK2 mutations. Journal of neurology 2011 1 258 (6): 1126-32. Valldeoriola Francesc, Gaig Carles, Muxí Africa, Navales Ignacio, Paredes Pilar, Lomeña Francisco, De la Cerda Andres, Buongiorno Mariateresa, Ezquerra Mario, Santacruz Pilar, Martí Maria Jose, Tolosa Eduar |
| Olfactory heterogeneity in LRRK2 related Parkinsonism. Movement disorders : official journal of the Movement Disorder Society 2010 Dec 25 (16): 2879-83. Silveira-Moriyama Laura, Munhoz Renato Pupi, de J Carvalho Margarete, Raskin Salmo, Rogaeva Ekaterina, de C Aguiar Patricia, Bressan Rodrigo A, Felicio Andre C, Barsottini Orlando G P, Andrade Luiz Augusto F, Chien Hsin F, Bonifati Vincenzo, Barbosa Egberto R, Teive Helio A, Lees Andrew |
| Hyposmia in G2019S LRRK2-related parkinsonism: clinical and pathologic data. Neurology 2008 Sep 71 (13): 1021-6. Silveira-Moriyama L, Guedes L C, Kingsbury A, Ayling H, Shaw K, Barbosa E R, Bonifati V, Quinn N P, Abou-Sleiman P, Wood N W, Petrie A, Sampaio C, Ferreira J J, Holton J, Revesz T, Lees A |
| High prevalence of LRRK2 mutations in familial and sporadic Parkinson's disease in Portugal. Movement disorders : official journal of the Movement Disorder Society 2007 Jun 22 (8): 1194-201. Ferreira Joaquim J, Guedes Leonor Correia, Rosa Mário Miguel, Coelho Miguel, van Doeselaar Marina, Schweiger Dorothea, Di Fonzo Alessio, Oostra Ben A, Sampaio Cristina, Bonifati Vincen |
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