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Frontal and associative visual areas related to visual hallucinations in dementia with Lewy bodies and Parkinson's disease with dementia. [electronic resource] by
- Sanchez-Castaneda, Cristina
- Rene, Ramon
- Ramirez-Ruiz, Blanca
- Campdelacreu, Jaume
- Gascon, Jordi
- Falcon, Carles
- Calopa, Matilde
- Jauma, Serge
- Juncadella, Montserrat
- Junque, Carme
Producer: 20100723
In:
Movement disorders : official journal of the Movement Disorder Society vol. 25
Availability: No items available.
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Correlations between gray matter reductions and cognitive deficits in dementia with Lewy Bodies and Parkinson's disease with dementia. [electronic resource] by
- Sanchez-Castaneda, Cristina
- Rene, Ramon
- Ramirez-Ruiz, Blanca
- Campdelacreu, Jaume
- Gascon, Jordi
- Falcon, Carles
- Calopa, Matilde
- Jauma, Serge
- Juncadella, Montserrat
- Junque, Carme
Producer: 20091204
In:
Movement disorders : official journal of the Movement Disorder Society vol. 24
Availability: No items available.
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Clinical and imaging markers in premotor LRRK2 G2019S mutation carriers. [electronic resource] by
- Vilas, Dolores
- Ispierto, Lourdes
- Álvarez, Ramiro
- Pont-Sunyer, Claustre
- Martí, María José
- Valldeoriola, Francesc
- Compta, Yaroslau
- de Fabregues, Oriol
- Hernández-Vara, Jorge
- Puente, Víctor
- Calopa, Matilde
- Jaumà, Serge
- Campdelacreu, Jaume
- Aguilar, Miquel
- Quílez, Pilar
- Casquero, Pilar
- Lomeña, Francisco
- Ríos, José
- Tolosa, Eduardo
Producer: 20160804
In:
Parkinsonism & related disorders vol. 21
Availability: No items available.
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Sleep Disorders in Parkinsonian and Nonparkinsonian LRRK2 Mutation Carriers. [electronic resource] by
- Pont-Sunyer, Claustre
- Iranzo, Alex
- Gaig, Carles
- Fernández-Arcos, Ana
- Vilas, Dolores
- Valldeoriola, Francesc
- Compta, Yaroslau
- Fernández-Santiago, Ruben
- Fernández, Manel
- Bayés, Angels
- Calopa, Matilde
- Casquero, Pilar
- de Fàbregues, Oriol
- Jaumà, Serge
- Puente, Victor
- Salamero, Manel
- José Martí, Maria
- Santamaría, Joan
- Tolosa, Eduard
Producer: 20160503
In:
PloS one vol. 10
Availability: No items available.
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Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification. [electronic resource] by
- Hsu, Sandy Chan
- Sears, Renee L
- Lemos, Roberta R
- Quintáns, Beatriz
- Huang, Alden
- Spiteri, Elizabeth
- Nevarez, Lisette
- Mamah, Catherine
- Zatz, Mayana
- Pierce, Kerrie D
- Fullerton, Janice M
- Adair, John C
- Berner, Jon E
- Bower, Matthew
- Brodaty, Henry
- Carmona, Olga
- Dobricić, Valerija
- Fogel, Brent L
- García-Estevez, Daniel
- Goldman, Jill
- Goudreau, John L
- Hopfer, Suellen
- Janković, Milena
- Jaumà, Serge
- Jen, Joanna C
- Kirdlarp, Suppachok
- Klepper, Joerg
- Kostić, Vladimir
- Lang, Anthony E
- Linglart, Agnès
- Maisenbacher, Melissa K
- Manyam, Bala V
- Mazzoni, Pietro
- Miedzybrodzka, Zofia
- Mitarnun, Witoon
- Mitchell, Philip B
- Mueller, Jennifer
- Novaković, Ivana
- Paucar, Martin
- Paulson, Henry
- Simpson, Sheila A
- Svenningsson, Per
- Tuite, Paul
- Vitek, Jerrold
- Wetchaphanphesat, Suppachok
- Williams, Charles
- Yang, Michele
- Schofield, Peter R
- de Oliveira, João R M
- Sobrido, María-Jesús
- Geschwind, Daniel H
- Coppola, Giovanni
Producer: 20130805
In:
Neurogenetics vol. 14
Availability: No items available.
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