Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Maria‐Jose Martí"'
Autor:
Azulay, Jean-Philippe, Balaguer, Ernest, Bhatia, Perminder, Bodis-Wollner, Ivan, Brownstone, Paul, Boulloche, Nicolas, Calegan, Gerald J., II, Castelnovo, Giovanni, Chou, Kelvin L., Corvol, Jean-Christophe, Danisi, Fabio, Defebvre, Luc, Desojo, Lydia Vela, Durif, Franck, Ehret, Reinhard, Evans, Bradley K., Forchetti, Concetta, Friedman, Joseph H., Fogel, Wolfgang, Garniga, Matilde Calopa, Gil, Ramon A., Ginsberg, Paul L., Glasberg, Mark R., Griffith, Alida, Groves, Jeffrey W., Gudesblatt, Mark, Hermanowicz, Neal, Herrera, Maria A., Houeto, Jean-Luc, Hutchman, Robert M., Isaacson, Stuart H., Jagadeesan, Singar, Jog, Mandar, Keegan, Andrew, Klostermann, Fabian, Krystkowiak, Pierre, Kulisevsky Bojarsky, Jaime, Kumar, Rajeev, Lacey, Dennis, Lasker, Bruce, LaVaccare, John, Lavallee, Michelle M., Piudo, Maria Rosario Luquin, Mahler, Andreas, Domenech, Maria José Martí, Martinez Castrillo, Juan Carlos, Mate, Laszlo J., Mendis, Tilak, Metman, Leonard Verhagen, Muhlack, Siegfried Martin, Müller, Thomas, Park, Ariane, Patton, James, Peckham, Elizabeth, Grandas Pérez, Francisco, Rabin, Marcie, Rascol, Olivier, Reifschneider, Gerd, Remy, Philippe, Rivera, Pablo Mir, Schwarz, Johannes, Roullet-Solignac, Isabelle, Salazar, Gabriel, Sergay, Stephen M., Sherman, Scott, Shubin, Richard, Spikol, Lorraine, Steigerwald, Frank, Tönges, Lars, Truong, Daniel D., Ugarte, Antonio, Vivancos Matellano, Francisco, Witte, Arnold, Zesiewicz, Theresa, Zauber, Sarah Elizabeth, deVries, Tina, Jaros, Mark, Quartel, Adrian, Jacobs, David
Publikováno v:
In Parkinsonism and Related Disorders March 2022 96:65-73
Autor:
Marta Soto, Alex Iranzo, Sara Lahoz, Manel Fernández, Mónica Serradell, Carles Gaig, Paula Melón, Maria‐Jose Martí, Joan Santamaría, Jordi Camps, Rubén Fernández‐Santiago, Mario Ezquerra
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 37(10)
Isolated rapid eye movement sleep behavior disorder (IRBD) is a well-established clinical risk factor for Lewy body diseases (LBDs), such as Parkinson's disease (PD) and dementia with Lewy bodies (DLB).To elucidate whether serum microRNA (miRNA) dere
Autor:
Viviana Torres, Jesica Pérez‐Montesino, Rubén Fernández‐Santiago, Manel Fernández, Ana Camara, Yaroslau Compta, María‐José Martí, Àlex Guerra Beltran, José Rios, Francesc Valldeoriola, Mario Ezquerra
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 11, Iss 8, Pp 2222-2229 (2024)
Abstract Impulse control disorders and their consequences display variability among individuals, indicating potential involvement of environmental and genetic factors. In this retrospective study, we analyzed a cohort of Parkinson's disease patients
Externí odkaz:
https://doaj.org/article/bf0de04c7cda432a871f493d306981d5
Autor:
Marta Soto, Manel Fernández, Paloma Bravo, Sara Lahoz, Alicia Garrido, Antonio Sánchez-Rodríguez, María Rivera-Sánchez, María Sierra, Paula Melón, Ana Roig-García, Anna Naito, Bradford Casey, Jordi Camps, Eduardo Tolosa, María-José Martí, Jon Infante, Mario Ezquerra, Rubén Fernández-Santiago
Publikováno v:
npj Parkinson's Disease, Vol 9, Iss 1, Pp 1-12 (2023)
Abstract The LRRK2 G2019S pathogenic mutation causes LRRK2-associated Parkinson’s disease (L2PD) with incomplete penetrance. LRRK2 non-manifesting carriers (L2NMC) are at PD high risk but predicting pheno-conversion is challenging given the lack of
Externí odkaz:
https://doaj.org/article/fc4ea8c201b04435b88fd67d9335edac
Autor:
Margalida Puigròs, Anna Calderon, Alexandra Pérez-Soriano, Cristina de Dios, Manel Fernández, Anna Colell, Maria-José Martí, Eduardo Tolosa, Ramon Trullas
Publikováno v:
Neurobiology of Disease, Vol 174, Iss , Pp 105885- (2022)
Mitochondrial dysfunction happens in both idiopathic (iPD) and LRRK2-related Parkinson's disease (LRRK2-PD). Nonetheless, previous studies suggested that a different type of mitochondrial pathology underlies the neurodegeneration in these two disorde
Externí odkaz:
https://doaj.org/article/ea2fbd6ab56e40a598e7f2f092c6d23e
Autor:
Carles, Gaig, Francesc, Valldeoriola, Ellen, Gelpi, Mario, Ezquerra, Sara, Llufriu, Mariateresa, Buongiorno, Maria Jesús, Rey, Maria Jose, Martí, Francesc, Graus, Eduardo, Tolosa
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 26(7)
Lewy body syndromes (mainly Parkinson's disease and dementia with Lewy bodies) share many clinical features and usually have a slowly progressive course. Some patients may show rapid symptoms progression.To evaluate clinical and neuropathological fea
Autor:
Marta Sánchez-Piñero, Mireia Corell, Alfonso Moriana, Pedro Castro-Valdecantos, María-José Martin-Palomo
Publikováno v:
Horticulturae, Vol 9, Iss 5, p 563 (2023)
The irrigation surface of olive orchards has increased over recent decades. In zones affected, deficit irrigation scheduling is a must. The aim of this work was to study water stress management based on reference equations for midday stem water poten
Externí odkaz:
https://doaj.org/article/bef10f2ee9104b0083cf357cb1142e1e
Publikováno v:
Education Sciences, Vol 12, Iss 10, p 667 (2022)
This paper analyses the relevance of religion for adolescents in the realm of peer relationships, both within and outside of educational institutions. The sample consisted of 385 young individuals attending different Secondary Education institutions
Externí odkaz:
https://doaj.org/article/03533157c83540859457e3cc53d0d3b1
Autor:
María-José Martín-Alonso, Luis G. Cal-Pereyra, Maximino Fernández-Caso, José-Ramiro González-Montaña
Publikováno v:
Revista Mexicana de Ciencias Pecuarias, Vol 10, Iss 3, Pp 729-755 (2019)
Reticular groove closure in ruminants is a primary mechanism, almost exclusive of lactating animals, which makes the passage of food from the orifice of cardia to the abomasum possible, thus avoiding unwanted fermentations in rumen and reticulum. In
Externí odkaz:
https://doaj.org/article/5bdca116365b4bddaa4a45e486211d99
Autor:
Teresa Botta-Orfila, Eduard Tolosa, Ellen Gelpi, Alex Sànchez-Pla, Maria-José Martí, Francesc Valldeoriola, Manel Fernández, Francesc Carmona, Mario Ezquerra
Publikováno v:
Neurobiology of Disease, Vol 45, Iss 1, Pp 462-468 (2012)
LRRK2 mutations are the most common genetic cause of Parkinson's disease (PD). We performed a whole-genome RNA profiling of putamen tissue from idiopathic PD (IPD), LRRK2-associated PD (G2019S mutation), neurologically healthy controls and one asympt
Externí odkaz:
https://doaj.org/article/0d3c6261a0344d73b4ceba88b81f0fb8