Seroprevalence of Toxoplasma gondii and Toxocara canis in a human rural population of Southern Rio Grande do Sul von Araújo, Adelita Campos, Villela, Marcos Marreiro, Sena-Lopes, Ângela, Farias, Nara Amélia da Rosa, Faria, Laura Maria Jorge de, Avila, Luciana Farias da Costa, Berne, Maria Elisabeth Aires, Borsuk, Sibele

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Diagnosis of Charcot-Marie-Tooth Disease von Banchs, Isabel, Casasnovas, Carlos, Albertí, Antonia, De Jorge, Laura, Povedano, Mònica, Montero, Jordi, Martínez-Matos, Juan Antonio, Volpini, Victor

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New Subtype of Spinocerebellar Ataxia With Altered Vertical Eye Movements Mapping to Chromosome 1p32 von Serrano-Munuera, Carmen, Corral-Juan, Marc, Stevanin, Giovanni, San Nicolás, Hector, Roig, Carles, Corral, Jordi, Campos, Berta, de Jorge, Laura, Morcillo-Suárez, Carlos, Navarro, Arcadi, Forlani, Sylvie, Durr, Alexandra, Kulisevsky, Jaime, Brice, Alexis, Sánchez, Ivelisse, Volpini, Victor, Matilla-Dueñas, Antoni

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Characterization of Toxoplasma gondii isolates from herds of sheep in southern Brazil reveals the archetypal type II genotype and new non-archetypal genotypes von da Silva Ramos, Tatiana, de Jesus Pena, Hilda Fátima, dos Santos Junior, Alceu Gonçalves, de Faria Santos, Laura Maria Jorge, Cademartori, Beatris Gonzales, Oliveira, Solange, Gennari, Solange Maria, da Silva Ramos Rocha, Andréa, da Rosa Farias, Nara Amélia

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Heterozygous STUB1 mutation causes familial ataxia with cognitive affective syndrome (SCA48) von Genis, David, Ortega-Cubero, Sara, San Nicolás, Hector, Corral, Jordi, Gardenyes, Josep, de Jorge, Laura, López, Eva, Campos, Berta, Lorenzo, Elena, Tonda, Raúl, Beltran, Sergi, Negre, Montserrat, Obón, María, Beltran, Brigitte, Fàbregas, Laura, Alemany, Berta, Márquez, Fabián, Ramió-Torrentà, Lluís, Gich, Jordi, Volpini, Víctor, Pastor, Pau

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Spinocerebellar ataxia type 2 in The Gambia: A case report von Almaguer-Mederos, Luis E, Sarr, Louise, Abascal, Jorge Vega, Aguilera-Rodríquez, Raúl, Martín, Maydelis Avíla, Khalil, M.I.A, Al-Jafari, Muhammed Ammar, de Jorge López, Laura, Volpini, Victor, Nyan, Ousman

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First case with Huntington's disease in The Gambia von Almaguer-Mederos, Luis E, Vega Abascal, Jorge, Ramos Cabrera, Asmell, García Quilez, Fátima, Betancourt Álvarez, Pablo, Miranda Rosales, Filiberto, Ferriol Ramírez, Ania, Khalil, M.I.A, de Jorge López, Laura, Volpini, Victor, Nyan, Ousman

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Diagnosis of Charcot-Marie-Tooth Disease von Volpini, Victor, Montero, Jordi, Povedano, Mònica, De Jorge, Laura, Albertí, Antonia, Casasnovas, Carlos, Banchs, Isabel, Martínez-Matos, Juan Antonio

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The metabotropic glutamate receptor 1, GRM1: evaluation as a candidate gene for inherited forms of cerebellar ataxia von Rossi, Pia Irene Anna, Vaccari, Carlotta Maria, Terracciano, Alessandra, Doria-Lamba, Laura, Facchinetti, Sabrina, Priolo, Manuela, Ayuso, Carmen, De Jorge, Laura, Gimelli, Stefania, Santorelli, Filippo Maria, Ravazzolo, Roberto, Puliti, Aldamaria

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A novel small deletion in PMP22 causes a mild hereditary neuropathy with liability to pressure palsies phenotype von Casasnovas, Carlos, Banchs, Isabel, De Jorge, Laura, Antónia albertí, Maria, Martínez–Campo, Yolanda, Povedano, Mónica, Montero, Jordi, Volpini, Victor

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New subtype of spinocerebellar ataxia with altered vertical eye movements mapping to chromosome 1p32 von Serrano, Carmen, Corral Juan, Marc, Stevanin, Giovanni, San Nicolás, Hector, Roig, Carles, Corral, Jordi, Campos, Berta, Jorge, Laura de, Morcillo Suárez, Carlos, 1969, Navarro i Cuartiellas, Arcadi, 1969, Forlani, Sylvie, Durr, Alexandra, Kulisevsky, Jaime J, Brice, Alexis, Sánchez, Ivelisse, Volpini, Victor, Matilla Dueñas, Antoni

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Patogenicidade e virulência de Toxoplasma gondii isolado de suínos de criação artesanal no sul do Brasil von Oliveira, Plínio Aguiar de, Oliveira, Fernando Caetano de, Faria, Laura Maria Jorge de, Cademartori, Beatris Gonzalez, Marcolongo-Pereira, Clairton, Coelho, Ana Carolina Barreto, Pappen, Felipe Geraldo, Farias, Nara Amélia

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Diagnosis of Charcot-Marie-Tooth disease von Banchs, Isabel, Casasnovas Pons, Carlos, Albertí, María A, Jorge, Laura de, Povedano, Mònica, Montero, Jordi, Martínez Matos, Juan Antonio, Volpini Bertrán, Víctor

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A novel small deletion in PMP22 causes a mild hereditary neuropathy with liability to pressure palsies phenotype von Casasnovas, Carlos, Banchs, Isabel, De Jorge, Laura, Antónia albertí, Maria, Martínez-Campo, Yolanda, Povedano, Mónica, Montero, Jordi, Volpini, Victor

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Spinocerebellar ataxia type 2 in The Gambia: A case report von Almaguer-Mederos, Luis E, Sarr, Louise, Abascal, Jorge Vega, Aguilera-Rodríquez, Raúl, Martín, Maydelis Avíla, Khalil, M I A, Al-Jafari, Muhammed Ammar, de Jorge López, Laura, Volpini, Victor, Nyan, Ousman

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First case with Huntington's disease in The Gambia von Almaguer-Mederos, Luis E, Vega Abascal, Jorge, Ramos Cabrera, Asmell, García Quilez, Fátima, Betancourt Álvarez, Pablo, Miranda Rosales, Filiberto, Ferriol Ramírez, Ania, Khalil, M I A, de Jorge López, Laura, Volpini, Victor, Nyan, Ousman

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Combining fsQCA and PLS-SEM to assess policyholders' attitude towards life settlements von de Andrés Sánchez, Jorge, Puchades, Laura González-Vila

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Progression of regional grey matter atrophy in multiple sclerosis von Eshaghi, Arman, Marinescu, Razvan V, Young, Alexandra L, Firth, Nicholas C, Prados, Ferran, Jorge Cardoso, M, Tur, Carmen, De Angelis, Floriana, Cawley, Niamh, Brownlee, Wallace J, De Stefano, Nicola, Laura Stromillo, M, Battaglini, Marco, Ruggieri, Serena, Gasperini, Claudio, Filippi, Massimo, Rocca, Maria A, Rovira, Alex, Sastre-Garriga, Jaume, Geurts, Jeroen J G, Vrenken, Hugo, Wottschel, Viktor, Leurs, Cyra E, Uitdehaag, Bernard, Pirpamer, Lukas, Enzinger, Christian, Ourselin, Sebastien, Gandini Wheeler-Kingshott, Claudia A, Chard, Declan, Thompson, Alan J, Barkhof, Frederik, Alexander, Daniel C, Ciccarelli, Olga

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Identification of risk features for complication in Gaucher's disease patients: a machine learning analysis of the Spanish registry of Gaucher disease von Andrade-Campos, Marcio M, de Frutos, Laura López, Cebolla, Jorge J, Serrano-Gonzalo, Irene, Medrano-Engay, Blanca, Roca-Espiau, Mercedes, Gomez-Barrera, Beatriz, Pérez-Heredia, Jorge, Iniguez, David, Giraldo, Pilar

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Observational registry of sorafenib use in clinical practice across Child-Pugh subgroups: The GIDEON study von Marrero, Jorge A, Kudo, Masatoshi, Venook, Alan P, Ye, Sheng-Long, Bronowicki, Jean-Pierre, Chen, Xiao-Ping, Dagher, Lucy, Furuse, Junji, Geschwind, Jean-Francois H, de Guevara, Laura Ladrón, Papandreou, Christos, Takayama, Tadatoshi, Sanyal, Arun J, Yoon, Seung Kew, Nakajima, Keiko, Lehr, Robert, Heldner, Stephanie, Lencioni, Riccardo

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