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A novel complex neurological phenotype due to a homozygous mutation in FDX2
A novel complex neurological phenotype due to a homozygous mutation in FDX2
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A novel complex neurological phenotype due to a homozygous mutation in FDX2

Gurgel-Giannetti, Juliana ; Lynch, David S ; Paiva, Anderson Rodrigues Brandão de ; Lucato, Leandro Tavares ; Yamamoto, Guilherme ; Thomsen, Christer ; Basu, Somsuvro ; Freua, Fernando ; Giannetti, Alexandre Varella ; de Assis, Bruno Della Ripa ; Ribeiro, Mara Dell Ospedale ; Barcelos, Isabella ; Sayão Souza, Katiane ; Monti, Fernanda ; Melo, Uirá Souto ; Amorim, Simone ; Silva, Leonardo G L ; Macedo-Souza, Lúcia Inês ; Vianna-Morgante, Angela M ; Hirano, Michio ; Van der Knaap, Marjo S ; Lill, Roland ; Vainzof, Mariz ; Oldfors, Anders ; Houlden, Henry ; Kok, Fernando

Brain (London, England : 1878), 2018-08, Vol.141 (8), p.2289-2298 [Periódico revisado por pares]

England: Oxford University Press

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2
Immune-Related Genetic Overlap Between Regional Gray Matter Reductions and Psychiatric Symptoms in Adolescents, and Gene-Set Validation in a Translational Model
Immune-Related Genetic Overlap Between Regional Gray Matter Reductions and Psychiatric Symptoms in Adolescents, and Gene-Set Validation in a Translational Model
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Immune-Related Genetic Overlap Between Regional Gray Matter Reductions and Psychiatric Symptoms in Adolescents, and Gene-Set Validation in a Translational Model

Penninck, Lukas ; Ibrahim, El Chérif ; Artiges, Eric ; Gorgievski, Victor ; Desrivières, Sylvane ; Farley, Severine ; Filippi, Irina ; de Macedo, Carlos E A ; Belzeaux, Raoul ; Banaschewski, Tobias ; Bokde, Arun L W ; Quinlan, Erin Burke ; Flor, Herta ; Grigis, Antoine ; Garavan, Hugh ; Gowland, Penny ; Heinz, Andreas ; Brühl, Rüdiger ; Nees, Frauke ; Papadopoulos Orfanos, Dimitri ; Paus, Tomáš ; Poustka, Luise ; Fröhner, Juliane H ; Smolka, Michael N ; Walter, Henrik ; Whelan, Robert ; Grenier, Julien ; Schumann, Gunter ; Paillère Martinot, Marie-Laure ; Tzavara, Eleni T ; Martinot, Jean-Luc

Frontiers in systems neuroscience, 2021-09, Vol.15, p.725413 [Periódico revisado por pares]

Switzerland: Frontiers

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3
Influence of IL1B , IL6 and IL10 gene variants and plasma fatty acid interaction on metabolic syndrome risk in a cross-sectional population-based study
Influence of IL1B , IL6 and IL10 gene variants and plasma fatty acid interaction on metabolic syndrome risk in a cross-sectional population-based study
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Influence of IL1B , IL6 and IL10 gene variants and plasma fatty acid interaction on metabolic syndrome risk in a cross-sectional population-based study

Maintinguer Norde, Marina ; Oki, Erica ; Ferreira Carioca, Antonio Augusto ; Teixeira Damasceno, Nágila Raquel ; Fisberg, Regina Mara ; Lobo Marchioni, Dirce Maria ; Rogero, Marcelo Macedo

Clinical nutrition (Edinburgh, Scotland), 2018-04, Vol.37 (2), p.659-666 [Periódico revisado por pares]

England: Elsevier Ltd

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4
Molecular identification of wild triatomines of the genus Rhodnius in the Bolivian Amazon: Strategy and current difficulties
Molecular identification of wild triatomines of the genus Rhodnius in the Bolivian Amazon: Strategy and current difficulties
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Molecular identification of wild triatomines of the genus Rhodnius in the Bolivian Amazon: Strategy and current difficulties

Brenière, Simone Frédérique ; Condori, Edwin Wily ; Buitrago, Rosio ; Sosa, Luis Fernando ; Macedo, Catarina Lopes ; Barnabé, Christian

Infection, genetics and evolution, 2017-07, Vol.51, p.1-9 [Periódico revisado por pares]

Netherlands: Elsevier B.V

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