SIGMAR1 gene mutation causing Distal Hereditary Motor Neuropathy in a Portuguese family

Por ALMENDRA, LUCIANO, LARANJEIRA, FRANCISCO, FERNÁNDEZ-MARMIESSE, ANA, NEGRÃO, LUÍS
Publicado no Acta Myol (2018)

Biomarkers and Imaging Findings of Anderson–Fabry Disease—What We Know Now

Por Beirão, Idalina, Cabrita, Ana, Torres, Márcia, Silva, Fernando, Aguiar, Patrício, Laranjeira, Francisco, Gomes, Ana Marta
Publicado no Diseases (2017)

Cost-Effective Control of Plant Disease When Epidemiological Knowledge Is Incomplete: Modelling Bahia Bark Scaling of Citrus

Por Cunniffe, Nik J., Laranjeira, Francisco F., Neri, Franco M., DeSimone, R. Erik, Gilligan, Christopher A.
Publicado em 2014

Data in support of a functional analysis of splicing mutations in the IDS gene and the use of antisense oligonucleotides to exploit an alternative therapy for MPS II

Por Matos, Liliana, Gonçalves, Vânia, Pinto, Eugénia, Laranjeira, Francisco, Prata, Maria João, Jordan, Peter, Desviat, Lourdes R., Pérez, Belén, Alves, Sandra
Publicado no Data Brief (2015)

Mutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast Brazil

Por Vieira Neto, Eduardo, Laranjeira, Francisco, Quelhas, Dulce, Ribeiro, Isaura, Seabra, Alexandre, Mineiro, Nicole, d. M. Carvalho, Lilian, Lacerda, Lúcia, G. Ribeiro, Márcia
Publicado no Mol Genet Genomic Med (2018)

Infantile Refsum Disease: Influence of Dietary Treatment on Plasma Phytanic Acid Levels

Por Sá, Maria João Nabais, Rocha, Júlio C., Almeida, Manuela F., Carmona, Carla, Martins, Esmeralda, Miranda, Vasco, Coutinho, Miguel, Ferreira, Rita, Pacheco, Sara, Laranjeira, Francisco, Ribeiro, Isaura, Fortuna, Ana Maria, Lacerda, Lúcia
Publicado no JIMD Rep (2015)