A rare case of a primary retroperitoneal mucinous cystic tumour with borderline malignancy and literature review

by Chaves, Mariana M, Castro, Rita, Mota-Vieira, Luisa, Carneiro, Vítor
Published in BMJ Case Rep (2019)

Three multiplex snapshot assays for SNP genotyping in candidate innate immune genes

by Esteves, Lisa M, Bulhões, Sara M, Brilhante, Maria J, Mota-Vieira, Luisa
Published 2013

Paternal Transmission of Small Supernumerary Marker Chromosome 15 Identified in Prenatal Diagnosis Due to Advanced Maternal Age

by Melo, Bruna C. S., Portocarrero, Ana, Alves, Cláudia, Sampaio, André, Mota-Vieira, Luisa
Published in Clin Med Insights Case Rep (2015)

Thrombotic genetic risk factors and warfarin pharmacogenetic variants in São Miguel's healthy population (Azores)

by Branco, Claudia C, Pereirinha, Tânia, Cabral, Rita, Pacheco, Paula R, Mota-Vieira, Luisa
Published 2009

HLA Class I and II profiles in São Miguel Island (Azores): genetic diversity and linkage disequilibrium

by Pacheco, Paula R, Branco, Claudia C, Gomes, Cidália T, Cabral, Rita, Mota-Vieira, Luisa
Published 2010

Linkage disequilibrium and diversity for three genomic regions in Azoreans and mainland Portuguese

by Branco, Claudia C., Pacheco, Paula R., Cabrol, Ester, Cabral, Rita, Vicente, Astrid M., Mota-Vieira, Luisa
Published 2009

A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report

by Argyropoulou, Zoe, Liu, Lu, Ozoemena, Linda, Branco, Claudia C., Senra, Raquel, Reis-Rego, Ângela, Mota-Vieira, Luisa
Published in BMC Dermatol (2018)

Evaluation of reference-based two-color methods for measurement of gene expression ratios using spotted cDNA microarrays

by Verjovski-Almeida Sergio, Mota-Vieira Luisa, Egidio Camila M, Vêncio Ricardo ZN, Peixoto Bernardo R, Reis Eduardo M
Published 2006-02-01

Evaluation of reference-based two-color methods for measurement of gene expression ratios using spotted cDNA microarrays

by Peixoto, Bernardo R, Vêncio, Ricardo ZN, Egidio, Camila M, Mota-Vieira, Luisa, Verjovski-Almeida, Sergio, Reis, Eduardo M
Published 2006

A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases

by Vaz, Sara O., Pires, Renato, Pires, Luís M., Carreira, Isabel M., Anjos, Rui, Maciel, Paula, Mota-Vieira, Luisa
Published in BMC Pediatr (2015)

A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?

by Dias Pereira, Bernardo, Nunes da Silva, Tiago, Bernardo, Ana Teresa, César, Rui, Vara Luiz, Henrique, Pacak, Karel, Mota-Vieira, Luísa
Published in Int J Endocrinol (2018)

Diagnosis of Human Leptospirosis in a Clinical Setting: Real-Time PCR High Resolution Melting Analysis for Detection of Leptospira at the Onset of Disease

by Esteves, Lisa M., Bulhões, Sara M., Branco, Claudia C., Carreira, Teresa, Vieira, Maria L., Gomes-Solecki, Maria, Mota-Vieira, Luisa
Published in Sci Rep (2018)

A comprehensive overview of the cystic fibrosis on the island of São Miguel (Azores, Portugal)

by Rosa, Joana, Gaspar-Silva, Patrícia, Pacheco, Paula, Silva, Conceição, Branco, Cláudia C., Vieira, Barbara S., Carreiro, Alexandra, Gonçalves, Juan, Mota-Vieira, Luisa
Published in BMC Pediatr (2020)

Human Leptospirosis: Seroreactivity and Genetic Susceptibility in the Population of São Miguel Island (Azores, Portugal)

by Esteves, Lisa M., Bulhões, Sara M., Branco, Claudia C., Mota, Francisco M., Paiva, Clara, Cabral, Rita, Vieira, Maria Luisa, Mota-Vieira, Luisa
Published 2014

Screening of copy number variants in the 22q11.2 region of congenital heart disease patients from the São Miguel Island, Azores, revealed the second patient with a triplication

by Pires, Renato, Pires, Luís M, Vaz, Sara O, Maciel, Paula, Anjos, Rui, Moniz, Raquel, Branco, Claudia C, Cabral, Rita, Carreira, Isabel M, Mota-Vieira, Luisa
Published in BMC Genet (2014)

DNA Methylation Is Correlated with Oxidative Stress in Myelodysplastic Syndrome—Relevance as Complementary Prognostic Biomarkers

by Gonçalves, Ana Cristina, Alves, Raquel, Baldeiras, Inês, Marques, Bárbara, Oliveiros, Bárbara, Pereira, Amélia, Nascimento Costa, José Manuel, Cortesão, Emília, Mota Vieira, Luisa, Sarmento Ribeiro, Ana Bela
Published in Cancers (Basel) (2021)

Carriers of the Complex Allele HFE c.[187C>G;340+4T>C] Have Increased Risk of Iron Overload in São Miguel Island Population (Azores, Portugal)

by Branco, Claudia C., Gomes, Cidália T., De Fez, Laura, Bulhões, Sara, Brilhante, Maria José, Pereirinha, Tânia, Cabral, Rita, Rego, Ana Catarina, Fraga, Cristina, Miguel, António G., Brasil, Gracinda, Macedo, Paula, Mota-Vieira, Luisa
Published in PLoS One (2015)

Low frequency of CD4(+)CD25(+ )Treg in SLE patients: a heritable trait associated with CTLA4 and TGFβ gene variants

by Barreto, Marta, Ferreira, Ricardo C, Lourenço, Lara, Moraes-Fontes, Maria F, Santos, Eugénia, Alves, Miguel, Carvalho, Cláudia, Martins, Berta, Andreia, Rita, Viana, João F, Vasconcelos, Carlos, Mota-Vieira, Luísa, Ferreira, Carlos, Demengeot, Jocelyne, Vicente, Astrid M
Published 2009

Epidemiology and genetic variability of respiratory syncytial virus in Portugal, 2014–2018

by Sáez-López, Emma, Cristóvão, Paula, Costa, Inês, Pechirra, Pedro, Conde, Patrícia, Guiomar, Raquel, Peres, Maria João, Viseu, Regina, Lopes, Paulo, Soares, Vânia, Vale, Fátima, Fonseca, Patricia, Freitas, Ludivina, Alves, Jose, Pessanha, Maria Ana, Toscano, Cristina, Mota-Vieira, Luísa, Veloso, Rita Cabral, Côrte-Real, Rita, Branquinho, Paula, Pereira‑Vaz, João, Rodrigues, Fernando, Cunha, Mário, Martins, Luís, Mota, Paula, Couto, Ana Rita, Bruges-Armas, Jácome, Almeida, Sofia, Rodrigues, Débora
Published in J Clin Virol (2019)

Clinical and Genetic Spectrum of Bartter Syndrome Type 3

by Seys, Elsa, Andrini, Olga, Keck, Mathilde, Mansour-Hendili, Lamisse, Courand, Pierre-Yves, Simian, Christophe, Deschenes, Georges, Kwon, Theresa, Bertholet-Thomas, Aurélia, Bobrie, Guillaume, Borde, Jean Sébastien, Bourdat-Michel, Guylhène, Decramer, Stéphane, Cailliez, Mathilde, Krug, Pauline, Cozette, Paul, Delbet, Jean Daniel, Dubourg, Laurence, Chaveau, Dominique, Fila, Marc, Jourde-Chiche, Noémie, Knebelmann, Bertrand, Lavocat, Marie-Pierre, Lemoine, Sandrine, Djeddi, Djamal, Llanas, Brigitte, Louillet, Ferielle, Merieau, Elodie, Mileva, Maria, Mota-Vieira, Luisa, Mousson, Christiane, Nobili, François, Novo, Robert, Roussey-Kesler, Gwenaëlle, Vrillon, Isabelle, Walsh, Stephen B., Teulon, Jacques, Blanchard, Anne, Vargas-Poussou, Rosa
Published in J Am Soc Nephrol (2017)