Enzyme immunoassays (EIA) for serodiagnosis of human leptospirosis: specific IgG3/IgG1 isotyping may further inform diagnosis of acute disease
Fortes-Gabriel, Elsa, Guedes, Mariana Soares, Shetty, Advait, Gomes, Charles Klazer, Carreira, Teresa, Vieira, Maria Luísa, Esteves, Lisa, Mota-Vieira, Luísa, Gomes-Solecki, Maria
Published in PLoS neglected tropical diseases (01.02.2022)
Published in PLoS neglected tropical diseases (01.02.2022)
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Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions
Oliveira, Guiomar, Ataíde, Assunção, Marques, Carla, Miguel, Teresa S, Coutinho, Ana Margarida, Mota‐Vieira, Luísa, Gonçalves, Esmeralda, Lopes, Nazaré Mendes, Rodrigues, Vitor, Carmona da Mota, Henrique, Vicente, Astrid Moura
Published in Developmental medicine and child neurology (01.10.2007)
Published in Developmental medicine and child neurology (01.10.2007)
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A Clinical Roadmap to Investigate the Genetic Basis of Pediatric Pheochromocytoma: Which Genes Should Physicians Think About?
Mota-Vieira, Luísa, Vara Luiz, Henrique, César, Rui, Bernardo, Ana Teresa, Nunes da Silva, Tiago, Dias Pereira, Bernardo, Pacak, Karel
Published in International journal of endocrinology (01.01.2018)
Published in International journal of endocrinology (01.01.2018)
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MECP2 coding sequence and 3′UTR variation in 172 unrelated autistic patients
Coutinho, Ana M., Oliveira, Guiomar, Katz, Cécile, Feng, Jinong, Yan, Jin, Yang, Chunmei, Marques, Carla, Ataíde, Assunção, Miguel, Teresa S., Borges, Luís, Almeida, Joana, Correia, Catarina, Currais, António, Bento, Celeste, Mota-Vieira, Luísa, Temudo, Teresa, Santos, Mónica, Maciel, Patrícia, Sommer, Steve S., Vicente, Astrid M.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2007)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2007)
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A new PAX8 mutation causing congenital hypothyroidism in three generations of a family is associated with abnormalities in the urogenital tract
Carvalho, Ana, Hermanns, Pia, Rodrigues, Ana-Luísa, Sousa, Isabel, Anselmo, João, Bikker, Hennie, Cabral, Rita, Pereira-Duarte, Carlos, Mota-Vieira, Luísa, Pohlenz, Joachim
Published in Thyroid (New York, N.Y.) (01.09.2013)
Published in Thyroid (New York, N.Y.) (01.09.2013)
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Epidemiology and genetic variability of respiratory syncytial virus in Portugal, 2014–2018
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 Journal of clinical virology (01.12.2019)
Published in Journal of clinical virology (01.12.2019)
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DNA Methylation Is Correlated with Oxidative Stress in Myelodysplastic Syndrome—Relevance as Complementary Prognostic Biomarkers
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 (23.06.2021)
Published in Cancers (23.06.2021)
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Prenatal sonographic diagnosis of isolated fetal ascites in cri‐du‐chat (5p‐) syndrome: A case report
Cardoso, Mariana C., Raposo, Maria Inês, Ormonde, Mariana, Monteiro, Rita, Sampaio, André, Cosme, Pedro, Mota‐Vieira, Luisa
Published in Journal of clinical ultrasound (01.05.2019)
Published in Journal of clinical ultrasound (01.05.2019)
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Genetic variants involved in oxidative stress, base excision repair, DNA methylation, and folate metabolism pathways influence myeloid neoplasias susceptibility and prognosis
Gonçalves, Ana Cristina, Alves, Raquel, Baldeiras, Inês, Cortesão, Emília, Carda, José Pedro, Branco, Claudia C., Oliveiros, Bárbara, Loureiro, Luísa, Pereira, Amélia, Nascimento Costa, José Manuel, Sarmento‐Ribeiro, Ana Bela, Mota‐Vieira, Luisa
Published in Molecular carcinogenesis (01.01.2017)
Published in Molecular carcinogenesis (01.01.2017)
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First isolation of human Leptospira strains, Azores, Portugal
Gonçalves, Ana T, Paiva, Clara, Melo-Mota, Francisco, Vieira, Maria Luísa, Carreira, Teresa, Nunes, Mónica S, Mota-Vieira, Luísa, Ahmed, Ahmed, Harstkeerl, Rudy A, Hyde, Karyne, Collares-Pereira, Margarida
Published in International journal of infectious diseases (01.09.2010)
Published in International journal of infectious diseases (01.09.2010)
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Journal Article
Diagnosis of Human Leptospirosis in a Clinical Setting: Real-Time PCR High Resolution Melting Analysis for Detection of Leptospira at the Onset of Disease
Esteves, Lisa M., Bulhões, Sara M., Branco, Claudia C., Carreira, Teresa, Vieira, Maria L., Gomes-Solecki, Maria, Mota-Vieira, Luisa
Published in Scientific reports (15.06.2018)
Published in Scientific reports (15.06.2018)
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Journal Article
Human leptospirosis: seroreactivity and genetic susceptibility in the population of São Miguel Island (Azores, Portugal)
Esteves, Lisa M, Bulhões, Sara M, Branco, Claudia C, Mota, Francisco M, Paiva, Clara, Cabral, Rita, Vieira, Maria Luisa, Mota-Vieira, Luisa
Published in PloS one (25.09.2014)
Published in PloS one (25.09.2014)
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Journal Article
MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients
Coutinho, Ana M., Oliveira, Guiomar, Katz, Cécile, Feng, Jinong, Yan, Jin, Yang, Chunmei, Marques, Carla, Ataíde, Assunção, Miguel, Teresa S., Borges, Luís, Almeida, Joana, Correia, Catarina, Currais, António, Bento, Celeste, Mota-Vieira, Luísa, Temudo, Teresa, Santos, Mónica, Maciel, P., Sommer, Steve S., Vicente, Astrid M.
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2007)
Published in American journal of medical genetics. Part B, Neuropsychiatric genetics (05.06.2007)
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Journal Article
Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFβ gene variants
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 in BMC immunology (27.01.2009)
Published in BMC immunology (27.01.2009)
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A comprehensive overview of the cystic fibrosis on the island of São Miguel (Azores, Portugal)
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 pediatrics (03.01.2020)
Published in BMC pediatrics (03.01.2020)
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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)
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 (26.10.2015)
Published in PloS one (26.10.2015)
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Journal Article
Enzyme immunoassays
Shetty, Advait, Gomes-Solecki, Maria, Fortes-Gabriel, Elsa, Esteves, Lisa, Vieira, Maria Luísa, Carreira, Teresa, Guedes, Mariana Soares, Mota-Vieira, Luísa, Gomes, Charles Klazer
Published in PLoS neglected tropical diseases (23.02.2022)
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Published in PLoS neglected tropical diseases (23.02.2022)
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Paternal Transmission of Small Supernumerary Marker Chromosome 15 Identified in Prenatal Diagnosis Due to Advanced Maternal Age
Melo, Bruna C. S., Portocarrero, Ana, Alves, Cláudia, Sampaio, André, Mota-Vieira, Luisa
Published in Clinical Medicine Insights: Case Reports (01.01.2015)
Published in Clinical Medicine Insights: Case Reports (01.01.2015)
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Journal Article
Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy
Chabrol, Elodie, Gourfinkel-An, Isabelle, Scheffer, Ingrid E, Picard, Fabienne, Couarch, Philippe, Berkovic, Samuel F, McMahon, Jacinta M, Bajaj, Nandita, Mota-Vieira, Luisa, Mota, Rui, Trouillard, Oriane, Depienne, Christel, Baulac, Michel, LeGuern, Eric, Baulac, Stéphanie
Published in Epilepsy research (01.08.2007)
Published in Epilepsy research (01.08.2007)
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