Population and Computational Analysis of the MGEA6 P521A Variation as a Risk Factor for Familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease)
Lemos, Roberta R., Oliveira, Danyllo F., Zatz, Mayana, Oliveira, João R. M.
Published in Journal of molecular neuroscience (01.03.2011)
Published in Journal of molecular neuroscience (01.03.2011)
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Exaggerated blood pressure response during exercise treadmill testing: functional and hemodynamic features, and risk factors
de Lima, Sandro G, de Albuquerque, Maria de F P M, de Oliveira, João R M, Ayres, Constância F J, da Cunha, José E G, de Oliveira, Danyllo F, de Lemos, Roberta R, de Souza, Manuela B R, e Silva, Odwaldo B
Published in Hypertension research (01.07.2012)
Published in Hypertension research (01.07.2012)
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Update and Mutational Analysis of SLC20A2: A Major Cause of Primary Familial Brain Calcification
Lemos, Roberta R., Ramos, Eliana M., Legati, Andrea, Nicolas, Gaël, Jenkinson, Emma M., Livingston, John H., Crow, Yanick J., Campion, Dominique, Coppola, Giovanni, Oliveira, João R. M.
Published in Human mutation (01.05.2015)
Published in Human mutation (01.05.2015)
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An Update on Primary Familial Brain Calcification
Lemos, Roberta R., Ferreira, J.B.M.M., Keasey, Matthew P., Oliveira, Joao R.M.
Published in International Review of Neurobiology (2013)
Published in International Review of Neurobiology (2013)
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Book Chapter
Journal Article
Brain calcifications and PCDH12 variants
Nicolas, Gaël, Sanchez-Contreras, Monica, Ramos, Eliana Marisa, Lemos, Roberta R, Ferreira, Joana, Moura, Denis, Sobrido, Maria J, Richard, Anne-Claire, Lopez, Alma Rosa, Legati, Andrea, Deleuze, Jean-François, Boland, Anne, Quenez, Olivier, Krystkowiak, Pierre, Favrole, Pascal, Geschwind, Daniel H, Aran, Adi, Segel, Reeval, Levy-Lahad, Ephrat, Dickson, Dennis W, Coppola, Giovanni, Rademakers, Rosa, de Oliveira, João R M
Published in Neurology. Genetics (01.08.2017)
Published in Neurology. Genetics (01.08.2017)
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Journal Article
Erratum to: Population and Computational Analysis of the MGEA6 P521A Variation as a Risk Factor for Familial Idiopathic Basal Ganglia Calcification (Fahr’s Disease)
Lemos, Roberta R., Oliveira, Danyllo F., Zatz, Mayana, Oliveira, João R. M.
Published in Journal of molecular neuroscience (01.03.2011)
Published in Journal of molecular neuroscience (01.03.2011)
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Journal Article
Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice
Keller, Annika, Westenberger, Ana, Sobrido, Maria J, García-Murias, Maria, Domingo, Aloysius, Sears, Renee L, Lemos, Roberta R, Ordoñez-Ugalde, Andres, Nicolas, Gael, da Cunha, José E Gomes, Rushing, Elisabeth J, Hugelshofer, Michael, Wurnig, Moritz C, Kaech, Andres, Reimann, Regina, Lohmann, Katja, Dobričić, Valerija, Carracedo, Angel, Petrović, Igor, Miyasaki, Janis M, Abakumova, Irina, Mäe, Maarja Andaloussi, Raschperger, Elisabeth, Zatz, Mayana, Zschiedrich, Katja, Klepper, Jörg, Spiteri, Elizabeth, Prieto, Jose M, Navas, Inmaculada, Preuss, Michael, Dering, Carmen, Janković, Milena, Paucar, Martin, Svenningsson, Per, Saliminejad, Kioomars, Khorshid, Hamid R K, Novaković, Ivana, Aguzzi, Adriano, Boss, Andreas, Le Ber, Isabelle, Defer, Gilles, Hannequin, Didier, Kostić, Vladimir S, Campion, Dominique, Geschwind, Daniel H, Coppola, Giovanni, Betsholtz, Christer, Klein, Christine, Oliveira, Joao R M
Published in Nature genetics (01.09.2013)
Published in Nature genetics (01.09.2013)
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Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification
Hsu, Sandy Chan, Sears, Renee L., Lemos, Roberta R., Quintáns, Beatriz, Huang, Alden, Spiteri, Elizabeth, Nevarez, Lisette, Mamah, Catherine, Zatz, Mayana, Pierce, Kerrie D., Fullerton, Janice M., Adair, John C., Berner, Jon E., Bower, Matthew, Brodaty, Henry, Carmona, Olga, Dobricić, Valerija, Fogel, Brent L., García-Estevez, Daniel, Goldman, Jill, Goudreau, John L., Hopfer, Suellen, Janković, Milena, Jaumà, Serge, Jen, Joanna C., Kirdlarp, Suppachok, Klepper, Joerg, Kostić, Vladimir, Lang, Anthony E., Linglart, Agnès, Maisenbacher, Melissa K., Manyam, Bala V., Mazzoni, Pietro, Miedzybrodzka, Zofia, Mitarnun, Witoon, Mitchell, Philip B., Mueller, Jennifer, Novaković, Ivana, Paucar, Martin, Paulson, Henry, Simpson, Sheila A., Svenningsson, Per, Tuite, Paul, Vitek, Jerrold, Wetchaphanphesat, Suppachok, Williams, Charles, Yang, Michele, Schofield, Peter R., de Oliveira, João R. M., Sobrido, María-Jesús, Geschwind, Daniel H., Coppola, Giovanni
Published in Neurogenetics (01.02.2013)
Published in Neurogenetics (01.02.2013)
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