Syndromes associated with mitochondrial DNA depletion

Por Nogueira, Célia, Almeida, Ligia S, Nesti, Claudia, Pezzini, Ilaria, Videira, Arnaldo, Vilarinho, Laura, Santorelli, Filippo M
Publicado em 2014

The impact of migration on women’s mental health in the postpartum period

Por Almeida, Lígia Moreira, Costa-Santos, Cristina, Caldas, José Peixoto, Dias, Sónia, Ayres-de-Campos, Diogo
Publicado no Rev Saude Publica (2016)

Clinical Severity of PGK1 Deficiency Due To a Novel p.E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t(3;14)(q26.33;q12), Disrupting NUBPL Gene

Por David, Dezső, Almeida, Lígia S., Maggi, Maristella, Araújo, Carlos, Imreh, Stefan, Valentini, Giovanna, Fekete, György, Haltrich, Irén
Publicado no JIMD Rep (2015)

Glial activation in the collagenase model of nociception associated with osteoarthritis

Por Adães, Sara, Almeida, Lígia, Potes, Catarina S, Ferreira, Ana Rita, Castro-Lopes, José M, Ferreira-Gomes, Joana, Neto, Fani L
Publicado no Mol Pain (2017)

Characterization of novel SLC6A8 variants with the use of splice-site analysis tools and implementation of a newly developed LOVD database

Por Betsalel, Ofir T, Rosenberg, Efraim H, Almeida, Ligia S, Kleefstra, Tjitske, Schwartz, Charles E, Valayannopoulos, Vassili, Abdul-Rahman, Omar, Poplawski, Nicola, Vilarinho, Laura, Wolf, Philipp, den Dunnen, Johan T, Jakobs, Cornelis, Salomons, Gajja S
Publicado em 2011

High Prevalence of SLC6A8 Deficiency in X-Linked Mental Retardation

Por Rosenberg, Efraim H., Almeida, Ligia S., Kleefstra, Tjitske, deGrauw, Rose S., Yntema, Helger G., Bahi, Nadia, Moraine, Claude, Ropers, Hans-Hilger, Fryns, Jean-Pierre, deGrauw, Ton J., Jakobs, Cornelis, Salomons, Gajja S.
Publicado em 2004