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Biochemistry Research International|October 21, 2011
Glycosaminoglycan storage disorders: a reviewMaria Francisca Coutinho, Lúcia Lacerda, Sandra AlvesCancers|July 15, 2026
Plasma Sphingomyelin as a Post-Treatment Monitoring Biomarker for Pathological Response in Locally Advanced Rectal CancerPedro Brandão, Lúcia Lacerda, Marisa D SantosCancers|January 11, 2024
Amino Acid Profiles in the Biological Fluids and Tumor Tissue of CRC PatientsMarisa Domingues Santos, Ivo Barros, Pedro Brandão, et al.BMJ Case Reports|September 24, 2015
Adolescent-onset Krabbe disease with an initial diagnosis of multiple sclerosis and a novel mutationJosé Tomás, João Durães, Lúcia Lacerda, et al.British Journal of Haematology|May 27, 2005
Evidence for a link between sphingolipid metabolism and expression of CD1d and MHC-class II: monocytes from Gaucher disease patients as a modelAndrea Balreira, Lúcia Lacerda, Clara Sá Miranda, et al.Pediatric Neurology|April 18, 2015
D-bifunctional protein deficiency: a cause of neonatal onset seizures and hypotoniaJoão Nascimento, Céu Mota, Lúcia Lacerda, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|October 7, 2016
Solving a case of allelic dropout in the GNPTAB gene: implications in the molecular diagnosis of mucolipidosis type III alpha/betaMaria Francisca Coutinho, Marisa Encarnação, Francisco Laranjeira, et al.Nature Clinical Practice. Cardiovascular Medicine|October 25, 2007
Cardiac Fabry's disease: an unusual cause of left ventricular hypertrophyJosé Pedro L Nunes, Ovídio Costa, Maria do Sameiro Faria, et al.Clinical Chemistry and Laboratory Medicine|April 2, 2002
Relationships between serum markers of monocyte/macrophage activation in type 1 Gaucher's diseaseJ Antonio Casal, Lúcia Lacerda, Luis F Pérez, et al.Molecular Genetics & Genomic Medicine|March 5, 2019
Genotype-phenotype correlations and BH<sub>4</sub> estimated responsiveness in patients with phenylketonuria from Rio de Janeiro, Southeast BrazilEduardo Vieira Neto, Francisco Laranjeira, Dulce Quelhas, et al.Pageof 2