Search Results - "Medeiros, A.M"

Looks like FH but it's not FH – Extended lipid profile of paediatric clinical FH patients reveals a different lipid profile in FH negative patients by Medeiros, A.M, Bourbon, M, Aguiar, P

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A biodegradable composite material based on polyhydroxybutyrate (PHB) and carnauba fibers by Melo, J.D.D., Carvalho, L.F.M., Medeiros, A.M., Souto, C.R.O., Paskocimas, C.A.

“…In this investigation, carnauba fibers obtained from the leaves of the carnauba palm tree were chemically modified and their potential for the development of a…”
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Construction of a new familial hypercholesterolaemia variant data base: A systematic review for a 2015 update by Azevedo, S, Chora, J.R, Alves, A.C, Medeiros, A.M, Bourbon, M

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Using percentiles to diagnose familial hypercholesterolemia in Portugal by Pereira, A, Alves, A.C, Medeiros, A.M, Mariano, C, Bourbon, M

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Mutational analysis of the Portuguese cohort with clinical diagnosis of FH by Medeiros, A.M, Alves, A.C, Bourbon, M

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Physicochemical characterization and evaluation of PGA bioflocculant in coagulation-flocculation and sedimentation processes by Campos, Valquíria, Fernandes, Ana R.A.C., Medeiros, Thales. A.M., Andrade, Erik L.

“…•PGα21Ca is a biopolymer flocculant containing γ-polyglutamic acid (γ-PGA).•PGα21Ca is composed of calcium sulfate (87%) and y-PGA (5.26%).•The results…”
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sdLDL/LDL ratio in familial combined hyperlipidaemia patients and familial hypercholesterolemia patients by Jamal, S, Alves, A.C, Medeiros, A.M, Bourbon, M

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In silico classification of ldlr variants leads to misdiagnosis of fh patients by Alves, A.C, Medeiros, A.M, Bourbon, M

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Genotype/phenotype of FH patients: differences in childhood and adulthood by Alves, A.C, Medeiros, A.M, Bourbon, M

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Dunnigan-type familial partial lipodystrophy in a large Portuguese kindred by Alves, A.C, Moldovan, O, Medeiros, A.M, Sousa, A.B, Bourbon, M

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Update of the Portuguese Familial Hypercholesterolaemia Study by Medeiros, A.M, Alves, A.C, Francisco, V, Bourbon, M

“…Abstract The main aim of the Portuguese Familial Hypercholesterolaemia Study is to identify the genetic cause of hypercholesterolaemia in individuals with a…”
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Functionally characterization of LDLR missense alterations found in clinical FH patients by Alves, A.C, Azevedo, S, Benito-Vicente, A, Etxebarria, A, Barros, P, Medeiros, A.M, Martin, C, Bourbon, M

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Will familial hypercholesterolaemia cohorts hide many more lisosomal acid lipase deficiency patients? by Chora, J.R, Alves, A.C, Medeiros, A.M, Mariano, C, Loubarinhas, G, Guerra, A, Mansilha, H, Bourbon, M

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Novel LDLR variants in Ibero-America: preliminary molecular results of familial hypercholesterolaemia in Ibero-America by Azevedo, S, Bañares, V, Schreier, L, Vázquez, A, Medeiros, A.M, Alves, A.C, Bourbon, M

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Novel LDLR variants in Ibero-America: Preliminary molecular results of familial hypercholesterolaemia in Ibero-America by Azevedo, S, Bañares, V, Schreier, L, Vázquez, A, Medeiros, A.M, Alves, A.C, Bourbon, M

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Genetic diagnosis of familial hypercholesterolaemia: The importance of an integrated analysis of clinical, molecular and functional data by Alves, A.C, Benito-Vicente, A, Etxebarria, A, Medeiros, A.M, Martin, C, Bourbon, M

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Familial hypercholesterolaemia in Portugal by Bourbon, M, Alves, A.C, Medeiros, A.M, Silva, S, Soutar, A.K

“…Abstract Familial hypercholesterolaemia (FH) is characterised clinically by an increased level of circulating LDL cholesterol that leads to lipid accumulation…”
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Genetic analysis of familial hypercholesterolaemia in Iberoamerican countries by Chora, J, Mata, P, Santos, R, Vázquez, A. Cárdenas, Stoll, M, Schreier, L, Cuevas, A, Alves, A.C, Medeiros, A.M, Isla, L. Perez, Jannes, C, Pereira, A, Dell'Oca, N, Reyes, X, Corral, P, Bañares, V, Magaña-Torres, T, Aguilar-Salinas, C, Alonso, R, Bourbon, M

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Comparison of different LDL-C genetic risk score in a sample of clinical FH patients by Medeiros, A.M., Alves, A.C.C., Bourbon, M.

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miRNA target-binding sites as regulators of genes involved in the lipid metabolism might explain the hypercholesterolaemia in FH patients by Medeiros, A.M., Enguita, F.J., Bourbon, M.

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