Fernando Andrade

Biochemistry, Genetics and Molecular Biology · Life Sciences

24h-index1.6kcitations78works3.32yr avg
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Research Topics

Metabolism and Genetic Disorders(34), Diet and metabolism studies(18), Mitochondrial Function and Pathology(10), Folate and B Vitamins Research(9), Lysosomal Storage Disorders Research(8)

Publications78 total

Reversible deficiencies of arylsulfatase B and alpha-galactosidase in Duchenne muscular dystrophy
Molecular Genetics and Metabolism·2025
ALTERAÇÕES OFTALMOLÓGICAS ASSOCIADAS AO ALBINISMO
Amplla Editora eBooks·2024
Revealing novel biomarkers for diagnosing chronic kidney disease in pediatric patients
Scientific Reports·2024· 10 citedOpen Access
Randomized Clinical Trial: Effects of β-Hydroxy-β-Methylbutyrate (HMB)-Enriched vs. HMB-Free Oral Nutritional Supplementation in Malnourished Cirrhotic Patients
Nutrients·2022· 22 citedOpen Access
Erythrocyte Membrane Nanomechanical Rigidity Is Decreased in Obese Patients
International Journal of Molecular Sciences·2022· 13 citedOpen Access
Urine Phenylacetylglutamine Determination in Patients with Hyperphenylalaninemia
Journal of Clinical Medicine·2021· 10 citedOpen Access
Treatment adherence in tyrosinemia type 1 patients
Orphanet Journal of Rare Diseases·2021· 26 citedOpen Access
Artrite Séptica Bilateral dos Ombros: Relato de Caso e Revisão da Literatura
Revista Científica Hospital Santa Izabel·2021Open Access
Hypophosphatasia screening in pediatric age based on records
Endocrinology&Metabolism International Journal·2021Open Access
Usefulness of urinary glycosaminoglycans assay for a mucopolysaccharidosis‐specific screening
Pediatrics International·2020· 14 cited
Vacuolated lymphocytes of blood smears in the diagnoses of lysosomal disorders
Molecular Genetics and Metabolism·2020
Expression levels of the mono carboxylate transporter MCT1 in erythrocytes from patients with Fabry disease and predominant hypertrophic myocardiopathy
Molecular Genetics and Metabolism·2020
Targeted Next-Generation Sequencing in Patients with Suggestive X-Linked Intellectual Disability
Genes·2020· 28 citedOpen Access
Implementation of an Affordable Method for MPS Diagnosis from Urine Screening to Enzymatic Confirmation: Results of a Pilot Study in Morocco
Clinical Laboratory·2020· 10 citedOpen Access
Oocytes of women who are obese or overweight have lower levels of n-3 polyunsaturated fatty acids compared with oocytes of women with normal weight
Fertility and Sterility·2020· 35 cited
Table of Contents
Fertility and Sterility·2020Open Access
Quantification of urinary derivatives of Phenylbutyric and Benzoic acids by LC-MS/MS as treatment compliance biomarkers in Urea Cycle disorders
Journal of Pharmaceutical and Biomedical Analysis·2019· 7 cited
Asymmetric dimethylarginine as a potential biomarker for management and follow-up of phenylketonuria
European Journal of Pediatrics·2019· 4 citedOpen Access
Effects of the amino acid derivatives, β-hydroxy-β-methylbutyrate, taurine, and N-methyltyramine, on triacylglycerol breakdown in fat cells
Journal of Physiology and Biochemistry·2019· 9 cited
Non-alcoholic fatty liver in hereditary fructose intolerance
Clinical Nutrition·2019· 45 citedOpen Access
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Frequent Co-authors

Luis Aldámiz‐Echevarría(39), María L. Couce(13), Sergio Lage(12), Pablo Sanjurjo(11), Marta Llarena(10), Domingo González‐Lamuño(9), José Angel Prieto(8), Javier Elorz(7), Isidro Vitoria(6), Javier Blasco‐Alonso(6), María A. Bueno(5), Jaime Dalmau(5), Carlos Losilla Alcalde(5), Mónica Ruiz(5), Juan Rodríguez‐Soriano(5), Ramón J. Barrio(5), José M. Arbones-Mainar(5), Christian Carpéné(5), David Gil(4), David González(4)