Silvia Meavilla - Concepedia

Author

Silvia Meavilla

Hospital Sant Joan de Déu Barcelona

Also Known As

P. Mayne, Philip Mayne, S Meavilla, S. Meavilla, Silvia María Meavilla, Silvia Meavilla

Publications

338

Citations

H-Index

Concepts

All Affiliations

Hospital Sant Joan de Déu Barcelona Centre for Biomedical Network Research on Rare Diseases Instituto de Salud Carlos III Vall d'Hebron Hospital Universitari Hospital Universitario 12 De Octubre

About

Silvia Meavilla is an author at Hospital Sant Joan de Déu Barcelona specializing in medicine, physiology, and metabolism.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	116
2	Metabolism	2	2	42
3	Health Sciences	1	1	29
4	Hepatology	1	1	29
5	Nephrology	1	1	13

Silvia Meavilla

Publications

250

Citations

H-Index

Page 1

	Year	Citations
Urea cycle disorders in Spain: an observational, cross-sectional and multicentric study of 104 cases Elena Martín‐Hernández, Luis Aldámiz‐Echevarría, E. Castejón-Ponce, Orphanet Journal of Rare Diseases	2014	49
Evolution of maple syrup urine disease in patients diagnosed by newborn screening versus late diagnosis María L. Couce, Federico Ramos, María A. Bueno, European Journal of Paediatric Neurology UrologyInherited Metabolic DiseaseDiagnosisPediatricsVersus Late Diagnosis	2015	39
Clinical and biochemical outcome after hydroxocobalamin dose escalation in a series of patients with cobalamin C deficiency Inês Vaz Matos, Esperanza Castejón, Silvia Meavilla, Molecular Genetics and Metabolism Translational MedicineHydroxocobalamin Dose EscalationCobalamin C DeficiencyMedicineBiochemical Outcome	2013	35
Plasma coenzyme Q10 status is impaired in selected genetic conditions Raquel Montero, Dèlia Yubero, Maria Cristina de Oliveira Salgado, Scientific Reports	2019	33
The Role of Liver Transplantation in Propionic Acidemia Jesús Quintero, Cristina Molera, Javier Juampérez, Liver Transplantation Hepatic ArteryMetabolic SyndromeThrombosisVenous ThrombosisHematology	2018	29
Implementation of second-tier tests in newborn screening for the detection of vitamin B12 related acquired and genetic disorders: results on 258,637 newborns Sonia Pajares, José Antonio Arranz, Aída Ormazábal, Orphanet Journal of Rare Diseases	2021	29
Assessment of plasma ammonia and glutamine concentrations in urea cycle disorders Mercedes Serrano, Aída Ormazábal, Marta Vilaseca, Clinical Biochemistry Plasma AmmoniaElectrolyte DisorderRenal FunctionMedicineGlutamine Concentrations	2011	13
Switching to Glycerol Phenylbutyrate in 48 Patients with Urea Cycle Disorders: Clinical Experience in Spain Elena Martín‐Hernández, Pilar Quijada‐Fraile, Patricia Correcher Medina, Journal of Clinical Medicine	2022	12
Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III Dèlia Yubero, Raquel Montero, Mar O’Callaghan, JIMD Reports	2015	11

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