Isidro Vitoria - Concepedia

Author

Isidro Vitoria

Hospital Universitari i Politècnic La Fe ORCID

Also Known As

I Vitoria Miñana, I. Vitoria, I. Vitoria Miñana, I. Vitoria-Miñana, I. Vitoria‐Miñana, Isidro Vitoria, Isidro Vitoria Miñana, Isidro Vitoria-Miñana, Isidro Vitoria‐Miñana, Vitoria I

Publications

1.3K

Citations

H-Index

Concepts

All Affiliations

Hospital Universitari i Politècnic La Fe Hospital Universitario Virgen del Rocío Hospital Universitario Miguel Servet Centre for Biomedical Network Research on Rare Diseases Hospital de Cruces

About

Isidro Vitoria is an author at Hospital Universitari i Politècnic La Fe specializing in medicine, clinical nutrition, and nutrition.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	16	477
2	Clinical Nutrition	8	8	234
3	Health Sciences	6	6	231
4	Public Health	5	5	122
5	Biochemistry	1	1	45

Isidro Vitoria

Publications

Citations

H-Index

Page 1

	Year	Citations
Molecular epidemiology, genotype–phenotype correlation and BH4 responsiveness in Spanish patients with phenylketonuria Luis Aldámiz‐Echevarría, Marta Llarena, María A. Bueno, Journal of Human Genetics UrologyMolecular EpidemiologyRenal PathologyGenetic EpidemiologyInherited Metabolic Disease	2016	69
Vitamin and mineral status in patients with hyperphenylalaninemia Vanesa Crujeiras Martínez, Luis Aldámiz‐Echevarría, Jaime Dalmau, Molecular Genetics and Metabolism NutritionNutritional RequirementClinical NutritionMineral StatusOsteoporosis	2015	58
Carbohydrate status in patients with phenylketonuria María L. Couce, Paula Sánchez‐Pintos, Isidro Vitoria, Orphanet Journal of Rare Diseases	2018	55
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
Non-alcoholic fatty liver in hereditary fructose intolerance Luis Aldámiz‐Echevarría, Javier de las Heras, María L. Couce, Clinical Nutrition ObesityMetabolic SyndromeMetabolic Associated SteatohepatitisHepatologyBiochemistry	2019	45
Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients Luis Aldámiz‐Echevarría, María A. Bueno, María L. Couce, Clinical Nutrition ObesityNutritionMetabolic SyndromeMalnutritionBody Composition	2013	43
Carnitine-Acylcarnitine Translocase Deficiency: Experience with Four Cases in Spain and Review of the Literature Isidro Vitoria, Elena Martín‐Hernández, Luis Peña Quintana, JIMD Reports	2014	42
Hyperhomocysteinemia in Adult Patients: A Treatable Metabolic Condition Domingo González‐Lamuño, Francisco Arrieta, Elena Dios Fuentes, Nutrients NutritionMetabolic DisorderHyperlipidemiaMetabolic SyndromeBiochemical Nutrition	2023	42
Molecular diagnosis of glycogen storage disease and disorders with overlapping clinical symptoms by massive parallel sequencing Ana Vega, Celia Medrano, Rosa Navarrete, Genetics in Medicine Clinical SymptomsSequencingMendelian DisorderMedicineGenetics	2016	39
Clinical and molecular diagnosis of non‐phosphomannomutase 2 N‐linked congenital disorders of glycosylation in Spain Celia Medrano, Ana Vega, Rosa Navarrete, Clinical Genetics	2019	38

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