M.T. García‐Silva

Author

M.T. García‐Silva

Also Known As

M T García-Silva, M Teresa García-Silva, M Teresa Garcı́a-Silva, M. Garcia‐Silva, M. T. Garcia-Silva, M. T. García‐Silva, M. Teresa García-Silva, M. Teresa García‐Silva, M.T. Garcia-Silva, M.T. García-Silva

Publications

850

Citations

H-Index

Concepts

All Affiliations

Hospital Universitario 12 De Octubre Research Institute Hospital 12 de Octubre Centre for Biomedical Network Research on Rare Diseases Hospital Sant Joan de Déu Barcelona Centro de Investigación Biomédica en Red

About

M.T. García‐Silva is an author at Hospital Universitario 12 De Octubre specializing in medicine, pathology, and molecular biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	458
2	Natural Sciences	2	2	111
3	Engineering	1	1	11
4	Biochemistry	1	1	77
5	Metabolism	1	1	77

M.T. García‐Silva

Publications

787

Citations

H-Index

Page 1

	Year	Citations
Apolipoprotein C-III Isofocusing in the Diagnosis of Genetic Defects in O-Glycan Biosynthesis Suzan Wopereis, Stephanie Grünewald, Éva Morava, Clinical Chemistry	2003	138
Therapeutic effects of docosahexaenoic acid ethyl ester in patients with generalized peroxisomal disorders Manuela Martínez, Élida Vázquez, M.T. García‐Silva, American Journal of Clinical Nutrition Docosahexaenoic AcidMedicineLipid PeroxidationTherapeutic EffectsGeneralized Peroxisomal Disorders	2000	119
Renal pathology in children with mitochondrial diseases Elena Martín‐Hernández, M.T. García‐Silva, Julia Vara, Pediatric Nephrology GlomerulonephritisUrologyMitochondrial FunctionMedicineKidney Failure	2005	108
MITOCHONDRIAL DISEASES ASSOCIATED WITH CEREBRAL FOLATE DEFICIENCY Àngels García‐Cazorla, Elizabeth Quadros, A. Nascimento, Neurology	2008	83
Secondary coenzyme Q 10 deficiencies in oxidative phosphorylation (OXPHOS) and non-OXPHOS disorders Dèlia Yubero, Raquel Montero, Miguel A. Martı́n, Mitochondrion BiochemistryNatural SciencesInherited Metabolic DiseaseNon-oxphos DisordersMolecular Biology	2016	77
Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease Paz Briones, Marta Vilaseca, M.T. García‐Silva, European Journal of Paediatric Neurology Mitochondrial MyopathyMendelian DisorderMitochondrial FunctionGenetic DisorderGenetics	2001	59
Congenital disorder of glycosylation (CDG) type Ie. A new patient M.T. García‐Silva, Gert Matthijs, Els Schollen, Journal of Inherited Metabolic Disease	2004	53
Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria M.T. García‐Silva, Antònia Ribes, Yolanda Campos, Pediatric Neurology Clinical FindingNeurological DisorderEthylmalonic AciduriaDiagnosisPathology	1997	50
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
Pathogenic mutations in the 5′ untranslated region of BCS1L mRNA in mitochondrial complex III deficiency M. Carmen Gil-Borlado, Maritza González-Hoyuela, Alberto Blázquez, Mitochondrion Mitochondrial FunctionUntranslated RegionNatural SciencesGeneticsBcs1l Mrna	2009	34

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