Beatriz San Millán - Concepedia

Author

Beatriz San Millán

University Hospital Complex Of Vigo ORCID

Also Known As

B Millán, B San Millán, B San‐Millán, B. San Millan, B. San Millan-Tejado, B. San Millán, Beatriz Millan, Beatriz Millán, Beatriz San Millan, Beatriz San Millán

Publications

933

Citations

H-Index

Concepts

All Affiliations

University Hospital Complex Of Vigo Centre for Biomedical Network Research on Rare Diseases Servicio Gallego de Salud Galicia Sur Biomedical Foundation Instituto de Investigación Sanitaria de Santiago

About

Beatriz San Millán is an author at University Hospital Complex Of Vigo specializing in medicine, pathology, and autoimmune disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	451
2	Natural Sciences	2	2	98
3	Engineering	1	1	39
4	Health Sciences	1	1	26
5	Social Sciences	1	1	17

Beatriz San Millán

Publications

705

Citations

H-Index

Page 1

	Year	Citations
Lafora bodies and neurological defects in malin-deficient mice correlate with impaired autophagy Olga Criado‐García, Carmen Aguado, Javier Machín Gayarre, Human Molecular Genetics MitophagyGlycogen BiosynthesisCell DeathCell AutophagyNeurological Defects	2011	150
Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36 Zachary T. McEachin, Tania F. Gendron, Nisha Raj, Neuron Autoimmune DiseaseProtein FoldingMedicineProteomicsImmunology	2020	72
A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy Saida Ortolano, Rosa Tarrı́o, Patricia Blanco, Neuromuscular Disorders Mendelian DisorderGenetic DisorderGeneticsPathologyMyosin Storage Myopathy	2011	51
Hexanucleotide Repeat Expansions in c9FTD/ALS and SCA36 Confer Selective Patterns of Neurodegeneration In Vivo Tiffany W. Todd, Zachary T. McEachin, Jeannie Chew, Cell Reports	2020	48
Light‐chain‐restricted germinal centres in reactive lymphadenitis: report of eight cases Syong Hyun Nam‐Cha, Beatriz San Millán, Manuela Mollejo, Histopathology	2008	46
Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC) R. Scalco, Alejandro Lucía, Alfredo Santalla, Orphanet Journal of Rare Diseases	2020	40
Molecular and clinical study of McArdle’s disease in a cohort of 123 European patients. Identification of 20 novel mutations Irene Viéitez, Susana Teijeira, José M. Fernández, Neuromuscular Disorders Molecular Diagnostic TechniquesEngineeringGenetic DisorderMedicineGenetics	2011	39
Acute Necrotizing Encephalopathy of Childhood: Report of a Spanish Case Beatriz San Millán, Susana Teijeira, Carmen Penin, Pediatric Neurology PediatricsNeurologyEncephalitisMedicineAcute Necrotizing Encephalopathy	2007	32
Clinical, pathological and genetic spectrum in 89 cases of mitochondrial progressive external ophthalmoplegia Claudia Rodríguez-López, Luis Miguel García‐Cárdaba, Alberto Blázquez, Journal of Medical Genetics	2020	31
Fabry disease in the Spanish population: observational study with detection of 77 patients Irene Viéitez, Olga Souto-Rodríguez, Lorena Fernández-Mosquera, Orphanet Journal of Rare Diseases	2018	27

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