Concepedia

Author

Susana Teijeira

University Hospital Complex Of VigoORCID

Also Known As

J C Rubio, S Teijeira, S. Teijeira, Susana Teijeira, Susana Teijeira Bautista, Susana Teijeira-Bautista

65

Publications

1.2K

Citations

20

H-Index

102

Concepts

All Affiliations

University Hospital Complex Of VigoHospital Xeral CaldeServicio Gallego de SaludGalicia Sur Biomedical FoundationCentre for Biomedical Network Research on Rare Diseases
ST

About

Susana Teijeira is an author at University Hospital Complex Of Vigo specializing in medicine, pathology, and neuromuscular pathology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

15

18

575

2

Health Sciences

2

2

36

3

Natural Sciences

2

2

152

4

Engineering

1

1

39

5

Public Health

1

1

10

Susana Teijeira

×

27

Publications

1.1K

Citations

20

H-Index

YearCitations

Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry

Alejandro Lucía, Jonatan R. Ruiz, Alfredo Santalla,

Journal of Neurology Neurosurgery & Psychiatry

2012

130

Long COVID in hospitalized and non-hospitalized patients in a large cohort in Northwest Spain, a prospective cohort study

Alexandre Pérez‐González, Alejandro Araújo-Ameijeiras, Alberto Fernández‐Villar,

Scientific Reports

2022

119

Molecular heterogeneity of myophosphorylase deficiency (Mcardle's disease): A genotype‐phenotype correlation study

Miguel A. Martı́n, Jenny L. Buchbinder, Roberto Fernández‐Hojas,

Annals of Neurology

2001

94

Oxidation of methionine residues in the prion protein by hydrogen peroxide

Jesús R. Requena, Mariana N. Dimitrova, Giuseppe Legname,

Archives of Biochemistry and Biophysics

2004

80

Chimeric Peptide Species Contribute to Divergent Dipeptide Repeat Pathology in c9ALS/FTD and SCA36

Zachary T. McEachin, Tania F. Gendron, Nisha Raj,

Neuron

2020

72

Permanent muscle weakness in M<scp>C</scp>Ardle disease

Aleksandra Nadaj‐Pakleza, C. Vincitorio, Pascal Laforêt,

Muscle & Nerve

2009

64

A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy

Saida Ortolano, Rosa Tarrı́o, Patricia Blanco,

Neuromuscular Disorders

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

Evaluation of heart involvement in gamma-sarcoglycanopathy (LGMD2C). A study of ten patients

Francisco Calvo, Susana Teijeira, J.M. Fernandez,

Neuromuscular Disorders

2000

43

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

2011

39

Page 1