Concepedia

Author

Eduardo López‐Laso

Hospital Universitario Reina SofíaORCID

Also Known As

E López-Laso, E. Lopez-Laso, E. López-Laso, E. López‐Laso, Eduardo Lopez-Laso, Eduardo Lopez‐Laso, Eduardo López Laso, Eduardo López-Laso, Eduardo López‐Laso, Maria López

66

Publications

2.7K

Citations

22

H-Index

55

Concepts

All Affiliations

Hospital Universitario Reina SofíaInstituto Maimónides de Investigación Biomédica de CórdobaHospital Sant Joan de Déu BarcelonaInstituto de Salud Carlos IIICentre for Biomedical Network Research on Rare Diseases
EL

About

Eduardo López‐Laso is an author at Hospital Universitario Reina Sofía specializing in medicine, neuropathology, and neurology.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

13

15

1.6K

2

Social Sciences

2

2

49

3

Public Health

1

1

29

4

Biochemistry

1

1

10

5

Biology

1

1

13

Eduardo López‐Laso

×

28

Publications

2.1K

Citations

18

H-Index

YearCitations

Frequency, symptoms, risk factors, and outcomes of autoimmune encephalitis after herpes simplex encephalitis: a prospective observational study and retrospective analysis

Thaís Armangué, Marianna Spatola, Alexandru Vlagea,

The Lancet Neurology

2018

622

Infection-Triggered Familial or Recurrent Cases of Acute Necrotizing Encephalopathy Caused by Mutations in a Component of the Nuclear Pore, RANBP2

Derek Neilson, Mark D. Adams, Caitlin M.D. Orr,

The American Journal of Human Genetics

2009

349

Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study

Thaís Armangué, Gemma Olivé-Cirera, Eugenia Martínez‐Hernández,

The Lancet Neurology

2020

314

X‐linked <i>NDUFA1</i> gene mutations associated with mitochondrial encephalomyopathy

Daniel Fernández-Moreira, Cristina Ugalde, Roel Smeets,

Annals of Neurology

2007

136

Dominant mutations in the cation channel gene transient receptor potential vanilloid 4 cause an unusual spectrum of neuropathies

M. Zimoń, Jonathan Baets, Michaela Auer‐Grumbach,

Brain

2010

133

The International Working Group on Neurotransmitter related Disorders (iNTD): A worldwide research project focused on primary and secondary neurotransmitter disorders

Thomas Opladen, Elisenda Cortès‐Saladelafont, Mario Mastrangelo,

Molecular Genetics and Metabolism Reports

2016

59

Unraveling the genetic landscape of autosomal recessive Charcot-Marie-Tooth neuropathies using a homozygosity mapping approach

M. Zimoń, Esra Battaloğlu, Yeşim Parman,

Neurogenetics

2014

42

Delineating the neurological phenotype in children with defects in the <scp><i>ECHS1</i></scp> or <scp><i>HIBCH</i></scp> gene

Laura Martí‐Sánchez, Heidy Baide‐Mairena, Anna Marcé‐Grau,

Journal of Inherited Metabolic Disease

2020

38

Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines

Oya Kuseyri Hübschmann, Gabriella Horváth, Elisenda Cortès‐Saladelafont,

Nature Communications

2021

37

Recommendations for the radiological diagnosis and follow-up of neuropathological abnormalities associated with tuberous sclerosis complex

Àlex Rovira, María Luz Ruiz-Falcó, Elena García-Esparza,

Journal of Neuro-Oncology

2014

34

Page 1