Publicacións en colaboración con investigadores/as de Heinrich Heine University Düsseldorf (20)

2022

  1. An International Perspective on Preceding Infections in Guillain-Barré Syndrome: The IGOS-1000 Cohort

    Neurology, Vol. 99, Núm. 12, pp. E1299-E1313

  2. Electrodiagnosis of Guillain-Barre syndrome in the International GBS Outcome Study: Differences in methods and reference values

    Clinical Neurophysiology, Vol. 138, pp. 231-240

2021

  1. Aetiology of acute respiratory infection in preschool children requiring hospitalisation in Europe-results from the PED-MERMAIDS multicentre case-control study

    BMJ Open Respiratory Research, Vol. 8, Núm. 1

2019

  1. Development of a new largely scalable in vitro prion propagation method for the production of infectious recombinant prions for high resolution structural studies

    PLoS Pathogens, Vol. 15, Núm. 10

  2. Proteomic studies reveal disrupted in schizophrenia 1 as a player in both neurodevelopment and synaptic function

    International Journal of Molecular Sciences, Vol. 20, Núm. 1

2018

  1. Regional variation of Guillain-Barré syndrome

    Brain, Vol. 141, Núm. 10, pp. 2866-2877

  2. Research update for articles published in EJCI in 2016

    European Journal of Clinical Investigation, Vol. 48, Núm. 10

2017

  1. International Guillain-Barré Syndrome Outcome Study: protocol of a prospective observational cohort study on clinical and biological predictors of disease course and outcome in Guillain-Barré syndrome

    Journal of the Peripheral Nervous System, Vol. 22, Núm. 2, pp. 68-76

2016

  1. Acute stimulation of brain mu opioid receptors inhibits glucose-stimulated insulin secretion via sympathetic innervation

    Neuropharmacology, Vol. 110, pp. 322-332

  2. The Priority position paper: Protecting Europe's food chain from prions

    Prion

2015

  1. Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation

    PLoS Genetics, Vol. 11, Núm. 7

  2. Mudd's disease (MAT I/III deficiency): A survey of data for MAT1A homozygotes and compound heterozygotes

    Orphanet Journal of Rare Diseases, Vol. 10, Núm. 1

2014

  1. Loss of Prion Protein Leads to Age-Dependent Behavioral Abnormalities and Changes in Cytoskeletal Protein Expression

    Molecular Neurobiology, Vol. 50, Núm. 3, pp. 923-936

2012

  1. Human and rat brain lipofuscin proteome

    Proteomics, Vol. 12, Núm. 15-16, pp. 2445-2454

  2. Proteomic, genomic and translational approaches identify CRMP1 for a role in schizophrenia and its underlying traits

    Human Molecular Genetics, Vol. 21, Núm. 20, pp. 4406-4418

2009

  1. Oligomer assembly of the C-terminal DISC1 domain (640-854) is controlled by self-association motifs and disease-associated polymorphism S704C

    Biochemistry, Vol. 48, Núm. 32, pp. 7746-7755

2008

  1. Insolubility of disrupted-in-schizophrenia 1 disrupts oligomer-dependent interactions with nuclear distribution element 1 and is associated with sporadic mental disease

    Journal of Neuroscience, Vol. 28, Núm. 15, pp. 3839-3845

2007

  1. APC Inactivation Associates With Abnormal Mitosis Completion and Concomitant BUB1B/MAD2L1 Up-Regulation

    Gastroenterology, Vol. 132, Núm. 7, pp. 2448-2458

2002

  1. Distant collaboration in drug discovery: The LINK3D project

    Journal of Computer-Aided Molecular Design, Vol. 16, Núm. 11, pp. 809-818

1999

  1. A limited repertoire of mutations of the luteinizing hormone (LH) receptor gene in familial and sporadic patients with male LH-independent precocious puberty

    Journal of Clinical Endocrinology and Metabolism, Vol. 84, Núm. 3, pp. 1136-1140