Publicacións en colaboración con investigadores/as de Heinrich Heine University Düsseldorf (16)

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

2020

  1. Comparison of a polyethylene glycol membrane and a collagen membrane for the treatment of bone dehiscence defects at bone level implants—A prospective, randomized, controlled, multicenter clinical trial

    Clinical Oral Implants Research, Vol. 31, Núm. 11, pp. 1105-1115

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

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. 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

  2. The state of psychogeriatrics in Europe: Challenges and opportunities in six European countries

    International Psychogeriatrics, Vol. 27, Núm. 8, pp. 1243-1246

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

2003

  1. Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin

    Nature Genetics, Vol. 34, Núm. 2, pp. 151-153

2000

  1. A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3

    American Journal of Human Genetics, Vol. 66, Núm. 6, pp. 1979-1983

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