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

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. Development of a Prediction Model for COVID-19 Acute Respiratory Distress Syndrome in Patients With Rheumatic Diseases: Results From the Global Rheumatology Alliance Registry

    ACR Open Rheumatology, Vol. 4, Núm. 10, pp. 872-882

  3. 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. 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

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

2011

  1. Development of quality indicators to evaluate the monitoring of SLE patients in routine clinical practice

    Autoimmunity Reviews, Vol. 10, Núm. 7, pp. 383-388

2010

  1. European league against rheumatism recommendations for monitoring patients with systemic lupus erythematosus in clinical practice and in observational studies

    Annals of the Rheumatic Diseases, Vol. 69, Núm. 7, pp. 1269-1274

2007

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

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

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