Complexo Hospitalario Universitario de Santiago
Centro de atención
Heinrich Heine University Düsseldorf
Düsseldorf, AlemaniaPublicacións en colaboración con investigadores/as de Heinrich Heine University Düsseldorf (16)
2022
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An International Perspective on Preceding Infections in Guillain-Barré Syndrome: The IGOS-1000 Cohort
Neurology, Vol. 99, Núm. 12, pp. E1299-E1313
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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
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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
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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
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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
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Regional variation of Guillain-Barré syndrome
Brain, Vol. 141, Núm. 10, pp. 2866-2877
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Research update for articles published in EJCI in 2016
European Journal of Clinical Investigation, Vol. 48, Núm. 10
2017
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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
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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
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The state of psychogeriatrics in Europe: Challenges and opportunities in six European countries
International Psychogeriatrics, Vol. 27, Núm. 8, pp. 1243-1246
2011
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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
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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
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APC Inactivation Associates With Abnormal Mitosis Completion and Concomitant BUB1B/MAD2L1 Up-Regulation
Gastroenterology, Vol. 132, Núm. 7, pp. 2448-2458
2003
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Hypotrichosis simplex of the scalp is associated with nonsense mutations in CDSN encoding corneodesmosin
Nature Genetics, Vol. 34, Núm. 2, pp. 151-153
2000
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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
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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