BIO Basque Health
Center
St George's, University of London
Londres, Reino UnidoPublications in collaboration with researchers from St George's, University of London (29)
2024
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Clinical and neuroradiological spectrum of biallelic variants in NOTCH3
eBioMedicine, Vol. 107
2023
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Causes of death in children with congenital anomalies up to age 10 in eight European countries
BMJ Paediatrics Open, Vol. 7, Núm. 1
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Diminishing benefits of urban living for children and adolescents’ growth and development
Nature, Vol. 615, Núm. 7954, pp. 874-883
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Ethics and legal requirements for data linkage in 14 European countries for children with congenital anomalies
BMJ Open, Vol. 13, Núm. 7
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Recent Advances and Potential Multi-Omics Approaches in the Early Phases of Inflammatory Bowel Disease
Journal of Clinical Medicine, Vol. 12, Núm. 10
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The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders
Brain, Vol. 146, Núm. 8, pp. 3273-3288
2022
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Temporal and geographical variations in survival of children born with congenital anomalies in Europe: A multi-registry cohort study
Paediatric and Perinatal Epidemiology, Vol. 36, Núm. 6, pp. 792-803
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Validation of the OAKS prognostic model for acute kidney injury after gastrointestinal surgery
BJS Open, Vol. 6, Núm. 1
2021
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Cardioversion in patients with newly diagnosed non-valvular atrial fibrillation: Observational study using prospectively collected registry data
BMJ, Vol. 375
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Heterogeneous contributions of change in population distribution of body mass index to change in obesity and underweight
eLife, Vol. 10
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Signal Detection in EUROmediCAT: Identification and Evaluation of Medication–Congenital Anomaly Associations and Use of VigiBase as a Complementary Source of Reference
Drug Safety, Vol. 44, Núm. 7, pp. 765-785
2020
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Recurrent De Novo NAHR Reciprocal Duplications in the ATAD3 Gene Cluster Cause a Neurogenetic Trait with Perturbed Cholesterol and Mitochondrial Metabolism
American Journal of Human Genetics, Vol. 106, Núm. 2, pp. 272-279
2019
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Management and 1-year outcomes of patients with newly diagnosed atrial fibrillation and chronic kidney disease: Results from the prospective garfield-af registry
Journal of the American Heart Association, Vol. 8, Núm. 3
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The phenotype of Sotos syndrome in adulthood: A review of 44 individuals
American Journal of Medical Genetics, Part C: Seminars in Medical Genetics, Vol. 181, Núm. 4, pp. 502-508
2018
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Effect of Systemic Hypertension With Versus Without Left Ventricular Hypertrophy on the Progression of Atrial Fibrillation (from the Euro Heart Survey)
American Journal of Cardiology, Vol. 122, Núm. 4, pp. 578-583
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Prediction of preterm delivery in symptomatic women using PAMG-1, fetal fibronectin and phiGFBP-1 tests: Systematic review and meta-analysis
Ultrasound in Obstetrics and Gynecology, Vol. 52, Núm. 4, pp. 442-451
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Risk profiles and one-year outcomes of patients with newly diagnosed atrial fibrillation in India: Insights from the GARFIELD-AF Registry
Indian Heart Journal, Vol. 70, Núm. 6, pp. 828-835
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The Tatton-Brown-Rahman Syndrome: A clinical study of 55 individuals with de novo constitutive DNMT3A variants [version 1; referees: 3 approved]
Wellcome Open Research, Vol. 3
2016
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Expression and function of Kv7.4 channels in rat cardiac mitochondria: Possible targets for cardioprotection
Cardiovascular Research, Vol. 110, Núm. 1, pp. 40-50
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Is prolonged infusion of piperacillin/tazobactam and meropenem in critically ill patients associated with improved pharmacokinetic/pharmacodynamic and patient outcomes? An observation from the Defining Antibiotic Levels in Intensive care unit patients (DALI) cohort
Journal of Antimicrobial Chemotherapy, Vol. 71, Núm. 1, pp. 196-207