Publicaciones en colaboración con investigadores/as de Hospital General de Niños Ricardo Gutierrez (27)

2023

  1. A second update on mapping the human genetic architecture of COVID-19

    Nature

  2. MicroRNA signature from extracellular vesicles of HCV/HIV co-infected individuals differs from HCV mono-infected

    Journal of Molecular Medicine, Vol. 101, Núm. 11, pp. 1409-1420

2022

  1. Identifying the research, advocacy, policy and implementation needs for the prevention and management of respiratory syncytial virus lower respiratory tract infection in low- and middle-income countries

    Frontiers in Pediatrics, Vol. 10

  2. Latin American Consensus on the Management of Sepsis in Children: Sociedad Latinoamericana de Cuidados Intensivos Pediátricos [Latin American Pediatric Intensive Care Society] (SLACIP) Task Force: Executive Summary

    Journal of Intensive Care Medicine, Vol. 37, Núm. 6, pp. 753-763

  3. Novel genes and sex differences in COVID-19 severity

    Human molecular genetics, Vol. 31, Núm. 22, pp. 3789-3806

2021

  1. Coronavirus disease 2019 in patients with inborn errors of immunity: An international study

    Journal of Allergy and Clinical Immunology, Vol. 147, Núm. 2, pp. 520-531

2019

  1. Development and validation of a composite disease activity score for measurement of muscle and skin involvement in juvenile dermatomyositis

    Rheumatology (United Kingdom), Vol. 58, Núm. 7, pp. 1196-1205

2018

  1. Development and Testing of a Hybrid Measure of Muscle Strength in Juvenile Dermatomyositis for Use in Routine Care

    Arthritis Care and Research, Vol. 70, Núm. 9, pp. 1312-1319

  2. Latin American consensus for pediatric cardiopulmonary resuscitation 2017: Latin American Pediatric Critical Care Society pediatric cardiopulmonary resuscitation committee

    Pediatric Critical Care Medicine, Vol. 19, Núm. 3, pp. E152-E156

2017

  1. Development and Initial Validation of the Macrophage Activation Syndrome/Primary Hemophagocytic Lymphohistiocytosis Score, a Diagnostic Tool that Differentiates Primary Hemophagocytic Lymphohistiocytosis from Macrophage Activation Syndrome

    Journal of Pediatrics, Vol. 189, pp. 72-78.e3

  2. Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation

    Journal of Allergy and Clinical Immunology, Vol. 139, Núm. 4, pp. 1282-1292

2016

  1. Mutations in pregnancy-associated plasma protein A2 cause short stature due to low IGF-I availability

    EMBO Molecular Medicine, Vol. 8, Núm. 4, pp. 363-374

  2. Treatment with recombinant human insulin-like growth factor-1 improves growth in patients with PAPP-A2 deficiency

    Journal of Clinical Endocrinology and Metabolism, Vol. 101, Núm. 11, pp. 3879-3883

2015

  1. Long-term evolution after in-hospital cardiac arrest in children: Prospective multicenter multinational study

    Resuscitation, Vol. 96, pp. 126-134

2014

  1. Cardiac arrest and resuscitation in the pediatric intensive care unit: A prospective multicenter multinational study

    Resuscitation, Vol. 85, Núm. 10, pp. 1380-1386

  2. Post return of spontaneous circulation factors associated with mortality in pediatric in-hospital cardiac arrest: A prospective multicenter multinational observational study

    Critical Care, Vol. 18, Núm. 6

  3. Shockable rhythms and defibrillation during in-hospital pediatric cardiac arrest

    Resuscitation, Vol. 85, Núm. 3, pp. 387-391

2012

  1. MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma

    Clinical Cancer Research, Vol. 18, Núm. 10, pp. 2828-2837

2010

  1. Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas

    JAMA - Journal of the American Medical Association, Vol. 304, Núm. 23, pp. 2611-2619

2006

  1. Factores asociados al pronóstico de los pacientes pediátricos ventilados mecánicamente. Un estudio internacional

    Medicina Intensiva, Vol. 30, Núm. 9, pp. 425-431