Disease: Holmes Collins syndrome
- A prognostic model for use before elective surgery to estimate the risk of postoperative pulmonary complications (GSU-Pulmonary Score): a development and validation study in three international cohorts
- Absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies: an autosomal recessive disorder
- Behavior Profiles at 2 Years for Children Born Extremely Preterm with Bronchopulmonary Dysplasia
- Consistency of neuropsychiatric syndromes across dementias: results from the European Alzheimer Disease Consortium. Part II
- Death following pulmonary complications of surgery before and during the SARS-CoV-2 pandemic
- Defining Incidence of Acute Compartment Syndrome in the Research Setting: A Proposed Method From the PACS Study
- Difficult or impossible facemask ventilation in children with difficult tracheal intubation: a retrospective analysis of the PeDI registry
- Efficacy and Safety of NVX-CoV2373 in Adults in the United States and Mexico
- Efficacy and Safety of the mRNA-1273 SARS-CoV-2 Vaccine
- Efficacy of the mRNA-1273 SARS-CoV-2 Vaccine at Completion of Blinded Phase
- Genomic reconstruction of the SARS-CoV-2 epidemic in England
- Homeobox genes and congenital malformations
- Identification of new epilepsy treatments: issues in preclinical methodology
- Immunomodulatory therapy in children with paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS, MIS-C; RECOVERY): a randomised, controlled, open-label, platform trial
- Incidence of cytomegalovirus retinitis in the era of highly active antiretroviral therapy
- Investigation of hospital discharge cases and SARS-CoV-2 introduction into Lothian care homes
- Neuropsychiatric syndromes in dementia. Results from the European Alzheimer Disease Consortium: part I
- Non-cytomegalovirus ocular opportunistic infections in patients with acquired immunodeficiency syndrome
- Outcomes of Preterm Infants following Discussions about Withdrawal or Withholding of Life Support
- Phenotypes, Developmental Basis, and Genetics of Pierre Robin Complex
- POLR1A variants underlie phenotypic heterogeneity in craniofacial, neural, and cardiac anomalies
- Potential impact of cardiology phone-consultation for patients risk-stratified by the HEART pathway
- Predicting Acute Compartment Syndrome (PACS): The Role of Continuous Monitoring
- Recurrent emergence of SARS-CoV-2 spike deletion H69/V70 and its role in the Alpha variant B.1.1.7
- SARS-CoV replicates in primary human alveolar type II cell cultures but not in type I-like cells
- SARS-CoV-2 evolution during treatment of chronic infection
- Some craniofacial dysostoses: (Pierre) Robin's syndrome, Treacher Collins' syndrome, and a digito-facial-mental retardation syndrome. Report of three cases
- Subcutaneous REGEN-COV Antibody Combination to Prevent Covid-19
- The low molecular weight protein tyrosine phosphatase promotes adipogenesis and subcutaneous adipocyte hypertrophy
- The prevalence and incidence of epiretinal membranes in eyes with inactive extramacular CMV retinitis
- The role of manual therapies in equine pain management
- Timing of postnatal steroids for bronchopulmonary dysplasia: association with pulmonary and neurodevelopmental outcomes
- Transgenomic metabolic interactions in a mouse disease model: interactions of Trichinella spiralis infection with dietary Lactobacillus paracasei supplementation