15 results match your criteria: "Great Ormond St Hospital for Children NHS Trust[Affiliation]"
Intensive Care Med
December 2017
Service of Neonatology and Pediatric Intensive Care, Department of Paediatrics, University Hospital of Geneva, Geneva, Switzerland.
Purpose: Much of the common practice in paediatric mechanical ventilation is based on personal experiences and what paediatric critical care practitioners have adopted from adult and neonatal experience. This presents a barrier to planning and interpretation of clinical trials on the use of specific and targeted interventions. We aim to establish a European consensus guideline on mechanical ventilation of critically children.
View Article and Find Full Text PDFEur J Pediatr
February 2017
Paediatric Intensive Care Unit, Great Ormond St Hospital for Children NHS Trust & Institute of Child Health, University College London, London, UK.
Unlabelled: Adolescents have specific healthcare needs distinct from adults or younger children secondary to anatomical, physiological and socio-behavioural differences. Healthcare providers have been slow to address this, leading the UK Department of Health (2011) to publish 'You're Welcome' quality criteria for services for young people. (In the UK, the term young people is preferred to adolescent.
View Article and Find Full Text PDFSci Rep
April 2016
Stem Cells and Regenerative Section, UCL Institute of Child Health, London WC1N 1EH, UK.
Expression of major histocompatibility antigens class-2 (MHC-II) under non-inflammatory conditions is not usually associated with the nervous system. Comparative analysis of immunogenicity of human embryonic/fetal brain-derived neural stem cells (hNSCs) and human mesenchymal stem cells with neurogenic potential from umbilical cord (UC-MSCs) and paediatric adipose tissue (ADSCs), while highlighting differences in their immunogenicity, led us to discover subsets of neural cells co-expressing the neural marker SOX2 and MHC-II antigen in vivo during human CNS development. MHC-II proteins in hNSCs are functional, and differently regulated upon differentiation along different lineages.
View Article and Find Full Text PDFStem Cell Res
July 2015
Stem Cells and Regenerative Medicine, UCL Institute of Child Health, London WC1N 1EH, UK. Electronic address:
Human somatic stem cells with neural differentiation potential can be valuable for developing cell-based therapies, including treatment of birth-related defects, while avoiding issues associated with cell reprogramming. Precisely defining the "identity" and differentiation potential of somatic stem cells from different sources, has proven difficult, given differences in sets of specific markers, protocols used and lack of side-by-side characterization of these cells in different studies. Therefore, we set to compare expression of mesenchymal and neural markers in human umbilical cord-derived mesenchymal stem cells (UC-MSCs), pediatric adipose-derived stem cells (p-ADSCs) in parallel with human neural stem cells (NSCs).
View Article and Find Full Text PDFThorax
May 2015
Manchester Adult cystic fibrosis Unit, Wythenshawe Hospital, University Hospitals, Manchester, UK.
J Clin Endocrinol Metab
December 2014
Developmental Endocrinology Research Group (K.S.A., M.T.D.), Clinical and Molecular Genetics Unit, University College London Institute of Child Health, London WC1N 1EH, United Kingdom; Department of Pediatric Endocrinology and Diabetes (A.A., F.R.), Oxford University Hospitals National Health Service (NHS) Trust, Oxford OX3 9DU, United Kingdom; School of Molecular and Biomedical Science (N.R., P.T.), The University of Adelaide, Adelaide SA 5005, Australia; Oxford Hemophilia and Thrombosis Centre (N.C., P.B.), and Departments of Clinical Genetics (C.N., H.S.) and Paediatric Hematology and Oncology (G.W.H.), Oxford University Hospitals NHS Trust, Oxford OX3 9DU, United Kingdom; Department of Radiology (A.S.L., D.S.), Great Ormond St Hospital for Children NHS Trust, London WC1N 1EH, United Kingdom.
Context: SOX3 is an early developmental transcription factor involved in pituitary development. In humans, over- and underdosage of SOX3 is associated with X-linked hypopituitarism with variable phenotypes ranging from isolated GH deficiency (GHD) to panhypopituitarism, with or without mental retardation and, in most cases, with reported pituitary imaging, an ectopic/undescended posterior pituitary.
Patient: We present a young patient with hemophilia B and developmental delay who had a 2.
Pediatr Nephrol
August 2014
Renal Unit, Great Ormond St Hospital for Children NHS Trust, Great Ormond St, London, WC1N 3JH, UK.
Background: The health related quality of life (HRQoL) of young adults treated for chronic kidney disease (CKD) stage 4/5 from infancy is unknown.
Methods: A HRQoL questionnaire was sent to all 41 patients aged >16 years from a previously characterised cohort of infants with CKD stage 4/5 born between 1986 and 1997. Patient scores were compared with a previously reported cohort of patients who needed renal replacement therapy (RRT) in mid childhood and in the normal population.
Nanomedicine
February 2014
Developmental Biology Unit, UCL Institute of Child Health, University College London (UCL), London, United Kingdom. Electronic address:
Unlabelled: Scaffold cellularization for cartilage engineering can aid implant properties, their retention and minimize repeated intervention, particularly in paediatric reconstructive craniofacial surgery. We developed novel bionanoscaffolds using paediatric adipose tissue-derived stem cells (hADSCs), an accessible autologous cell source, and POSS-PCU. Little is known about cellular responses to this nanomaterial, though it was used in human.
View Article and Find Full Text PDFJ Plast Reconstr Aesthet Surg
September 2010
Department of Plastic Surgery, Great Ormond St. Hospital for Children NHS Trust, Great Ormond St, London WC1N 3JH, UK.
Background: Current techniques of autologous ear reconstruction involve the soft tissue coverage of a carved costal cartilage framework. However, assessment of the morbidity associated with this donor site has been little documented. This study describes a method to reconstruct the defect and analyses the outcomes with or without donor site reconstitution.
View Article and Find Full Text PDFCirculation
March 2001
Vascular Physiology Unit, Great Ormond St Hospital for Children NHS Trust, London, UK.
Background: Low birth weight is related to increased risk of coronary heart disease in adults and recently has been associated with vascular endothelial dysfunction in children. We investigated whether the relation between birth weight and endothelial function was still present in early adult life and whether there was an interaction with emerging risk factors.
Methods And Results: In 315 adults (165 women, 150 men, aged 20 to 28 years), high-resolution ultrasound was used to determine endothelium-dependent and -independent vascular responses of the brachial artery.
Eur Child Adolesc Psychiatry
September 1999
Neurosciences Unit, Institute of Child Health and Great Ormond St. Hospital for Children NHS Trust, Mecklenburgh Sq., UK-London WCI 2AP.
One third of children with autistic spectrum disorders (or pervasive developmental disorders) enter that state by regression from a more normal prior development at the onset of epilepsy or epileptiform abnormality in the electroencephalogram. In a very small proportion structural lesions of the temporal lobes are discovered. These form part of the sample of children coming to a surgical treatment programme.
View Article and Find Full Text PDFJ Nucl Med
March 1999
Department of Radiology, Great Ormond St. Hospital for Children NHS Trust, London, UK.
Unlabelled: In view of the established role of 111In-antimyosin in the detection of heart muscle pathology, radiation dose estimates were made for this substance. Biodistribution and biokinetic data were obtained from our studies, which failed to show abnormal uptake of 111In-antimyosin in localized sites of skeletal muscle involvement in patients with idiopathic inflammatory myopathies.
Methods: After intravenous administration of 74 MBq (2 mCi) 111In-antimyosin, gamma camera scintigraphy was performed in 12 adult patients with inflammatory muscle disease and in 2 control patients.