A5081272186- Medical History and Innovations
- History of Medicine Studies
- Empathy and Medical Education
- History of Medical Practice
- Historical Psychiatry and Medical Practices
- Grief, Bereavement, and Mental Health
- Historical Studies on Reproduction, Gender, Health, and Societal Changes
- Migration, Policy, and Dickens Studies
- Genetic Syndromes and Imprinting
- Anatomy and Medical Technology
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Assisted Reproductive Technology and Twin Pregnancy
- Organ Donation and Transplantation
- Health and Conflict Studies
- Spanish Literature and Culture Studies
- Autopsy Techniques and Outcomes
- Innovations in Medical Education
- Neuroscience and Neuropharmacology Research
- Neurology and Historical Studies
- Diversity and Career in Medicine
- Historical and Modern Theater Studies
- Gestational Trophoblastic Disease Studies
- Genetic Neurodegenerative Diseases
- Genomic variations and chromosomal abnormalities
Newcastle upon Tyne Hospitals NHS Foundation Trust
2021-2025
Centre for Life
2013-2022
Manchester University NHS Foundation Trust
2021
Newcastle upon Tyne Hospital
2018-2021
King's College London
2000-2020
Digital Research Alliance of Canada
2020
Cornell University
2016
Lancet Laboratories
2000-2015
University of Nottingham
2011
University of Hong Kong
2010
Before 1832 dissection was a feared and hated punishment for murder. The Anatomy Act requisitioned instead the corpses of poor, transferring penalty from murder to poverty. contributed terrible fear Victorian workhouse influences attitudes towards death even today. This is an unputdownable analysis which draws on many disciplines explore fundamental issues folklore science, life political struggles surrounding ownership body in 19th century. 'This heartfelt dilemma whose history movingly...
Variants in SCN8A are associated with a spectrum of epilepsies and neurodevelopmental disorders. Ataxia as predominant symptom variation has not been well studied. We set out to investigate disease mechanisms genotype-phenotype correlations SCN8A-related ataxia.
Witteveen-Kolk syndrome (OMIM 613406) is a recently defined neurodevelopmental caused by heterozygous loss-of-function variants in SIN3A. We define the clinical and phenotypes related to SIN3A-haploinsufficiency 28 unreported patients. Patients with SIN3A adversely affecting protein function have mild intellectual disability, growth feeding difficulties. Involvement of multidisciplinary team including geneticist, paediatrician neurologist should be considered managing these described here...
Abstract When a nurse or doctor unpacks wound, they take away the dressings to see how things look beneath. Historians unpack present by looking behind it, try discern roots and causes. Here, transplantation is seen in long historical perspective (since sixteenth century) taking funerary culture of British Isles, judicial use dissection as punishment, bodysnatching, itself, history bodily donation, an attempt help provide some understanding modern phenomena, such organ shortage. The...
Marine chlorophytes of the genus Chlorella are unicellular algae capable accumulating a high proportion cellular lipids that can be used for biodiesel production. In this study, we examined broad physiological capabilities subtropical strain (C596) sp. "SAG-211-18" including its heterotrophic growth and tolerance to low salt. We found alga replicates more slowly at diluted salt concentrations grow on wide range carbon substrates in dark. then sequenced RNA C596 elucidate key metabolic genes...
<h3>Introduction</h3> There is little described in the current COVID-19 literature about outcomes of patients discharged from hospital following pneumonia. We describe rapid establishment a 'virtual ward' (VW) for follow-up with suspected or confirmed diagnosis pneumonia pneumonitis upon discharge, characteristics and first 300 patient referrals. <h3>Methods</h3> Admitted confirmed/suspected pneumonia/pneumonitis were referred electronically to VW on discharge. Pulse oximeters provided if...
transfusion or injections, and there was no history of venereal infection genital ulceration.The other antibody positive heterosexual man an intravenous drug user.When the beginning October compared with mid- November increase over 300% in people attending clinic who required counselling for HIV test.By end December this had fallen slightly, but surge publicity at February we are expecting a further dramatic requests testing.Our staff, particular health advisers, working under enormous...
Oxford University Press, New York, 2008 Correspondence: Alta Kendall, BSN, RNC-NIC, Tacoma General Hospital (Multicare), Tacoma, WA 98405 ([email protected]).
Abstract To delineate further the clinical phenotype of Lamb–Shaffer Syndrome (LSS) 16 unpublished patients with heterozygous variation in SOX5 were identified either through UK Decipher database or study team was contacted by clinicians directly. Clinical phenotyping tables completed for each patient their responsible geneticist. Photos and features compared to assess key phenotypes genotype–phenotype correlation. We report variants all which meet American College Medical...
SCN2A-related disorders include intellectual disability, autism spectrum disorder, seizures, episodic ataxia, and schizophrenia. In this study, the phenotype-genotype association in was further delineated by collecting detailed clinical molecular characteristics. Using previously proposed genotype-phenotype hypotheses based on variant function position, potential of phenotype prediction from variants found examined. Patients were identified through Deciphering Developmental Disorders study...