Zobrazeno 1 - 10
of 348
pro vyhledávání: '"Robert, Wynn"'
Autor:
Paul Harmatz, Robert Wynn, Ashish Gupta, Sandhya Kharbanda, Caroline Lindemans, Rebecca Ahrens-Nicklas, Peter van Hasselt, Troy Lund, Timothy Olson, Francesca Tucci, Leonie Martin, Nathalie Boeglin, Jean Brooks, Su Syonmez, Laura Campbell, Simon Jones, Paul Orchard, Maria Ester Bernardo
Publikováno v:
Genetics in Medicine Open, Vol 2, Iss , Pp 100914- (2024)
Externí odkaz:
https://doaj.org/article/70e16dbba1ce45d1b98e1211c66c59e6
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
Allogeneic hematopoietic stem cell transplantation (HSCT) has been an important and efficacious treatment for acute leukemia in children for over 60 years. It works primarily through the graft-vs.-leukemia (GVL) effect, in which donor T-cells and oth
Externí odkaz:
https://doaj.org/article/3761552dce2f4ad79fafa2991a3dced7
Autor:
Aimee Donald, Cecilia Kämpe Björkvall, Ashok Vellodi, GAUCHERITE Consortium, Timothy M. Cox, Derralyn Hughes, Simon A. Jones, Robert Wynn, Maciej Machaczka
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Neuronopathic Gaucher Disease (nGD) describes the condition of a subgroup of patients with the Lysosomal Storage Disorder (LSD), Gaucher disease with involvement of the central nervous system (CNS) which results from inherited def
Externí odkaz:
https://doaj.org/article/87856b3cd87144b293aea32047560137
Autor:
Farrukh Shah, Paul Telfer, Mark Velangi, Shivan Pancham, Robert Wynn, Sally Pollard, Elizabeth Chalmers, Jonathan Kell, Angela M. Carter, Joe Hickey, Clark Paramore, Minesh Jobanputra, Kate Ryan
Publikováno v:
eJHaem, Vol 2, Iss 4, Pp 738-749 (2021)
Abstract Objectives We evaluated routine healthcare management, clinical status and patient‐ and carer‐reported outcomes in UK paediatric and adult patients with transfusion‐dependent β‐thalassaemia (TDT). Methods A multi‐centre, observati
Externí odkaz:
https://doaj.org/article/0e55f29da6df4ad2860859fcc13a2116
Autor:
Arthavan Selvanathan, Jane Kinsella, Francesca Moore, Robert Wynn, Simon Jones, Peter J. Shaw, Bridget Wilcken, Kaustuv Bhattacharya
Publikováno v:
JIMD Reports, Vol 61, Iss 1, Pp 3-11 (2021)
Abstract Aspartylglucosaminuria (AGU) (OMIM #208400) is a recessively inherited disorder of glycoprotein catabolism, a subset of the lysosomal storage disorders (LSDs). Deficiency of the enzyme glycosylasparaginase (E.C. 3.5.1.26) leads to accumulati
Externí odkaz:
https://doaj.org/article/3767fcb1821f4f51af28d77354e8df76
Autor:
Robert Wynn Jones
Palaeontology, the scientific study of fossils, has developed from a descriptive science to an analytical science used to interpret relationships between Earth and life history. This book provides a comprehensive and thematic treatment of applied pal
Autor:
John Girdlestone, Meera Raymond, Bronwen Shaw, Sameer Tulpule, Vikesh R. Devlia, Robert Danby, Trudy Ahyee, Aurore Saudemont, Rachael Hough, Paul Veys, Annalisa Ruggeri, Ajay Vora, David I. Marks, Brenda Gibson, Robert Wynn, Alejandro Madrigal, Cristina V. Navarrete
Publikováno v:
eJHaem, Vol 1, Iss 1, Pp 208-218 (2020)
Abstract To obtain a qualitative as well as quantitative view immune reconstitution following umbilical cord blood (UCB) transplantation of paediatric patients, we utilised a broad panel of flow cytometry markers to monitor the phenotypes of lymphoid
Externí odkaz:
https://doaj.org/article/5e08f9b7f453485e971b21e158fc84b1