Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Angela Guzys"'
Autor:
Angela Guzys, Susan M. Reid, Christie Bolch, Dinah S. Reddihough, Mark Teoh, Ricardo Palma-Dias, Alison Fung, Stephen Cole, Ryan Hodges, Michael Fahey, Susan P. Walker
Publikováno v:
BMC Pregnancy and Childbirth, Vol 23, Iss 1, Pp 1-11 (2023)
Abstract Background Fetoscopic laser coagulation of placental anastomoses reverses the pathological process in twin-to-twin transfusion syndrome, thereby increasing survival, but there are a paucity of studies addressing long-term neurodevelopmental
Externí odkaz:
https://doaj.org/article/7b9334eca4e542cab8a2612a5b78efa4
Autor:
Christie Bolch, Michael Fahey, Dinah Reddihough, Katrina Williams, Susan Reid, Angela Guzys, Stephen Cole, Andrew Edwards, Alison Fung, Ryan Hodges, Ricardo Palma-Dias, Mark Teoh, Susan Walker
Publikováno v:
BMC Pediatrics, Vol 18, Iss 1, Pp 1-11 (2018)
Abstract Background Twin-to-twin transfusion syndrome (TTTS) is a serious complication of 10–15% of twin or triplet pregnancies in which multiple fetuses share a single placenta. Communicating placental vessels allow one fetus (the donor) to pump b
Externí odkaz:
https://doaj.org/article/0985fefc0dfb40a9922e6754a1c9b6bb
Autor:
Gina L. Hinwood, Hayley Loftus, Daisy A. Shepherd, Angela Guzys, Dinah S. Reddihough, Susan M. Reid
Publikováno v:
Developmental medicine and child neurologyREFERENCES.
To provide an updated description of the rates, trends, and predictors of mortality of individuals with cerebral palsy (CP), born in the Australian state of Victoria between 1970 and 2012.Data were extracted for 4807 individuals (2091 females; 2716 m
Publikováno v:
Developmental Medicine & Child Neurology. 62:346-353
To determine: the effectiveness of three anticholinergic medications in reducing drooling in children with developmental disabilities (such as cerebral palsy, intellectual disability, and autism spectrum disorder), the frequency and nature of side ef
Autor:
Margarita Moreno-Betancur, Susan M Reid, Angela Guzys, David J. Amor, Daisy A Shepherd, Niels Vos, David E. Godler
Publikováno v:
Genes
Volume 11
Issue 7
Genes, Vol 11, Iss 736, p 736 (2020)
Volume 11
Issue 7
Genes, Vol 11, Iss 736, p 736 (2020)
Prader&ndash
Willi syndrome (PWS) is a rare disorder caused by the loss of expression of genes on the paternal copy of chromosome 15q11-13. The main molecular subtypes of PWS are the deletion of 15q11-13 and non-deletion, and differences in neur
Willi syndrome (PWS) is a rare disorder caused by the loss of expression of genes on the paternal copy of chromosome 15q11-13. The main molecular subtypes of PWS are the deletion of 15q11-13 and non-deletion, and differences in neur
Autor:
Susan M Reid, David K. Chong, Bruce R. Johnstone, Angela Guzys, Dinah Reddihough, Christine Westbury
Publikováno v:
Journal of plastic, reconstructiveaesthetic surgery : JPRAS. 72(7)
Sialorrhea is a common problem in children with disability, often negatively affecting socialization, self-esteem, and burden of care. Saliva control surgery is an available option to manage this problem, particularly when other conservative methods