Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Roshini Nayyar"'
Publikováno v:
JIMD Reports, Vol 63, Iss 3, Pp 216-220 (2022)
Abstract Glycogen storage disease type IIIa (GSD‐IIIa) is an autosomal recessive disorder that impairs glycogenolysis, producing ketotic hypoglycaemia, hepatomegaly, cardiac and skeletal myopathy. During pregnancy, increased metabolic demand requir
Externí odkaz:
https://doaj.org/article/045ec7261ed64d1b861c7c7b662771d4
Publikováno v:
Clinical Case Reports, Vol 9, Iss 5, Pp n/a-n/a (2021)
Abstract Although rare, literature demonstrates evidence that vascular anastomoses do occur in dichorionic twins. Therefore, twin anemia polycythemia sequence should be considered as a differential diagnoses in dichorionic twins if there is suspicion
Externí odkaz:
https://doaj.org/article/7d85bdd61a0843d4b5d3fd8e89921bbb
Autor:
Supuni Kapurubandara, Sarah J Melov, Evangeline R Shalou, Monika Mukerji, Stephen Yim, Ujvala Rao, Zain Battikhi, Nirusha Karunaratne, Roshini Nayyar, Thushari I Alahakoon
Publikováno v:
PLoS ONE, Vol 12, Iss 2, p e0171829 (2017)
It is estimated that everyday 7000 women worldwide have their pregnancy end with a stillbirth, however, research and data collection on stillbirth remains underfunded. This stillbirth case series audit investigates an apparent rise in stillbirths at
Externí odkaz:
https://doaj.org/article/e9e48782e557412d99f97262993fc4bd
Autor:
Sarah Asmaa Gebara, Sarah Jane Melov, Thushari Indika Alahakoon, Gary Sholler, Roshini Nayyar
Publikováno v:
Australian and New Zealand Journal of Obstetrics and Gynaecology. 63:212-218
Fetal heart block (FHB) occurs in approximately 1:20 000 births and is associated with significant morbidity and mortality. Vaginal delivery with intrapartum fetal scalp lactate monitoring is offered as an option at our centre for selected cases, in
Publikováno v:
Australian and New Zealand Journal of Obstetrics and Gynaecology. 63:66-73
Pulmonary arterial hypertension (PAH) is a high-risk condition during pregnancy, with recent literature describing mortality rates of up to 23%.To describe the course and outcomes of pregnancy for women with PAH in a major Australian metropolitan ref
Bladder exstrophy (BE) is a congenital genito-urinary malformation where there is a defect in the abdominal wall resulting in a protruding open bladder with exposed mucosa [1]. Several reconstructive procedures are required to correct the anomalies r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9d6fb964ab187684c8e1ad714b525e6
https://doi.org/10.21203/rs.3.rs-2679626/v1
https://doi.org/10.21203/rs.3.rs-2679626/v1
Autor:
Christine Thuy-Trang Tran, Maria-Elisabeth Smet, Jonathan Forsey, Andreas Zankl, Roshini Nayyar
Publikováno v:
Fetal Diagnosis and Therapy. 49:479-485
Introduction: Bruck syndrome is a rare autosomal recessive disease characterized by multiple joint contractures, bone fragility, and fractures. Two genes have been associated with Bruck syndrome, FKBP10 and PLOD2, though they are phenotypically indis
Publikováno v:
Obstetric Anesthesia Digest. 43:29-30
Placenta accreta spectrum (PAS) has a high risk of maternal morbidity, and requires meticulous antenatal and peripartum management.To compare the management and outcomes of PAS between women with and without antenatally suspected disease, and to eval
Publikováno v:
Australian and New Zealand Journal of Obstetrics and Gynaecology. 61:217-222
Background Vasa praevia (VP) is a rare obstetric condition in which unprotected fetal vessels transverse the cervix, are vulnerable to rupture during labour and may result in rapid exsanguination of the fetus. Antenatal diagnosis of VP has resulted i
Publikováno v:
Current Women s Health Reviews. 16:327-333
Background: The discovery of the benefits of antenatal corticosteroids (ACS) for preterm infants was one of the most significant developments in obstetric care. However, due to the difficulty in predicting preterm delivery, optimal use of ACS, is cha