User profiles for Jessica Sand

Jessica L Sandy

The Children's Hospital at Westmead
Verified email at health.nsw.gov.au
Cited by 65

[PDF][PDF] An iPSC line from human pancreatic ductal adenocarcinoma undergoes early to invasive stages of pancreatic cancer progression

…, CX Yuan, KJ Won, G Donahue, J Sands… - Cell reports, 2013 - cell.com
Pancreatic ductal adenocarcinoma (PDAC) carries a dismal prognosis and lacks a human
cell model of early disease progression. When human PDAC cells are injected into …

Chronic kidney disease guideline implementation in primary care: a qualitative report from the TRANSLATE CKD study

BM Vest, TRM York, J Sand, CH Fox… - The Journal of the …, 2015 - Am Board Family Med
Background: Primary care physicians (PCPs) are optimally situated to identify and manage
early stage chronic kidney disease (CKD). Nonetheless, studies have documented …

Thyroid nodules in children and adolescents: Investigation and management

JL Sandy, A Titmuss, S Hameed… - … of Paediatrics and …, 2022 - Wiley Online Library
Clinically detectable thyroid nodules are less common in children than adults. However,
they are associated with an increased risk of malignancy. Therefore, thorough evaluation of …

Rapid increases in observed incidence and prevalence of Type 1 diabetes in children and youth in Mali, 2007–2016

JL Sandy, S Besançon, AT Sidibé… - Pediatric …, 2021 - Wiley Online Library
Aims Determine incidence, prevalence and mortality of Type 1 diabetes (T1D) in children
and youth <25 years (y) in Mali during the first 10 years of the Santé Diabète/Life for a Child …

Is knowledge translation without patient or community engagement flawed?

…, JM Westfall, M Felzien, J Braden, J Sand - Family …, 2017 - academic.oup.com
Background. The engagement of patients/individuals and/or communities has become
increasingly important in all aspects of the research process. Objective. The aim of this …

Clinical practice guidelines for paediatric X‐linked hypophosphataemia in the era of burosumab

JL Sandy, PJ Simm, A Biggin, CP Rodda… - … of Paediatrics and …, 2022 - Wiley Online Library
X‐linked hypophosphataemia (XLH), the most common inherited form of rickets, is caused
by a PHEX gene mutation that leads to excessive serum levels of fibroblast growth factor 23 (…

[HTML][HTML] Prevalence and characteristics of paediatric X-linked hypophosphataemia in Australia and New Zealand: Results from the Australian and the New Zealand …

JL Sandy, C Nunez, BJ Wheeler, C Jefferies, A Morris… - Bone, 2023 - Elsevier
… Author links open overlay panel Jessica L. Sandy a b , Carlos Nunez c d , Benjamin J.
Wheeler e , Craig Jefferies f , Anne Morris c d , Aris Siafarikas g h i , Christine P. Rodda j k , Peter …

Demographic, Clinical, Management, and Outcome Characteristics of 8,004 Young Children With Type 1 Diabetes

JL Sandy, SR Tittel, S Rompicherla, B Karges… - Diabetes …, 2024 - Am Diabetes Assoc
OBJECTIVE To compare demographic, clinical, and therapeutic characteristics of children
with type 1 diabetes age <6 years across three international registries: Diabetes Prospective …

The North American Primary Care Research Group's patient and clinician engagement program (pace): demystifying patient engagement through a dyad model

J Sand, M Felzien, R Haeme, H Tapp… - Family …, 2017 - academic.oup.com
Background. Community engagement in research is essential for translating the best
evidence into community and clinical practice to improve the health and well-being of the …

Expanding the phenotype of Bruck syndrome: Severe limb deformity, arthrogryposis, congenital cardiac disease and pulmonary hemorrhage

JL Sandy, D Perez, S Goh, J Forsey… - American Journal of …, 2023 - Wiley Online Library
Bruck syndrome is a rare collagen disorder with autosomal recessive inheritance caused by
pathogenic variants in either FKBP10 or PLOD2 genes. It is characterized by bone fragility …