User profiles for Jessica Sand
Jessica L SandyThe 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 …
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 …
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 …
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 …
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 …
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
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 (…
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 …
… 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 …
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 …
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 …
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 …
pathogenic variants in either FKBP10 or PLOD2 genes. It is characterized by bone fragility …