Carolyn Jane Ellaway (Carolyn Ellaway)

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 5

Top Topics

Molecular Docking

Subarachnoid Hemorrhage

Autism Spectrum Disorder

Anti Inflammatory

Top Venues

Internal medicine journal

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Kathleen M Nicholls, Charles Denaro, Michel C Tchan, Carolyn Jane Ellaway, Drago Bratkovic, Sheridan Campbell, Megan Fookes, Mark Thomas
Fabry-specific treatment in Australia: time to align eligibility criteria with international best practices. Internal medicine journal (2024)
Kathleen M Nicholls, Charles Denaro, Michel C Tchan, Carolyn Jane Ellaway, Drago Bratkovic, Sheridan Campbell, Megan Fookes, Mark Thomas
Fabry-specific treatment in Australia: time to align eligibility criteria with international best practices. Internal medicine journal 54 (6) (2024)
Andrew Paul Fennell, Anne Elizabeth Baxter, Samuel Frank Berkovic, Carolyn Jane Ellaway, Caitlin Forwood, Michael Stephen Hildebrand, Smitha Kumble, Colina McKeown, David Mowat, Gemma Poke, Sulekha Rajagopalan, Brigid M Regan, Ingrid Eileen Scheffer, Zornitza Stark, Chloe Alice Stutterd, Tiong Yang Tan, Ella Jane Wilkins, Alison Yeung, Matthew Frank Hunter
The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome. American journal of medical genetics. Part A 188 (12) (2022)
Carolyn M Sue, Shanti Balasubramaniam, Drago Bratkovic, Catherine Bonifant, John Chrisodoulou, David John Coman, Karen Crawley, Fabienne Edema-Hildebrand, Carolyn Jane Ellaway, Roula Ghaoui, Maina Kava, Lisa S Kearns, Joy Lee, Christina Liang, David A Mackey, Sean Murray, Merrilee Needham, Rocio Rius, Jacqui Russell, Nicholas J C Smith, Dominic Thyagarajan, Christine Wools
Patient care standards for primary mitochondrial disease in Australia: an Australian adaptation of the Mitochondrial Medicine Society recommendations. Internal medicine journal (2021)
Simranpreet Kaur, Nicole J Van Bergen, Kristen J Verhey, Cameron J Nowell, Breane Budaitis, Yang Yue, Carolyn Jane Ellaway, Nicola Brunetti-Pierri, Gerarda Cappuccio, Irene Bruno, Lia Boyle, Vincenzo Nigro, Anna Laura Torella, Tony Roscioli, Mark J Cowley, Sean Massey, Rhea Sonawane, Matthew D Burton, Bitten Schönewolf-Greulich, Zeynep Tümer, Wendy K Chung, Wendy Anne Gold, John Chrisodoulou
Expansion of the phenotypic spectrum of de novo missense variants in kinesin family member 1A (KIF1A). Human mutation 41 (10) (2020)