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Author/Creator Craig, Jamie E.

11. Eosinophilic Vasculitis and Arteritic Anterior Ischemic Optic Neuropathy Associated With Anti-PD-L1 Therapy. Issue 1 (27th January 2022)

Authors:
Berry, Ella C.; Mullany, Sean; Quinlivan, Alannah; Craig, Amelia; New-Tolley, Julia; Slattery, James; Sukumaran, Shawgi; Klebe, Sonja; Craig, Jamie E.; Siggs, Owen M.; Wechalekar, Mihir D.
Journal:
Journal of immunotherapy
Issue:
Volume 45:Issue 1(2022)
Page Start:
51
Record Type:
Journal Article
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12. Eosinophilic Vasculitis and Arteritic Anterior Ischemic Optic Neuropathy Associated With Anti-PD-L1 Therapy. Issue 1 (January 2022)

Authors:
Berry, Ella C.; Mullany, Sean; Quinlivan, Alannah; Craig, Amelia; New-Tolley, Julia; Slattery, James; Sukumaran, Shawgi; Klebe, Sonja; Craig, Jamie E.; Siggs, Owen M.; Wechalekar, Mihir D.
Journal:
Journal of immunotherapy
Issue:
Volume 45:Issue 1(2022)
Page Start:
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗

15. Genetic Dissection of Acute Anterior Uveitis Reveals Similarities and Differences in Associations Observed With Ankylosing Spondylitis. Issue 1 (January 2015)

Authors:
Robinson, Philip C.; Claushuis, Theodora A. M.; Cortes, Adrian; Martin, Tammy M.; Evans, David M.; Leo, Paul; Mukhopadhyay, Pamela; Bradbury, Linda A.; Cremin, Katie; Harris, Jessica; Maksymowych, Walter P.; Inman, Robert D.; Rahman, Proton; Haroon, Nigil; Gensler, Lianne; Powell, Joseph E.; van ...
Journal:
Arthritis & rheumatology
Issue:
Volume 67:Issue 1(2015)
Page Start:
140
Record Type:
Journal Article
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16. Gene‐specific facial dysmorphism in Axenfeld‐Rieger syndrome caused by FOXC1 and PITX2 variants. Issue 2 (24th November 2020)

Authors:
Souzeau, Emmanuelle; Siggs, Owen M.; Pasutto, Francesca; Knight, Lachlan S. W.; Perez‐Jurado, Luis A.; McGregor, Lesley; Le Blanc, Shannon; Barnett, Christopher P.; Liebelt, Jan; Craig, Jamie E.
Journal:
American journal of medical genetics
Issue:
Volume 185:Issue 2(2021)
Page Start:
434
Record Type:
Journal Article
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18. Identification of a Novel Oligomerization Disrupting Mutation in CRYΑA Associated with Congenital Cataract in a South Australian Family. Issue 3 (17th January 2013)

Authors:
Laurie, Kate J.; Dave, Alpana; Straga, Tania; Souzeau, Emmanuelle; Chataway, Timothy; Sykes, Matthew J.; Casey, Theresa; Teo, Theodosia; Pater, John; Craig, Jamie E.; Sharma, Shiwani; Burdon, Kathryn P.
Journal:
Human mutation
Issue:
Volume 34:Issue 3(2013:Mar.)
Page Start:
435
Record Type:
Journal Article
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19. Identification of novel mutations causing pediatric cataract in Bhutan, Cambodia, and Sri Lanka. Issue 4 (16th May 2018)

Authors:
Javadiyan, Shari; Lucas, Sionne E. M.; Wangmo, Dechen; Ngy, Meng; Edussuriya, Kapila; Craig, Jamie E.; Rudkin, Adam; Casson, Robert; Selva, Dinesh; Sharma, Shiwani; Lower, Karen M.; Meucke, James; Burdon, Kathryn P.
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 6:Issue 4(2018)
Page Start:
555
Record Type:
Journal Article
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