Search Results - "Procopis, Peter"

DHDDS and NUS1: A Converging Pathway and Common Phenotype.

Authors: Williams, Laura J. Waller, Sophie Qiu, Jessica et al.

Source: Movement Disorders Clinical Practice. Jan2024, Vol. 11 Issue 1, p76-85. 10p.

NAD(P)HX dehydratase (NAXD) deficiency: a novel neurodegenerative disorder exacerbated by febrile illnesses.

Authors: Bergen, Nicole J Van Guo, Yiran Rankin, Julia et al.

Source: Brain: A Journal of Neurology; Jan2019, Vol. 142 Issue 1, p50-58, 9p

GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome.

Authors: Sankaran, Bindu Parayil Gupta, Sachin Tchan, Michel et al.

Source: Orphanet Journal of Rare Diseases. 11/3/2021, Vol. 16 Issue 1, p1-12. 12p.

Examination Paediatrics; A Guide to Paediatric Training.

Authors: Procopis, Peter G.

Source: Journal of paediatrics and child health Apr2007; Vol. 43 (4).

Journal Info: Publisher: Wiley-Blackwell ISSN: 1034-4810

Book Reviews: 4.

Authors: Procopis, Peter

Source: Journal of paediatrics and child health Jan2006; Vol. 42 (1/2).

Journal Info: Publisher: Wiley-Blackwell ISSN: 1034-4810