Stewart Rust
Overview
Explore the profile of Stewart Rust including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
204
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Recent Articles
1.
Schwahn B, Hart C, Smith L, Hart A, Fairbanks L, Arenas-Hernandez M, et al.
Mol Genet Metab
. 2024 Nov;
143(4):108598.
PMID: 39488078
We report the first, and so far, only index patient with neonatal onset MoCD type A who was diagnosed and treated early enough with cPMP to avoid severe brain injury...
2.
Muenzer J, Burton B, Harmatz P, Gutierrez-Solana L, Ruiz-Garcia M, Jones S, et al.
J Inherit Metab Dis
. 2024 Sep;
PMID: 39252529
Mucopolysaccharidosis II (MPS II; Hunter syndrome; OMIM 309900) is a rare, X-linked, heterogeneous lysosomal storage disease. Approximately two-thirds of patients develop cognitive impairment, which is difficult to assess in clinical...
3.
Lum S, Will A, Church H, Mercer J, Tylee K, Poulton K, et al.
Blood Cell Ther
. 2023 Oct;
2(2):31-35.
PMID: 37885827
Hematopoietic cell transplantation (HCT) confers a long-term disease-modifying therapy for transplant-permissive inherited metabolic diseases (IMDs). We examined the overall survival (OS) and engrafted survival (ES) of children with IMDs, who...
4.
Horgan C, Watts K, Ram D, Rust S, Hutton R, Jones S, et al.
JIMD Rep
. 2023 Sep;
64(5):346-352.
PMID: 37701322
Metachromatic leukodystrophy (MLD) results from ARSA gene mutations. Affected individuals meet early milestones before neurological deterioration and early death. Atidarsagene autotemcel (arsa-cel), an autologous haematopoietic stem cell gene therapy (HSC-GT)...
5.
Chen C, Methley A, Naicker R, Rust S, Stepien K
Mol Genet Metab
. 2023 Jan;
138(2):106980.
PMID: 36709537
A systematic review of Randomised Controlled Trials in adult mucopolysaccharidoses (MPSs) was conducted to inform neuropsychology service development at a large tertiary Lysosomal Storage Diseases centre. Studies including psychological endpoints...
6.
Hassall S, Smith D, Rust S, Wittkowski A
J Inherit Metab Dis
. 2022 Feb;
45(3):406-416.
PMID: 35124835
Lysosomal storage disorders are rare multiorgan, degenerative conditions requiring invasive treatment. Rare disorders pose unique challenges; therefore, exploring their impact is crucial for understanding family needs. This novel review aimed...
7.
Wijburg F, Heap F, Rust S, de Ruijter J, Tump E, Marchal J, et al.
Mol Genet Metab
. 2021 Oct;
134(4):317-322.
PMID: 34600820
Introduction: Currently, there is no effective therapy for mucopolysaccharidosis IIIA (MPS IIIA). Intravenously-administered enzyme replacement therapies, while effective in other forms of MPS without neurological involvement, have not been successful...
8.
Ghosh A, Rust S, Langford-Smith K, Weisberg D, Canal M, Breen C, et al.
J Inherit Metab Dis
. 2021 May;
44(5):1248-1262.
PMID: 34047372
The aim of this study was to evaluate the efficacy of high dose genistein aglycone in Sanfilippo syndrome (mucopolysaccharidosis type III). High doses of genistein aglycone have been shown to...
9.
Haselhurst J, Moss K, Rust S, Oliver J, Hughes R, McGrath C, et al.
Clin Child Psychol Psychiatry
. 2020 Nov;
26(1):51-63.
PMID: 33233929
Background: Parents of children with chronic health conditions can face many challenges. The Tree of Life narrative therapy group intervention aims to connect parents with their skills and resources before...
10.
van der Lee J, Morton J, Adams H, Clarke L, Eisengart J, Escolar M, et al.
Mol Genet Metab
. 2020 Sep;
131(1-2):181-196.
PMID: 32917509
Neurological dysfunction represents a significant clinical component of many of the mucopolysaccharidoses (also known as MPS disorders). The accurate and consistent assessment of neuropsychological function is essential to gain a...