Patricia Crock
Overview
Explore the profile of Patricia Crock including associated specialties, affiliations and a list of published articles.
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23
Citations
413
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Recent Articles
1.
Groeneweg S, van Geest F, Martin M, Dias M, Frazer J, Medina-Gomez C, et al.
Nat Commun
. 2025 Mar;
16(1):2479.
PMID: 40075072
Predicting and quantifying phenotypic consequences of genetic variants in rare disorders is a major challenge, particularly pertinent for 'actionable' genes such as thyroid hormone transporter MCT8 (encoded by the X-linked...
2.
Sanchez-Bezanilla S, Beard D, Hood R, Aberg N, Crock P, Walker F, et al.
Neural Plast
. 2022 Apr;
2022:9983042.
PMID: 35465399
Aims: We have shown that growth hormone (GH) treatment poststroke increases neuroplasticity in peri-infarct areas and the hippocampus, improving motor and cognitive outcomes. We aimed to explore the mechanisms of...
3.
Choong C, Nixon G, Blackmore A, Chen W, Jacoby P, Leonard H, et al.
Eur J Pediatr
. 2022 Mar;
181(6):2491-2500.
PMID: 35316366
Individuals with Prader-Willi syndrome (PWS) often have excessive daytime sleepiness and emotional/behavioral disturbances. The objective of this study was to examine whether daytime sleepiness was associated with these emotional/behavioral problems,...
4.
van Geest F, Groeneweg S, van den Akker E, Bacos I, Barca D, van den Berg S, et al.
J Clin Endocrinol Metab
. 2021 Oct;
107(3):e1136-e1147.
PMID: 34679181
Context: Patients with mutations in thyroid hormone transporter MCT8 have developmental delay and chronic thyrotoxicosis associated with being underweight and having cardiovascular dysfunction. Objective: Our previous trial showed improvement of...
5.
Mackay J, Nixon G, Lafferty A, Ambler G, Kapur N, Bergman P, et al.
J Autism Dev Disord
. 2021 Sep;
52(9):3877-3889.
PMID: 34498151
Prader-Willi syndrome (PWS) is a rare genetic disorder characterised by neurodevelopmental delays, hyperphagia, difficulties with social communication and challenging behaviours. Individuals require intensive supervision from caregivers which may negatively affect...
6.
Caudri D, Nixon G, Nielsen A, Mai L, Hafekost C, Kapur N, et al.
J Paediatr Child Health
. 2021 Aug;
58(2):248-255.
PMID: 34397126
Aim: In children with Prader-Willi syndrome (PWS), growth hormone (GH) improves height and body composition; however, may be associated with worsening sleep-disordered breathing (SDB). Some studies have reported less SDB...
7.
Sanchez-Bezanilla S, Aberg N, Crock P, Walker F, Nilsson M, Isgaard J, et al.
Int J Mol Sci
. 2020 Jul;
21(12).
PMID: 32604953
Cognitive impairment is common after stroke, and disturbances in hippocampal function are often involved, even in remote non-hippocampal injuries. In terms of hippocampal function, growth hormone (GH) is known to...
8.
Groeneweg S, van Geest F, Abaci A, Alcantud A, Ambegaonkar G, Armour C, et al.
Lancet Diabetes Endocrinol
. 2020 Jun;
8(7):594-605.
PMID: 32559475
Background: Disordered thyroid hormone transport, due to mutations in the SLC16A2 gene encoding monocarboxylate transporter 8 (MCT8), is characterised by intellectual and motor disability resulting from cerebral hypothyroidism and chronic...
9.
Sanchez-Bezanilla S, Aberg N, Crock P, Walker F, Nilsson M, Isgaard J, et al.
Int J Mol Sci
. 2020 Jan;
21(2).
PMID: 31963456
Motor impairment is the most common and widely recognised clinical outcome after stroke. Current clinical practice in stroke rehabilitation focuses mainly on physical therapy, with no pharmacological intervention approved to...
10.
Mackay J, McCallum Z, Ambler G, Vora K, Nixon G, Bergman P, et al.
J Paediatr Child Health
. 2019 Jul;
55(9):1029-1037.
PMID: 31257692
Prader-Willi syndrome (PWS) is a rare genetic condition with multi-system involvement. The literature was reviewed to describe neurodevelopment and the behavioural phenotype, endocrine and metabolic disorders and respiratory and sleep...