Articles with public access mandates - Monique RyanLearn more
OverallNIHNHMRCNIHRMRCDoDARCTelethonUSEDMedical Research Future Fund, AustraliaDFGYorkshire Cancer Research, UKGovernment of SpainSNSFFWOAcademy of FinlandCancer Research UKDFIDWellcomeGovernment of ItalyCIHRINSERMFCTBHFEuropean CommissionLeducq Foundation, USAFRQSGenome CanadaESRCPCORIPancreatic Cancer, UKSiegel Rare Neuroimmune AssociationCitizen’s United for Research in Epilepsy
Not available anywhere: 20
De novo LMNA mutations cause a new form of congenital muscular dystrophy
S Quijano‐Roy, B Mbieleu, CG Bönnemann, PY Jeannet, J Colomer, ...
Annals of Neurology: Official Journal of the American Neurological …, 2008
Mandates: National Institute of Health and Medical Research, France
An open-label trial in Friedreich ataxia suggests clinical benefit with high-dose resveratrol, without effect on frataxin levels
EM Yiu, G Tai, RE Peverill, KJ Lee, KD Croft, TA Mori, ...
Journal of neurology 262, 1344-1353, 2015
Mandates: National Health and Medical Research Council, Australia
Pediatric Guillain-Barré syndrome
MM Ryan
Current Opinion in Pediatrics 25 (6), 689-693, 2013
Mandates: National Health and Medical Research Council, Australia
Binaural speech processing in individuals with auditory neuropathy
G Rance, MM Ryan, P Carew, LA Corben, E Yiu, J Tan, MB Delatycki
Neuroscience 226, 227-235, 2012
Mandates: National Health and Medical Research Council, Australia
Peripheral nerve ultrasound in pediatric Charcot-Marie-Tooth disease type 1A
EM Yiu, CR Brockley, KJ Lee, K Carroll, K De Valle, R Kennedy, P Rao, ...
Neurology 84 (6), 569-574, 2015
Mandates: National Health and Medical Research Council, Australia
Describing nutrition in spinal muscular atrophy: A systematic review
GE Moore, AW Lindenmayer, GA McConchie, MM Ryan, ZE Davidson
Neuromuscular Disorders 26 (7), 395-404, 2016
Mandates: National Health and Medical Research Council, Australia
Acute flaccid myelitis in childhood: a retrospective cohort study
EW Andersen, AJ Kornberg, JL Freeman, RJ Leventer, MM Ryan
European journal of neurology 24 (8), 1077-1083, 2017
Mandates: National Health and Medical Research Council, Australia
Mutations in the cyclic adenosine monophosphate response element of the tyrosine hydroxylase gene
MM Verbeek, GCH Steenbergen‐Spanjers, MAAP Willemsen, FA Hol, ...
Annals of neurology 62 (4), 422-426, 2007
Mandates: Swiss National Science Foundation
Genetic, radiologic, and clinical variability in Brown-Vialetto-van Laere syndrome
IR Woodcock, MP Menezes, L Coleman, J Yaplito-Lee, H Peters, ...
Seminars in Pediatric Neurology 26, 2-9, 2018
Mandates: National Health and Medical Research Council, Australia
A diagnostic approach to recurrent myalgia and rhabdomyolysis in children
EK Chan, AJ Kornberg, MM Ryan
Archives of Disease in Childhood 100 (8), 793-797, 2015
Mandates: National Health and Medical Research Council, Australia
Acute flaccid myelitis: a clinical review
OC Murphy, CA Pardo
Seminars in neurology 40 (02), 211-218, 2020
Mandates: Siegel Rare Neuroimmune Association
The effects of calf massage in boys with Duchenne muscular dystrophy: a prospective interventional study
K Carroll, EM Yiu, MM Ryan, RA Kennedy, K de Valle
Disability and rehabilitation 43 (26), 3803-3809, 2021
Mandates: National Health and Medical Research Council, Australia
A homozygous UBA5 pathogenic variant causes a fatal congenital neuropathy
M Cabrera-Serrano, DJ Coote, D Azmanov, H Goullee, E Andersen, ...
Journal of medical genetics 57 (12), 835-842, 2020
Mandates: National Health and Medical Research Council, Australia, Government of Spain
Pathogenic mechanisms underlying X-linked Charcot-Marie-Tooth neuropathy (CMTX6) in patients with a pyruvate dehydrogenase kinase 3 mutation
G Perez-Siles, C Ly, A Grant, AP Drew, EM Yiu, MM Ryan, DT Chuang, ...
Neurobiology of disease 94, 237-244, 2016
Mandates: US National Institutes of Health, National Health and Medical Research …
Autosomal dominant congenital spinal muscular atrophy–A possible developmental deficiency of motor neurones?
S Reddel, RA Ouvrier, G Nicholson, I Dierick, J Irobi, V Timmerman, ...
Neuromuscular Disorders 18 (7), 530-535, 2008
Mandates: Research Foundation (Flanders)
Physical activity and the use of standard and complementary therapies in Duchenne and Becker muscular dystrophies
KL Valle, ZE Davidson, RA Kennedy, MM Ryan, KM Carroll
Journal of pediatric rehabilitation medicine 9 (1), 55-63, 2016
Mandates: National Health and Medical Research Council, Australia
Development of clinical practice guidelines for allied health and nursing assessment and management of Duchenne muscular dystrophy
ZE Davidson, P Bray, K Rose, MJ Rodrigues, L Corben, KN North, ...
Disability and Rehabilitation 44 (19), 5450-5467, 2022
Mandates: National Health and Medical Research Council, Australia, UK Medical Research …
Infantile-onset myelin protein zero–related demyelinating neuropathy presenting as an upper extremity monoplegia
EM Yiu, J Wanigasinghe, MT Mackay, M Gonzales, GA Nicholson, ...
Seminars in Pediatric Neurology 26, 52-55, 2018
Mandates: National Health and Medical Research Council, Australia
Effect of a multicomponent nutritional supplement on functional outcomes for Duchenne muscular dystrophy: a randomized controlled trial
ZE Davidson, I Hughes, MM Ryan, AJ Kornberg, AG Cairns, K Jones, ...
Clinical Nutrition 40 (7), 4702-4711, 2021
Mandates: National Health and Medical Research Council, Australia
Safety and efficacy of intra-erythrocyte dexamethasone sodium phosphate in children with ataxia telangiectasia (ATTeST): a multicentre, randomised, double-blind, placebo …
S Zielen, T Crawford, L Benatti, M Magnani, M Kieslich, M Ryan, I Meyts, ...
The Lancet Neurology 23 (9), 871-882, 2024
Mandates: European Commission
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