Cookies on this website

We use cookies to ensure that we give you the best experience on our website. If you click 'Accept all cookies' we'll assume that you are happy to receive all cookies and you won't see this message again. If you click 'Reject all non-essential cookies' only necessary cookies providing core functionality such as security, network management, and accessibility will be enabled. Click 'Find out more' for information on how to change your cookie settings.

Search results (14)

« Back to Publications

Evaluation atraumatique de modèles murins de maladies musculaires génétiques

Martins Bach AB., (2026)

Exploring the relationship between cognitive performance and magnetic resonance imaging diffusion parameters in elderly individuals

Rodrigues MAS. et al, (2025), einstein (São Paulo), 23

TDP-43-M323K causes abnormal brain development and progressive cognitive and motor deficits associated with mislocalised and increased levels of TDP-43

Godoy-Corchuelo JM. et al, (2023)

Mutation in the FUS nuclear localisation signal domain causes neurodevelopmental and systemic metabolic alterations

Ali Z. et al, (2023), Disease Models & Mechanisms, 16

FUSDelta14 mutation impairs normal brain development and causes systemic metabolic alterations

Godoy-Corchuelo JM. et al, (2023)

7,8-dihydroxyflavone enhances long-term spatial memory and alters brain volume in wildtype mice.

Rawlings-Mortimer F. et al, (2023), Front Syst Neurosci, 17

Phenotypic and genetic associations of quantitative magnetic susceptibility in UK Biobank brain imaging

Wang C. et al, (2022), Nature Neuroscience, 25, 818 - 831

Non-invasive assessment of skeletal muscle fibrosis in mice using nuclear magnetic resonance imaging and ultrasound shear wave elastography

Martins-Bach AB. et al, (2021), Scientific Reports, 11

Nuclear defects in skeletal muscle from a Dynamin 2-linked centronuclear myopathy mouse model

Fongy A. et al, (2019), Scientific Reports, 9

Structural and Functional Alterations of Skeletal Muscle Microvasculature in Dystrophin-Deficient mdx Mice

Latroche C. et al, (2015), The American Journal of Pathology, 185, 2482 - 2494

A normal life without muscle dystrophin

Zatz M. et al, (2015), Neuromuscular Disorders, 25, 371 - 374

Quantitative T2 Combined with Texture Analysis of Nuclear Magnetic Resonance Images Identify Different Degrees of Muscle Involvement in Three Mouse Models of Muscle Dystrophy: mdx, Largemyd and mdx/Largemyd

Martins-Bach AB. et al, (2015), PLOS ONE, 10, e0117835 - e0117835

Dmdmdx/Largemyd: a new mouse model of neuromuscular diseases useful for studying physiopathological mechanisms and testing therapies

Martins PCM. et al, (2013), Disease Models & Mechanisms

Metabolic profile of dystrophic mdx mouse muscles analyzed with in vitro magnetic resonance spectroscopy (MRS)

Martins-Bach AB. et al, (2012), Magnetic Resonance Imaging, 30, 1167 - 1176