Fukutin-related protein (FKRP) is a putative glycosyltransferase that mediate O-linked glycosylation of the α-dystroglycan. Mutations in the FKRP gene cause a spectrum of diseases ranging from a limb girdle muscular dystrophy 2I (LGMD2I), to severe Walker-Warburg or muscle-eye-brain forms and a congenital muscular dystrophy (with or without...
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2014 (v1)PublicationUploaded on: March 27, 2023
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2024 (v1)Publication
Chemotherapy and radiotherapy are widely used in the treatment of central nervous system tumors and acute lymphocytic leukemia even in the pediatric population. However, such treatments run the risk of a broad spectrum of cognitive and neurological deficits. Even though the correlation with cognitive decline is still not clear,...
Uploaded on: July 3, 2024 -
2022 (v1)Publication
N-methyl-D-aspartate receptors (NMDAR) are di-or tri-heterotetrameric ligand-gated ion channels composed of two obligate glycine-binding GluN1 subunits and two glutamate-binding GluN2 or GluN3 subunits, encoded by GRIN1, GRIN2A-D, and GRIN3A-B receptor genes respectively. Each NMDA receptor subtype has different temporal and spatial expression...
Uploaded on: February 14, 2024 -
2015 (v1)Publication
Magnetic Resonance (MR) Imaging and Spectroscopy of the muscle is a valuable tool in the diagnosis and monitoring of Neuromuscular Disorders (NMD). New Ultra-High Field (UHF) 7 T MRI systems, with their enhanced Signal-to-Noise Ratio, may offer increased image quality in terms of spatial resolution and/or shorter scanning time compared to lower...
Uploaded on: April 14, 2023 -
2022 (v1)Publication
IntroductionStroke-like syndrome (SLS) is a rare subacute neurological complication of intrathecal or high-dose (>= 500 mg) Methotrexate (MTX) administration. Its clinical features, evoking acute cerebral ischaemia with fluctuating course symptoms and a possible spontaneous resolution, have elicited interest among the scientific community....
Uploaded on: February 14, 2024 -
2018 (v1)Publication
The aim of the study was to establish 24 month changes in upper limb function using a revised version of the performance of upper limb test (PUL 2.0) in a large cohort of ambulant and non-ambulant boys with Duchenne muscular dystrophy and to identify possible trajectories of progression. Of the 187 patients studied, 87 were ambulant (age range:...
Uploaded on: October 11, 2023 -
2024 (v1)Publication
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Uploaded on: October 11, 2024