Search Results - "Bolaño, C."
-
1
O04 Myoguide.org: a web-based portal supporting the analysis of MRIs for the diagnosis of neuromuscular patients
Published in Neuromuscular disorders : NMD (01-10-2023)“…Muscle magnetic resonance imaging (MRI) is a useful tool to study muscle structure in patients with genetic neuromuscular diseases (NMDs), as it can easily…”
Get full text
Journal Article -
2
P123 MRI based criteria to differentiate dysferlinopathies from other genetic muscle diseases
Published in Neuromuscular disorders : NMD (01-10-2023)“…Muscle MRI is a useful tool for the diagnosis of neuromuscular diseases as it identifies selective patterns of pathology that are characteristic of a specific…”
Get full text
Journal Article -
3
674P Quantification of skeletal muscle glycogen in late onset Pompe patients using carbon MR spectroscopy at 3 Tesla
Published in Neuromuscular disorders : NMD (01-10-2024)“…Pompe disease is a rare genetic disorder resulting from a deficiency of the enzyme alpha-glucosidase. Late onset Pompe patients (LOPD) develop slowly…”
Get full text
Journal Article -
4
P124 A series of dysferlinopathy patients showing fluctuations in muscle fat fraction and contractile cross-sectional area values (cCSA) over a 3-year follow-up period
Published in Neuromuscular disorders : NMD (01-10-2023)“…Dysferlinopathy is produced by mutations in the DYSF gene causing loss of dysferlin expression leading to progressive muscle weakness. Patients show different…”
Get full text
Journal Article -
5
281P Prognostic significance of ACTN3 genotype in Duchenne muscular dystrophy: findings from an Argentine patient cohort
Published in Neuromuscular disorders : NMD (01-10-2024)“…A wide phenotypic spectrum exists among DMD patients, with genetic modifiers seen as a putative cause of this variability. The main aim was to evaluate the…”
Get full text
Journal Article -
6
P.111 Nusinersen in children and adults with spinal muscular atrophy in Argentina: Real world experienc
Published in Neuromuscular disorders : NMD (01-10-2022)Get full text
Journal Article -
7
224P Psychosocial discussions in neuromuscular clinics from a professional lens: evidence from a service evaluation regarding barriers to discussions
Published in Neuromuscular disorders : NMD (01-10-2024)“…Neuromuscular disorders have a high symptom burden and are frequently associated with many adverse psychosocial outcomes, particularly reduced quality of life…”
Get full text
Journal Article -
8
P246 Non-glucocorticoid related comorbidities in adults with Duchenne muscular dystrophy
Published in Neuromuscular disorders : NMD (01-10-2023)“…Life expectancy in individuals with Duchenne muscular dystrophy (DMD) has been extended due to implementation of multidisciplinary care. This has led to an…”
Get full text
Journal Article -
9
P243 Functional abilities, respiratory and cardiac function in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids
Published in Neuromuscular disorders : NMD (01-10-2023)“…According to care recommendations for Duchenne muscular dystrophy (DMD), glucocorticoids should be continued after loss of ambulation. However, their effect in…”
Get full text
Journal Article -
10
Axial involvement as a prominent feature in SMPX-related distal myopathy
Published in Neuromuscular disorders : NMD (01-06-2024)Get full text
Journal Article -
11
Effects of buspirone on influenza A virus infection in stressed mice
Published in Life sciences (1973) (1995)“…Experiments were conducted to evaluate the effects of chronic buspirone (1 mg/kg/day) on the influenza A (PR-8/34) virus specific immune injury in CD-1 mice…”
Get more information
Journal Article -
12
Allelopathic Effects of Tree Species on Some Soil Microbial Populations and Herbaceous Plants
Published in Biologia plantarum (01-01-2001)“…The allelopathic potential of four tree species on soil microbial populations and some herbaceous plants (two understory species and one general biotest…”
Get full text
Journal Article -
13
655P Predictive modelling of dysferlinopathy progression: a longitudinal fat fraction analysis
Published in Neuromuscular disorders : NMD (01-10-2024)“…Skeletal muscle quantitative muscle magnetic resonance imaging (MRI) is sensitive to changes in fat content over time. The Dysferlinopathy Clinical Outcome…”
Get full text
Journal Article -
14
P122 Longitudinal Dixon Magnetic Resonance Imaging in dysferlinopathy patients can provide a powerful tool in assessing outcomes of therapeutic interventions
Published in Neuromuscular disorders : NMD (01-10-2023)“…Fat replacement in muscles measured by Dixon MRI provides an excellent marker for disease progression in dysferlinopathy patients. Although no specific…”
Get full text
Journal Article -
15
MUSCLE IMAGING – MRI
Published in Neuromuscular disorders : NMD (01-10-2020)Get full text
Journal Article -
16
MUSCLE IMAGING – MRI: P.162 The use of muscle MRI in the diagnosis of neuromuscular diseases
Published in Neuromuscular disorders : NMD (01-10-2020)Get full text
Journal Article -
17
653P Rapid quantitative assessment of sodium dynamics after exercise using 23Na-MRI in dysferlinopathy and healthy controls
Published in Neuromuscular disorders : NMD (01-10-2024)“…Dysferlin plays a key role in cell membrane repair, and its absence or malfunction in patients with dysferlin-deficient limb girdle muscular dystrophy leads to…”
Get full text
Journal Article -
18
631P Respiratory function and trajectories in facioscapulohumeral muscular dystrophy (FSHD): a clinical audit
Published in Neuromuscular disorders : NMD (01-10-2024)“…Facioscapulohumeral Muscular Dystrophy (FSHD) is a slowly progressive autosomal dominant neuromuscular condition causing asymmetrical muscle weakness mostly…”
Get full text
Journal Article -
19
208P Are people living with neuromuscular disorders in the north of England satisfied with National Health Service wheelchair service provision?
Published in Neuromuscular disorders : NMD (01-10-2024)“…People living with neuromuscular disorders (NMD) often describe weakness, reduced mobility, falls, pain and fatigue as factors requiring mobility support with…”
Get full text
Journal Article -
20