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UnknownImmunological Profiles in Parry-Romberg Syndrome: A Case-Control Study.
Not available
S-EPMC10932088 | biostudies-literature
UnknownHereditary inclusion-body myopathy with sparing of the quadriceps: the many tiles of an incomplete puzzle.
Not available
S-EPMC3235839 | biostudies-literature
UnknownLongitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy.
Not available
S-EPMC4799716 | biostudies-literature
UnknownMyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle.
Not available
S-EPMC1636567 | biostudies-literature
UnknownUpper limb disease evolution in exon 53 skipping eligible patients with Duchenne muscular dystrophy.
Not available
S-EPMC8528463 | biostudies-literature
UnknownPABPN1 (GCN)11 as a Dominant Allele in Oculopharyngeal Muscular Dystrophy -Consequences in Clinical Diagnosis and Genetic Counselling.
Not available
S-EPMC5271460 | biostudies-literature
UnknownRimeporide as a first- in-class NHE-1 inhibitor: Results of a phase Ib trial in young patients with Duchenne Muscular Dystrophy.
Not available
S-EPMC7482441 | biostudies-literature
UnknownNon-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype.
Not available
S-EPMC5240539 | biostudies-literature
UnknownUpper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial.
Not available
S-EPMC4393256 | biostudies-literature
UnknownA negative feedback loop between fibroadipogenic progenitors and muscle fibres involving endothelin promotes human muscle fibrosis.
Not available
S-EPMC9178170 | biostudies-literature
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