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Isolation of Human Adult Stem Cells from Muscle Biopsy for Future Treatment of Urinary Incontinence
PURPOSE: To find a suitable and cost-effective technique for isolation and culture of muscle-derived stem cells (MDSCs) obtained from muscle biopsy in large quantities.MATERIALS AND METHODS: A small muscle biopsy was taken from 10 donor rectus muscles in
Farzaneh Sharifiaghdas +2 more
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Needle muscle biopsy and its application
Needle muscle biopsy is a straightforward and reliable minimally-invasive technique. During the past century, the needle biopsy can provide adequate samples and the technique has gradually gained wider acceptance. Compared with open biopsy, needle biopsy
Meng-long CHEN, Cheng ZHANG
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IntroductionConventionally, we rely on transurethral resection of bladder tumour (TURBT) for local staging of muscle-invasive bladder cancer (MIBC). However, the procedure is limited by its staging inaccuracy which may delay the definitive treatment of ...
Jeremy Yuen-Chun Teoh +10 more
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This short overview recalls the basic principles and technical aspects of skin and skeletal muscle biopsies in humans with paying special attention to the stages of these procedures essential for further correct morphological diagnosis.
Dorota Dziewulska +2 more
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Resistance-Based Muscle Therapy, Frailty, and Muscle Biopsy Findings in Kidney Transplant Candidates: A Clinical Trial. [PDF]
Bartlett ST +14 more
europepmc +3 more sources
Muscle biopsy: what and why and when?
Skeletal muscle biopsy remains an important investigative tool in the diagnosis of a variety of muscle disorders. Traditionally, someone with a limb-girdle muscle weakness, myopathic changes on electrophysiology and raised serum creatine kinase (CK ...
J. Walters, A. Baborie
semanticscholar +1 more source
Recently, percutaneous microbiopsy needles have been used as a less invasive alternative to the Bergstrom needle for obtaining human skeletal muscle biopsy to assess changes in protein content, gene expression, and enzymatic activities.
Patrick J. Drouin +3 more
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Characterization of early disease status in treatment-naive male paediatric patients with Fabry disease enrolled in a randomized clinical trial. [PDF]
Trial designThis analysis characterizes the degree of early organ involvement in a cohort of oligo-symptomatic untreated young patients with Fabry disease enrolled in an ongoing randomized, open-label, parallel-group, phase 3B clinical trial.MethodsMales
An Haack, Kristina +17 more
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Diverse myopathological features in the congenital myasthenia syndrome with GFPT1 mutation
Introduction Mutations in the GFPT1 gene are associated with a particular subtype of congenital myasthenia syndrome (CMS) called limb‐girdle myasthenia with tubular aggregates.
Kaiyan Jiang +9 more
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