Zobrazeno 1 - 10
of 870
pro vyhledávání: '"Muscle MRI"'
Autor:
Usha Sinha, Shantanu Sinha
Publikováno v:
Tomography, Vol 10, Iss 9, Pp 1411-1438 (2024)
This review is focused on the current status of quantitative MRI (qMRI) of skeletal muscle. The first section covers the techniques of qMRI in muscle with the focus on each quantitative parameter, the corresponding imaging sequence, discussion of the
Externí odkaz:
https://doaj.org/article/acfa47cf12e64c1db5f7a15bd39547db
Autor:
Mainak Bardhan, Kiran Polavarapu, Dipti Baskar, Veeramani Preethish-Kumar, Seena Vengalil, Saraswati Nashi, Valakunja H. Ganaraja, Dinesh Sharma, Karthik Kulanthaivelu, B.N. Nandeesh, Atchayaram Nalini
Publikováno v:
Global Medical Genetics, Vol 11, Iss 02, Pp 167-174 (2024)
Introduction VMA21-related myopathy is one of the rare forms of slowly progressive myopathy observed in males. Till now, there have been only a handful of reports, mainly from Europe and America, and two reports from India.
Externí odkaz:
https://doaj.org/article/6b926896a46547af87bc6f517017fd4d
Publikováno v:
BMC Musculoskeletal Disorders, Vol 25, Iss 1, Pp 1-7 (2024)
Abstract Background A few patients with inflammatory myopathy showed anti-mitochondrial antibody (AMA) positivity. This study aimed to report the clinical and pathological findings with vacuoles in 3 cases of such patients. Methods Three cases with m
Externí odkaz:
https://doaj.org/article/b1c684394d2446afa249fb8a3eaa3d53
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Autor:
Ryo Morishima, Benedikt Schoser
Publikováno v:
Muscles, Vol 2, Iss 4, Pp 374-388 (2023)
Skeletal muscle MRI studies in limb-girdle muscular dystrophy (LGMD) have increased over the past decades, improving the utility of MRI as a differential diagnostic tool. Nevertheless, the relative rarity of individual genotypes limits the scope of w
Externí odkaz:
https://doaj.org/article/296cd39842184d36ad14b7d562932eb4
Autor:
Andrey F. Vasilenko, Maria I. Karpova, Maria V. Shestakova, Yulia V. Putintseva, Olga V. Podobed, Gleb Yu. Novikov, Igor V. Kochetkov
Publikováno v:
Клинический разбор в общей медицине, Vol 4, Iss 10, Pp 76-82 (2023)
Kennedy disease is a rare neuromuscular disease associated with damage of androgen receptor gene and inherited by the X-linked recessive type. Its clinic features is characterized by a complex of neurological and extraneural disorders, including extr
Externí odkaz:
https://doaj.org/article/12cdafd863f54c9aa5b6443e231893c9
Autor:
Claire L Wood, Kieren G Hollingsworth, Edrina Bokaie, Eric Hughes, Robert Muni-Lofra, Anna Mayhew, Rod T Mitchell, Michela Guglieri, Joseph McElvaney, Timothy D Cheetham, Volker Straub
Publikováno v:
Endocrine Connections, Vol 12, Iss 12, Pp 1-12 (2023)
Glucocorticoids (GCs) reduce inflammation and preserve muscle function in boys with Duchenne muscular dystrophy (DMD) but cause pubertal delay. Pubertal induction with testosterone is recommended but longer-term outcome is unknown. Objective: To asse
Externí odkaz:
https://doaj.org/article/db405beaad49493dbc40bf202b1d89db
Autor:
Klaus Engelke, Oliver Chaudry, Lena Gast, Mootaz AB. Eldib, Ling Wang, Jean-Denis Laredo, Georg Schett, Armin M. Nagel
Publikováno v:
Journal of Orthopaedic Translation, Vol 42, Iss , Pp 57-72 (2023)
Background: Magnetic resonance imaging (MRI) is the dominant 3D imaging modality to quantify muscle properties in skeletal muscle disorders, in inherited and acquired muscle diseases, and in sarcopenia, in cachexia and frailty. Methods: This review c
Externí odkaz:
https://doaj.org/article/0614ebc09fea4b1e95865b688fa81e5f
Publikováno v:
Frontiers in Neurology, Vol 14 (2023)
ObjectivesThis study aimed to assess the feasibility of a machine learning-based radiomics tools to discriminate between Limb-girdle muscular dystrophy R2 (LGMDR2) and immune-mediated necrotizing myopathy (IMNM) using lower-limb muscle magnetic reson
Externí odkaz:
https://doaj.org/article/c487971b4ea5441cb4c90de83ec2ff00
Autor:
Jon Christiansen, Anne-Katrin Güttsches, Ulrike Schara-Schmidt, Matthias Vorgerd, Christoph Heute, Corinna Preusse, Werner Stenzel, Andreas Roos
Publikováno v:
Genes and Diseases, Vol 9, Iss 6, Pp 1506-1520 (2022)
Anoctamin-5 (ANO5) is a multi-pass membrane protein localized to the sarcolemma and the sarcoplasmic reticulum. Mutations were linked to rare autosomal recessive muscle diseases. Here, we summarize the clinical spectrum, imaging data and molecular re
Externí odkaz:
https://doaj.org/article/fd7fc8e1d2884268b14f0f49d33cfa0b