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Physiopathology of vesico-ureteral reflux.
Arena S, Iacona R, Impellizzeri P, Russo T, Marseglia L, Gitto E, Romeo C. Arena S, et al. Ital J Pediatr. 2016 Nov 29;42(1):103. doi: 10.1186/s13052-016-0316-x. Ital J Pediatr. 2016. PMID: 27899160 Free PMC article. Review.
Vescico-Ureteral Reflux (VUR) is a common condition in childhood, caused by a congenital anomaly at the Vescico-Ureteral Junction (VUJ) level. It seems that the main cause could be an abnormal embryological development occurred during the early stage of fetal life.R …
Vescico-Ureteral Reflux (VUR) is a common condition in childhood, caused by a congenital anomaly at the Vescico-Ureteral Junction (VU …
The role of the dystrophin glycoprotein complex on the neuromuscular system.
Belhasan DC, Akaaboune M. Belhasan DC, et al. Neurosci Lett. 2020 Mar 23;722:134833. doi: 10.1016/j.neulet.2020.134833. Epub 2020 Feb 10. Neurosci Lett. 2020. PMID: 32057921 Free PMC article. Review.
This complex is critical in maintaining the structural integrity of muscle fibers and the stability of the neuromuscular synapse. The DGC consists of dystrophin and its utrophin homolog, as well as dystroglycans, sarcoglycans, sarcospan, syntrophins, and dyst …
This complex is critical in maintaining the structural integrity of muscle fibers and the stability of the neuromuscular synap …
Current knowledge of dystrophin and dystrophin-associated proteins in the retina.
Ueda H, Baba T, Ohno S. Ueda H, et al. Histol Histopathol. 2000 Jul;15(3):753-60. doi: 10.14670/HH-15.753. Histol Histopathol. 2000. PMID: 10963120 Review.
DMD gene product, dystrophin, is a submembranous cytoskeletal protein and many dystrophin-associated proteins (DAPs) have been identified, such as utrophin, dystroglycans, sarcoglycans, syntrophins and dystrobrevins. Dystrophin and DAPs are very important proteins not only …
DMD gene product, dystrophin, is a submembranous cytoskeletal protein and many dystrophin-associated proteins (DAPs) have been identified, s …
Clinical and morphological phenotype of the filamin myopathy: a study of 31 German patients.
Kley RA, Hellenbroich Y, van der Ven PF, Fürst DO, Huebner A, Bruchertseifer V, Peters SA, Heyer CM, Kirschner J, Schröder R, Fischer D, Müller K, Tolksdorf K, Eger K, Germing A, Brodherr T, Reum C, Walter MC, Lochmüller H, Ketelsen UP, Vorgerd M. Kley RA, et al. Brain. 2007 Dec;130(Pt 12):3250-64. doi: 10.1093/brain/awm271. Brain. 2007. PMID: 18055494 Review.
Mutations in the filamin C gene (FLNC) cause a myofibrillar myopathy (MFM), morphologically characterized by focal myofibrillar destruction and abnormal accumulation of several proteins within skeletal muscle fibres. ...Patients frequently developed respirato …
Mutations in the filamin C gene (FLNC) cause a myofibrillar myopathy (MFM), morphologically characterized by focal myofibrillar destruction …
[Muscle pathologic diagnosis--mechanism in muscle fiber degeneration].
Nonaka I. Nonaka I. Rinsho Shinkeigaku. 1994 Dec;34(12):1279-81. Rinsho Shinkeigaku. 1994. PMID: 7774135 Review. Japanese.
In various neuromuscular diseases, the most significant muscle degeneration is muscle fiber necrosis as seen in Duchenne muscular dystrophy (DMD). ...The muscle fiber then undergoes necrosis and allows macrophage invasion, followed by muscle …
In various neuromuscular diseases, the most significant muscle degeneration is muscle fiber necrosis as seen in Duchenn …