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1993 4
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Showing results for (((spinal) AND muscular) AND atrophy) AND ("2011/01/01"[Date - Publication] : "2021/12/31"[Date - Publication])
Your search for (((pinal) AND muscular) AND astrophy) AND ("2011/01/01"[Date - Publication] : "2021/12/31"[Date - Publication]) retrieved no results
Hirayama disease.
Huang YL, Chen CJ. Huang YL, et al. Neuroimaging Clin N Am. 2011 Nov;21(4):939-50, ix-x. doi: 10.1016/j.nic.2011.07.009. Neuroimaging Clin N Am. 2011. PMID: 22032508 Free article. Review.
Hirayama disease (juvenile muscular atrophy of distal upper extremity) is a cervical myelopathy. Predominantly affecting male adolescents, it is characterized by progressive muscular weakness and atrophy of distal upper limbs, followed by spontaneous a …
Hirayama disease (juvenile muscular atrophy of distal upper extremity) is a cervical myelopathy. Predominantly affecting male …
Spinal Muscular Atrophy Treatments, Newborn Screening, and the Creation of a Neurogenetics Urgency.
Butterfield RJ. Butterfield RJ. Semin Pediatr Neurol. 2021 Jul;38:100899. doi: 10.1016/j.spen.2021.100899. Epub 2021 May 29. Semin Pediatr Neurol. 2021. PMID: 34183144 Free PMC article. Review.
Spinal muscular atrophy (SMA) is a progressive neuromuscular disorder characterized by loss of motor neurons leading to muscle weakness and atrophy. ...
Spinal muscular atrophy (SMA) is a progressive neuromuscular disorder characterized by loss of motor neurons leading to …
Respiratory management of children with spinal muscular atrophy (SMA).
Fauroux B, Griffon L, Amaddeo A, Stremler N, Mazenq J, Khirani S, Baravalle-Einaudi M. Fauroux B, et al. Arch Pediatr. 2020 Dec;27(7S):7S29-7S34. doi: 10.1016/S0929-693X(20)30274-8. Arch Pediatr. 2020. PMID: 33357594 Review.
Spinal muscular atrophy (SMA) causes a predominantly bilateral proximal muscle weakness and atrophy. ...
Spinal muscular atrophy (SMA) causes a predominantly bilateral proximal muscle weakness and atrophy. ...
Spinal Muscular Atrophy Revisited.
Dubowitz V. Dubowitz V. Neuromuscul Disord. 2019 Jun;29(6):413-414. doi: 10.1016/j.nmd.2019.06.008. Neuromuscul Disord. 2019. PMID: 31227066 No abstract available.
Infantile spinal muscular atrophy (SMA).
Chabrol B, Desguerre I. Chabrol B, et al. Arch Pediatr. 2020 Dec;27(7S):7S1-7S2. doi: 10.1016/S0929-693X(20)30268-2. Arch Pediatr. 2020. PMID: 33357590 No abstract available.
Muscle type and fiber type specificity in muscle wasting.
Ciciliot S, Rossi AC, Dyar KA, Blaauw B, Schiaffino S. Ciciliot S, et al. Int J Biochem Cell Biol. 2013 Oct;45(10):2191-9. doi: 10.1016/j.biocel.2013.05.016. Epub 2013 May 21. Int J Biochem Cell Biol. 2013. PMID: 23702032 Review.
Muscle wasting occurs in a variety of conditions, including both genetic diseases, such as muscular dystrophies, and acquired disorders, ranging from muscle disuse to cancer cachexia, from heart failure to aging sarcopenia. ...For example, muscle disuse, such as spinal …
Muscle wasting occurs in a variety of conditions, including both genetic diseases, such as muscular dystrophies, and acquired disorde …
[SMA: from gene discovery to gene therapy].
Barkats M. Barkats M. Med Sci (Paris). 2020 Feb;36(2):137-140. doi: 10.1051/medsci/2020010. Epub 2020 Mar 4. Med Sci (Paris). 2020. PMID: 32129749 Free article. Review. French.
Spinal muscular atrophy (SMA) is the most common genetic disease leading to infant mortality. This neuro-muscular disorder is caused by the loss or mutation of the telomeric copy of the 'survival of motor neuron' (Smn) gene, termed SMN1. ...
Spinal muscular atrophy (SMA) is the most common genetic disease leading to infant mortality. This neuro-muscular …
Targeting the myostatin signaling pathway to treat muscle loss and metabolic dysfunction.
Lee SJ. Lee SJ. J Clin Invest. 2021 May 3;131(9):e148372. doi: 10.1172/JCI148372. J Clin Invest. 2021. PMID: 33938454 Free PMC article. Review.
Considerable progress has been made in elucidating key components of this regulatory system, and in parallel with this effort has been the development of numerous biologics that have been tested in clinical trials for a wide range of indications, including muscular dystrop …
Considerable progress has been made in elucidating key components of this regulatory system, and in parallel with this effort has been the d …
Muscle wasting in disease: molecular mechanisms and promising therapies.
Cohen S, Nathan JA, Goldberg AL. Cohen S, et al. Nat Rev Drug Discov. 2015 Jan;14(1):58-74. doi: 10.1038/nrd4467. Nat Rev Drug Discov. 2015. PMID: 25549588 Review.
Atrophy occurs in specific muscles with inactivity (for example, during plaster cast immobilization) or denervation (for example, in patients with spinal cord injuries). ...This loss of muscle function can lead to reduced quality of life, increased morbidity and mor …
Atrophy occurs in specific muscles with inactivity (for example, during plaster cast immobilization) or denervation (for example, in …
Denervation-activated STAT3-IL-6 signalling in fibro-adipogenic progenitors promotes myofibres atrophy and fibrosis.
Madaro L, Passafaro M, Sala D, Etxaniz U, Lugarini F, Proietti D, Alfonsi MV, Nicoletti C, Gatto S, De Bardi M, Rojas-García R, Giordani L, Marinelli S, Pagliarini V, Sette C, Sacco A, Puri PL. Madaro L, et al. Nat Cell Biol. 2018 Aug;20(8):917-927. doi: 10.1038/s41556-018-0151-y. Epub 2018 Jul 26. Nat Cell Biol. 2018. PMID: 30050118 Free PMC article.
Denervation-activated FAPs exhibited persistent STAT3 activation and secreted elevated levels of IL-6, which promoted muscle atrophy and fibrosis. FAPs with aberrant activation of STAT3-IL-6 signalling were also found in mouse models of spinal cord injury, spinal …
Denervation-activated FAPs exhibited persistent STAT3 activation and secreted elevated levels of IL-6, which promoted muscle atrophy …
4,686 results