一加就喷出
发表于 2025-3-23 10:29:54
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Flawless
发表于 2025-3-23 15:07:06
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欢乐中国
发表于 2025-3-23 20:25:47
Limb-Girdle Muscular Dystrophy Type 2Dein defect was recognized to cause the original patients with Duchenne-like females or males and later also a variety of phenotypes in adult cases. Some of them have been treated also with steroids for their similarities to Duchenne dystrophy pathogenesis.
狂怒
发表于 2025-3-24 00:42:04
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NAUT
发表于 2025-3-24 02:40:31
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发怨言
发表于 2025-3-24 07:53:01
https://doi.org/10.1007/978-3-322-98829-4inactivation pattern may result in large groups of negative fibers. Conversely, the skeletal muscle is a syncytium where regeneration is possible, and some nuclei can migrate and compensate for the lack of dystrophin. In the DMD carrier here described, the most relevant sign was dilated cardiomyopathy that required cardiac transplantation.
我悲伤
发表于 2025-3-24 14:17:42
Das Vernehmlassungsverfahren in der Schweizfferent clinical forms, which are now often referred to as laminopathies, include the autosomal dominant form of Emery-Dreifuss muscular dystrophy type 2 and the allelic LGMD1B, familial partial lipodystrophy, axonal neuropathy (CMT2B1), mandibulo-sacral disease, premature ageing (progeria), and restrictive dermopathy.
摇摆
发表于 2025-3-24 15:35:09
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Debark
发表于 2025-3-24 22:02:09
https://doi.org/10.1007/978-3-642-51378-7ed ubiquitin-proteasomal and autophagic degradation in part secondary due to high levels of regeneration and inflammation. The detection of dysferlin deficiency in muscle offers an important diagnostic tool, which has allowed the molecular diagnosis of dysferlinopathy in most patients.
ADORE
发表于 2025-3-25 01:08:28
https://doi.org/10.1007/978-3-322-91962-5rum CK, and mild muscle weakness. Muscle biopsy showed dystrophic changes, inflammatory changes, and severely decreased alpha-dystroglycan. Brain MRI, ophthalmologic examination, and cognitive development were normal.