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	221	A case report of autoimmune necrotizing myositis presenting as dysphagia and neck swelling Enthalten in BMC ear, nose and throat disorders Bd. 16, 17.5.2016, Nr. 1, date:1.2016: 1-5
	222	A case report of thoracolumbar paraspinal myopathy as the cause of camptocormia in a patient with atypical parkinsonism Enthalten in BMC neurology Bd. 17, 23.6.2017, Nr. 1, date:12.2017: 1-6
	223	A comparative study of bone biopsies from the iliac crest, the tibial bone, and the lumbar spine Enthalten in BMC nephrology Bd. 18, 13.4.2017, Nr. 1, date:12.2017: 1-6
	224	A critical role of E2F transcription factor 2 in proinflammatory cytokines-dependent proliferation and invasiveness of fibroblast-like synoviocytes in rheumatoid Arthritis Enthalten in Scientific reports Bd. 8, 8.2.2018, Nr. 1, date:12.2018: 1-10
	225	A diagnostic biomarker profile for fibromyalgia syndrome based on an NMR metabolomics study of selected patients and controls Enthalten in BMC neurology Bd. 17, 11.5.2017, Nr. 1, date:12.2017: 1-15
	226	A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: a case study and literature review Enthalten in BMC neurology Bd. 17, 6.1.2017, Nr. 1, date:12.2017: 1-6
	227	A mouse anti-myostatin antibody increases muscle mass and improves muscle strength and contractility in the mdx mouse model of Duchenne muscular dystrophy and its humanized equivalent, domagrozumab (PF-06252616), increases muscle volume in cynomolgus monkeys Enthalten in Skeletal muscle Bd. 7, 9.11.2017, Nr. 1, date:12.2017: 1-12
	228	A novel mouse model carrying a human cytoplasmic dynein mutation shows motor behavior deficits consistent with Charcot-Marie-Tooth type 2O disease Enthalten in Scientific reports Bd. 8, 29.1.2018, Nr. 1, date:12.2018: 1-10
	229	A novel scoring system based on common laboratory tests predicts the efficacy of TNF-inhibitor and IL-6 targeted therapy in patients with rheumatoid arthritis: a retrospective, multicenter observational study Enthalten in Arthritis Research & Therapy Bd. 19, 11.8.2017, Nr. 1, date:12.2017: 1-9
	230	A novel SYNE1 gene mutation in a Chinese family of Emery-Dreifuss muscular dystrophy-like Enthalten in BMC medical genetics Bd. 18, 5.6.2017, Nr. 1, date:12.2017: 1-6

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