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A marine lipopeptides-producing Bacillus amyloliquefaciens HY2-1 with a broad-spectrum antifungal and antibacterial activity and its fermentation kinetics study.
- Published in:
- World Journal of Microbiology & Biotechnology, 2023, v. 39, n. 8, p. 1, doi. 10.1007/s11274-023-03643-y
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- Publication type:
- Article
Advances in quantitative MRI of hereditary myopathies.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2021, v. 21, n. 6, p. 448, doi. 10.3969/j.issn.1672-6731.2021.06.004
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- Publication type:
- Article
Characteristics of fatty infiltration and edema of muscle MRI in Duchenne muscular dystrophy patients.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2018, v. 18, n. 7, p. 501
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- Publication type:
- Article
Clinical characteristics and MTMR13/SBF2 gene mutation analysis of a Charcot-Marie-Tooth disease type 4B2 Chinese family.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2018, v. 18, n. 8, p. 582, doi. 10.3969/j.issn.1672-6731.2018.08.005
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- Publication type:
- Article
Limb?girdle muscular dystrophy type 2D: clinical and genetic analysis of a family.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2017, v. 17, n. 8, p. 609, doi. 10.3969/j.issn.1672-6731.2017.08.010
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- Publication type:
- Article
Clinical study of DMD gene point mutation causing Becker muscular dystrophy.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2015, v. 15, n. 6, p. 442, doi. 10.3969/j.issn.1672-6731.2015.06.005
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- Publication type:
- Article
Study on T2 mapping in thigh muscles of patients with Duchenne muscular dystrophy.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2015, v. 15, n. 6, p. 437, doi. 10.3969/j.issn.1672-6731.2015.06.004
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- Publication type:
- Article
Clinical characteristics and gene mutation analysis of riboflavin - responsive lipid storage myopathy: report of 3 cases in 2 families and review of literature.
- Published in:
- 2014
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- Publication type:
- Case Study
Clinical features and genetic analysis of 7 patients with late - onset glycogen storage disease type II.
- Published in:
- Chinese Journal of Contemporary Neurology & Neurosurgery, 2014, v. 14, n. 5, p. 405, doi. 10.3969/j.issn.1672.6731.2014.05.008
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- Publication type:
- Article
Clinical characteristics and gene mutation analysis of riboflavin - responsive lipid storage myopathy: report of 3 cases in 2 families and review of literature.
- Published in:
- 2014
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- Publication type:
- Journal Article