警察在苦笑
发表于 2025-3-21 18:59:50
书目名称Inherited Neuromuscular Diseases影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0466465<br><br> <br><br>书目名称Inherited Neuromuscular Diseases读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0466465<br><br> <br><br>
投票
发表于 2025-3-22 00:04:40
Advances in Experimental Medicine and Biologyhttp://image.papertrans.cn/i/image/466465.jpg
神圣不可
发表于 2025-3-22 04:06:21
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Intentional
发表于 2025-3-22 05:06:25
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hidebound
发表于 2025-3-22 09:45:07
978-94-007-3056-4The Editor(s) (if applicable) and The Author(s), under exclusive license to Springer Nature B.V. 200
confide
发表于 2025-3-22 14:15:55
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Creditee
发表于 2025-3-22 19:40:28
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Jocose
发表于 2025-3-22 22:24:47
Standards of Care for Duchenne Muscular Dystrophy: Brief Treat-NMD Recommendations,d on the generation of brief standards of care for DMD, which are presented here and are available via the TREAT-NMD website (.). Guidelines are presented for diagnostics, neurological follow up, gastrointestinal and nutritional issues, respiratory and cardiac care as well as orthopaedics, rehabilitation, psychosocial interventions and oral care.
fulmination
发表于 2025-3-23 02:50:04
Phenotype and Clinical Evolution of Charcot-Marie-Tooth Disease Type 1A Duplication,d early childhood; (iii) proximal lower-limb musculature involvement as a late phenotypic feature; and (iv) minimal adult phenotype. We also briefly revise genetic, electrophysiological, pathological and neuroimaging data of the disease.
absolve
发表于 2025-3-23 06:23:35
Pathology and Diagnosis of Muscular Dystrophies,approach, necessary to conduct genetic studies and to offer an appropriate genetic counseling. The application of molecular medicine in genetic muscular dystrophies also brings great expectations to the therapeutic management of these patients.