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Titlebook: JIMD Reports, Volume 36; Eva Morava,Matthias Baumgartner,Verena Peters Book 2017 Society for the Study of Inborn Errors of Metabolism (SSI

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發(fā)表于 2025-3-21 17:41:26 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱JIMD Reports, Volume 36
編輯Eva Morava,Matthias Baumgartner,Verena Peters
視頻videohttp://file.papertrans.cn/501/500074/500074.mp4
概述Unique collection of case and research reports on rare metabolic disorders.Contains unusual or previously unrecorded features relevant to metabolic disorders.All contributions rigorously peer-reviewed
叢書名稱JIMD Reports
圖書封面Titlebook: JIMD Reports, Volume 36;  Eva Morava,Matthias Baumgartner,Verena Peters Book 2017 Society for the Study of Inborn Errors of Metabolism (SSI
描述JIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinical or biochemical features of a Mendelian disorder.
出版日期Book 2017
關鍵詞inherited metabolic diseases; pediatrics; medical genetics; Mendelian disorder; endocrinology; metabolic
版次1
doihttps://doi.org/10.1007/978-3-662-56138-6
isbn_softcover978-3-662-56137-9
isbn_ebook978-3-662-56138-6Series ISSN 2192-8304 Series E-ISSN 2192-8312
issn_series 2192-8304
copyrightSociety for the Study of Inborn Errors of Metabolism (SSIEM) 2017
The information of publication is updating

書目名稱JIMD Reports, Volume 36影響因子(影響力)




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書目名稱JIMD Reports, Volume 36網絡公開度學科排名




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書目名稱JIMD Reports, Volume 36被引頻次學科排名




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2192-8304 tabolic disorders.All contributions rigorously peer-reviewedJIMD Reports publishes case and short research reports in the area of inherited metabolic disorders. Case reports highlight some unusual or previously unrecorded feature relevant to the disorder, or serve as an important reminder of clinica
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Irreversibility of Symptoms with Biotin Therapy in an Adult with Profound Biotinidase Deficiency,ting further damage in those who already exhibit irreversible neurological damage. Newborn screening for the disorder would have avoided years of clinical symptoms that now appear to be irreversible with biotin treatment.
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Eva Morava,Matthias Baumgartner,Verena PetersUnique collection of case and research reports on rare metabolic disorders.Contains unusual or previously unrecorded features relevant to metabolic disorders.All contributions rigorously peer-reviewed
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JIMD Reportshttp://image.papertrans.cn/j/image/500074.jpg
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https://doi.org/10.1007/978-3-662-56138-6inherited metabolic diseases; pediatrics; medical genetics; Mendelian disorder; endocrinology; metabolic
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