DIGN
发表于 2025-3-21 18:22:52
书目名称JIMD Reports, Volume 33影响因子(影响力)<br> http://figure.impactfactor.cn/if/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33影响因子(影响力)学科排名<br> http://figure.impactfactor.cn/ifr/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33网络公开度<br> http://figure.impactfactor.cn/at/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33网络公开度学科排名<br> http://figure.impactfactor.cn/atr/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33被引频次<br> http://figure.impactfactor.cn/tc/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33被引频次学科排名<br> http://figure.impactfactor.cn/tcr/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33年度引用<br> http://figure.impactfactor.cn/ii/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33年度引用学科排名<br> http://figure.impactfactor.cn/iir/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33读者反馈<br> http://figure.impactfactor.cn/5y/?ISSN=BK0500071<br><br> <br><br>书目名称JIMD Reports, Volume 33读者反馈学科排名<br> http://figure.impactfactor.cn/5yr/?ISSN=BK0500071<br><br> <br><br>
Arboreal
发表于 2025-3-22 00:15:34
2192-8304 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.978-3-662-55011-3978-3-662-55012-0Series ISSN 2192-8304 Series E-ISSN 2192-8312
FRAX-tool
发表于 2025-3-22 04:10:23
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发怨言
发表于 2025-3-22 06:28:34
Brain White Matter Integrity Mediates the Relationship Between Phenylalanine Control and Executiveprocessing, and MD in the PPO mediated the relationship between Phe exposure and working memory. These exploratory findings demonstrate the importance of using sophisticated modeling procedures to understand the interplay among metabolic control, neural factors, and functional outcomes in individuals with PKU.
Additive
发表于 2025-3-22 09:30:47
Mutations: Is Pontocerebellar Hypoplasia Type 6 a Mitochondrial Encephalopathy?,ns beyond the first report of PCH6 by Edvardson and colleagues. We propose to classify .-associated phenotypes as an early onset mitochondrial encephalopathy, since this is more in agreement with both clinical presentation and underlying genetic cause.
Dri727
发表于 2025-3-22 13:09:45
Missed Newborn Screening Case of Carnitine Palmitoyltransferase-II Deficiency,of disease. We conclude that (1) not all cases of CPT-II deficiency are currently detected through newborn screening, even when blood is appropriately collected on day 2 of life and (2) CPT-II deficiency should be kept on the differential for patients presenting with rhabdomyolysis, even if the newborn screening results were normal.
MIR
发表于 2025-3-22 17:38:19
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ARCH
发表于 2025-3-23 00:55:54
JIMD Reports, Volume 33978-3-662-55012-0Series ISSN 2192-8304 Series E-ISSN 2192-8312
反馈
发表于 2025-3-23 04:55:25
Eva Morava (Editor-in-Chief),Matthias Baumgartner,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
指耕作
发表于 2025-3-23 08:00:38
JIMD Reportshttp://image.papertrans.cn/j/image/500071.jpg