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Titlebook: JIMD Reports, Volume 32; Eva Morava (Editor-in-Chief),Matthias Baumgartner, Book 2017 SSIEM and Springer-Verlag Berlin Heidelberg 2017 inh

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發(fā)表于 2025-3-21 17:15:35 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書目名稱JIMD Reports, Volume 32
編輯Eva Morava (Editor-in-Chief),Matthias Baumgartner,
視頻videohttp://file.papertrans.cn/501/500070/500070.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 32;  Eva Morava (Editor-in-Chief),Matthias Baumgartner, Book 2017 SSIEM and Springer-Verlag Berlin Heidelberg 2017 inh
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(guān)鍵詞inherited metabolic diseases; pediatrics; medical genetics; Mendelian disorder; endocrinology; metabolic
版次1
doihttps://doi.org/10.1007/978-3-662-54385-6
isbn_softcover978-3-662-54384-9
isbn_ebook978-3-662-54385-6Series ISSN 2192-8304 Series E-ISSN 2192-8312
issn_series 2192-8304
copyrightSSIEM and Springer-Verlag Berlin Heidelberg 2017
The information of publication is updating

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Four Years of Diagnostic Challenges with Tetrahydrobiopterin Deficiencies in Iranian Patients,otometry. Differential diagnosis was conducted for PKU, transient HPA, and BH. deficiencies..Our results indicated that out of 76 cases involving BH. deficiencies, 37 had 6-pyruvoyl-tetrahydropterin synthase (PTPS) deficiency, 35 had DHPR deficiency, 1 case had pterin-4a-carbinolamine dehydratase (P
板凳
發(fā)表于 2025-3-22 04:02:19 | 只看該作者
Endurance Exercise Training in Young Adults with Barth Syndrome: A Pilot Study,ercise testing or training for any participant. Peak oxygen consumption modestly (~5%) improved in three or four participants. Mean quality of life questions regarding dyspnea and side effects from medications significantly improved following exercise training. Mean resting heart function or skeleta
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Reliable Diagnosis of Carnitine Palmitoyltransferase Type IA Deficiency by Analysis of Plasma Acylcristic (ROC) curves were calculated based on samples of the whole patient population.. Concentrations of C0 in plasma were normal in all CPT-IA deficient patient samples. ROC analyses showed highest diagnostic values for C18:0-ac, C18:1-ac, and ∑lc-ac (AUC 1.000) and lowest for C0 (AUC 0.738). Combi
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發(fā)表于 2025-3-22 16:39:34 | 只看該作者
Relationships Between Childhood Experiences and Adulthood Outcomes in Women with PKU: A Qualitativehood factors have a combined, long-term impact. These findings have significant clinical implications, suggesting that early psychosocial intervention relating to these identified childhood experiences has the potential to enhance positive outcomes for adults with PKU.
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發(fā)表于 2025-3-22 19:00:52 | 只看該作者
,The Effect of S-Adenosylmethionine on Self-Mutilation in a Patient with Lesch–Nyhan Disease,total of 1,762 events of self-mutilation were recorded, of which 1,281 events were in the placebo period and 481 in the verum period. The daily mean of events was 8.6 with placebo and 4.5 with SAM corresponding to a 50?% decrease in self-mutilation events under SAM treatment (.?
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Low Protein Formula: Consequences of Quantitative Effects of Pre-analytical Factors on Amino Acid Co 4.5?h and the daily protein intake. Dependant variables were the amino acid concentrations. The combined effect was calculated with the natural logarithm of the amino acid concentration..: Most amino acids fitted a significant exponential decrease due to the sampling delay, except of aspartate, ci
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發(fā)表于 2025-3-23 05:17:15 | 只看該作者
A Multiplatform Metabolomics Approach to Characterize Plasma Levels of Phenylalanine and Tyrosine iabolic pattern from 118 metabolites and we built excellent multivariate models to explain Phe, Tyr concentrations and PKU diagnosis. Common metabolites of these models were identified: Gln, Arg, succinate and alpha aminobutyric acid. Univariate analysis showed an inverse correlation between Arg, alp
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發(fā)表于 2025-3-23 05:49:27 | 只看該作者
Japanese Male Siblings with 2-Methyl-3-Hydroxybutyryl-CoA Dehydrogenase Deficiency (HSD10 Disease) was not elevated. HSD10 disease was suspected based on urinary organic acid data. The patient had a novel hemizygous c.470C>T (p.A157V) mutation in the . gene. His mother was a heterozygous carrier of this mutation. The patient’s older brother also had the c.470C>T (p.A157V) mutation. Neurological
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