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Titlebook: JIMD Reports, Volume 37; Eva Morava,Matthias Baumgartner,Verena Peters Book 2017 Society for the Study of Inborn Errors of Metabolism (SSI

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樓主: cobble
21#
發(fā)表于 2025-3-25 04:10:51 | 只看該作者
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發(fā)表于 2025-3-25 09:42:55 | 只看該作者
Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features i with a mutation of . gene, coding for an accessory subunits of complex I, was described. Here, we present an additional description of a child with Leigh syndrome harboring a homozygous mutation in ., providing insights in clinical, biochemical, and neuroradiologic features for future earlier recognition.
23#
發(fā)表于 2025-3-25 15:13:00 | 只看該作者
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.978-3-662-56358-8978-3-662-56359-5Series ISSN 2192-8304 Series E-ISSN 2192-8312
24#
發(fā)表于 2025-3-25 19:46:43 | 只看該作者
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發(fā)表于 2025-3-25 21:07:37 | 只看該作者
26#
發(fā)表于 2025-3-26 01:58:39 | 只看該作者
Favourable Outcome in Two Pregnancies in a Patient with 3-Hydroxy-3-Methylglutaryl-CoA Lyase Deficiweight/d was given. Meals were taken every 3?h. Additionally, 70?g of starch was given at midnight to maintain normoglycemia at night time. Peripartum, a complete parenteral nutrition, was delivered through a central venous catheter. The patient delivered a healthy male infant by Caesarean section a
27#
發(fā)表于 2025-3-26 06:13:20 | 只看該作者
Guanidinoacetate Methyltransferase Activity in Lymphocytes, for a Fast Diagnosis,. The formed .H.-.C.-creatine was butylated and subsequently measured by liquid chromatography tandem mass-spectrometry (LC-MS/MS).... We measured GAMT enzyme activity in lymphocyte extracts of 24 controls, 3 GAMT deficient patients and of 2 parents proven to be carrier. Because GAMT activity decrea
28#
發(fā)表于 2025-3-26 08:33:09 | 只看該作者
29#
發(fā)表于 2025-3-26 14:27:47 | 只看該作者
30#
發(fā)表于 2025-3-26 20:08:36 | 只看該作者
Normal Neurological Development During Infancy Despite Massive Hyperammonemia in Early Treated NAGSy. Under long-term treatment with NCG, the patient developed normally at last follow-up at 7 months of age..In conclusion, the standard neonatal situation of a neurologically compromised newborn turned out as a treatable rare inborn error of metabolism. In all neonates with somnolence and coma and h
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