Medley
发表于 2025-3-25 04:10:51
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FISC
发表于 2025-3-25 09:42:55
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.
BOAST
发表于 2025-3-25 15:13:00
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
变量
发表于 2025-3-25 19:46:43
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一窝小鸟
发表于 2025-3-25 21:07:37
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negligence
发表于 2025-3-26 01:58:39
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
avarice
发表于 2025-3-26 06:13:20
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
斗志
发表于 2025-3-26 08:33:09
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xanthelasma
发表于 2025-3-26 14:27:47
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Classify
发表于 2025-3-26 20:08:36
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