碌碌之人
发表于 2025-3-26 22:12:37
Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?,ted in an in-frame insertion of 21 base pairs (c.2059-21_c.2059-1) of intron 16 of DPYD. Family investigation showed that the asymptomatic father was also homozygous for the same mutation and enzymatic and biochemical findings were similar to his severely affected son. When the child deteriorated cl
夹克怕包裹
发表于 2025-3-27 01:25:34
Potential Misdiagnosis of Hyperhomocysteinemia due to Cystathionine Beta-Synthase Deficiency Duringhen exposed to high homocysteine and methionine has increased synthesis of cystathionine which cannot be cleared because the fetus lacks cystathionine gamma-lyase, and thus cystathionine is returned to the mother’s circulation. This situation could lead to a misdiagnosis of the cause of hyperhomocys
vasculitis
发表于 2025-3-27 06:27:50
Clinical and Molecular Variability in Patients with , Variants and Liver Phosphorylase b Kinase Defked liver PhK deficiency caused by mutations in .. We found that there is variability in the severity of clinical features, including hypoglycemia and growth. We also report additional . variants that were identified in 24 patients suspected to have liver PhK deficiency. The basis of the clinical va
Torrid
发表于 2025-3-27 12:42:38
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无聊的人
发表于 2025-3-27 14:33:57
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inflame
发表于 2025-3-27 21:16:02
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evasive
发表于 2025-3-28 00:38:30
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使激动
发表于 2025-3-28 04:07:48
Systematic Review and Meta-analysis of Intelligence Quotient in Early-Treated Individuals with Clasvariates (age or gender) as fixed effects where appropriate...: Four articles were included in this meta-analysis. Data of 87 individuals (median age 13 years, range 3–38 years) were used to assess mean FSIQ in CG. The FSIQ ranged from 47 to 122, and the mean score was 87 (95% CI, 81–94). Forty-five
哄骗
发表于 2025-3-28 09:35:25
David Santosa,Markus G. Donner,Stephan vom Dahl,Markus Fleisch,Thomas Hoehn,Ertan Mayatepek,Katrin H
外科医生
发表于 2025-3-28 14:30:28
Carla Ruiz-Andrés,Elena Sellés,Angela Arias,Laura Gort,The Spanish LAL Deficiency Working Group