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41% of presentation samples had antibodies that only recognise these N-terminal domains.
ADAMTS13 antigen levels were lower in presentation samples of patients who died (median 1.0% vs. 5.5%).
All presentation samples were taken before plasma exchange or rituximab were commenced.
We therefore analysed plasma ADAMTS13 antigen levels in 91 acquired TTP presentation samples.
We obtained presentation samples from 102 patients of whom 72 were found to be informative at the MAOA locus.
Analysis of the prognostic implications of domain specificity of anti-ADAMTS13 was performed on the 62 first presentation samples.
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Three patients did not have an INR determined from the presentation sample.
In three patients with ALL (= 25%) we reproducibly detected identical clonotypic marker in the presentation sample and in the neonatal blood spot on the Guthrie card.
Table 3 also summarizes the predictive performance for miR-122, HMGB1, K18, and GLDH quantified from the first presentation sample to reflect ALI in patients admitted to the hospital emergency room later than 8 hours following overdose (n = 62).
The university's good intentions came with some concerns: it's not easy to share the lecture notes, slide presentations, sample tests, syllabuses and reading lists that go into an M.I.T. course.
We assayed 104 presentation myeloma samples for the presence of MYC translocations using the capture assay followed by massively parallel sequencing.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com