Suggestions(1)
Exact(1)
In Study 2 (N = 43), a number of changes were introduced to a group assignment task (double presentation, inclusion of decoys) that allowed a more rigorous test of the predicted item-specific memory effects.
Similar(59)
Samples (blood, sputum and urine) were taken within 24 h of first presentation and inclusion in the CAPNETZ study.
Venous blood samples were collected within 24 h after first presentation and inclusion in the CAPNETZ study and stored centrally at -70°C.
Samples (blood, sputum and urine) were collected within 24 h of first presentation and inclusion in the CAPNETZ study, and CRB and CRB-65 scores were determined for all patients at the time of enrollment.
Usability testing informed amendments to the user interface, graphical risk presentations and inclusion of additional features (Table 1) to produce a beta prototype.> Data collected on contact forms and automatically logged data on use of COMPASS by clinicians are summarised in Table 2.
At the index presentation, presenting patients who meet the inclusion criteria will be identified by the triage nurse or treating clinician and invited to participate in the study.
Thus, to alert and help the physicians, especially radiologists, in diagnosing female genito-urinary malformations, these mentioned aspects will be reviewed briefly as well as the clinical presentation, catalogation and inclusion of female genital malformations in the embryological and clinical classification [8] and in other current classification systems.
These observations might reflect the requirement for fever at presentation as an inclusion criterion for this subanalysis, which may exclude certain populations from being assessed [ 11].
These inherent differences in individual neuronal populations also could partially explain some of the disordered presentation of αS inclusion pathology in human brains.
23 Ten studies defined specific time from onset of symptoms to presentation as an inclusion criterion, which ranged from four hours 39 to 24 hours.
Six missense mutations in the αS gene, SNCA, resulting in six different amino acid substitutions (A30P, E46K, H50Q, G51D, A53T, and A53E) have been identified that can cause PD with or without additional clinical features such as dementia reflecting a more widespread presentation of αS inclusion pathology typical of dementia with LBs (DLB) [ 5, 96, 107, 116, 145, 150, 151, 194].
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