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To identify subgroups at risk for long-term probable PTSD, risk factors for the development of probable PTSD one and two year following injury were assessed.
This study aimed to assess how various cognitive, neuroimaging and genetic measures collected at baseline can be used to predict the development of probable AD dementia at 24 months in a sample of elderly participants obtained from ADNI.
The flowchart depicting injury patients with and without symptoms at one and two years following injury allowed us to gain insight into the development of probable PTSD over time in a sample of severely injured trauma patients.
By assessing a series of normative cutoff scores from cognitive test results, the number of episodic memory and non-memory tests used to assess cognitive performance, and other commonly used neuroimaging and genetic biomarkers, a set of recommended criteria was established which may be used in future investigations to improve prediction for the development of probable AD in the elderly.
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We report on an immunocompromised patient, followed-up from the start of a symptomatic acute Q fever episode to the development and treatment of probable chronic Q fever.
This methodological innovation facilitated a fairly reliable mathematical statistical description of (probable) development in the social systems.
Thus, in about 20% of the patients, the time delay between the development of the disease entity of probable Ménière's disease was more than 5 years.
The most probable development of the future HVDC grid has been defined: the grid is not expected to be built at once, but rather to develop in an organic way.
He started the drum beat early too, signing onto a 1998 letter to President Clinton drafted by the neo-conservative Project for the New American Century that laid out the all arguments we are still hearing today about Hussein probable development of WMDs and the urgent need to remove him from office.
This is what leads to a probable development of papillae in some patients [ 5].
Murine monoclonal antibodies are not suitable for development as therapeutic agents in humans because of their short half-lives and the probable development of neutralizing antibodies due to the immunogenicity of the mouse protein.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com