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Median interval from diagnosis to study entry was 0 month (range, 0 62 months).
Indexing disease progression at study entry with individuals at-risk for Huntington disease.
Clinical characteristics at study entry were similar between groups.
Participants provided signed, written informed consent prior to study entry.
Data were collected at study entry and six weeks postnatal.
All participants signed an informed consent form before study entry.
Informed consent was obtained from the patients at study entry.
At study entry no patient was under mechanical ventilation (MV).
The groups were similar in all characteristics upon study entry.
Twenty-seven percent had started HAART prior to study entry.
All patients provided written informed consent prior to study entry.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com