UPDRS III UPDRS scale (motor score). Scale from: 0 to 56. · people with Parkinson's disease
1 finding from 1 review
UPDRS ADL score · people with Parkinson's disease
1 finding from 1 review
Change in disability score · children with SMA types II and III
1 finding from 1 review
Muscle strength · children with SMA types II and III
1 finding from 1 review
Acquiring the ability to stand or walk · children with SMA types II and III
The review found no eligible studies for this question.
1 finding from 1 review
no estimate extracted
Studies not reported
No studies found
Change in quality of life · children with SMA types II and III
1 finding from 1 review
Change in pulmonary function · children with SMA types II and III
1 finding from 1 review
Time from beginning of treatment until death or full‐time ventilation · children with SMA types II and III
1 finding from 1 review
Adverse events related to treatment · children with SMA types II and III
1 finding from 1 review
Intervention not reported
Creatine phosphate 1g/day · patients with heart failure
1 finding from 1 review
Intervention not reported
Creatine 20g/day for 6 weeks · patients with heart failure
1 finding from 1 review
Intervention not reported
Creatine 20g/day for 10 days · patients with heart failure
1 finding from 1 review
Intervention not reported
Myopathy: proportion with changed serum creatine kinase levels (>10x ULN) ‐ at all time points · children with familial hypercholesterolemia
1 finding from 1 review
Intervention not reported
hour Plasma Creatine Phosphokinase · patients with acute coronary syndrome
1 finding from 1 review
Intervention not reported
hour Plasma Creatine Phosphate · patients with acute coronary syndrome
1 finding from 1 review
Intervention not reported
Maximum Plasma Creatine Phosphate · patients with acute coronary syndrome
1 finding from 1 review
Intervention not reported
Maximum voluntary contraction in dystrophinopathies % · patients with muscular dystrophies
1 finding from 1 review
Intervention not reported
Adverse events in glycogen storage disease type V · patients with metabolic myopathies
1 finding from 1 review
Intervention not reported
Aggregate functional performance time (AFPT), intention‐to‐treat analysis % · patients with idiopathic inflammatory myopathies
1 finding from 1 review
Intervention not reported
AFPT, valid compliant completer analysis % · patients with idiopathic inflammatory myopathies
1 finding from 1 review