CandeSpartan Study Candesartan Spanish Response-prediction and Tolerability study
Observational study on response predictors and tolerability of Candesartan in usual clinical practice
INTRODUCTION:
Migraine is a neurological disease with a prevalence of 14% of the population 1, 2. It is the second
Spinal muscular atrophy is an autosomal recessive disease of varying severity that destroys motor neurons, resulting in atrophy and weakness of the voluntary muscles. Around 95% of the cases demonstrate a homozygous deletion/mutation involving exon 7 in SMN1 (survival motor neuron 1), resulting in
Adult Chinese patients with known focal or suspected liver lesions, referred for magnetic resonance imaging (MRI) for further diagnostic work-up, who have undergone or are scheduled to undergo a defined SOR procedure, within one month before or after the study MRI.
The data for the Secondary Outcome
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