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It can unmask or exacerbate underlying musculoskeletal conditions that were previously asymptomatic or mild

This gradual approach minimizes gastrointestinal side effects and allows patients to adjust to the medication

In conclusion: Our study identified five families and four different mutations in the HAE population of Bosnia and Herzegovina, confirming the heterogeneity of mutations in the SERPING1 gene that cause C1 INH HAE in the human population

As medications, research and technology continue to reshape healthcare, the need for professionals who understand both human performance and nutrition will only grow