Cargando…
Familial Hypercholesterolemia in Patients with Acute Coronary Syndrome: Genetic Insights from EXPLORE-J
Aim: Genetic testing can provide a definitive diagnosis of familial hypercholesterolemia (FH). However, accessibility of genetic testing may be limited in certain countries where it is not considered “standard of care,” including Japan. In addition, mutations responsible for FH cannot be identified...
Autores principales: | Harada-Shiba, Mariko, Ako, Junya, Hirayama, Atsushi, Nakamura, Masato, Nohara, Atsushi, Sato, Kayoko, Murakami, Yoshitaka, Koshida, Ryusuke, Ozaki, Asuka, Arai, Hidenori |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Japan Atherosclerosis Society
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9371751/ https://www.ncbi.nlm.nih.gov/pubmed/34526433 http://dx.doi.org/10.5551/jat.62989 |
Ejemplares similares
-
Lipid Management and 2-Year Clinical Outcomes in Japanese Patients with Acute Coronary Syndrome: EXPLORE-J
por: Nakamura, Masato, et al.
Publicado: (2021) -
Investigation into Lipid Management in Acute Coronary Syndrome Patients from the EXPLORE-J Study
por: Nakamura, Masato, et al.
Publicado: (2019) -
Exploration into lipid management and persistent risk in patients hospitalised for acute coronary syndrome in Japan (EXPLORE-J): protocol for a prospective observational study
por: Nakamura, Masato, et al.
Publicado: (2017) -
Guidelines for Diagnosis and Treatment of Familial Hypercholesterolemia 2017
por: Harada-Shiba, Mariko, et al.
Publicado: (2018) -
Guidance for Pediatric Familial Hypercholesterolemia 2017
por: Harada-Shiba, Mariko, et al.
Publicado: (2018)