Liver disease epidemiology and burden in patients with alterations in plasma protein metabolism: German retrospective insurance claims analysis

BACKGROUND: Alpha-1 antitrypsin deficiency is a rare genetic disease and a leading cause of inherited alterations in plasma protein metabolism (APPM). AIM: To understand the prevalence, burden and progression of liver disease in patients with APPM including alpha-1 antitrypsin deficiency. METHODS: W...

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Detalles Bibliográficos
Autores principales: Picker, Nils, Hagiwara, May, Baumann, Severin, Marins, Ed G, Wilke, Thomas, Ren, Kaili, Maywald, Ulf, Karki, Chitra, Strnad, Pavel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Retrospective Study
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642430/
https://www.ncbi.nlm.nih.gov/pubmed/37970617
http://dx.doi.org/10.4254/wjh.v15.i10.1127

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10642430/
https://www.ncbi.nlm.nih.gov/pubmed/37970617
http://dx.doi.org/10.4254/wjh.v15.i10.1127

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