Cargando…
High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes
BACKGROUND AND OBJECTIVES: Our goal was to study hereditary transthyretin-related amyloidosis (hATTR) in Crete, Greece. METHODS: We aimed at ascertaining all hATTR cases in Crete, an island of 0.62 million people. For this, we evaluated patients with polyneuropathy, autonomic involvement, cardiomyop...
Autores principales: | Tzagournissakis, Minas, Foukarakis, Emmanouil, Samonakis, Dimitrios, Tsilimbaris, Miltiadis, Michaelidou, Kleita, Mathioudakis, Lambros, Marinis, Anastasios, Giannakoudakis, Emmanouil, Spanaki, Cleanthe, Skoula, Irene, Erimaki, Sofia, Amoiridis, Georgios, Koutsis, Georgios, Koukouraki, Sofia, Stylianou, Kostas, Plaitakis, Andreas, Mitsias, Panayiotis D., Zaganas, Ioannis |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465837/ https://www.ncbi.nlm.nih.gov/pubmed/36101541 http://dx.doi.org/10.1212/NXG.0000000000200013 |
Ejemplares similares
-
Familial amyloidotic polyneuropathy in Crete, Greece
por: Tzagournissakis, Minas, et al.
Publicado: (2015) -
Whole exome sequencing establishes diagnosis of Charcot–Marie–Tooth 4J, 1C, and X1 subtypes
por: Michaelidou, Kleita, et al.
Publicado: (2020) -
Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients
por: Zaganas, Ioannis, et al.
Publicado: (2020) -
The Glutamate Dehydrogenase Pathway and Its Roles in Cell and Tissue Biology in Health and Disease
por: Plaitakis, Andreas, et al.
Publicado: (2017) -
Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes
por: Zaganas, Ioannis, et al.
Publicado: (2021)