Detalhe da pesquisa
1.
Molecular epidemiology of hereditary ataxia in Finland.
BMC Neurol
; 21(1): 382, 2021 Oct 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34600502
2.
Late-onset and classic phenotypes of Fabry disease in males with the GLA-Thr410Ala mutation.
Open Heart
; 10(1)2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36927868
3.
Metabolite Signature in the Carriers of Pathogenic Genetic Variants for Cardiomyopathy: A Population-Based METSIM Study.
Metabolites
; 12(5)2022 May 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35629941
4.
Clinical and Genetic Characterization of 153 Patients with Persistent or Transient Congenital Hyperinsulinism.
J Clin Endocrinol Metab
; 105(4)2020 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32170320
5.
Genetic basis and outcome in a nationwide study of Finnish patients with hypertrophic cardiomyopathy.
ESC Heart Fail
; 6(2): 436-445, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30775854
6.
Clinical, Genetic, and Biochemical Characteristics of Early-Onset Diabetes in the Finnish Population.
J Clin Endocrinol Metab
; 101(8): 3018-26, 2016 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27167055