Detalhe da pesquisa
1.
Deciphering genetic signatures by whole exome sequencing in a case of co-prevalence of severe renal hypouricemia and diabetes with impaired insulin secretion.
BMC Med Genet
; 21(1): 91, 2020 05 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32375679
2.
Genetic and Functional Analyses of Patients with Marked Hypo-High-Density Lipoprotein Cholesterolemia.
J Atheroscler Thromb
; 2024 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38538338
3.
L-Asparaginase-Induced Continuous Hyperglycemia With Type 1 Diabetes-Related Antibodies and HLA Genotypes: A Case Study.
Cureus
; 14(10): e30067, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36381756
4.
A case of NASH with genetic predisposition successfully treated with an SGLT2 inhibitor: a possible involvement of mitochondrial dysfunction.
Endocrinol Diabetes Metab Case Rep
; 20222022 Dec 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36571472