Detalhe da pesquisa
1.
[Congenital hyperinsulinism: Loss of B-cell self-control]. / Vrozený hyperinzulinizmus: kdyz B-bunka ztratí sebekontrolu.
Vnitr Lek
; 62(11 Suppl 4): S72-76, 2016.
Artigo
em Tcheco
| MEDLINE | ID: mdl-27921429
2.
Quality of Life and Treatment Satisfaction in Participants with Maturity-Onset Diabetes of the Young: A Comparison to Other Major Forms of Diabetes.
Exp Clin Endocrinol Diabetes
; 130(2): 85-93, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-32722819
3.
Congenital Hyperinsulinism Caused by Novel Homozygous KATP Channel Gene Variants May Be Linked to Unexplained Neonatal Deaths among Kurdish Consanguineous Families.
Horm Res Paediatr
; 93(1): 58-65, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32203961
4.
Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial.
Lancet Diabetes Endocrinol
; 7(9): 695-706, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31377265
5.
Could a combination of heterozygous ABCC8 and KCNJ11 mutations cause congenital hyperinsulinism?
J Pediatr Endocrinol Metab
; 30(12): 1311-1315, 2017 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-29127764
6.
Severe Hyperinsulinaemic Hypoglycaemia in Beckwith-Wiedemann Syndrome due to Paternal Uniparental Disomy of 11p15.5 Managed with Sirolimus Therapy.
Horm Res Paediatr
; 85(5): 353-7, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26863215
7.
The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia.
J Clin Res Pediatr Endocrinol
; 7(2): 86-97, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26316429
8.
High Incidence of Heterozygous ABCC8 and HNF1A Mutations in Czech Patients With Congenital Hyperinsulinism.
J Clin Endocrinol Metab
; 100(12): E1540-9, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26431509