Detalhe da pesquisa
1.
Hyperglycaemia-related complications at the time of diagnosis can cause permanent neurological disability in children with neonatal diabetes.
Diabet Med
; 34(7): 1000-1004, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28173619
2.
Psychiatric morbidity in children with KCNJ11 neonatal diabetes.
Diabet Med
; 33(10): 1387-91, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27086753
3.
HNF1B deletions in patients with young-onset diabetes but no known renal disease.
Diabet Med
; 30(1): 114-7, 2013 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-22587559
4.
Heterozygous ABCC8 mutations are a cause of MODY.
Diabetologia
; 55(1): 123-7, 2012 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21989597
5.
Neuropsychological impairments in children with KCNJ11 neonatal diabetes.
Diabet Med
; 34(8): 1171-1173, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28477417
6.
Maturity-onset diabetes of the young (MODY): how many cases are we missing?
Diabetologia
; 53(12): 2504-8, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20499044
7.
A comparison of tonographic-trace simulations achieved by two systems: nonlinear elastic and linear viscoelastic.
IEEE Trans Biomed Eng
; 18(2): 97-103, 1971 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-5576069
8.
Continue with long term sulfonylureas in patients with mutations in the KCNJ11 gene when there is evidence of response even if insulin treatment is still required.
Diabetes Res Clin Pract
; 100(3): e63, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-23608551
9.
Partial and whole gene deletion mutations of the GCK and HNF1A genes in maturity-onset diabetes of the young.
Diabetologia
; 50(11): 2313-7, 2007 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-17828387
10.
Circular mitochondrial DNA molecules from petite mutants of Saccharomyces cerevisiae: resolution by polyacrylamide gel electrophoresis.
Mol Biol Rep
; 4(2): 101-4, 1978 Jun 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-355858