Detalhe da pesquisa
1.
A novel NEUROG3 mutation in neonatal diabetes associated with a neuro-intestinal syndrome.
Pediatr Diabetes
; 19(3): 381-387, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28940958
2.
Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes.
Pediatr Diabetes
; 19(3): 559-565, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29159931
3.
Diabetes knowledge in adolescents with type 1 diabetes and their parents and glycemic control.
Pediatr Diabetes
; 18(7): 559-565, 2017 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27726250
4.
Revisiting autoimmune gastritis in children and adolescents with type 1 diabetes.
Pediatr Diabetes
; 18(8): 772-776, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28004477
5.
Insulin regimens, diabetes knowledge, quality of life, and HbA1c in children and adolescents with type 1 diabetes.
Pediatr Diabetes
; 18(5): 340-347, 2017 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-27161814
6.
A unique CD8(+) T lymphocyte signature in pediatric type 1 diabetes.
J Autoimmun
; 73: 54-63, 2016 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-27318739
7.
Bone imaging findings in genetic and acquired lipodystrophic syndromes: an imaging study of 24 cases.
Skeletal Radiol
; 45(11): 1495-506, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27631079
8.
GAD65 antigen therapy in recently diagnosed type 1 diabetes mellitus.
N Engl J Med
; 366(5): 433-42, 2012 Feb 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-22296077
9.
Changes in insulin therapy regimens over 10 yr in children and adolescents with type 1 diabetes attending diabetes camps.
Pediatr Diabetes
; 15(5): 329-35, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24016246
10.
Recommendations for age-appropriate education of children and adolescents with diabetes and their parents in the European Union.
Pediatr Diabetes
; 13 Suppl 16: 20-8, 2012 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22931221
11.
Comorbidity and metabolic context are crucial factors determining neurological sequelae of hypoglycaemia.
Dev Med Child Neurol
; 54(11): 1012-7, 2012 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-22924392
12.
Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.
N Engl J Med
; 355(5): 467-77, 2006 Aug 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-16885550
13.
Developmental methylation program and concerted expression of Stx11 in mouse tissues.
Mamm Genome
; 20(3): 131-9, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19169743
14.
Glucose tolerance and insulin secretion, morbidity, and death in patients with cystic fibrosis.
J Pediatr
; 152(4): 540-5, 545.e1, 2008 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-18346512
15.
High Prevalence of Polycystic Ovary Syndrome in Type 1 Diabetes Mellitus Adolescents: Is There a Difference Depending on the NIH and Rotterdam Criteria?
Horm Res Paediatr
; 87(5): 333-341, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28437788
16.
The Knudson's two-hit model and timing of somatic mutation may account for the phenotypic diversity of focal congenital hyperinsulinism.
J Clin Endocrinol Metab
; 91(10): 4118-23, 2006 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-16882742
17.
Congenital hyperinsulinism: pancreatic [18F]fluoro-L-dihydroxyphenylalanine (DOPA) positron emission tomography and immunohistochemistry study of DOPA decarboxylase and insulin secretion.
J Clin Endocrinol Metab
; 91(3): 933-40, 2006 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-16403819
18.
KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features.
Eur J Hum Genet
; 14(7): 824-30, 2006 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-16670688
19.
Prevalence of mutations in AGPAT2 among human lipodystrophies.
Diabetes
; 52(6): 1573-8, 2003 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-12765973
20.
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.
Diabetes
; 53(7): 1876-83, 2004 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-15220213