Search details
1.
Two novel mutations in the EIF2AK3 gene in children with Wolcott-Rallison syndrome.
Pediatr Diabetes
; 12(3 Pt 1): 187-91, 2011 May.
Article
in English
| MEDLINE | ID: mdl-21518408
2.
COMPLEXITY OF PEDIATRIC CHRONIC DISEASE: CROSS-SECTIONAL STUDY WITH 16,237 PATIENTS FOLLOWED BY MULTIPLE MEDICAL SPECIALTIES.
Rev Paul Pediatr
; 38: e2018101, 2020.
Article
in English, Portuguese
| MEDLINE | ID: mdl-31778404
3.
Pitfalls in the diagnosis of insulin autoimmune syndrome (Hirata's disease) in a hypoglycemic child: a case report and review of the literature.
J Pediatr Endocrinol Metab
; 32(4): 421-428, 2019 Apr 24.
Article
in English
| MEDLINE | ID: mdl-30862762
4.
Translation and validation of Pediatric Quality of Life Inventory™ 3.0 Diabetes Module (PedsQL™ 3.0 Diabetes Module) in Brazil-Portuguese language.
J Pediatr (Rio J)
; 94(6): 680-688, 2018.
Article
in English
| MEDLINE | ID: mdl-29144963
5.
Translation and validation of diabetes self-management profile (DSMP) into Brazilian Portuguese language: first instrument to assess type 1 diabetes self-management in a pediatric population.
Diabetol Metab Syndr
; 9: 51, 2017.
Article
in English
| MEDLINE | ID: mdl-28702090
6.
Maturity-onset diabetes of the young (MODY) in Brazil: Establishment of a national registry and appraisal of available genetic and clinical data.
Diabetes Res Clin Pract
; 123: 134-142, 2017 Jan.
Article
in English
| MEDLINE | ID: mdl-28012402
7.
Clinical and molecular data from 61 Brazilian cases of Congenital Hyperinsulinemic Hypoglycemia.
Diabetol Metab Syndr
; 7: 5, 2015.
Article
in English
| MEDLINE | ID: mdl-25972930
8.
Complexity of pediatric chronic disease: cross-sectional study with 16,237 patients followed by multiple medical specialties / Complexidade da doença crônica pediátrica: estudo tranversal com 16.237 pacientes seguidos por múltiplas especialidades médicas
Rev. Paul. Pediatr. (Ed. Port., Online)
; 38: e2018101, 2020. tab
Article
in English, Portuguese
| LILACS, SES-SP | ID: biblio-1136725
9.
Health-related quality of life in patients with type 1 diabetes mellitus in the different geographical regions of Brazil: data from the Brazilian Type 1 Diabetes Study Group.
Diabetol Metab Syndr
; 7: 87, 2015.
Article
in English
| MEDLINE | ID: mdl-26448787
10.
Severe hypercalcemia in a 9-year-old Brazilian girl due to a novel inactivating mutation of the calcium-sensing receptor.
J Clin Endocrinol Metab
; 89(12): 5936-41, 2004 Dec.
Article
in English
| MEDLINE | ID: mdl-15579740
11.
Precocious puberty: an endocrine manifestation in congenital toxoplasmosis.
J Pediatr Endocrinol Metab
; 15(9): 1487-90, 2002.
Article
in English
| MEDLINE | ID: mdl-12503855
12.
[Evaluation of 2 home monitoring schemes in patients with type 1 diabetes mellitus]. / Avaliação de dois esquemas de monitorização domiciliar em pacientes com diabetes mellitus do tipo 1.
Rev Esc Enferm USP
; 36(4): 317-23, 2002 Dec.
Article
in Portuguese
| MEDLINE | ID: mdl-12876842
13.
[Home glycemic profiles as an strategy for insulin therapy adjustments in patients with type 1 diabetes mellitus]. / Caracterização dos perfis glicêmicos domiciliares como estratégia para os ajustes insulinoterápicos em pacientes com diabetes mellitus do tipo 1.
Rev Esc Enferm USP
; 37(1): 62-71, 2003 Mar.
Article
in Portuguese
| MEDLINE | ID: mdl-12968431
14.
Translation and validation of Pediatric Quality of Life InventoryTM 3 0 Diabetes Module (PedsQLTM 3 0 Diabetes Module) in Brazil-Portuguese language / Tradução e validação do Pediatric Quality of Life InventoryTM 3 0 Diabetes Module (PedsQLTM 3 0 Diabetes Module) para a língua portuguesa do Brasil
J. pediatr. (Rio J.)
; 94(6): 680-688, Nov.-Dec. 2018. tab, graf
Article
in English
| LILACS | ID: biblio-976016
15.
A novel glucokinase deletion (p.Lys32del) and five previously described mutations co-segregate with the phenotype of mild familial hyperglycaemia (MODY2) in Brazilian families.
Diabetes Res Clin Pract
; 100(2): e42-5, 2013 May.
Article
in English
| MEDLINE | ID: mdl-23433541
16.
Economic status and clinical care in young type 1 diabetes patients: a nationwide multicenter study in Brazil.
Acta Diabetol
; 50(5): 743-52, 2013 Oct.
Article
in English
| MEDLINE | ID: mdl-22688518
17.
Novel mutation in MCT8 gene in a Brazilian boy with thyroid hormone resistance and severe neurologic abnormalities.
Arq Bras Endocrinol Metabol
; 55(1): 60-6, 2011 Feb.
Article
in English
| MEDLINE | ID: mdl-21468521
18.
Congenital hyperinsulinism in Brazilian neonates: a study of histology, KATP channel genes, and proliferation of ß cells.
Pediatr Dev Pathol
; 13(5): 375-84, 2010.
Article
in English
| MEDLINE | ID: mdl-20482375
19.
Efficacy of photographic educational materials for carbohydrate counting training of adolescents with diabetes mellitus / Eficacia de materiales educativos fotográficos para entrenar a adolescentes con diabetes mellitus con el conteo de carbohidratos
Nutr. hosp
; 29(2): 344-349, 2014. ilus, tab
Article
in English
| IBECS (Spain) | ID: ibc-120593
20.
Identification of novel mutations of the WFS1 gene in Brazilian patients with Wolfram syndrome.
Eur J Endocrinol
; 160(2): 309-16, 2009 Feb.
Article
in English
| MEDLINE | ID: mdl-19042979