Detalles de la búsqueda
1.
CTLA4, SH2B3, and CLEC16A diversely affect the progression of early islet autoimmunity in relatives of Type 1 diabetes patients.
Clin Exp Immunol
; 211(3): 224-232, 2023 03 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-36622793
2.
Genetic variation at ERBB3/IKZF4 and sexual dimorphism in epitope spreading in single autoantibody-positive relatives.
Diabetologia
; 64(11): 2511-2516, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34448034
3.
Diabetic ketoacidosis in children newly diagnosed with type 1 diabetes mellitus: Role of demographic, clinical, and biochemical features along with genetic and immunological markers as risk factors. A 20-year experience in a tertiary Belgian center.
Pediatr Diabetes
; 20(5): 584-593, 2019 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-31038262
4.
Efficacy and safety of a 4-year combination therapy of growth hormone and gonadotropin-releasing hormone analogue in pubertal girls with short predicted adult height.
Front Endocrinol (Lausanne)
; 14: 1113750, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-37008942
5.
Comparison Between Continuous Versus Flash Glucose Monitoring in Children, Adolescents, and Young Adults with Type 1 Diabetes: An 8-Week Prospective Randomized Trial.
Diabetes Ther
; 13(9): 1671-1681, 2022 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-35870074
6.
Six Novel Variants in the MKRN3 Gene Causing Central Precocious Puberty.
J Endocr Soc
; 7(1): bvac168, 2022 Nov 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-36438546
7.
Anti-SARS-CoV-2 antibodies in new-onset type 1 diabetes in children during pandemic in Belgium.
J Pediatr Endocrinol Metab
; 34(10): 1319-1322, 2021 Oct 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-34280962
8.
The Retina in Patients With Triple A Syndrome: A Window Into Neurodegeneration?
Front Endocrinol (Lausanne)
; 12: 729056, 2021.
Artículo
en Inglés
| MEDLINE | ID: mdl-34867779
9.
[Neonatal diabetes: a case of pancreatic beta cell agenesis and a 38-year follow-up of a permanent neonatal diabetes mellitus]. / Diabètes néonatals: un cas d'agénésie des cellules beta et suivi pendant 38 ans d'un diabète néonatal permanent.
Rev Med Brux
; 31(2 Suppl): S109-12, 2010.
Artículo
en Francés
| MEDLINE | ID: mdl-21812222
10.
[Severe hypoglycemia in children and adolescents with type 1 diabetes: risks factors and management]. / Hypoglycémies sévères chez les jeunes diabétiques de type 1: facteurs de risque et traitement.
Rev Med Brux
; 31(2 Suppl): S65-70, 2010.
Artículo
en Francés
| MEDLINE | ID: mdl-21812217
11.
[Diabetic ketoacidosis: diagnosis, management, prevention]. / L'acidocétose diabétique: diagnostic, prise en charge, prévention.
Rev Med Brux
; 31(2 Suppl): S71-6, 2010.
Artículo
en Francés
| MEDLINE | ID: mdl-21812218
12.
Flash Glucose Monitoring Accepted in Daily Life of Children and Adolescents with Type 1 Diabetes and Reduction of Severe Hypoglycemia in Real-Life Use.
Diabetes Technol Ther
; 21(6): 329-335, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-31058545
13.
Criteria for First-Year Growth Response to Growth Hormone Treatment in Prepubertal Children With Growth Hormone Deficiency: Do They Predict Poor Adult Height Outcome?
Front Endocrinol (Lausanne)
; 10: 792, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-31849835
14.
Atypical Rothmund-Thomson syndrome in a patient with compound heterozygous mutations in RECQL4 gene and phenotypic features in RECQL4 syndromes.
Eur J Pediatr
; 167(2): 175-81, 2008 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-17372760
15.
Accelerated Progression to Type 1 Diabetes in the Presence of HLA-A*24 and -B*18 Is Restricted to Multiple Islet Autoantibody-Positive Individuals With Distinct HLA-DQ and Autoantibody Risk Profiles.
Diabetes Care
; 41(5): 1076-1083, 2018 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-29545461
16.
Congenital Hypothyroidism: Long-Term Experience with Early and High Levothyroxine Dosage.
Horm Res Paediatr
; 85(3): 188-97, 2016.
Artículo
en Inglés
| MEDLINE | ID: mdl-26881423
17.
Insulin sensitivity modulates the growth response during the first year of high-dose growth hormone treatment in short prepubertal children born small for gestational age.
Horm Res Paediatr
; 78(1): 24-30, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22832126
18.
Growth retardation in untreated autosomal dominant familial neurohypophyseal diabetes insipidus caused by one recurring and two novel mutations in the vasopressin-neurophysin II gene.
Eur J Endocrinol
; 164(2): 179-87, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21088058
19.
Genetic deficiency of tartrate-resistant acid phosphatase associated with skeletal dysplasia, cerebral calcifications and autoimmunity.
Nat Genet
; 43(2): 132-7, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21217752
20.
Phenotypical, biological, and molecular heterogeneity of 5α-reductase deficiency: an extensive international experience of 55 patients.
J Clin Endocrinol Metab
; 96(2): 296-307, 2011 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-21147889