Detalles de la búsqueda
1.
Natural history of Wolcott-Rallison syndrome: A systematic review and follow-up study.
Liver Int;
44(3): 811-822, 2024 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-38230874
2.
A Specific CNOT1 Mutation Results in a Novel Syndrome of Pancreatic Agenesis and Holoprosencephaly through Impaired Pancreatic and Neurological Development.
Am J Hum Genet;
104(5): 985-989, 2019 05 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31006513
3.
A randomized clinical trial of the efficacy and safety of sitagliptin as initial oral therapy in youth with type 2 diabetes.
Pediatr Diabetes;
23(2): 173-182, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34779087
4.
Efficacy and safety of the addition of sitagliptin to treatment of youth with type 2 diabetes and inadequate glycemic control on metformin without or with insulin.
Pediatr Diabetes;
23(2): 183-193, 2022 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-34779103
5.
Short stature with low insulin-like growth factor 1 availability due to pregnancy-associated plasma protein A2 deficiency in a Saudi family.
Clin Genet;
100(5): 601-606, 2021 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-34272725
6.
Glucose management for exercise using continuous glucose monitoring (CGM) and intermittently scanned CGM (isCGM) systems in type 1 diabetes: position statement of the European Association for the Study of Diabetes (EASD) and of the International Society for Pediatric and Adolescent Diabetes (ISPAD) endorsed by JDRF and supported by the American Diabetes Association (ADA).
Diabetologia;
63(12): 2501-2520, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-33047169
7.
Glucose management for exercise using continuous glucose monitoring (CGM) and intermittently scanned CGM (isCGM) systems in type 1 diabetes: position statement of the European Association for the Study of Diabetes (EASD) and of the International Society for Pediatric and Adolescent Diabetes (ISPAD) endorsed by JDRF and supported by the American Diabetes Association (ADA).
Pediatr Diabetes;
21(8): 1375-1393, 2020 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-33047481
8.
Acidosis and Deafness in Patients with Recessive Mutations in FOXI1.
J Am Soc Nephrol;
29(3): 1041-1048, 2018 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-29242249
9.
Ramadan fasting in children.
J Pak Med Assoc;
69(5): 745-746, 2019 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-31105303
10.
Paediatric insulin injection technique: The softer side.
J Pak Med Assoc;
68(8): 1270-1272, 2018 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-30108402
11.
ISPAD Clinical Practice Consensus Guidelines 2022: Ramadan and other religious fasting by young people with diabetes.
Pediatr Diabetes;
23(8): 1512-1528, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-36537522
12.
Glucose management for exercise using continuous glucose monitoring: should sex and prandial state be additional considerations? Reply to Yardley JE and Sigal RJ [letter].
Diabetologia;
64(4): 935-938, 2021 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-33538843
13.
Genetic characteristics, clinical spectrum, and incidence of neonatal diabetes in the Emirate of AbuDhabi, United Arab Emirates.
Am J Med Genet A;
170(3): 602-9, 2016 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26463504
14.
ISPAD Clinical Practice Consensus Guidelines: Fasting during Ramadan by young people with diabetes.
Pediatr Diabetes;
21(1): 5-17, 2020 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31659852
15.
National growth charts for United Arab Emirates children with Down syndrome from birth to 15 years of age.
J Epidemiol;
25(1): 20-9, 2015.
Artículo
en Inglés
| MEDLINE | ID: mdl-25196167
16.
Characteristics of adolescents referred for bariatric surgery in Abu Dhabi, United Arab Emirates.
Front Pediatr;
12: 1297251, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38523841
17.
Analysis of disease characteristics of a large patient cohort with congenital generalized lipodystrophy from the Middle East and North Africa.
Orphanet J Rare Dis;
19(1): 118, 2024 Mar 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-38481246
18.
Recessive mutations in the INS gene result in neonatal diabetes through reduced insulin biosynthesis.
Proc Natl Acad Sci U S A;
107(7): 3105-10, 2010 Feb 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-20133622
19.
Whole-Exome Sequencing in Family Trios Reveals De Novo Mutations Associated with Type 1 Diabetes Mellitus.
Biology (Basel);
12(3)2023 Mar 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36979105
20.
International Consensus Guideline on Small for Gestational Age: Etiology and Management From Infancy to Early Adulthood.
Endocr Rev;
44(3): 539-565, 2023 05 08.
Artículo
en Inglés
| MEDLINE | ID: mdl-36635911