Detalhe da pesquisa
1.
Bisphosphonate treatment at spondylo-ocular syndrome due to a novel compound heterozygote variant in XYLT2 and review of the literature.
Am J Med Genet A
; 191(6): 1581-1585, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36815763
2.
Clinical, biochemical, and echocardiographic evaluation of neonates with vitamin D deficiency due to maternal vitamin D deficiency.
Cardiol Young
; 32(1): 88-93, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-33941295
3.
Severe Hypercalcemia in a Child With Acute Lymphoblastic Leukemia Relapse: Successful Management With Combination of Calcitonin and Bisphosphonate.
J Pediatr Hematol Oncol
; 38(3): 232-4, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26907650
4.
Comparison of the optical coherence tomography-angiography (OCT-A) vascular measurements between molecularly confirmed MODY and age-matched healthy controls.
Acta Diabetol
; 61(7): 917-924, 2024 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-38565685
5.
Benign transient hyperphosphatasemia in the pediatric population: a single center cohort study.
J Pediatr Endocrinol Metab
; 2024 May 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-38800840
6.
The Relationship Between Internet Usage Style and Internet Addiction and Food Addiction in Obese Children Compared to Healthy Children.
Turk Arch Pediatr
; 58(2): 205-211, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36856359
7.
Comparison of internet usage and internet addiction scores in healthy children and children with type 1 diabetes mellitus.
J Pediatr Endocrinol Metab
; 36(5): 435-440, 2023 May 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37013724
8.
Body mass index evolution and ovarian function in adolescent girls who received GnRH agonist treatment for central precocious puberty or early and fast puberty.
J Pediatr Endocrinol Metab
; 36(11): 1044-1051, 2023 Nov 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-37735929
9.
The First Case of 4H Syndrome with Type 1 Diabetes Mellitus.
J Clin Res Pediatr Endocrinol
; 2023 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-36974356
10.
Novel sphingosine-1-phosphate lyase mutation causes multisystemic diseases: case report.
Turk J Pediatr
; 65(6): 1025-1032, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38204317
11.
Acromesomelic dysplasia-Maroteaux type, nine patients with two novel NPR2 variants.
J Pediatr Endocrinol Metab
; 34(9): 1115-1121, 2021 Sep 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-34162036
12.
Identification of Three Novel and One Known Mutation in the WFS1 Gene in Four Unrelated Turkish Families: The Role of Homozygosity Mapping in the Early Diagnosis
J Clin Res Pediatr Endocrinol
; 13(1): 34-43, 2021 02 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-32938580
13.
Clinical Characteristics and Long-term Follow-up of Patients with Diabetes Due To PTF1A Enhancer Mutations.
J Clin Endocrinol Metab
; 105(12)2020 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32893856
14.
Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology.
Int J Pediatr Endocrinol
; 2017: 9, 2017.
Artigo
em Inglês
| MEDLINE | ID: mdl-28855921
15.
Severe hyponatremia and repeated intestinal resections for intestinal dysmotility mimicking congenital aganglionic megacolon due to delay in the diagnosis of congenital hypothyroidism.
Ann Pediatr Endocrinol Metab
; 21(4): 230-234, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28164077
16.
Platelet aggregation, secretion, and coagulation changes in children with asthma.
Blood Coagul Fibrinolysis
; 25(7): 738-44, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-24842314