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1.
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation.
Am J Hum Genet
; 92(1): 131-6, 2013 Jan 10.
Article
in English
| MEDLINE | ID: mdl-23273570
2.
Gastric carcinoid tumor in a 14-year old girl.
Scand J Gastroenterol
; 49(11): 1391-3, 2014 Nov.
Article
in English
| MEDLINE | ID: mdl-25180819
3.
Adherence to growth hormone therapy: results of a multicenter study.
Endocr Pract
; 20(1): 46-51, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24013997
4.
Pathophysiology of critical illness hyperglycemia in children.
J Pediatr Endocrinol Metab
; 26(7-8): 715-20, 2013.
Article
in English
| MEDLINE | ID: mdl-23640956
5.
The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD?
Eur J Pediatr
; 171(10): 1497-502, 2012 Oct.
Article
in English
| MEDLINE | ID: mdl-22644991
6.
Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents.
J Pediatr Endocrinol Metab
; 24(1-2): 21-4, 2011.
Article
in English
| MEDLINE | ID: mdl-21528810
7.
The endocrine spectrum of intracranial cysts in childhood and review of the literature.
J Pediatr Endocrinol Metab
; 24(11-12): 867-75, 2011.
Article
in English
| MEDLINE | ID: mdl-22308834
8.
Characteristics and prevalence of non-classical congenital adrenal hyperplasia with a V2811 mutation in patients with premature pubarche.
J Pediatr Endocrinol Metab
; 24(11-12): 965-70, 2011.
Article
in English
| MEDLINE | ID: mdl-22308849
9.
Primary adrenal insufficiency in a child after busulfan and cyclophosphamide-based conditioning for hematopoietic stem cell transplantation.
J Pediatr Endocrinol Metab
; 24(9-10): 853-5, 2011.
Article
in English
| MEDLINE | ID: mdl-22145493
10.
Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell.
J Pediatr Endocrinol Metab
; 24(11-12): 1019-23, 2011.
Article
in English
| MEDLINE | ID: mdl-22308858
11.
Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant.
J Pediatr Endocrinol Metab
; 24(11-12): 1077-80, 2011.
Article
in English
| MEDLINE | ID: mdl-22308870
12.
A novel mutation of 5alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment.
Eur J Pediatr
; 169(8): 991-5, 2010 Aug.
Article
in English
| MEDLINE | ID: mdl-20179965
13.
The effect of colchicine on physical growth in children with familial mediterranean fever.
Eur J Pediatr
; 169(7): 825-8, 2010 Jul.
Article
in English
| MEDLINE | ID: mdl-20016916
14.
Amiodarone-induced thyrotoxicosis in children and adolescents is a possible outcome in patients with low iodine intake.
J Pediatr Endocrinol Metab
; 23(4): 363-8, 2010 Apr.
Article
in English
| MEDLINE | ID: mdl-20583541
15.
Effect of interferon therapy on glucose metabolism in children with chronic hepatitis B.
Turk J Pediatr
; 52(6): 594-601, 2010.
Article
in English
| MEDLINE | ID: mdl-21428191
16.
Final height of patients with classical congenital adrenal hyperplasia.
Turk J Pediatr
; 51(6): 539-44, 2009.
Article
in English
| MEDLINE | ID: mdl-20196386
17.
Persistently raised thyroid stimulating hormone in adequately treated congenital hypothyroidism on long-term follow-up.
J Pediatr Endocrinol Metab
; 21(3): 251-6, 2008 Mar.
Article
in English
| MEDLINE | ID: mdl-18540252
18.
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome.
Pediatr Int
; 50(2): 172-4, 2008 Apr.
Article
in English
| MEDLINE | ID: mdl-18353053
19.
Evaluation of glucose homeostasis in transfusion-dependent thalassemic patients.
Pediatr Hematol Oncol
; 25(7): 630-7, 2008 Sep.
Article
in English
| MEDLINE | ID: mdl-18850475
20.
The incidence and evolution of thyroid dysfunction during interferon-alpha therapy in children with chronic hepatitis B infection.
J Pediatr Endocrinol Metab
; 20(2): 237-45, 2007 Feb.
Article
in English
| MEDLINE | ID: mdl-17396441