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journal of clinical research in pediatric endocrinology
  
سال:2016 - دوره:8 - شماره:4
  
 
A case of vitamin d-dependent rickets type 1a with a novel mutation in the uzbek population
- صفحه:484-489
  
 
A critical appraisal of growth hormone therapy in growth hormone deficiency and turner syndrome patients in turkey
- صفحه:490-495
  
 
A novel homozygous mutation in the KCNJ11 gene of a neonate with congenital hyperinsulinism and successful management with sirolimus
- صفحه:478-481
  
 
A novel missense mutation in the CLPP gene causing perrault syndrome type 3 in a turkish family
- صفحه:472-477
  
 
A p.(glu809lys) mutation in the WFS1 gene associated with wolfram-like syndrome: A case report
- صفحه:482-483
  
 
Association between common genetic variants and polycystic ovary syndrome risk in a chinese han population
- صفحه:405-410
  
 
Breast-milk iodine concentrations,iodine status,and thyroid function of breastfed infants aged 2-4 months and their mothers residing in a south african township
- صفحه:381-391
  
 
Complex glycerol kinase deficiency and adrenocortical insufficiency in two neonates
- صفحه:468-471
  
 
Current status of childhood hyperinsulinemic hypoglycemia in turkey
- صفحه:375-380
  
 
Development and validation of a pediatric endocrine knowledge assessment questionnaire: Impact of ac pediatric endocrine knowledge assessment questionnaire intervention study
- صفحه:411-418
  
 
Effect of cytokine signaling 3 gene polymorphisms in childhood obesity
- صفحه:452-460
  
 
Lower plasma ghrelin levels are found in women with diabetes-complicated pregnancies
- صفحه:425-431
  
 
Luteinizing hormone secretion during gonadotropin-releasing hormone stimulation tests in obese girls with central precocious puberty
- صفحه:392-398
  
 
Prevalence of vitamin d deficiency and calcium homeostasis in saudi children
- صفحه:461-467
  
 
Pseudohypoparathyroidism type 1a-subclinical hypothyroidism and rapid weight gain as early clinical signs: A clinical review of 10 cases
- صفحه:432-438
  
 
The effect of congenital and postnatal hypothyroidism on depression-like behaviors in juvenile rats
- صفحه:439-444
  
 
The role of osteopontin in the pathogenesis and complications of type 1 diabetes mellitus in children
- صفحه:399-404
  
 
The13c-glucose breath test for insulin resistance assessment in adolescents: Comparison with fasting and post-glucose stimulus surrogate markers of insulin resistance
- صفحه:419-424
  
 
Vitamin D deficiency in pediatric fracture patients: Prevalence,risk factors,and vitamin D supplementation
- صفحه:445-451
  
 
Wolcott-rallison syndrome with novel EIF2AK3 gene mutation
- صفحه:496-497
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