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journal of clinical research in pediatric endocrinology
  
سال:2016 - دوره:8 - شماره:2
  
 
A newly-discovered mutation in the RFX6 gene of the rare Mitchell-Riley syndrome
- صفحه:246-249
  
 
A novel c.554+5C>T mutation in the DUOXA2 gene combined with p.R885Q mutation in the DUOX2 gene causing congenital hypothyroidism
- صفحه:224-227
  
 
A novel mutation in human androgen receptor gene causing partial androgen insensitivity syndrome in a patient presenting with gynecomastia at puberty
- صفحه:232-235
  
 
A novel mutation in thyroid peroxidase gene causing congenital goitrous hypothyroidism in a German-Thai patient
- صفحه:241-245
  
 
A novel null mutation in P450 aromatase gene (CYP19A1) associated with development of hypoplastic ovaries in humans
- صفحه:205-210
  
 
Association of DENND1A gene polymorphisms with polycystic ovary syndrome: A meta-analysis
- صفحه:135-143
  
 
Bone mineral density in adolescent girls with hypogonadotropic and hypergonadotropic hypogonadism
- صفحه:163-169
  
 
Cellular trace element changes in type 1 diabetes patients
- صفحه:180-186
  
 
Clinical and genetic characteristics,management and long-term follow-up of turkish patients with congenital hyperinsulinism
- صفحه:197-204
  
 
Early presentation of Hyperinsulinism/hyperammonemia syndrome in three Serbian patients
- صفحه:228-231
  
 
Editor’s note
  
 
Effects of thyroid autoimmunity on early atherosclerosis in euthyroid girls with Hashimoto’s thyroiditis
- صفحه:150-156
  
 
Gonadotropin-releasing hormone analogue treatment in females with moderately early puberty: No effect on final height
- صفحه:211-217
  
 
Homozygous ALA65Pro mutation with V89L polymorphism in SRD5A2 deficiency
- صفحه:218-223
  
 
Idiopathic hypogonadotropic hypogonadism caused by inactivating mutations in SRA1
- صفحه:125-134
  
 
Investigation of SHOX gene mutations in Turkish patients with idiopathic short stature
- صفحه:144-149
  
 
Long-term outcome after robotic-assisted gastroplication in adolescents: Hunger hormone and food preference changes two case reports
- صفحه:250-256
  
 
Maternal obesity and its short-and long-term maternal and infantile effects
- صفحه:114-124
  
 
Menstrual characteristics of pubertal girls: A questionnaire-based study in Turkey
- صفحه:192-196
  
 
Neonatal thyroid-stimulating hormone screening as a monitoring tool for iodine deficiency in Turkey
- صفحه:187-191
  
 
Phenotype,sex of rearing,gender re-assignment,and response to medical treatment in extended family members with a novel mutation in the SRD5A2 gene
- صفحه:236-240
  
 
Thyroid function and thyroid autoimmunity in relation to weight status and cardiovascular risk factors in children and adolescents: A population-based study
- صفحه:157-162
  
 
Transient congenital hypothyroidism in Turkey: An analysis on frequency and natural course
- صفحه:170-179
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