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Bircan

İffet Bircan

Genetics of Obesity

(J Clin Res Pediatr Endocrinol 2009; 1: -)

Wolcott-Rallison Syndrome Due to a Novel Mutation (R491X) in EIF2AK3 Gene

(J Clin Res Pediatr Endocrinol 2012; 4: -)

Urinary Bisphenol A Levels in Girls with Idiopathic Central Precocious Puberty

(J Clin Res Pediatr Endocrinol 2014; 6: -)

A Combination of Nifedipine and Octreotide Treatment in an Hyperinsulinemic Hypoglycemic Infant

(J Clin Res Pediatr Endocrinol 2014; 6: 119-121)

Current Practice in Diagnosis and Treatment of Growth Hormone Deficiency in Childhood: A Survey from Turkey

(J Clin Res Pediatr Endocrinol 2015; 7: 37-44)

An Infantile Hypophosphatasia Patient with a Homozygous Mutation in the ALPS Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 79-79)

Pyridoxine-Responsive Seizures in Infantile Hypophosphatasia and a Novel Homozygous Mutation in ALPL Gene

(J Clin Res Pediatr Endocrinol 2016; 8: 360-364)

Clinical and Molecular Genetic Analysis in Three Children with Wolfram Syndrome: A Novel WFS1 Mutation (c.2534T>A)

(J Clin Res Pediatr Endocrinol 2017; 9: 80-84)

Evaluation of the Response to the First Two Years of Growth Hormone Treatment in Kabuki Make-Up Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 7-7)
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