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Çelmeli

Gamze Çelmeli

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

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

The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study

(J Clin Res Pediatr Endocrinol 2016; 8: 305-312)

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)

Basal Serum Neurokinin B Levels in Differentiating Idiopathic Central Precocious Puberty from Premature Thelarche

(J Clin Res Pediatr Endocrinol 2017; 9: 101-105)

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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