AUTHOR INDEX

A B C Ç D E F G H I İ J K L M N O Ö P R S Ş T U Ü V Y Z
Ibardolaza

Milagros Ibardolaza

Inflammatory Cytokine Profiles During Exercise in Obese, Diabetic, and Healthy Children

(J Clin Res Pediatr Endocrinol 2011; 3: -)
Ibrahim

Niema A. Ibrahim

A Case of Achondrogenesis Type 2/Hypochondrogenesis Due to a De Novo Mutation in the COL2A1 Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 80-80)
Ibukunoluwa

Fakunle Ibukunoluwa

Phenotype, Sex of Rearing, Gender Re-Assignment, and Response to Medical Treatment in Extended Family Members with a Novel Mutation in the SRD5A2 Gene

(J Clin Res Pediatr Endocrinol 2016; 8: 236-240)
Index

Author Index

2009 Author Index

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

2010 Author Index

(J Clin Res Pediatr Endocrinol 2010; 2: -)

2009 Referee Index

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

2010 Referee Index

(J Clin Res Pediatr Endocrinol 2010; 2: -)

2009 Subject Index

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

2010 Subject Index

(J Clin Res Pediatr Endocrinol 2010; 2: -)
Ingelfinger

Julie R Ingelfinger

Averting the Legacy of Kidney Disease-Focus on Childhood

(J Clin Res Pediatr Endocrinol 2016; 8: 108-113)
Ishizu

Katsura Ishizu

Polyarthritis Caused by Methimazole in Two Japanese Patients with Graves’ Disease

(J Clin Res Pediatr Endocrinol 2013; 5: -)
Işgüven

Pınar Işgüven

Microcephalic Osteodysplastic Primordial Dwarfism Type Two

(J Clin Res Pediatr Endocrinol 2015; 7: 71-71)
Işık

Emregül Işık

Severe Congenital Insulin Resistance Syndrome Due to a Compound Heterozygous c.836G>A & c.1268+2T>A Mutation in Insulin Receptor (INSR) Gene

(J Clin Res Pediatr Endocrinol 2015; 7: 85-85)

Two Siblings with Microcephalic Osteodysplastic Primordial Dwarfism Type II (MOPD II)

(J Clin Res Pediatr Endocrinol 2017; 9: 10-10)

Six 11-Beta Hydroxylase Deficiency Patients: Identification of Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 26-26)

Mutation Spectrum of GCK, HNF1A, and HNF1B in MODY Patients and 40 Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 22-22)

Anthropometric Measurements and Complications of Achondroplasia Patients

(J Clin Res Pediatr Endocrinol 2017; 9: 22-22)

The Mutation Spectrum of DHCR7 Gene and Two Novel Mutations

(J Clin Res Pediatr Endocrinol 2017; 9: 21-22)

POU1F1 and PROP1 Gene Mutations in 4 Cases of Combined Pituitary Hormone Deficiency

(J Clin Res Pediatr Endocrinol 2017; 9: 20-21)

HOXC4 Gene is Possibly Responsible for Lin-Gettig Syndrome

(J Clin Res Pediatr Endocrinol 2017; 9: 20-20)

A Case of SHOX Gene Deletion Diagnosed By Microarray

(J Clin Res Pediatr Endocrinol 2017; 9: 20-20)

Is Hyperpigmentation on the First Day of Life Always Associated with IMAGe Syndrome?

(J Clin Res Pediatr Endocrinol 2014; 6: 266-268)
Işıkay

Sedat Işıkay

Pseudohypoparathyroidism Presenting with Ventricular Arrhythmia: A Case Report

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

Masako Izawa

Polyarthritis Caused by Methimazole in Two Japanese Patients with Graves’ Disease

(J Clin Res Pediatr Endocrinol 2013; 5: -)
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