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
J.G.Mackay

Deborah J.G.Mackay

Transient Neonatal Diabetes Mellitus in a Turkish Patient with Three Novel Homozygous Variants in the ZFP57 Gene

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

Andrew Jackson

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

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

Jill Jacobson

Morning Cortisol Levels Affected by Sex and Pubertal Status in Children and Young Adults

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

Bahar Jafari

Functioning Adrenocortical Tumors in 
Children-Secretory Behavior

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

Sevinç Jaferova

A Case of Vitamin D-Dependent Rickets Type 1A with a Novel Mutation in the Uzbek Population

(J Clin Res Pediatr Endocrinol 2016; 8: 484-489)
Jain

Rajesh Jain

Isolated Cushing’s Syndrome in Early Infancy Due to Left Adrenal Adenoma: An Unusual Aetiology

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

Medical Management of Thyroid Ectopia: Report of Three Cases

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

Javad Javaheri

Epidemiology of Congenital Hypothyroidism in Markazi Province, Iran

(J Clin Res Pediatr Endocrinol 2014; 6: 105-110)
Jayasekara

Rohan W. Jayasekara

An Infant Born to a Mother with Gestational Diabetes Presenting with 49,XXXXY Syndrome and Renal Agenesis-A Case Report

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

Musharraf Jelani

A Novel Missense Mutation in the CLPP Gene Causing Perrault Syndrome Type 3 in a Turkish Family

(J Clin Res Pediatr Endocrinol 2016; 8: 472-477)
Jessup

Ashley B. Jessup

Effects of Diabetic Ketoacidosis on Visual and Verbal Neurocognitive Function in Young Patients Presenting with New-Onset Type 1 Diabetes

(J Clin Res Pediatr Endocrinol 2015; 7: 203-210)
Jin

Tianbo Jin

Association of DENND1A Gene Polymorphisms with Polycystic Ovary Syndrome: A Meta-Analysis

(J Clin Res Pediatr Endocrinol 2016; 8: 135-143)

Association between Common Genetic Variants and Polycystic Ovary Syndrome Risk in a Chinese Han Population

(J Clin Res Pediatr Endocrinol 2016; 8: 405-410)
Jones

Jeremy Jones

Optimising Outcome in Congenital Hypothyroidism; Current Opinions on Best Practice in Initial Assessment and Subsequent Management

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

Matthew Jonhson

A Diabetic Infant with Homozygous LRBA Mutation: The Youngest Patient Reported

(J Clin Res Pediatr Endocrinol 2016; 8: 16-16)
Joustra

Sjoerd Joustra

Delayed Adrenarche may be an Additional Feature of Immunoglobulin Super Family Member 1 Deficiency Syndrome

(J Clin Res Pediatr Endocrinol 2016; 8: 86-91)
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