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Nacak

Muradiye Nacak

The Possible Role of Mitochondrial Uncoupling Protein 2 (UCP2) Gene on the Development of Metabolic Syndrome and Platelet Count in Obese Children/Adolescents - A Preliminary Study

(J Clin Res Pediatr Endocrinol 2015; 7: 66-66)

A Preliminary Study of the Possible Role of Cannabinoid Receptor-1 (CNR1) Gene Polymorphisms in the Development of Morbid Obesity in Obese Children

(J Clin Res Pediatr Endocrinol 2015; 7: 87-87)
Naeem

Muhammad Naeem

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)
Nagasatyavani

Mudiganti Nagasatyavani

An Unusual Combination of Klinefelter Syndrome and Growth Hormone Deficiency in a Prepubertal Child

(J Clin Res Pediatr Endocrinol 2014; 6: 187-189)
Nagender

Jakka Nagender

An Unusual Combination of Klinefelter Syndrome and Growth Hormone Deficiency in a Prepubertal Child

(J Clin Res Pediatr Endocrinol 2014; 6: 187-189)
Nair

Mohandas Nair

Identification of Novel ROR2 Gene Mutations in Indian Children with Robinow Syndrome

(J Clin Res Pediatr Endocrinol 2014; 6: 79-83)

Monogenic Diabetes Secondary to Congenital Lipodystrophy in a 14-year-old Yemeni Girl-Case Report

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

Akie Nakamura

Early Onset of Liver Steatosis in a Japanese Girl with Maturity-Onset Diabetes of the Young Type 3 (MODY3)

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

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

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

A Novel De Novo GATA Binding Protein 3 Mutation in a Turkish Boy with Hypoparathyroidism, Deafness, and Renal Dysplasia Syndrome

(J Clin Res Pediatr Endocrinol 2015; 7: 344-348)
Nakasatien

Soontaree Nakasatien

A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient

(J Clin Res Pediatr Endocrinol 2016; 8: 241-245)
Nalbantoğlu

Özlem Nalbantoğlu

A Case with Infantile-Onset Pancytopenia and Hyperglycemia Associated with SLC19A2 Mutation

(J Clin Res Pediatr Endocrinol 2015; 7: 89-89)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Osteopetrosis of Infancy

(J Clin Res Pediatr Endocrinol 2015; 7: 356-357)
Nalbantoğlu Elmas

Özlem Nalbantoğlu Elmas

Tuberculous Meningitis Associated with Diabetic Ketoacidosis

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

Importance of Insulin Immunoassays in the Diagnosis of Factitious Hypoglycemia

(J Clin Res Pediatr Endocrinol 2014; 6: 258-261)

46,XY Complete Gonadal Dysgenesis: A Case Report

(J Clin Res Pediatr Endocrinol 2015; 7: 65-65)

A Case with Acrodysostosis and Hormone Resistance

(J Clin Res Pediatr Endocrinol 2015; 7: 75-75)

Genetic Diagnosis Using Whole Exome Analysis in Two Cases with Malignant Infantile Osteopetrosis

(J Clin Res Pediatr Endocrinol 2015; 7: 76-76)
Namwongprom

Sirianong Namwongprom

Radioactive Iodine for Thyrotoxicosis in Childhood and Adolescence: Treatment and Outcomes

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

Relationship Between Total Body Adiposity Assessed by Dual-Energy X-ray Absorptiometry, Birth Weight and Metabolic Syndrome in Young Thai Adults

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

Relationship Between Body Composition Parameters and Metabolic Syndrome in Young Thai Adults

(J Clin Res Pediatr Endocrinol 2014; 6: 227-232)
Naruse

Yuki Naruse

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

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

José R. Navarro-Betancourt

The 13C-Glucose Breath Test for Insulin Resistance Assessment in Adolescents: Comparison with Fasting and Post-Glucose Stimulus Surrogate Markers of Insulin Resistance

(J Clin Res Pediatr Endocrinol 2016; 8: 419-424)
Nayır

Ahmet Nayır

Neutrophil Gelatinase-Associated Lipocalin as an Early Sign of Diabetic Kidney Injury in Children

(J Clin Res Pediatr Endocrinol 2015; 7: 274-279)
Nemec

Vladimir Nemec

Normal Bone Turnover in Transient Hyperphosphatasemia

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

Maria I. New

CYP21A2 Gene Mutations in Congenital Adrenal Hyperplasia: Genotype-phenotype correlation in Turkish children - Original Article

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

Olcay Neyzi

Puberty and Pubertal Growth in Healthy Turkish Girls: No evidence for secular trend - Original Article

(J Clin Res Pediatr Endocrinol 2008; 1: -)

Anthropometric Studies on the Turkish 
Population - A Historical Review

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

Z-Score Reference Values for Height in Turkish Children Aged 6 to 18 Years

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

Epidemiologic Features of Type 1 Diabetic Patients between 0 and 18 Years of Age in İstanbul City

(J Clin Res Pediatr Endocrinol 2015; 7: 49-56)

Reference Values for Weight, Height, Head Circumference, and Body Mass Index in Turkish Children

(J Clin Res Pediatr Endocrinol 2015; 7: 280-293)

A Critical Appraisal of Growth Hormone Therapy in Growth Hormone Deficiency and Turner Syndrome Patients in Turkey

(J Clin Res Pediatr Endocrinol 2016; 8: 490-495)
Nicoletti

Annalisa Nicoletti

Current Loss-of-Function Mutations in the Thyrotropin Receptor Gene: When to Investigate, Clinical Effects, and Treatment

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

Hiroko Nihei

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

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

Kathryn Noyes

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