Concepedia

Author

Heves Kırmızıbekmez

Zeynep Kamil HospitalORCID

Also Known As

H. Kırmızıbekmez, Heves KIRMIZIBEKMEZ, Heves Kirmizibekmez, Heves Kırmızıbekmez, KIRMIZIBEKMEZ, Heves, Kirmizibekmez, Heves

93

Publications

406

Citations

12

H-Index

38

Concepts

All Affiliations

Zeynep Kamil HospitalÜmraniye Eğitim ve Araştırma HastanesiKocaeli ÜniversitesiEducation Training And ResearchOwl Research Institute
HK

About

Heves Kırmızıbekmez is an author at Zeynep Kamil Hospital specializing in medicine, public health, and pediatrics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

4

4

72

2

Public Health

3

3

58

3

Health Sciences

1

1

14

4

Diabetes

1

1

14

5

Hepatology

1

1

14

Heves Kırmızıbekmez

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10

Publications

186

Citations

10

H-Index

YearCitations

Genetic and Clinical Characteristics of Patients with Vitamin D Dependent Rickets Type 1A

Fatma Dursun, Gamze Özgürhan, Heves Kırmızıbekmez,

Journal of Clinical Research in Pediatric Endocrinology

2019

30

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

Fatma Dursun, Hussein Sheikh Ali Mohamoud, Noreen Karim,

Journal of Clinical Research in Pediatric Endocrinology

2016

26

Autoimmune Polyglandular Syndrome Type 2: A Rare Condition in Childhood

Heves Kırmızıbekmez, Gül Yeşiltepe Mutlu, Nafiye Urgancı,

Journal of Clinical Research in Pediatric Endocrinology

2015

22

Metabolic Bone Disease of Prematurity: Report of Four Cases

Gül Yeşiltepe Mutlu, Heves Kırmızıbekmez, Elif Özsu,

Journal of Clinical Research in Pediatric Endocrinology

2014

21

Developmental Defects of the Thyroid Gland: Relationship with Advanced Maternal Age

Heves Kırmızıbekmez, Ayla Güven, Metin Yıldız,

Journal of Clinical Research in Pediatric Endocrinology

2012

21

Incidence of Type 1 Diabetes in Children Aged Below 18 Years During 2013-2015 in Northwest Turkey

Şükran Poyrazoğlu, Rüveyde Bundak, Zehra Yavaş Abal,

Journal of Clinical Research in Pediatric Endocrinology

2018

16

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

Gül Yeşiltepe Mutlu, Heves Kırmızıbekmez, Akie Nakamura,

Journal of Clinical Research in Pediatric Endocrinology

2015

15

Hepatopathies in children and adolescents with type 1 diabetes

Firdevs Aydın, Nelgin Gerenlı, Fatma Dursun,

Journal of Pediatric Endocrinology and Metabolism

2019

14

Pure gonadal dysgenesis (Swyer syndrome) due to microdeletion in the SRY gene: a case report

Gül Yeşiltepe Mutlu, Heves Kırmızıbekmez, Hatip Aydın,

Journal of Pediatric Endocrinology and Metabolism

2014

11

Atypical Presentation of Hashimoto’s Disease in an Adolescent: Thyroid-Associated Ophthalmopathy

Heves Kırmızıbekmez, Gül Yeşiltepe Mutlu, Fatma Dursun,

Journal of Clinical Research in Pediatric Endocrinology

2014

10

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