Mahmut Çöker - Concepedia

Author

Mahmut Çöker

Also Known As

A Or8-58 Cicognani, Coker Mahmut, Coker, Mahmut, H. Güven, M Coker, M. Coker, M. Çoker, MAHMUT ÇOKER, MAhmut Çöker, Mahmut Coker

195

Publications

2.3K

Citations

H-Index

129

Concepts

All Affiliations

Ege University University Children's Hospital Zurich Wilhelmina Children's Hospital University Medical Center Freiburg Johannes Gutenberg University Mainz

MÇ

About

Mahmut Çöker is an author at Ege University specializing in medicine, pediatrics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	26	647
2	Health Sciences	6	6	261
3	Public Health	6	6	249
4	Engineering	1	1	18
5	Nursing	1	1	11

Mahmut Çöker

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
A Phase 3 Trial of Sebelipase Alfa in Lysosomal Acid Lipase Deficiency Barbara K. Burton, Manisha Balwani, François Feillet, New England Journal of Medicine	2015	238
Clinical course of sly syndrome (mucopolysaccharidosis type VII) Adriana M. Montaño, Lock Hock Ngu, Robert D. Steiner, Journal of Medical Genetics	2016	162
Idiopathic Hyperphosphatasia and <i>TNFRSF11B</i> Mutations: Relationships Between Phenotype and Genotype Belinda Chong, Madhuri Hegde, Matthew Fawkner, Journal of Bone and Mineral Research	2003	120
Burden of disease in patients with Morquio A syndrome: results from an international patient-reported outcomes survey Christian J. Hendriksz, Christine Lavery, Mahmut Çöker, Orphanet Journal of Rare Diseases	2014	92
Bone Mineral Density of Healthy Turkish Children and Adolescents Damla Gökşen, Şükran Darcan, Mahmut Çöker, Journal of Clinical Densitometry Bone DiseaseNutritionBody CompositionBone HealthAdolescent Nutrition	2006	85
The effect of childhood obesity on respiratory function tests and airway hyperresponsiveness. Zülal Ülger, Esen Demir, Remziye Tanaç, PubMed AsthmaPhysical ActivityPediatric Lung DiseaseObesityBody Composition	2006	81
The missing “link”: an autosomal recessive short stature syndrome caused by a hypofunctional XYLT1 mutation Julia Schreml, Burak Durmaz, Özgür Çoğulu, Human Genetics Developmental BiologyMendelian Disorder“ Link ”Hypofunctional Xylt1 MutationGenetic Disorder	2013	77
Alterations of blood pressure in type 1 diabetic children and adolescents Şükran Darcan, Damla Gökşen, Erkin Serdaroğlu, Pediatric Nephrology Metabolic SyndromeHypertensionType 1Diabetic ChildrenDiabetes Management	2006	54
The oral manifestations of Maroteaux-Lamy syndrome (mucopolysaccharidosis VI): A case report Ali Rıza Alpöz, Mahmut Çöker, Elif Celen, Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology Maroteaux-lamy SyndromePathologyOral ManifestationsCase Report	2006	54
Carglumic acid enhances rapid ammonia detoxification in classical organic acidurias with a favourable risk-benefit profile: a retrospective observational study Vassili Valayannopoulos, Julien Baruteau, María Bueno Delgado, Orphanet Journal of Rare Diseases	2016	45

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