Enver Şimşek - Concepedia

Author

Enver Şimşek

Also Known As

E Simsek, E. S. Simsek, E. Simsek, E. ŞimŞek, ENVER SIMSEK, Emrullah Simsek, Emrullah Şimşek, Enver Simsek, Enver Simşek, Enver SİMSEK

118

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Eskişehir Osmangazi University Istanbul University Marmara University Bolu Abant İzzet Baysal University Düzce Üniversitesi

EŞ

About

Enver Şimşek is an author at Eskişehir Osmangazi University specializing in medicine, pediatrics, and obstetrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	12	17	325
2	Public Health	5	5	96
3	Health Sciences	2	2	47
4	Education	1	1	18
5	Clinical Nutrition	1	1	14

Enver Şimşek

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
A new mutation of the <i>fukutin</i> gene in a non‐Japanese patient Mieko Yoshioka, Kazuhiro Kobayashi, Enver Şimşek, Annals of Neurology	2003	98
Sonographic Assessment of the Normal Limits and Percentile Curves of Liver, Spleen, and Kidney Dimensions in Healthy School-Aged Children Alp Alper Şafak, Enver Şimşek, Talat Bahçebaşı Journal of Ultrasound in Medicine	2005	95
Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From Turkey Hüseyin Önay, Tevfik Demir, Samim Özen, The Journal of Clinical Endocrinology & Metabolism	2016	94
Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: Outcomes of Extended Pilot Study in 241,083 Infants Tülay Güran, Başak Tezel, Meltem Didem Çakır, Journal of Clinical Research in Pediatric Endocrinology	2020	71
Quality-of-Life Evaluation of Healthy Siblings of Children with Chronic Illness Meltem Dinleyici, Kürşat Bora Çarman, Canan Özdemir, Balkan Medical Journal	2019	67
Wolfram (DIDMOAD) syndrome: a multidisciplinary clinical study in nine Turkish patients and review of the literature Enver Şimşek, Tülay Şimşek, S TekgüT, Acta Paediatrica	2003	65
Genome-Wide Homozygosity Analysis Reveals <i>HADH</i> Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in Consanguineous Pedigrees Sarah E. Flanagan, Ann‐Marie Patch, Jonathan M. Locke, The Journal of Clinical Endocrinology & Metabolism	2011	58
Turner Syndrome and Associated Problems in Turkish Children: A Multicenter Study Ediz Yeşilkaya, Abdullah Bereket, Feyza Darendelıler, Journal of Clinical Research in Pediatric Endocrinology	2015	56
Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase Amanda Heslegrave, Ritika R. Kapoor, Simon Eaton, Orphanet Journal of Rare Diseases	2012	50
UROLOGICAL MANIFESTATIONS OF THE WOLFRAM SYNDROME: OBSERVATIONS IN 14 PATIENTS Serdar Tekgül, Ömer Öge, Enver Şimşek, The Journal of Urology	1999	49

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