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Enver Şimşek
Enver Şimşek
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Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Sonographic assessment of the normal limits and percentile curves of liver, spleen, and kidney dimensions in healthy school‐aged children
AA Safak, E Simsek, T Bahcebasi
Journal of ultrasound in medicine 24 (10), 1359-1364, 2005
1642005
The prevalence of overweight and obese children aged 6–17 years in the West Black Sea region of Turkey
E Simsek, S Akpinar, T Bahcebasi, DA Senses, K Kocabay
International journal of clinical practice 62 (7), 1033-1038, 2008
1252008
A new mutation of the fukutin gene in a non‐Japanese patient
F Silan, M Yoshioka, K Kobayashi, E Simsek, M Tunc, M Alper, M Cam, ...
Annals of Neurology: Official Journal of the American Neurological …, 2003
1222003
Neonatal screening for congenital hypothyroidism in West Black Sea area, Turkey
E Simsek, M Karabay, K Kocabay
International journal of clinical practice 59 (3), 336-341, 2005
982005
Natural history of congenital generalized lipodystrophy: a nationwide study from Turkey
B Akinci, H Onay, T Demir, S Ozen, H Kayserili, G Akinci, B Nur, B Tuysuz, ...
The Journal of Clinical Endocrinology & Metabolism 101 (7), 2759-2767, 2016
862016
Turner syndrome and associated problems in Turkish children: a multicenter study
E Yeşilkaya, A Bereket, F Darendeliler, F Baş, Ş Poyrazoğlu, BK Aydın, ...
Journal of Clinical Research in Pediatric Endocrinology 7 (1), 27, 2015
782015
Genome-Wide Homozygosity Analysis Reveals HADH Mutations as a Common Cause of Diazoxide-Responsive Hyperinsulinemic-Hypoglycemia in …
SE Flanagan, AM Patch, JM Locke, T Akcay, E Simsek, M Alaei, Z Yekta, ...
The Journal of Clinical Endocrinology & Metabolism 96 (3), E498-E502, 2011
752011
Iodine deficiency in Turkey
N Yordam, A Özön, A Alikaşifoğlu, A Özgen, N Ceren, Y Zafer, E Şimşek
European journal of pediatrics 158, 501-505, 1999
731999
Wolfram (DIDMOAD) syndrome: a multidisciplinary clinical study in nine Turkish patients and review of the literature
E Simsek, T Simsek, S TekgüT, S Hosal, V Seyrantepe, G Aktan
Acta Paediatrica 92 (1), 55-61, 2003
712003
Childhood obesity-related cardiovascular risk factors and carotid intima-media thickness
E Simşek, H Balta, Z Balta, Y Dallar
The Turkish journal of pediatrics 52 (6), 602-611, 2010
602010
A novel thyroid hormone receptor-β mutation that fails to bind nuclear receptor corepressor in a patient as an apparent cause of severe, predominantly pituitary resistance to …
SY Wu, RN Cohen, E Simsek, DA Senses, NE Yar, H Grasberger, J Noel, ...
The Journal of Clinical Endocrinology & Metabolism 91 (5), 1887-1895, 2006
472006
Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA Dehydrogenase
AJ Heslegrave, RR Kapoor, S Eaton, B Chadefaux, T Akcay, E Simsek, ...
Orphanet journal of rare diseases 7, 1-6, 2012
382012
Congenital hypothyroidism and iodine status in Turkey: a comparison between the data obtained from an epidemiological study in school-aged children and neonatal screening for …
E Simşek, M Karabay, A Safak, K Kocabay
Pediatric endocrinology reviews: PER 1, 155-161, 2003
372003
Effectiveness of two different methods for pain reduction during insulin injection in children with Type 1 diabetes: Buzzy and ShotBlocker
N Canbulat Sahiner, AS Turkmen, A Acikgoz, E Simsek, B Kirel
Worldviews on Evidence‐Based Nursing 15 (6), 464-470, 2018
362018
Utility of ApoB/ApoA1 ratio for the prediction of cardiovascular risk in children with metabolic syndrome
S Savas Erdeve, E Simsek, Y Dallar, Z Biyikli
The Indian Journal of Pediatrics 77, 1261-1265, 2010
362010
Neonatal screening for congenital adrenal hyperplasia in Turkey: a pilot study with 38,935 infants
T Güran, B Tezel, F Gürbüz, BS Eklioğlu, N Hatipoğlu, C Kara, E Şimşek, ...
Journal of clinical research in pediatric endocrinology 11 (1), 13, 2019
342019
Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoea
C Binay, E Simsek, O Cilingir, Z Yuksel, O Kutlay, S Artan
International Journal of Endocrinology 2014, 2014
342014
Two frameshift mutations in MKRN3 in Turkish patients with familial central precocious puberty
E Simsek, M Demiral, S Ceylaner, B Kırel
Hormone research in paediatrics 87 (6), 405-411, 2017
322017
The growth characteristics of patients with noonan syndrome: results of three years of growth hormone treatment: a nationwide multicenter study
Z Şıklar, M Genens, Ş Poyrazoğlu, F Baş, F Darendeliler, R Bundak, ...
Journal of Clinical Research in Pediatric Endocrinology 8 (3), 305, 2016
322016
Pituitary hyperplasia mimicking pituitary macroadenoma in two adolescent patients with long-standing primary hypothyroidism: case reports and review of literature
E Simşek, T Simşek, S Savaş-Erdeve, B Erdoğmuş, M Döşoğlu
The Turkish journal of pediatrics 51 (6), 624-630, 2009
312009
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