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Enver Simsek

Showing results (21-30 of 36) with videos related to

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Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2003
Sensitivity of iodine deficiency indicators and iodine status in TurkeyEnver Simsek, Alper Safak, Ozlem Yavuz, et al.
International Journal of Endocrinology|April 30, 2014
Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoeaCigdem Binay, Enver Simsek, Oguz Cilingir, et al.
Molecular Syndromology|February 6, 2025
Key Clinical and X-Ray Characteristics for the Diagnosis of Kenny-Caffey Syndrome Types 1 and 2Enver Simsek, Sumeyye Emel Eren, Atilla Cayir, et al.
International Journal of Endocrinology|July 20, 2012
Procoagulant and anticoagulant factors in childhood hypothyroidismNevin Kilic, Yildiz Dallar, Enver Simsek, et al.
Hormone Research in Paediatrics|January 10, 2019
Clinical, Histochemical, and Molecular Study of Three Turkish Siblings Diagnosed with H Syndrome, and Literature ReviewEnver Simsek, Tulay Simsek, Makbule Eren, et al.
European Journal of Radiology|March 22, 2007
Evaluation of the thyroid blood flow with Doppler ultrasonography in healthy school-aged childrenBurhan Yazici, Enver Simsek, Besir Erdogmus, et al.
Orphanet Journal of Rare Diseases|May 16, 2012
Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA DehydrogenaseAmanda J Heslegrave, Ritika R Kapoor, Simon Eaton, et al.
The Journal of Clinical Endocrinology and Metabolism|February 9, 2006
A novel thyroid hormone receptor-beta mutation that fails to bind nuclear receptor corepressor in a patient as an apparent cause of severe, predominantly pituitary resistance to thyroid hormoneSharon Y Wu, Ronald N Cohen, Enver Simsek, et al.
Annals of Neurology|February 26, 2003
A new mutation of the fukutin gene in a non-Japanese patientFatma Silan, Mieko Yoshioka, Kazuhiro Kobayashi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2011
Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigreesSarah E Flanagan, Ann-Marie Patch, Jonathan M Locke, et al.
Pageof 4

Showing results (21-30 of 36) with videos related to

Sort By:
Pageof 4
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 26, 2003
Sensitivity of iodine deficiency indicators and iodine status in TurkeyEnver Simsek, Alper Safak, Ozlem Yavuz, et al.
International Journal of Endocrinology|April 30, 2014
Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoeaCigdem Binay, Enver Simsek, Oguz Cilingir, et al.
Molecular Syndromology|February 6, 2025
Key Clinical and X-Ray Characteristics for the Diagnosis of Kenny-Caffey Syndrome Types 1 and 2Enver Simsek, Sumeyye Emel Eren, Atilla Cayir, et al.
International Journal of Endocrinology|July 20, 2012
Procoagulant and anticoagulant factors in childhood hypothyroidismNevin Kilic, Yildiz Dallar, Enver Simsek, et al.
Hormone Research in Paediatrics|January 10, 2019
Clinical, Histochemical, and Molecular Study of Three Turkish Siblings Diagnosed with H Syndrome, and Literature ReviewEnver Simsek, Tulay Simsek, Makbule Eren, et al.
European Journal of Radiology|March 22, 2007
Evaluation of the thyroid blood flow with Doppler ultrasonography in healthy school-aged childrenBurhan Yazici, Enver Simsek, Besir Erdogmus, et al.
Orphanet Journal of Rare Diseases|May 16, 2012
Leucine-sensitive hyperinsulinaemic hypoglycaemia in patients with loss of function mutations in 3-Hydroxyacyl-CoA DehydrogenaseAmanda J Heslegrave, Ritika R Kapoor, Simon Eaton, et al.
The Journal of Clinical Endocrinology and Metabolism|February 9, 2006
A novel thyroid hormone receptor-beta mutation that fails to bind nuclear receptor corepressor in a patient as an apparent cause of severe, predominantly pituitary resistance to thyroid hormoneSharon Y Wu, Ronald N Cohen, Enver Simsek, et al.
Annals of Neurology|February 26, 2003
A new mutation of the fukutin gene in a non-Japanese patientFatma Silan, Mieko Yoshioka, Kazuhiro Kobayashi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 22, 2011
Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigreesSarah E Flanagan, Ann-Marie Patch, Jonathan M Locke, et al.
Pageof 4