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Enver Simsek

Showing results (31-40 of 36) with videos related to

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Human Genetics|January 23, 2022
Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humansA Kemal Topaloglu, Enver Simsek, Matthew A Kocher, et al.
BMC Medical Genetics|June 20, 2018
SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case reportShoko Horita, Enver Simsek, Tulay Simsek, et al.
Molecular Vision|January 5, 2011
Novel mutations in the USH1C gene in Usher syndrome patientsMaría José Aparisi, Gema García-García, Teresa Jaijo, et al.
Journal of Neuroendocrinology|February 16, 2022
PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadismBradley A Welch, Hyun-Ju Cho, Seyit Ahmet Ucakturk, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2016
Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From TurkeyBaris Akinci, Huseyin Onay, Tevfik Demir, et al.
Frontiers in Pediatrics|July 18, 2022
Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in TurkeyEylem Kiral, Birgul Kirel, Merve Havan, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Human Genetics|January 23, 2022
Inactivating NHLH2 variants cause idiopathic hypogonadotropic hypogonadism and obesity in humansA Kemal Topaloglu, Enver Simsek, Matthew A Kocher, et al.
BMC Medical Genetics|June 20, 2018
SLC4A4 compound heterozygous mutations in exon-intron boundary regions presenting with severe proximal renal tubular acidosis and extrarenal symptoms coexisting with Turner's syndrome: a case reportShoko Horita, Enver Simsek, Tulay Simsek, et al.
Molecular Vision|January 5, 2011
Novel mutations in the USH1C gene in Usher syndrome patientsMaría José Aparisi, Gema García-García, Teresa Jaijo, et al.
Journal of Neuroendocrinology|February 16, 2022
PLXNB1 mutations in the etiology of idiopathic hypogonadotropic hypogonadismBradley A Welch, Hyun-Ju Cho, Seyit Ahmet Ucakturk, et al.
The Journal of Clinical Endocrinology and Metabolism|May 5, 2016
Natural History of Congenital Generalized Lipodystrophy: A Nationwide Study From TurkeyBaris Akinci, Huseyin Onay, Tevfik Demir, et al.
Frontiers in Pediatrics|July 18, 2022
Increased Severe Cases and New-Onset Type 1 Diabetes Among Children Presenting With Diabetic Ketoacidosis During First Year of COVID-19 Pandemic in TurkeyEylem Kiral, Birgul Kirel, Merve Havan, et al.
Pageof 4