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Ágnes Sallai

Showing results (1-10 of 7) with videos related to

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Orvosi Hetilap|July 3, 2018
[Examination of sex chromosome abnormalities in childhood]Éva Pinti, Anna Lengyel, Ágnes Sallai, et al.
Orvosi Hetilap|November 6, 2022
Diagnostics and follow-up strategy for Silver–Russell syndrome based on a case report showing familial accumulationÁrpád Ferenc Kovács, Nikolett Jusztina Beniczky, Rita Ágnes Bertalan, et al.
Orvosi Hetilap|March 6, 2022
Pediatric adrenocortical adenoma presenting with Cushing’s syndromeBence Bukovszky, Zsófia Gács, Zoltán Jenővári, et al.
Orvosi Hetilap|June 18, 2019
[Angioid streaks in systemic disease]Dorottya Kriskó, Andrea Popper-Sachetti, Ágnes Sallai, et al.
Frontiers in Endocrinology|March 18, 2026
Male sex assignment in severely virilized 46,XX children with congenital adrenal hyperplasiaNikolett Jusztina Beniczky, Emma Lenke Magyar, Ágnes Sallai, et al.
Orvosi Hetilap|January 9, 2018
[Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome]Orsolya Dóra Ács, Bálint Péterfia, Péter Hollósi, et al.
Orvosi Hetilap|August 22, 2017
[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study]Anna Dávid, Henriett Butz, Zita Halász, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Orvosi Hetilap|July 3, 2018
[Examination of sex chromosome abnormalities in childhood]Éva Pinti, Anna Lengyel, Ágnes Sallai, et al.
Orvosi Hetilap|November 6, 2022
Diagnostics and follow-up strategy for Silver–Russell syndrome based on a case report showing familial accumulationÁrpád Ferenc Kovács, Nikolett Jusztina Beniczky, Rita Ágnes Bertalan, et al.
Orvosi Hetilap|March 6, 2022
Pediatric adrenocortical adenoma presenting with Cushing’s syndromeBence Bukovszky, Zsófia Gács, Zoltán Jenővári, et al.
Orvosi Hetilap|June 18, 2019
[Angioid streaks in systemic disease]Dorottya Kriskó, Andrea Popper-Sachetti, Ágnes Sallai, et al.
Frontiers in Endocrinology|March 18, 2026
Male sex assignment in severely virilized 46,XX children with congenital adrenal hyperplasiaNikolett Jusztina Beniczky, Emma Lenke Magyar, Ágnes Sallai, et al.
Orvosi Hetilap|January 9, 2018
[Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome]Orsolya Dóra Ács, Bálint Péterfia, Péter Hollósi, et al.
Orvosi Hetilap|August 22, 2017
[The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study]Anna Dávid, Henriett Butz, Zita Halász, et al.
Pageof 1