Agnes E. Sallai, Ph.D.
Affiliations: | 2009 | Semmelweis Egyetem, Hungary |
Area:
Oncology, Endocrinology BiologyGoogle:
"Agnes Sallai"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Karoly Racz | grad student | 2009 | Semmelweis Egyetem | |
| (Molekularis genetikai vizsgalatok jelentosege endokrin daganatok megelozeseben.) | ||||
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Publications
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| Kovács ÁF, Beniczky NJ, Bertalan RÁ, et al. (2022) [Diagnostics and follow-up strategy for Silver–Russell syndrome based on a case report showing familial accumulation]. Orvosi Hetilap. 163: 1775-1781 |
| Bukovszky B, Gács Z, Jenővári Z, et al. (2022) Pediatric adrenocortical adenoma presenting with Cushing’s syndrome Orvosi Hetilap. 163: 407-412 |
| McElreavey K, Jorgensen A, Eozenou C, et al. (2019) Pathogenic variants in the DEAH-box RNA helicase DHX37 are a frequent cause of 46,XY gonadal dysgenesis and 46,XY testicular regression syndrome. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Kriskó D, Popper-Sachetti A, Sallai Á, et al. (2019) [Angioid streaks in systemic disease]. Orvosi Hetilap. 160: 994-1000 |
| Pinti É, Lengyel A, Sallai Á, et al. (2018) [Examination of sex chromosome abnormalities in childhood]. Orvosi Hetilap. 159: 1121-1128 |
| Ács OD, Péterfia B, Hollósi P, et al. (2018) [Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome]. Orvosi Hetilap. 159: 64-69 |
| Dávid A, Butz H, Halász Z, et al. (2017) [The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study]. Orvosi Hetilap. 158: 1351-1356 |
| Dusatkova P, Pfäffle R, Brown MR, et al. (2015) Genesis of two most prevalent PROP1 gene variants causing combined pituitary hormone deficiency in 21 populations. European Journal of Human Genetics : Ejhg |
| Virágh K, Tőke J, Sallai A, et al. (2014) Gradual development of brachydactyly in pseudohypoparathyroidism. The Journal of Clinical Endocrinology and Metabolism. 99: 1945-6 |
| Bertalan R, Sallai A, Sólyom J, et al. (2010) Hyperthyroidism caused by a germline activating mutation of the thyrotropin receptor gene: difficulties in diagnosis and therapy. Thyroid : Official Journal of the American Thyroid Association. 20: 327-32 |