| International consensus on the diagnosis and management of pediatric patients with hereditary angioedema with C1 inhibitor deficiency H Farkas, I Martinez‐Saguer, K Bork, T Bowen, T Craig, M Frank, ... Allergy 72 (2), 300-313, 2017 | 215 | 2017 |
| Real-world estimates of adrenal insufficiency–related adverse events in children with congenital adrenal hyperplasia SR Ali, J Bryce, H Haghpanahan, JD Lewsey, LE Tan, N Atapattu, ... The Journal of Clinical Endocrinology & Metabolism 106 (1), e192-e203, 2021 | 33 | 2021 |
| Cushing’s syndrome in a child with pancreatic acinar cell carcinoma G Illyés, A Luczay, G Benyó, A Kálmán, K Borka, K Köves, K Racz, ... Endocrine Pathology 18, 95-102, 2007 | 30 | 2007 |
| International practice of corticosteroid replacement therapy in congenital adrenal hyperplasia: data from the I-CAH registry I Bacila, N Freeman, E Daniel, M Sandrk, J Bryce, SR Ali, Z Yavas Abali, ... European journal of endocrinology 184 (4), 553-563, 2021 | 27 | 2021 |
| Potential advantage of N363S glucocorticoid receptor polymorphism in 21-hydroxylase deficiency A Luczay, D Török, A Ferenczi, J Majnik, J Sólyom, G Fekete European journal of endocrinology 154 (6), 859-864, 2006 | 24 | 2006 |
| Methylation status of CYP27B1 and IGF2 correlate to BMI SDS in children with obesity O Ács, B Péterfia, P Hollósi, A Luczay, D Török, A Szabó Obesity Facts 10 (4), 353-362, 2017 | 22 | 2017 |
| NSD1 duplication in Silver–Russell syndrome (SRS): molecular karyotyping in patients with SRS features J Sachwitz, R Meyer, G Fekete, S Spranger, A Matulevičienė, V Kučinskas, ... Clinical Genetics 91 (1), 73-78, 2017 | 21 | 2017 |
| Some GCR polymorphisms (N363S, ER22/23EK, and Bcl-1) may influence steroid-induced toxicities and survival rates in children with ALL O Eipel, M Hegyi, K Csordás, K Németh, A Luczay, D Török, M Csóka, ... Journal of pediatric hematology/oncology 38 (5), 334-340, 2016 | 14 | 2016 |
| Latent autoimmune diabetes in adults (LADA): part of the clinical spectrum of type-1 diabetes mellitus of autoimmune origin P Panczel, N Hosszufalusi, B Bornemisza, L Horvath, L Janoskuti, G Füst, ... Orvosi hetilap 142 (46), 2571-2578, 2001 | 14 | 2001 |
| Detection of antibodies against pancreatic islet cells in clinical practice P Panczel, O Külkey, A Luczay, B Bornemisza, G Illyes, T Halmos, ... Orvosi Hetilap 140 (48), 2695-2701, 1999 | 14 | 1999 |
| The influence of treatment, age at onset, and metabolic control on height in children and adolescents with type 1 diabetes—A SWEET collaborative study J Svensson, A Schwandt, D Pacaud, J Beltrand, NH Birkebaek, ... Pediatric diabetes 19 (8), 1441-1450, 2018 | 12 | 2018 |
| A unique haplotype of RCCX copy number variation: from the clinics of congenital adrenal hyperplasia to evolutionary genetics M Doleschall, A Luczay, K Koncz, K Hadzsiev, É Erhardt, Á Szilágyi, ... European Journal of Human Genetics 25 (6), 702-710, 2017 | 12 | 2017 |
| A comprehensive analysis of Hungarian MODY patients—part I: gene panel sequencing reveals pathogenic mutations in HNF1A, HNF1B, HNF4A, ABCC8 and INS genes Z Gaál, Z Szűcs, I Kántor, A Luczay, P Tóth-Heyn, O Benn, E Felszeghy, ... Life 11 (8), 755, 2021 | 10 | 2021 |
| Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia M Doleschall, D Török, K Mészáros, A Luczay, Z Halász, K Németh, ... Orvosi Hetilap 159 (7), 269-277, 2018 | 9 | 2018 |
| A comprehensive analysis of Hungarian MODY patients—part II: Glucokinase MODY is the most prevalent subtype responsible for about 70% of confirmed cases Z Gaál, Z Szűcs, I Kántor, A Luczay, P Tóth-Heyn, O Benn, E Felszeghy, ... Life 11 (8), 771, 2021 | 8 | 2021 |
| The prevalence of SHOX gene deletion in children with idiopathic short stature. A multicentric study A Dávid, H Butz, Z Halász, D Török, G Nyirő, Á Muzsnai, V Csákváry, ... Orvosi Hetilap 158 (34), 1351-1356, 2017 | 8 | 2017 |
| Anti-SARS-CoV-2 Seropositivity Among Children With Newly Diagnosed Type 1 Diabetes Mellitus: A Case-Control Study V Herczeg, A Luczay, N Ténai, G Czine, P Tóth-Heyn Indian Pediatrics 59 (10), 809-810, 2022 | 7 | 2022 |
| Diabetic ketoacidosis in childhood D Krikovszky, A Luczay, A Körner, L Madacsy Orvosi Hetilap 141 (4), 173-177, 2000 | 7 | 2000 |
| Altered erythrocyte sodium‐lithium counter‐transport and Na+/K+‐ATPase activity in cystic fibrosis A Luczay, B Vásárhelyi, M Dobos, K Holics, R Ujhelyi, T Tulassay Acta Pædiatrica 86 (3), 245-247, 1997 | 7 | 1997 |
| Similar cause, different phenotype: SOX9 enhancer duplication in a family E Pinti, H Piko, A Lengyel, A Luczay, V Karcagi, G Fekete, I Haltrich Hormone Research in Paediatrics 92 (5), 335-339, 2020 | 6 | 2020 |
