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| Personal data sheet |
 Print previewpersonal data approved: 2022. X. 17. | Publications |
2022
 from data base, 2022. X. 17. |
Barsi Adam, Beke Artur, Sarman Beatrix: Case report: A particularly rare case of endogenous hyperinsulinemic hypoglycemia complicated with pregnancy treated with short-acting somatostatin analog injections, FRONTIERS IN ENDOCRINOLOGY 13: 964481
type of document: Journal paper/Article
language: English
URL |
2021
from data base, 2022. X. 17. |
Tidrenczel Zsolt, Hajdu Julia, Simonyi Atene, Szabo Istvan, Acs Nandor, Demeter Janos, Beke Artur: Trends in the prenatal diagnosis of trisomy 21 show younger maternal age and shift in the distribution of congenital heart disease over a 20-year period, AMERICAN JOURNAL OF MEDICAL GENETICS PART A 185: (6) pp. 1732-1742.
type of document: Journal paper/Article
language: English
URL |
2021
from data base, 2022. X. 17. |
Simonyi A., Eros F.R., Hajdu J., Beke A.: Effectiveness of fetal ultrasound diagnostics in cardiac malformations and association with polyhydramnios and oligohydramnios, QUANTITATIVE IMAGING IN MEDICINE AND SURGERY 11: (7) pp. 2994-3004.
type of document: Journal paper/Article
language: English
URL |
2019
from data base, 2022. X. 17. |
Tidrenczel Zsolt, Tardy Erika P., Pikó Henriett, Sarkadi Edina, Böjtös Ildikó, Demeter János, Simon Judit, Kósa János P., Beke Artúr: Prenatal Diagnosis of 4q Terminal Deletion and Review of the Literature, CYTOGENETIC AND GENOME RESEARCH 158: (2) pp. 63-73.
type of document: Journal paper/Article
number of independent citations: 4
language: English
URL |
2018
from data base, 2022. X. 17. |
Beke A, Piko H, Haltrich I, Karcagi V, Rigo J Jr, Molnar MJ, Fekete G: Study of patterns of inheritance of premature ovarian failure syndrome carrying maternal and paternal premutations, BMC MEDICAL GENETICS 19: (1) 113
type of document: Journal paper/Article
language: English
URL |
2014
from data base, 2022. X. 17. |
Beke A, Eros FR, Pete B, Szabo I, Gorbe E, Rigo J Jr: Efficacy of prenatal ultrasonography in diagnosing urogenital developmental anomalies in newborns., BMC PREGNANCY AND CHILDBIRTH 14: 82
type of document: Journal paper/Article
number of independent citations: 6
language: English
URL |
2013
from data base, 2022. X. 17. |
Beke A, Piko H, Haltrich I, Csomor J, Matolcsy A, Fekete G, Rigo J Jr, Karcagi V: Molecular cytogenetic analysis of Xq critical regions in premature ovarian failure., MOLECULAR CYTOGENETICS 6: (1) 62
type of document: Journal paper/Article
number of independent citations: 25
language: English
URL |
2011
from data base, 2022. X. 17. |
Beke A, Latkóczy K, Nagy GR, Dudnyikova A, Csaba A, Szabó I, Papp C, Rigó J Jr: Comparison of prevalence of toxoplasma and cytomegalovirus infection in cases with fetal ultrasound markers in the second trimester of pregnancy, PRENATAL DIAGNOSIS 31: (10) pp. 945-948.
type of document: Journal paper/Article
number of independent citations: 14
language: English
URL |
2009
from data base, 2022. X. 17. |
Beke A, Joó JG, Csaba Á, Lázár L, Bán Z, Papp Cs, Tóth-Pál E, Papp Z: Incidence of chromosomal abnormalities in the presence of fetal subcutaneous oedema, such as nuchal oedema, cystic hygroma and non-immune hydrops, FETAL DIAGNOSIS AND THERAPY 25: (1) pp. 83-92.
type of document: Journal paper/Article
number of independent citations: 26
language: English
URL |
2008
from data base, 2022. X. 17. |
Beke A, Barakonyi E, Belics Z, Joó JG, Csaba Á, Papp Cs, Tóth-Pál E, Papp Z: Risk of chromosome abnormalities in the presence of bilateral or unilateral choroid plexus cysts, FETAL DIAGNOSIS AND THERAPY 23: (3) pp. 185-191.
type of document: Journal paper/Article
number of independent citations: 23
language: English
URL |
| | Number of independent citations to these publications: | 98 |
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