Items where Author is "Madar, László"

Article

Madar, László and Majoros, Viktória and Szűcs, Zsuzsanna and Nagy, Orsolya and Babicz, Tamás and Butz, Henriett and Patócs, Attila and Balogh, István and Koczok, Katalin (2023) Double Heterozygosity for Rare Deleterious Variants in the BRCA1 and BRCA2 Genes in a Hungarian Patient with Breast Cancer. International Journal of Molecular Sciences, 24 (20). No.-15334. ISSN 1422-0067

Deák, Anna and Koczok, Katalin and Bessenyei, Beáta and Szűcs, Zsuzsanna and Madar, László and Csorba, Gabriella and Orosz, Orsolya and Laki, István and Halász, Adrien and Marsal, Géza and Balogh, István (2022) A magyar Cystás Fibrosis Regiszter genetikai revíziója. ORVOSI HETILAP, 163 (51). pp. 2052-2059. ISSN 0030-6002

Szabó, Tamás and Pethő-Orosz, Petronella Éva and Balogh, Eszter and Jávorszky, Eszter and Máttyus, István and Bereczki, Csaba and Maróti, Zoltán and Kalmár, Tibor and Szabó, Attila and Reusz, György and Várkonyi, Ildikó and Orosz, Orsolya and Madar, László and Balla, György and Kappelmayer, János and Tory, Kálmán and Balogh, István (2018) Comprehensive genetic testing in children with a clinical diagnosis of ARPKD identifies phenocopies. PEDIATRIC NEPHROLOGY, 33 (10). pp. 1713-1721. ISSN 0931-041X

Koczok, Katalin and Gombos, Éva and Madar, László and Török, Olga and Balogh, István (2018) Interfering effect of maternal cell contamination on invasive prenatal molecular genetic testing. PRENATAL DIAGNOSIS, 38 (9). pp. 713-719. ISSN 0197-3851

Zádori, Dénes and Szpisjak, László and Madar, László and Varga, Viktória Evelin and Csányi, Bernadett and Bencsik, Krisztina and Balogh, István and Harangi, Mariann and Kereszty, Éva and Vécsei, László and Klivényi, Péter (2017) Different phenotypes in identical twins with cerebrotendinous xanthomatosis: case series. NEUROLOGICAL SCIENCES, 38 (3). pp. 481-483. ISSN 1590-1874

Varga, Viktória Evelin and Katkó, Mónika and Harangi, János and Balogh, István and Kapás, István and Madar, László and Seres, Ildikó and Molnár, Mária Judit and Paragh, György and Kovács, G. Gábor and Harangi, Mariann (2014) Egy ritka, veleszületett neurodegeneratív betegség: a cerebrotendinosus xanthomatosis laboratóriumi diagnosztikája | Laboratory diagnosis of a rare congenital neurodegenerative disease: cerebrotendinous xanthomatosis. Orvosi Hetilap, 155 (21). pp. 811-816. ISSN 0030-6002