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| Personal data sheet |
 Print previewVALIDITY EXPIRED
personal data approved: 2021. IV. 13. | Publications |
2021
 from data base, 2021. IV. 12. |
Kovács Árpád Ferenc, Ponyi Andrea, Constantin Tamás, Kovács Gábor, Németh Krisztina, Varga Edit, Lengyel Anna, Pinti Éva, Horváth Zsuzsanna, Bereczki Dániel, Kádár Krisztina, Medvecz Márta, Anker Pálma, Erdõs Melinda, Molnár Mária Judit, Müller Veronika, Seres Éva, Müllner Katalin, Széchey Rita, Vastagh Ildikó, Reismann Péter, Gyimesi Tamás, Nyolczas Noémi, Noszek László, Hadzsiev Kinga, Faludi Réka, Wittmann István, Takács Hedvig, Sepp Róbert, Maródi László, Fekete György: Fabry-betegség – diagnosztikai útmutató, GYERMEKGYÓGYÁSZAT 72: (2) pp. 73-84.
type of document:
language: Hungarian
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2020
from data base, 2021. IV. 12. |
Eßinger Carla, Karch Stephanie, Moog Ute, Fekete György, Lengyel Anna, Pinti Eva, Eggermann Thomas, Begemann Matthias: Frequency of KCNQ1 variants causing loss of methylation of Imprinting Centre 2 in Beckwith-Wiedemann syndrome, CLINICAL EPIGENETICS 12: (1) 63
type of document: Journal paper/Article
language: English
URL |
2019
from data base, 2021. IV. 12. |
Hennermann Julia B, Arash-Kaps Laila, Fekete György, Schaaf Andreas, Busch Andreas, Frischmuth Thomas: Pharmacokinetics, pharmacodynamics, and safety of moss-aGalactosidase A in patients with Fabry disease, JOURNAL OF INHERITED METABOLIC DISEASE 42: (3) pp. 527-533.
type of document: Journal paper/Article
number of independent citations: 5
language: English
URL |
2019
from data base, 2021. IV. 12. |
Haltrich Irén, Fekete György: Új diagnosztikai módszerek a ritka betegségek felismerésében [Modern Diagnostic Techniques for Diagnosis of Rare Diseases], MAGYAR TUDOMÁNY 180: (5) pp. 669-678.
type of document: Journal paper/Article
language: Hungarian
URL |
2019
from data base, 2021. IV. 12. |
Madar László, Szakszon Katalin, Pfliegler György, Szabó Gabriella P, Brúgós Boglárka, Ronen Natali, Papp Judit, Zahuczky Katalin, Szakos Erzsébet, Fekete György, Oláh Éva, Koczok Katalin, Balogh István: FBN1 gene mutations in 26 Hungarian patients with suspected Marfan syndrome or related fibrillinopathies, JOURNAL OF BIOTECHNOLOGY 301: pp. 105-111.
type of document: Journal paper/Article
language: English
URL |
2018
from data base, 2021. IV. 12. |
Acs OD, Peterfia B, Hollosi P, Haltrich I, Sallai A, Luczay A, Buiting K, Horsthemke B, Torok D, Szabo A, Fekete G: Elsődleges genetikai vizsgálat Prader–Willi-szindróma igazolására [Rapid first-tier genetic diagnosis in patients with Prader-Willi syndrome], ORVOSI HETILAP 159: (2) pp. 64-69.
type of document: Journal paper/Article
language: Hungarian
URL |
2018
from data base, 2021. IV. 12. |
Kiss N, Haluszka D, Lőrincz K, Kuroli E, Hársing J, Mayer B, Kárpáti S, Fekete G, Szipőcs R, Wikonkál N, Medvecz M: Ex vivo nonlinear microscopy imaging of Ehlers–Danlos syndrome-affected skin, ARCHIVES OF DERMATOLOGICAL RESEARCH 310: (5) pp. 463-473.
type of document: Journal paper/Article
language: English
URL |
2017
from data base, 2021. IV. 12. |
Meyer R, Soellner L, Begemann M, Dicks S, Fekete G, Rahner N, Zerres K, Elbracht M, Eggermann T: Targeted Next Generation Sequencing Approach in Patients Referred for Silver-Russell Syndrome Testing Increases the Mutation Detection Rate and Provides Decisive Information for Clinical Management, JOURNAL OF PEDIATRICS 187: pp. 206-212.
type of document: Journal paper/Article
number of independent citations: 8
language: English
URL |
2017
from data base, 2021. IV. 12. |
Odler B, Cseh A, Constantin T, Fekete G, Losonczy G, Tamasi L, Benke K, Szilveszter B, Muller V: Long time enzyme replacement therapy stabilizes obstructive lung disease and alters peripheral immune cell subsets in Fabry patients, CLINICAL RESPIRATORY JOURNAL 11: (6) pp. 942-950.
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL |
2015
from data base, 2021. IV. 12. |
Haltrich I, Piko H, Pamjav H, Somogyi A, Volgyi A, David D, Beke A, Garamvolgyi Z, Kiss E, Karcagi V, Fekete G: Complex X chromosome rearrangement associated with multiorgan autoimmunity, MOLECULAR CYTOGENETICS 8: 51
type of document: Journal paper/Article
number of independent citations: 6
language: English
URL |
| | Number of independent citations to these publications: | 26 |
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