 Print previewpersonal data approved: 2022. I. 12. | Publications |
2020
 from data base, 2022. I. 12. |
Erdos Melinda, Jakobicz Eszter, Soltesz Beata, Toth Beata, Bata-Csorgo Zsuzsanna, Marodi Laszlo: Recurrent, Severe Aphthous Stomatitis and Mucosal Ulcers as Primary Manifestations of a NovelSTAT1Gain-of-Function Mutation, FRONTIERS IN IMMUNOLOGY 11: 967
type of document: Journal paper/Article
number of independent citations: 4
language: English
URL |
2019
from data base, 2022. I. 12. |
Sediva A, Bataneant M, Belevtsev M, Blaziene A, Ciznar P, Förster-Waldl E, Kelecic J, Marodi J, Naumova E, Nasrullayeva G, Ress K, Serban M, Sitkaustiene B, Toth B, Modell V, Modell F, Tenembaum V, Marković M, Avcin T: Primary immunodeficiencies in Central and Eastern Europe-the power of networking Report on the activity of the Jeffrey Modell Foundation Centers Network in Central and Eastern Europe, IMMUNOLOGIC RESEARCH 67: (4-5) pp. 358-367.
type of document: Journal paper/Article
number of independent citations: 1
language: English
URL |
2018
from data base, 2022. I. 12. |
Mosdosi B, Toth B: Autoinflammatiós kórképek, ORVOSI HETILAP 159: (23) pp. 898-907.
type of document: Journal paper/Article
language: Hungarian
URL |
2018
from data base, 2022. I. 12. |
Vida Livia, Ottóffy Gábor, Rózsai Barnabás, Stankovics József, Tóth Beáta, Nyúl Zoltán, Kajtár Béla: X kromoszómához kötött limfoproliferatív betegség (X LP): Az Epstein–Barr-vírus (EBV) találkozása egy ritka génhibával, HEMATOLÓGIA-TRANSZFUZIOLÓGIA 51: (2) pp. 86-91.
type of document: Journal paper/Article
language: Hungarian
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2017
from data base, 2022. I. 12. |
Tóth Beáta, Kappelmayer János: Genetikai vizsgálatok jelentősége primer immundeficienciában., FOCUS MEDICINAE 3: pp. 18-22.
type of document: Journal paper/Article
language: Angol, Magyar
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2015
from data base, 2022. I. 12. |
Soltesz B, Toth B, Sarkadi AK, Erdos M, Marodi L: The Evolving View of IL-17-Mediated Immunity in Defense Against Mucocutaneous Candidiasis in Humans., INTERNATIONAL REVIEWS OF IMMUNOLOGY 34: (4) pp. 348-363.
type of document: Journal paper/Article
number of independent citations: 8
language: English
URL |
2015
from data base, 2022. I. 12. |
Gulacsy V, Soltesz B, Petrescu C, Bataneant M, Gyimesi E, Serban M, Marodi L, Toth B: A novel large deletion and single nucleotide insertion in the Wiskott-Aldrich syndrome protein gene., EUROPEAN JOURNAL OF HAEMATOLOGY 95: (1) pp. 93-98.
type of document: Journal paper/Article
language: English
URL |
2015
from data base, 2022. I. 12. |
Tóth B, Soltész B, Gyimesi E, Csorba G, Veres A, Lányi Á, Kovács G, Maródi L, Erdős M: Severe XLP phenotype caused by a novel intronic mutation int he SH2D1A gene, JOURNAL OF CLINICAL IMMUNOLOGY 35: (1) pp. 26-31.
type of document: Journal paper/Article
number of independent citations: 2
language: English
URL |
2013
from data base, 2022. I. 12. |
Tóth B, Pistár Z, Csorba G, Balogh I, Kovács T, Erdős M, Maródi L: Novel dedicator of cytokinesis 8 mutations identified by multiplex ligation-dependent probe amplification, EUROPEAN JOURNAL OF HAEMATOLOGY 91: (4) pp. 369-375.
type of document: Journal paper/Article
number of independent citations: 2
language: English
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2012
from data base, 2022. I. 12. |
Tóth B, Erdős M, Székely A, Ritli L, Bagossi P, Sümegi J, Maródi L: Molecular genetic characterization of novel sphingomyelin phosphodiesterase 1 mutations causing Niemann–Pick disease, JOURNAL OF INHERITED METABOLIC DISEASE REPORTS 3: pp. 125-129.
type of document: Journal paper/Article
number of independent citations: 6
language: English
URL |
| | Number of independent citations to these publications: | 23 |
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