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personal data approved: 2021. I. 22.
Personal data
Melinda Erdős
name Melinda Erdős
name of institution
doctoral school
SE Károly Rácz Doctoral School of Clinical Medicine (Announcer of research topic)
DE Gyula Petrányi Doctoral School of Allergy and Clinical Immunology (Academic staff member)
the share of work in the different doctoral schools. SE Károly Rácz Doctoral School of Clinical Medicine 50%
DE Gyula Petrányi Doctoral School of Allergy and Clinical Immunology 50%
accreditation statement submitted to: University of Debrecen
Contact details
E-mail address melinda.erdosyahoo.com
Academic title
scientific degree, title Ph.D.
year degree was obtained 2006
discipline to which degree belongs clinical medicine
institution granting the degree University of Debrecen
scientific degree, title Habilitation
year degree was obtained 2012
discipline to which degree belongs clinical medicine
institution granting the degree University of Debrecen
Employment
2015 - Semmelweis University, Budapest
university professor or researcher
Thesis topic supervisor
number of doctoral students supervised until now 4
number of students who fulfilled course requirements 2
students who obtained their degrees:
Adrien Katalin Sarkadi PhD 2014  GPDSACI

completed course requirement:
Annamária Székely (PhD) 2012/08  
  Thesis topic proposals
Research
research area Primary immunodeficiencies, Infectious immunology, Lysosomal storage disorders
research field in which current research is conducted clinical medicine
Publications
2021

Erdős Melinda, Lányi Árpád, Balázs György, Casanova Jean-Laurent, Boisson Bertrand, Maródi László: Inherited TOP2B Mutation: Possible Confirmation of Mutational Hotspots in the TOPRIM Domain, JOURNAL OF CLINICAL IMMUNOLOGY 41: 10.1007/s10875-020-00963-8
type of document: Journal paper/Article
language: English
URL 
2021

Erdős Melinda: Niemann-Pick-betegség: Saját megfigyelések és új terápiás lehetoségek, ORVOSI HETILAP 162: (2) pp. 74-80.
type of document: Journal paper/Article
language: Angol, Magyar
URL 
2020

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: 1
language: English
URL 
2018

Erdős Melinda: A súlyos kombinált immundefektusok újszülöttkori szűrővizsgálata, ORVOSI HETILAP 159: (23) pp. 948-956.
type of document: Journal paper/Review paper
language: Hungarian
URL 
2018

Erdős Melinda: Molekuláris genetikai vizsgálatok primer immundefektusokban, ORVOSI HETILAP pp. 2095-2112.
type of document: Journal paper/Article
language: Hungarian
2010

Maródi L, Erdős M: Dectin-1 deficiency and mucocutaneous fungal infections, NEW ENGLAND JOURNAL OF MEDICINE 362: (4) pp. 367-368.
type of document:
number of independent citations: 7
language: English
2008

Erdős M, Lakos G, Dérfalvi B, Notarangelo LD, Durandy A, Maródi L: Molecular genetic analysis of Hungarian patients with the hyper-immunoglobulin M syndrome, MOLECULAR IMMUNOLOGY 45: (1) pp. 278-282.
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL 
2008

Erdős M, Németh K, Tóth B, Constantin T, Rákóczi É, Ponyi A, Dajnoki A, Grubits J, Pintér I, Garzuly F, Hahn K, Bencsik K, Vécsei L, Fekete G, Maródi L: Novel sequence variants of the α-galactosidase A gene in patients with Fabry disease, MOLECULAR GENETICS AND METABOLISM 95: (4) pp. 224-228.
type of document: Journal paper/Article
number of independent citations: 5
language: English
URL 
2007

Erdős M, Hodanova K, Palicz A, Stolnaja L, Dvorakova L, Hrebicek M, Maródi L: Genetic and clinical features of patients with Gaucher disease in Hungary, BLOOD CELLS MOLECULES AND DISEASES 39: (1) pp. 119-123.
type of document: Journal paper/Article
number of independent citations: 16
language: English
URL 
2005

Erdős M, Úzvölgyi É, Nemes Z, Török O, Rákóczi É, Went-Sümegi N, Sümegi J, Maródi L: Characterization of a disease-causing mutation of SH2D1A in a family with X-linked lymphoproliferative disease., HUMAN MUTATION 25: (5) pp. 506-510.
type of document: Journal paper/Article
number of independent citations: 8
language: English
URL 
Number of independent citations to these publications:44 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
104
number of scientific publications:
104
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
17 
scientific publications published abroad that meet the accreditation criteria:
54
publications not in Hungarian, published in Hungary, meeting the accreditation criteria:
7
number of independent citations to scientific publications and creative works:
523

 
All rights reserved © 2007, Hungarian Doctoral Council. Doctoral Council registration number at commissioner for data protection: 02003/0001. Program version: 2.2358 ( 2017. X. 31. )