Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Emöke Endreffy"'
Autor:
Elisa Alonso-Perez, Marian Suarez-Gestal, Manuel Calaza, Josep Ordi-Ros, Eva Balada, Marc Bijl, Chryssa Papasteriades, Patricia Carreira, Fotini N Skopouli, Torsten Witte, Emöke Endreffy, Maurizio Marchini, Sergio Migliaresi, Gian Domenico Sebastiani, Maria Jose Santos, Ana Suarez, Francisco J Blanco, Nadia Barizzone, Rudolf Pullmann, Sarka Ruzickova, Bernard R Lauwerys, Juan J Gomez-Reino, Antonio Gonzalez, European Consortium of SLE DNA Collections
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45356 (2012)
IntroductionSystemic Lupus Erythematosus (SLE) shows a spectrum of clinical manifestations that complicate its diagnosis, treatment and research. This variability is likely related with environmental exposures and genetic factors among which known SL
Externí odkaz:
https://doaj.org/article/d692975c5ef74c0bb689b2d428e6b30c
Publikováno v:
The Laryngoscope. 110(3 Pt 1)
Objectives/Hypothesis Genetic etiology is suspected in the development of nasal polyposis on the basis of familial aggregation. This study investigated whether there is an association between HLA-DRB1, -DQA1, and -DQB1 alleles and developing nasal po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d95719da63f42f6a86dbc4623fa4de1
https://pubmed.ncbi.nlm.nih.gov/10718431
https://pubmed.ncbi.nlm.nih.gov/10718431
Autor:
AS Charonis, IB Petri, I Haszon, Sándor Túri, P Szenohradszky, RJ Butkowski, Béla Iványi, Emöke Endreffy, Tibor Kalmár
Publikováno v:
Scopus-Elsevier
Childhood membranous nephropathy (MNP) with anti-tubular basement membrane (anti-TBM) nephritis is a rare disorder that may have extrarenal manifestations. This article describes a new case to be added to the 10 previously reported. A renal biopsy sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::96a0b4f6401c1c91ccc9d4979182de3d
https://pubmed.ncbi.nlm.nih.gov/9856526
https://pubmed.ncbi.nlm.nih.gov/9856526
Duchenne and Becker muscular dystrophies are among the most severe and frequent inherited disorders. Being still incurable, medical treatment is concentrated on the carrier diagnosis of the members of the affected families. Here we report the results
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af17bfd9d53b56accde1906e0947d3e7
http://publicatio.bibl.u-szeged.hu/10218/
http://publicatio.bibl.u-szeged.hu/10218/
Autor:
Sándor Sonkodi, Jenö Ormos, Marta Magyari, Sándor Túri, Béla Iványi, Gábor Zsurka, Emöke Endreffy, Pál Venetianer
Publikováno v:
Human genetics. 99(4)
Renal biopsy of two children and a maternal relative, diagnosed with severe progressive tubulointerstitial nephritis, has shown the presence of distorted mitochondria. Mitochondrial DNA from the blood of these patients was analysed. No major deletion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6616613895a8794dbdb24d996be65bea
https://pubmed.ncbi.nlm.nih.gov/9099838
https://pubmed.ncbi.nlm.nih.gov/9099838
Akademický článek
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Akademický článek
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Autor:
Alonso-Perez, Elisa, Suarez-Gestal, Marian, Calaza, Manuel, Blanco, Francisco J., Suarez, Ana, Santos, Maria Jose, Papasteriades, Chryssa, Carreira, Patricia, Pullmann, Rudolf, Ordi-Ros8, Josep, Marchini, Maurizio, Skopouli, Fotini N., Bijl, Marc, Barrizone, Nadia, Sebastiani, Gian Domenico, Migliaresi, Sergio, Witte, Torsten, Lauwerys, Bernard R., Kovacs, Attila, Ruzickova, Sarka
Publikováno v:
Arthritis Research & Therapy; 2014, Vol. 16 Issue 3, p1-19, 19p
Autor:
Shaikh, Sajid A., Strauss, John, King, Nicole, Bulgin, Natalie L., Vetró, Ágnes, Kiss, Enikö, George, Charles J., Kovacs, Maria, Barr, Cathy L., Kennedy, James L.
Publikováno v:
Psychiatric Genetics; Apr2008, Vol. 18 Issue 2, p47-52, 6p