• 1157 Citations
  • 18 h-Index
1975 …2017

Research output per year

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Research Output

  • 1157 Citations
  • 18 h-Index
  • 74 Article
  • 6 Letter
  • 3 Review article
  • 1 Short survey
2017

Plasma alpha-L-fucosidase activity in chronic inflammation and autoimmune disorders in a pediatric cohort of hospitalized patients

Endreffy, I., Bjørklund, G., Szerafin, L., Chirumbolo, S., Urbina, M. A. & Endreffy, E., Oct 1 2017, In : Immunologic Research. 65, 5, p. 1025-1030 6 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
2016

Acid glycosaminoglycan (aGAG) excretion is increased in children with autism spectrum disorder, and it can be controlled by diet

Endreffy, I., Bjørklund, G., Dicső, F., Urbina, M. A. & Endreffy, E., Apr 1 2016, In : Metabolic Brain Disease. 31, 2, p. 273-278 6 p.

Research output: Contribution to journalArticle

14 Citations (Scopus)

Efficient targeted next generation sequencing-based workflow for differential diagnosis of Alport-related disorders

Kovács, G., Kalmár, T., Endreffy, E., Ondrik, Z., Iványi, B., Rikker, C., Haszon, I., Túri, S., Sinkó, M., Bereczki, C. & Maróti, Z., Mar 2016, In : PloS one. 11, 3, e0149241.

Research output: Contribution to journalArticle

6 Citations (Scopus)

Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA

BIOLUPUS and GENLES Networks, Jan 1 2016, In : Annals of the rheumatic diseases. 75, 1, p. 242-252 11 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)
2015

Genetic associations of leptin-related polymorphisms with systemic lupus erythematosus

The members of GENLES Network & The BIOLUPUS network, Dec 1 2015, In : Clinical Immunology. 161, 2, p. 157-162 6 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)

Impact of single nucleotide polymorphisms of cytarabine metabolic genes on drug toxicity in childhood acute lymphoblastic leukemia

Gabor, K. M., Schermann, G., Lautner-Csorba, O., Rarosi, F., Erdelyi, D. J., Endreffy, E., Berek, K., Bartyik, K., Bereczki, C., Szalai, C. & Semsei, A. F., Apr 1 2015, In : Pediatric Blood and Cancer. 62, 4, p. 622-628 7 p.

Research output: Contribution to journalArticle

8 Citations (Scopus)

PXK locus in systemic lupus erythematosus: Fine mapping and functional analysis reveals novel susceptibility gene ABHD6

Oparina, N. Y., Delgado-Vega, A. M., Martinez-Bueno, M., Magro-Checa, C., Fernández, C., Ortega Castro, R., Pons-Estel, B. A., D'Alfonso, S., Sebastiani, G. D., Witte, T., Lauwerys, B. R., Endreffy, E., Kovács, L., Escudero, A., López-Pedrera, C., Vasconcelos, C., Da Silva, B. M., Frostegård, J., Truedsson, L., Martin, J. & 7 others, Raya, E., Ortego-Centeno, N., Aguirre, M. D. L. A., Garrido, E. D. R., Palma, M. J. C., Alarcon-Riquelme, M. E. & Kozyrev, S. V., Mar 1 2015, In : Annals of the rheumatic diseases. 74, 3, e14.

Research output: Contribution to journalArticle

13 Citations (Scopus)
2014

Lack of replication of higher genetic risk load in men than in women with systemic lupus erythematosus

Alonso-Perez, E., Suarez-Gestal, M., Calaza, M., Blanco, F. J., Suarez, A., Santos, M. J., Papasteriades, C., Carreira, P., Pullmann, R., Ordi-Ros, J., Marchini, M., Skopouli, F. N., Bijl, M., Barrizone, N., Sebastiani, G. D., Migliaresi, S., Witte, T., Lauwerys, B. R., Kovacs, A., Ruzickova, S. & 15 others, Gomez-Reino, J. J., Gonzalez, A., Liz, M., Kappou-Rigatou, I., Beretta, L., Balada, E., Kallenberg, C. G., Vinagre, F., Mavromati, M., Gutierrez, C., Rego, I., D'Alfonso, S., Schmidt, R. E., Endreffy, E. & Dostal, C., Jun 19 2014, In : Arthritis Research and Therapy. 16, 3, R128.

Research output: Contribution to journalArticle

5 Citations (Scopus)
2013

Congenital myasthenic syndromes and transient myasthenia gravis

Gajda, A., Szabó, H., Gergev, G., Karcagi, V., Szabó, N., Endreffy, E., Túri, S. & Sztriha, L., May 30 2013, In : Ideggyogyaszati szemle. 66, 5-6, p. 200-203 4 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Early detection of Angelman syndrome resulting from de novo paternal isodisomic 15q UPD and review of comparable cases

Horváth, E., Horváth, Z., Isaszegi, D., Gergev, G., Nagy, N., Szabó, J., Sztriha, L., Széll, M. & Endreffy, E., Sep 11 2013, In : Molecular Cytogenetics. 6, 1, 35.

Research output: Contribution to journalArticle

8 Citations (Scopus)

Preferential Binding to Elk-1 by SLE-Associated IL10 Risk Allele Upregulates IL10 Expression

Sakurai, D., Zhao, J., Deng, Y., Kelly, J. A., Brown, E. E., Harley, J. B., Bae, S. C., Alarcn-Riquelme, M. E., Edberg, J. C., Kimberly, R. P., Ramsey-Goldman, R., Petri, M. A., Reveille, J. D., Vilá, L. M., Alarcón, G. S., Kaufman, K. M., Vyse, T. J., Jacob, C. O., Gaffney, P. M., Sivils, K. M. & 128 others, James, J. A., Kamen, D. L., Gilkeson, G. S., Niewold, T. B., Merrill, J. T., Scofield, R. H., Criswell, L. A., Stevens, A. M., Boackle, S. A., Kim, J. H., Choi, J., Pons-Estel, B. A., Freedman, B. I., Anaya, J. M., Martin, J., Yu, C. Y., Chang, D. M., Song, Y. W., Langefeld, C. D., Chen, W., Grossman, J. M., Cantor, R. M., Hahn, B. H., Tsao, B. P., Frostegård, J., Truedsson, L., de Ramón, E., Sabio, J. M., Martin, J., Ortego-Centeno, N., CAllejas, J. L., González-Escribano, M. F., Sánchez-Román, J., D'Alfonso, S., Migliarese, S., Sebastiani, G. D., Galeazzi, M., Witte, T., Lauwerys, B. R., Endreffy, E., Kovács, L., Vasconcelos, C., da Silva, B. M., Scherbarth, H. R., Marino, P. C., Motta, E. L., Gamron, S., Drenkard, C., Menso, E., Allievi, A., Tate, G. A., Presas, J. L., Palatnik, S. A., Abdala, M., Bearzotti, M., Alvarellos, A., Caeiro, F., Bertoli, A., Paira, S., Roverano, S., Graf, C. E., Bertero, E., Caprarulo, C., Buchanan, G., Guillerón, C., Grimaudo, S., Manni, J., Catoggio, L. J., Soriano, E. R., Santos, C. D., Prigione, C., Ramos, F. A., Navarro, S. M., Berbotto, G. A., Jorfen, M., Romero, E. J., Garcia, M. A., Marcos, J. C., Marcos, A. I., Perandones, C. E., Eimon, A., Parque, S., Battagliotti, C. G., Acevedo, E., Cucho, M., de la Torre, I. G., Ríos, M. C., Moctezuma, J. F., Ceceña, M. M., Scherbarth, H. R., Marino, P. C., Motta, E. L., Gamron, S., Drenkard, C., Menso, E., Allievi, A., Tate, G. A., Presas, J. L., Palatnik, S. A., Abdala, M., Bearzotti, M., Alvarellos, A., Caeiro, F., Bertoli, A., Paira, S., Roverano, S., Graf, C. E., Bertero, E., Caprarulo, C., Buchanan, G., Guillerón, C., Grimaudo, S., Manni, J., Catoggio, L. J., Soriano, E. R., Santos, C. D., Prigione, C., Ramos, F. A., Navarro, S. M., Berbotto, G. A., Jorfen, M., Romero, E. J., Garcia, M. A., Marcos, J. C., Marcos, A. I., Perandones, C. E., Eimon, A. & Battagliotti, C. G., Oct 1 2013, In : PLoS genetics. 9, 10, e1003870.

Research output: Contribution to journalArticle

25 Citations (Scopus)
2012

Analysis of autosomal genes reveals gene-sex interactions and higher total genetic risk in men with systemic lupus erythematosus

Hughes, T., Adler, A., Merrill, J. T., Kelly, J. A., Kaufman, K. M., Williams, A., Langefeld, C. D., Gilkeson, G. S., Sanchez, E., Martin, J., Boackle, S. A., Stevens, A. M., Alarcón, G. S., Niewold, T. B., Brown, E. E., Kimberly, R. P., Edberg, J. C., Ramsey-Goldman, R., Petri, M., Reveille, J. D. & 31 others, Criswell, L. A., Vilá, L. M., Jacob, C. O., Gaffney, P. M., Moser, K. L., Vyse, T. J., Alarcón-Riquelme, M. E., James, J. A., Tsao, B. P., Scofield, R. H., Harley, J. B., Richardson, B. C., Sawalha, A. H., Frostegård, J., Truedsson, L., De Ramón, E., Sabio, J. M., González-Escribano, M. F., Ortego-Centeno, N., Callejas, J. L., Sánchez-Román, J., D'Alfonso, S., Migliarese, S., Sebastiani, G. D., Galeazzi, M., Witte, T., Lauwerys, B. R., Endreffy, E., Kovács, L., Vasconcelos, C. & Da Silva, B. M., May 1 2012, In : Annals of the rheumatic diseases. 71, 5, p. 694-699 6 p.

Research output: Contribution to journalArticle

47 Citations (Scopus)

Changes in NADPH oxidase mRNA level can be detected in blood at inhaled corticosteroid treated asthmatic children

Ökrös, Z., Endreffy, E., Novak, Z., Maroti, Z., Monostori, P., Varga, I. S., Király, A. & Turi, S., Nov 2 2012, In : Life sciences. 91, 19-20, p. 907-911 5 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)

Fine mapping and conditional analysis identify a new mutation in the autoimmunity susceptibility gene BLK that leads to reduced half-life of the BLK protein

Delgado-Vega, A. M., Dozmorov, M. G., Quirós, M. B., Wu, Y. Y., Martínez-García, B., Kozyrev, S. V., Frostegård, J., Truedsson, L., De Ramón, E., González-Escribano, M. F., Ortego-Centeno, N., Pons-Estel, B. A., D'Alfonso, S., Sebastiani, G. D., Witte, T., Lauwerys, B. R., Endreffy, E., Kovács, L., Vasconcelos, C., Da Silva, B. M. & 4 others, Wren, J. D., Martin, J., Castillejo-López, C. & Alarcón-Riquelme, M. E., Jul 1 2012, In : Annals of the rheumatic diseases. 71, 7, p. 1219-1226 8 p.

Research output: Contribution to journalArticle

22 Citations (Scopus)

Further Evidence of Subphenotype Association with Systemic Lupus Erythematosus Susceptibility Loci: A European Cases Only Study

Alonso-Perez, E., Suarez-Gestal, M., Calaza, M., Ordi-Ros, J., Balada, E., Bijl, M., Papasteriades, C., Carreira, P., Skopouli, F. N., Witte, T., Endreffy, E., Marchini, M., Migliaresi, S., Sebastiani, G. D., Santos, M. J., Suarez, A., Blanco, F. J., Barizzone, N., Pullmann, R., Ruzickova, S. & 17 others, Lauwerys, B. R., Gomez-Reino, J. J., Gonzalez, A., Liz, M., Schmidt, R. E., Kappou-Rigatou, I., Scorza, R., Kovacs, A., Balada, E., Kallenberg, C. G., Vinagre, F., Dostal, C., Pullmann, R., Mavromati, M., D'Alfonso, S., Gutierrez, C. & Rego, I., Sep 26 2012, In : PloS one. 7, 9, e45356.

Research output: Contribution to journalArticle

24 Citations (Scopus)

Genetic association of miRNA-146a with systemic lupus erythematosus in Europeans through decreased expression of the gene

Löfgren, S. E., Frostegård, J., Truedsson, L., Pons-Estel, B. A., D'Alfonso, S., Witte, T., Lauwerys, B. R., Endreffy, E., Kovács, L., Vasconcelos, C., Martins Da Silva, B., Kozyrev, S. V. & Alarcón-Riquelme, M. E., Apr 1 2012, In : Genes and Immunity. 13, 3, p. 268-274 7 p.

Research output: Contribution to journalArticle

94 Citations (Scopus)

Mutation analysis of alpha-galactosidase A gene in Hungarian fabry patients

László, A., Török, L., Raffai, S., Török, É., Sallay, É., Endreffy, E., Morvai, L. & Van Amstel, J. K. P., Jan 30 2012, In : Ideggyogyaszati szemle. 65, 1-2, p. 35-39 5 p.

Research output: Contribution to journalArticle

2011

Collagen type IV nephropathy: Genetic heterogeneity examinations in affected Hungarian families

Endreffy, E., Ondrik, Z., Iványi, B., Maróti, Z., Bereczki, C., Haszon, I., Györke, Z., Worum, E., Németh, K., Rikker, C., Ökrös, Z. & Túri, S., Feb 1 2011, In : Molecular and Cellular Probes. 25, 1, p. 28-34 7 p.

Research output: Contribution to journalArticle

4 Citations (Scopus)

Genetic polymorphisms and the risk of progressive renal failure in elderly Hungarian patients

Zsom, M., Fülöp, T., Zsom, L., Baráth, Á., Maróti, Z. & Endreffy, E., Oct 1 2011, In : Hemodialysis International. 15, 4, p. 501-508 8 p.

Research output: Contribution to journalArticle

19 Citations (Scopus)

Haplotype analysis of the apolipoprotein A5 gene in obese pediatric patients

Horvatovich, K., Bokor, S., Baráth, Á., Maász, A., Kisfali, P., Járomi, L., Polgár, N., Tóth, D., Répásy, J., Endreffy, E., Molnár, D. & Melegh, B., Jun 1 2011, In : International Journal of Pediatric Obesity. 6, 2 -2, p. e318-e325

Research output: Contribution to journalArticle

23 Citations (Scopus)
2010

A 3′-untranslated region variant is associated with impaired expression of CD226 in T and natural killer T cells and is associated with susceptibility to systemic lupus erythematosus

Löfgren, S. E., Delgado-Vega, A. M., Gallant, C. J., Sánchez, E., Truedsson, L., De Ramón Garrido, E., Sabio, J. M., González-Escribano, M. F., Pons-Estel, B. A., D'Alfonso, S., Witte, T., Lauwerys, B. R., Endreffy, E., Kovács, L., Vasconcelos, C., Martins Da Silva, B., Martín, J., Alarcón-Riquelme, M. E. & Kozyrev, S. V., Nov 1 2010, In : Arthritis and rheumatism. 62, 11, p. 3404-3414 11 p.

Research output: Contribution to journalArticle

44 Citations (Scopus)

Molecular genetic mutation analysis in menkes-disease with prenatal diagnosis

László, A., Endreffy, E., Tümer, Z., Horn, N. & Szabó, J., Jan 30 2010, In : Ideggyogyaszati szemle. 63, 1-2, p. 48-51 4 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Paraoxonase 1 activities and polymorphisms in autism spectrum disorders

Paşca, S. P., Dronca, E., Nemeş, B., Kaucsár, T., Endreffy, E., Iftene, F., Benga, I., Cornean, R. & Dronca, M., Mar 1 2010, In : Journal of Cellular and Molecular Medicine. 14, 3, p. 600-607 8 p.

Research output: Contribution to journalArticle

17 Citations (Scopus)
2009

Genetically determined neuromuscular disorders of some Roma families living in Hungary

Laszlo, A., Mayer, P., Kobor, J., Racz, K., Talosi, G., Endreffy, E., Herczegfalvi, A., Hortobagyi, T., Tiszlavicz, L., Bereg, E., Katona, M., Szabo, J. & Karcagi, V., Jan 30 2009, In : Ideggyogyaszati szemle. 62, 1-2, p. 41-47 7 p.

Research output: Contribution to journalArticle

3 Citations (Scopus)

One carbon metabolism disturbances and the C677T MTHFR gene polymorphism in children with autism spectrum disorders

Paşca, S. P., Dronca, E., Kaucsár, T., Crǎciun, E. C., Endreffy, E., Ferencz, B. K., Iftene, F., Benga, I., Cornean, R., Banerjee, R. & Dronca, M., Oct 1 2009, In : Journal of Cellular and Molecular Medicine. 13, 10, p. 4229-4238 10 p.

Research output: Contribution to journalArticle

71 Citations (Scopus)

Replication of recently identified systemic lupus erythematosus genetic associations: A case-control study

Suarez-Gestal, M., Calaza, M., Endreffy, E., Pullmann, R., Ordi-Ros, J., Domenico Sebastiani, G., Ruzickova, S., Jose Santos, M., Papasteriades, C., Marchini, M., Skopouli, F. N., Suarez, A., Blanco, F. J., D'Alfonso, S., Bijl, M., Carreira, P., Witte, T., Migliaresi, S., Gomez-Reino, J. J., Gonzalez, A. & 12 others, Kovacs, A., Balada, E., Dostal, C., Vinagre, F., Kappou-Rigatou, I., Scorza, R., Mavromati, M., Gutierrez, C., Rego, I., Barizzone, N., Kallenberg, C. G. & Schmidt, R. E., May 14 2009, In : Arthritis Research and Therapy. 11, 3, 69.

Research output: Contribution to journalArticle

108 Citations (Scopus)
3 Citations (Scopus)
2008

First case of compound heterozygosity in ALS2 gene in infantile-onset ascending spastic paralysis with bulbar involvement

Sztriha, L., Panzeri, C., Kálmánchey, R., Szabó, R., Endreffy, E., Túri, S., Baschirotto, C., Bresolin, N., Vekerdy, Z. & Bassi, M. T., Jun 1 2008, In : Clinical Genetics. 73, 6, p. 591-593 3 p.

Research output: Contribution to journalLetter

12 Citations (Scopus)

Increased heme oxygenase-1 expression in premature infants with respiratory distress syndrome

Farkas, I., Maróti, Z., Katona, M., Endreffy, E., Monostori, P., Máder, K. & Túri, S., Dec 1 2008, In : European Journal of Pediatrics. 167, 12, p. 1379-1383 5 p.

Research output: Contribution to journalArticle

9 Citations (Scopus)
2007

Bias in association studies of systemic lupus erythematosus susceptibility due to geographical variation in the frequency of a programmed cell death 1 polymorphism across Europe

Ferreiros-Vidal, I., D'Alfonso, S., Papasteriades, C., Skopouli, F. N., Marchini, M., Scorza, R., Migliaresi, S., Sebastiani, G. D., Endreffy, E., Mavromati, M., Kappou-Rigatou, I., Ruzickova, S., Dostal, C., Schmidt, R. E., Witte, T., Gomez-Reino, J. J. & Gonzalez, A., Mar 1 2007, In : Genes and Immunity. 8, 2, p. 138-146 9 p.

Research output: Contribution to journalArticle

31 Citations (Scopus)

Endothelin-1 gene and endothelial nitric oxide synthase gene polymorphisms in adolescents with juvenile and obesity-associated hypertension

Baráth, Á., Endreffy, E., Bereczki, C., Gellén, B., Szücs, B., Németh, I. & Túri, S., Mar 1 2007, In : Acta physiologica Hungarica. 94, 1-2, p. 49-66 18 p.

Research output: Contribution to journalArticle

17 Citations (Scopus)

Myotubularis myopathi. Esetismertetés és irodalmi áttekintés

Translated title of the contribution: Myotubular myopathy. Case report and review of the literatureKovács, S. K., Korcsik, J., Szabó, H., Bódi, I., Katona, M., Bereg, E., Endreffy, E., Túri, S., Hortobágyi, T. & Sztriha, L., Sep 16 2007, In : Orvosi hetilap. 148, 37, p. 1757-1762 6 p.

Research output: Contribution to journalArticle

Opposed independent effects and epistasis in the complex association of IRF5 to SLE

Ferreiro-Neira, I., Calaza, M., Alonso-Perez, E., Marchini, M., Scorza, R., Sebastiani, G. D., Blanco, F. J., Rego, I., Pullmann, R., Pullmann, R., Kallenberg, C. G., Bijl, M., Skopouli, F. N., Mavromati, M., Migliaresi, S., Barizzone, N., Ruzickova, S., Dostal, C., Schmidt, R. E., Witte, T. & 9 others, Papasteriades, C., Kappou-Rigatou, I., Endreffy, E., Kovacs, A., Ordi-Ros, J., Balada, E., Carreira, P., Gomez-Reino, J. J. & Gonzalez, A., Jul 1 2007, In : Genes and Immunity. 8, 5, p. 429-438 10 p.

Research output: Contribution to journalArticle

52 Citations (Scopus)
2006

HLA class II allele polymorphism in Hungarian patients with primary Sjögren's syndrome [1]

Kovács, A., Endreffy, E., Petri, I., Kovács, L. & Pokorny, G., Feb 1 2006, In : Scandinavian Journal of Rheumatology. 35, 1, p. 75-76 2 p.

Research output: Contribution to journalLetter

6 Citations (Scopus)
16 Citations (Scopus)

The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosis

Laki, J., Laki, I., Németh, K., Újhelyi, R., Bede, O., Endreffy, E., Bolbás, K., Gyurkovits, K., Csiszér, E., Sólyom, E., Dobra, G., Halász, A., Pozsonyi, É., Rajczy, K., Prohászka, Z., Fekete, G. & Füst, G., Nov 1 2006, In : International Immunology. 18, 11, p. 1585-1590 6 p.

Research output: Contribution to journalArticle

27 Citations (Scopus)
2005

A gyermekkori rákos betegséget túlélok késoi renalis glomerularis és tubularis funkciója: Bárdi Edit és munkatársai közleményének kivonata

Edit, B., Anna, O. V., Katalin, B., Emöke, E., Csaba, J., János, K. & Csongor, K., Dec 1 2005, In : Lege Artis Medicinae. 15, 6, 1 p.

Research output: Contribution to journalShort survey

IV-es típusú kollagén nephropathiák: A vékony bazális membrán nephropathiától az Alport-szindrómáig

Translated title of the contribution: Collagen type IV nephropathy: From thin basement membrane nephropathy to Alport syndromeEndreffy, E., Ondrik, Z., Kemény, É., Vas, Z., Maróti, Z., Lencse, G., Bereczki, C., Haszon, I., Túri, S. & Iványi, B., Dec 1 2005, In : Orvosi hetilap. 146, 52, p. 2647-2653 7 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Quantitative cytomegalovirus load in urine and clinical outcome in neonates [3]

Nagy, A., Tálosi, G., Streitman, K., Pintér, S., Endreffy, E. & Pusztai, R., Apr 2005, In : Journal of Clinical Virology. 32, 4, p. 340-341 2 p.

Research output: Contribution to journalLetter

2004

Erythema nodosum in association with celiac disease

Bartyik, K., Várkonyi, Á., Kirschner, Á., Endreffy, E., Túri, S. & Karg, E., May 1 2004, In : Pediatric Dermatology. 21, 3, p. 227-230 4 p.

Research output: Contribution to journalArticle

15 Citations (Scopus)

Heme oxygenase 1 expression in young uremic patients on hemodialysis

Maróti, Z., Németh, I., Túri, S., Karg, E., Ugocsai, P. & Endreffy, E., Apr 1 2004, In : Pediatric Nephrology. 19, 4, p. 426-431 6 p.

Research output: Contribution to journalArticle

6 Citations (Scopus)

Hemoxigenáz-1 génexpresszió érett és koraszülött újszülöttekben

Translated title of the contribution: HO-1 expression in premature and mature neonates during the first week of lifeFarkas, I., Maróti, Z., Katona, M., Orvos, H., Németh, I., Endreffy, E., Pál, A. & Túri, S., Oct 22 2004, In : Magyar Noorvosok Lapja. 67, 5, p. 251-255 5 p.

Research output: Contribution to journalReview article

Incidence and outcome of congenital cytomegalovirus infection in selected groups of preterm and full-term neonates under intensive care

Nagy, A., Endreffy E., E., Streitman, K., Pintér, S. & Pusztai, R., Nov 1 2004, In : In Vivo. 18, 6, p. 819-824 6 p.

Research output: Contribution to journalArticle

14 Citations (Scopus)

Late effects on renal glomerular and tubular function in childhood cancer survivors

Bárdi, E., Oláh, A. V., Bartyik, K., Endreffy, E., Jenei, C., Kappelmayer, J. & Kiss, C., Nov 1 2004, In : Pediatric Blood and Cancer. 43, 6, p. 668-673 6 p.

Research output: Contribution to journalArticle

43 Citations (Scopus)

Leiden mutation, bed rest and infection: Simultaneous triggers for maternal deep-vein thrombosis and neonatal intracranial hemorrhage?

Sikovanyecz, J., Orvos, H., Pál, A., Katona, M., Endreffy, E., Horváth, E. & Szabó, J., Apr 23 2004, In : Fetal Diagnosis and Therapy. 19, 3, p. 275-277 3 p.

Research output: Contribution to journalArticle

13 Citations (Scopus)
2003

Clinical and genetical aspects of autosomal dominantly inherited osteogenesis imperfecta tarda

László, A., Endreffy, E., Bossányi, A. & Maróti, Z., Dec 1 2003, In : Acta Biologica Szegediensis. 47, 1-4, p. 41-45 5 p.

Research output: Contribution to journalArticle

1 Citation (Scopus)

Heme oxygenase 1 (HMOX1) gene expression in hemodialysed uremic patients

Maróti, Z., Túri, S., Németh, I., Karg, E., Ugocsai, P. & Endreffy, E., Dec 1 2003, In : Acta Biologica Szegediensis. 47, 1-4, p. 147-151 5 p.

Research output: Contribution to journalArticle

HLA class II allele polymorphism in Hungarian patients with systemic lupus erythematosus [2]

Endreffy, E., Kovács, A., Kovács, L. & Pokorny, G., Oct 1 2003, In : Annals of the rheumatic diseases. 62, 10, p. 1017-1018 2 p.

Research output: Contribution to journalLetter

13 Citations (Scopus)

Neonatal screening for biotinidase deficiency in Hungary: Clinical, biochemical and molecular studies

László, Á., Schuller, É. Á., Sallay, É., Endreffy, E., Somogyi, C., Várkonyi, Á., Havass, Z., Jansen, K. P. & Wolf, B., Dec 1 2003, In : Journal of inherited metabolic disease. 26, 7, p. 693-698 6 p.

Research output: Contribution to journalArticle

12 Citations (Scopus)

Renin-angiotensin gene polymorphism in children with uremia and essential hypertension

Papp, F., Friedman, A. L., Bereczki, C., Haszon, I., Kiss, É., Endreffy, E. & Túri, S., Feb 1 2003, In : Pediatric Nephrology. 18, 2, p. 150-154 5 p.

Research output: Contribution to journalArticle

18 Citations (Scopus)