Endreffy E - Search Results

1

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. Sikovanyecz J, et al. Among authors: endreffy e. Fetal Diagn Ther. 2004 May-Jun;19(3):275-7. doi: 10.1159/000076711. Fetal Diagn Ther. 2004. PMID: 15067240

2

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. Horváth E, et al. Among authors: endreffy e. Mol Cytogenet. 2013 Sep 8;6(1):35. doi: 10.1186/1755-8166-6-35. Mol Cytogenet. 2013. PMID: 24011290 Free PMC article.

3

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. Farkas I, et al. Among authors: endreffy e. Eur J Pediatr. 2008 Dec;167(12):1379-83. doi: 10.1007/s00431-008-0673-6. Epub 2008 Feb 27. Eur J Pediatr. 2008. PMID: 18301921

4

Molecular genetic mutation analysis in Menkes-disease with prenatal diagnosis.

László A, Endreffy E, Tümer Z, Horn N, Szabó J. László A, et al. Among authors: endreffy e. Ideggyogy Sz. 2010 Jan 30;63(1-2):48-51. Ideggyogy Sz. 2010. PMID: 20420124

5

Human cytomegalovirus gB genotype 1 is dominant in congenital infections in South Hungary.

Lukácsi A, Taródi B, Endreffy E, Bábinszki A, Pál A, Pusztai R. Lukácsi A, et al. Among authors: endreffy e. J Med Virol. 2001 Nov;65(3):537-42. J Med Virol. 2001. PMID: 11596091

6

[Myotubular myopathy. Case report and review of the literature].

Kovács SK, Korcsik J, Szabó H, Bódi I, Katona M, Bereg E, Endreffy E, Túri S, Hortobágyi T, Sztriha L. Kovács SK, et al. Among authors: endreffy e. Orv Hetil. 2007 Sep 16;148(37):1757-62. doi: 10.1556/OH.2007.28054. Orv Hetil. 2007. PMID: 17827085 Review. Hungarian.

7

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

Nagy A, Endreffy E, Streitman K, Pintér S, Pusztai R. Nagy A, et al. Among authors: endreffy e. In Vivo. 2004 Nov-Dec;18(6):819-23. In Vivo. 2004. PMID: 15646827 Free article.

8

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

László A, Schuler EA, Sallay E, Endreffy E, Somogyi C, Várkonyi A, Havass Z, Jansen KP, Wolf B. László A, et al. Among authors: endreffy e. J Inherit Metab Dis. 2003;26(7):693-8. doi: 10.1023/b:boli.0000005622.89660.59. J Inherit Metab Dis. 2003. PMID: 14707518

9

Erythema nodosum in association with celiac disease.

Bartyik K, Várkonyi A, Kirschner A, Endreffy E, Túri S, Karg E. Bartyik K, et al. Among authors: endreffy e. Pediatr Dermatol. 2004 May-Jun;21(3):227-30. doi: 10.1111/j.0736-8046.2004.21307.x. Pediatr Dermatol. 2004. PMID: 15165200

10

Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis.

Zsurka G, Ormos J, Iványi B, Túri S, Endreffy E, Magyari M, Sonkodi S, Venetianer P. Zsurka G, et al. Among authors: endreffy e. Hum Genet. 1997 Apr;99(4):484-7. doi: 10.1007/s004390050393. Hum Genet. 1997. PMID: 9099838

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