Publications by authors named "Agnes Schuler"

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High frequencies of biotinidase (BTD) gene mutations in the Hungarian population.
Ilona Milánkovics, Krisztina Németh, Csilla Somogyi, Agnes Schuler, György Fekete

J Inherit Metab Dis· December 2010

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Molecular and clinical analysis of patients with classic and Duarte galactosemia in western Hungary.
Ilona Milánkovics, Agnes Schuler, Eniko Kámory, Béla Csókay, Flóra Fodor

Wien Klin Wochenschr· February 2010

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[Frequencies of the Los Angeles and Duarte galactose-1-phosphate uridyltransferase variant alleles in the Hungarian population].
Ilona Milánkovics, Agnes Schuler, Krisztina Németh, Csilla Somogyi, György Fekete

Orv Hetil· July 2009

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[Convulsions in neonatal period and infancy with rare etiology (neurogenetic disease)].
Andrea Nagy, Zsuzsa Szever, Zsuzsa Kormos, Emoke Székely, Edit Tóth, Agnes Schuler

Ideggyogy Sz· November 2008

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Outcome and long-term follow-up of 36 patients with tetrahydrobiopterin deficiency.
Leandra Jäggi, Marcel R Zurflüh, Agnes Schuler, Alberto Ponzone, Francesco Porta

Mol Genet Metab· March 2008

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Mutations causing biotinidase deficiency in children ascertained by newborn screening in Western Hungary.
Ilona Milánkovics, Eniko Kámory, Béla Csókay, Flóra Fodor, Csilla Somogyi, Agnes Schuler

Mol Genet Metab· March 2007

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Genetic variants of TNF-[FC12]a, IL-1beta, IL-4 receptor [FC12]a-chain, IL-6 and IL-10 genes are not risk factors for sepsis in low-birth-weight infants.
András Treszl, István Kocsis, Miklós Szathmári, Agnes Schuler, Erika Héninger

Biol Neonate· December 2003

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Lower prevalence of IL-4 receptor alpha-chain gene G variant in very-low-birth-weight infants with necrotizing enterocolitis.
András Treszl, Erika Héninger, Attila Kálmán, Agnes Schuler, Tivadar Tulassay

J Pediatr Surg· September 2003

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Interleukin genetic variants and the risk of renal failure in infants with infection.
András Treszl, Péter Tóth-Heyn, István Kocsis, András Nobilis, Agnes Schuler

Pediatr Nephrol· September 2002

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