Á. Schuler

发表

G protein in very low birth weight infants

B. Vásárhelyi, I. Kocsis, Á. Schuler, 2000, The Lancet.

Genetic variants of the tumour necrosis factor‐alpha promoter gene do not influence the development of necrotizing enterocolitis

B. Vásárhelyi, I. Kocsis, Á. Schuler, 2001, Acta paediatrica.

Deprenyl in 6-Pyruvoyl Tetrahydropterin Synthase Deficiency

Á. Schuler, N. Blau, M. Spada, 1995 .

Lower prevalence of IL-4 receptor α-chain gene 1902G variant in very-low-birth-weight infants with necrotizing enterocolitis

B. Vásárhelyi, Á. Schuler, T. Tulassay, 2003 .

Genetic Variants of TNF-α, IL-1β, IL-4 Receptor α-Chain, IL-6 and IL-10 Genes Are Not Risk Factors for Sepsis in Low-Birth-Weight Infants

B. Vásárhelyi, I. Kocsis, Á. Schuler, 2003, Neonatology.

Maternal mild hyperphenylalaninaemia: an international survey of offspring outcome

S. Waisbren, Á. Schuler, E. Allred, 1994, The Lancet.

In vivo latex phagocytosis primes the Kupffer cells and hepatic neutrophils to generate superoxide anion

Á. Schuler, J. Spitzer, Z. Spolarics, 1992, Journal of leukocyte biology.

Outcome and long-term follow-up of 36 patients with tetrahydrobiopterin deficiency.

M. Baumgartner, Á. Schuler, N. Blau, 2008, Molecular genetics and metabolism.

High frequencies of biotinidase (BTD) gene mutations in the Hungarian population

Á. Schuler, G. Fekete, K. Németh, 2010, Journal of Inherited Metabolic Disease.

Mutations causing biotinidase deficiency in children ascertained by newborn screening in Western Hungary.

Á. Schuler, E. Kámory, B. Csókay, 2007, Molecular genetics and metabolism.

Molecular and clinical analysis of patients with classic and Duarte galactosemia in western Hungary

Á. Schuler, E. Kámory, B. Csókay, 2010, Wiener klinische Wochenschrift.

[Frequencies of the Los Angeles and Duarte galactose-1-phosphate uridyltransferase variant alleles in the Hungarian population].

Á. Schuler, G. Fekete, K. Németh, 2009, Orvosi hetilap.

In vivo metabolic response of hepatic nonparenchymal cells and leukocytes to granulocyte‐macrophage colony‐stimulating factor

Á. Schuler, J. Spitzer, C. Lang, 1992, Journal of leukocyte biology.

Distribution of Q188R and N314D mutations in the Hungarian galactosemic population.

Á. Schuler, B. Melegh, A. Horváth, 2000, Human Mutation.

Tumor necrosis factor-alpha stimulates superoxide anion generation by perfused rat liver and Kupffer cells.

Á. Schuler, J. Spitzer, Z. Spolarics, 1991, The American journal of physiology.

Upregulation of glucose metabolism by granulocyte-monocyte colony-stimulating factor.

Á. Schuler, J. Spitzer, C. Lang, 1991, Life sciences.

Interleukin genetic variants and the risk of renal failure in infants with infection

B. Vásárhelyi, I. Kocsis, Á. Schuler, 2002, Pediatric Nephrology.

Tumor Necrosis Factor Increases In Vivo Glucose Uptake in Hepatic Nonparenchymal Cells

Á. Schuler, J. Spitzer, C. Lang, 1991, Journal of leukocyte biology.

Lower prevalence of IL-4 receptor alpha-chain gene G variant in very-low-birth-weight infants with necrotizing enterocolitis.

B. Vásárhelyi, Á. Schuler, T. Tulassay, 2003, Journal of pediatric surgery.

Deprenyl in the treatment of patients with tetrahydrobiopterin deficiencies

P. Barsi, Á. Schuler, N. Blau, 2000, Journal of Inherited Metabolic Disease.

A longitudinal study of phenylketonuria based on the data of the Budapest Screening Center

Á. Schuler, M. Mate, C. Somogyi, 2009, European Journal of Pediatrics.

Cognitive development related to metabolic phenotype and mutation genotype in 25 Hungarian patients with phenylketonuria

Simon S. Woo, Á. Schuler, R. Eisensmith, 1994, Journal of Inherited Metabolic Disease.

Variance of ACE and AT1 receptor gene does not influence the risk of neonatal acute renal failure

B. Vásárhelyi, I. Kocsis, Á. Schuler, 2001, Pediatric Nephrology.

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.

B. Vásárhelyi, I. Kocsis, Á. Schuler, 2003, Biology of the neonate.