Z. Almássy

发表

MEDICAL INFORMATION SYSTEM FOR DIAGNOSING DIABETES MELLITUS AND HEARING DISORDER IN CHILDREN

G. Katona, L. Kovács, K. Papp, 2005 .

Mortality and cause of death in mucopolysaccharidosis type II—a historical review based on data from the Hunter Outcome Survey (HOS)

C. Hendriksz, U. Ramaswami, R. Giugliani, 2009, Journal of Inherited Metabolic Disease.

The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers

D. Zafeiriou, Z. Gucev, I. Pećin, 2021, Orphanet Journal of Rare Diseases.

Consensus statement on enzyme replacement therapy for mucopolysaccharidosis IVA in Central and South-Eastern European countries

Z. Gucev, B. Kieć-Wilk, A. Tylki-Szymańska, 2022, Orphanet Journal of Rare Diseases.

Correlation of GAA Genotype and Acid-α-Glucosidase Enzyme Activity in Hungarian Patients with Pompe Disease

L. Kerényi, Z. Almássy, M. Molnár, 2021, Life.

[Clinical manifestations, course and outcome of enzyme replacement therapy in Hungarian patients with Pompe's disease].

I. György, Z. Illés, Z. Almássy, 2011, Orvosi hetilap.

No mutation in the gene for Noonan syndrome, PTPN11, in 18 patients with Costello syndrome

H. Bolz, D. Wieczorek, K. Kutsche, 2003, American journal of medical genetics. Part A.

Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease

L. de Meirleir, J. Zeman, P. Hensman, 2011, Orphanet journal of rare diseases.

The HLA 8.1 ancestral haplotype is strongly linked to the C allele of -429T>C promoter polymorphism of receptor of the advanced glycation endproduct (RAGE) gene. Haplotype-independent association of the -429C allele with high hemoglobinA1C levels in diabetic patients.

Yee-Ling Wu, G. Füst, L. Madácsy, 2007, Molecular immunology.

[Cartilage-hair hypoplasia].

B. Tóth, L. Maródi, Z. Almássy, 2008, Orvosi hetilap.

Differences in the laboratory parameters of obese and healthy Hungarian children and their use in automatic classification

L. Kovács, Z. Benyó, L. Szilágyi, 2010, 2010 Annual International Conference of the IEEE Engineering in Medicine and Biology.

Nonalcoholic Fatty Liver Disease (NAFLD)

G. Baffy, A. Pár, I. Tornai, 2017 .

Polymorphism in the promoter region of the apolipoprotein A5 gene is associated with an increased susceptibility for coronary artery disease.

Z. Prohászka, C. Szalai, Marton Keszei, 2004, Atherosclerosis.

Analyzing a novel model of human blood glucose system at molecular levels

Levente Kovács, András György, Zoltán Benyó, 2009, 2009 European Control Conference (ECC).

[The long-term follow-up of enzyme replacement treatment in late onset Pompe disease].

L. Kerényi, Z. Almássy, L. Dézsi, 2020, Ideggyogyaszati szemle.

The Psychometric Properties of the Hungarian Version of the Proactive Coping Inventory: Reliability, Construct Validity and Factor Structure

E. Greenglass, G. Papp, Z. Almássy, 2014 .