Istvan Balogh
Cited by
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Val34Leu polymorphism of plasma factor XIII: biochemistry and epidemiology in familial thrombophilia
I Balogh, G Szôke, L Kárpáti, U Wartiovaara, E Katona, I Komáromi, ...
Blood, The Journal of the American Society of Hematology 96 (7), 2479-2486, 2000
Analysis of Gas6 in human platelets and plasma
I Balogh, S Hafizi, J Stenhoff, K Hansson, B Dahlbäck
Arteriosclerosis, thrombosis, and vascular biology 25 (6), 1280-1286, 2005
Effect of Val34Leu polymorphism on the activation of the coagulation factor XIII-A
U Wartiovaara, H Mikkola, G Szoke, G Haramura, L Karpati, I Balogh, ...
Thrombosis and haemostasis 84 (10), 595-600, 2000
A modified, optimized kinetic photometric assay for the determination of blood coagulation factor XIII activity in plasma
L Karpati, B Penke, E Katona, I Balogh, G Vámosi, L Muszbek
Clinical chemistry 46 (12), 1946-1955, 2000
Novel and recurrent STAT3 mutations in hyper-IgE syndrome patients from different ethnic groups
H Jiao, B Tóth, M Erdős, I Fransson, É Rákóczi, I Balogh, Z Magyarics, ...
Molecular immunology 46 (1), 202-206, 2008
A European spectrum of pharmacogenomic biomarkers: implications for clinical pharmacogenomics
C Mizzi, E Dalabira, J Kumuthini, N Dzimiri, I Balogh, N Başak, R Böhm, ...
PloS one 11 (9), e0162866, 2016
Factor V Leiden as a risk factor for miscarriage and reduced fertility
SN Bare, R Poka, I Balogh, E Ajzner
Australian and New Zealand Journal of Obstetrics and Gynaecology 40 (2), 186-190, 2000
The P28T mutation in the GALK1 gene accounts for galactokinase deficiency in Roma (Gypsy) patients across Europe
M Hunter, E Heyer, F Austerlitz, D Angelicheva, V Nedkova, P Briones, ...
Pediatric research 51 (5), 602-606, 2002
Severe coagulation factor V deficiency caused by 2 novel frameshift mutations: 2952delT in exon 13 and 5493insG in exon 16 of factor 5 gene
E Ajzner, I Balogh, T Szabó, A Marosi, G Haramura, L Muszbek
Blood, The Journal of the American Society of Hematology 99 (2), 702-705, 2002
The effect of small molecules on sterol homeostasis: measuring 7-dehydrocholesterol in Dhcr7-deficient Neuro2a cells and human fibroblasts
Z Korade, HYH Kim, KA Tallman, W Liu, K Koczok, I Balogh, L Xu, ...
Journal of medicinal chemistry 59 (3), 1102-1115, 2016
Anti‐factor V auto‐antibody in the plasma and platelets of a patient with repeated gastrointestinal bleeding
E Ajzner, I Balogh, G Haramura, Z Boda, K Kalmar, G Pfliegler, ...
Journal of Thrombosis and Haemostasis 1 (5), 943-949, 2003
Analysis of the population heterogeneity in Hungary using fifteen forensically informative STR markers
B Egyed, S Füredi, M Angyal, I Balogh, L Kalmar, Z Padar
Forensic science international 158 (2-3), 244-249, 2006
Analysis of complement factor H Y402H, LOC387715, HTRA1 polymorphisms and ApoE alleles with susceptibility to age‐related macular degeneration in Hungarian patients
G Losonczy, Á Fekete, Z Vokó, L Takács, I Káldi, É Ajzner, M Kasza, ...
Acta ophthalmologica 89 (3), 255-262, 2011
Human epididymis protein 4: a novel serum inflammatory biomarker in cystic fibrosis
B Nagy Jr, B Nagy, L Fila, LA Clarke, F Gönczy, O Bede, D Nagy, ...
Chest 150 (3), 661-672, 2016
Complete recovery from psychosis upon miglustat treatment in a juvenile Niemann–Pick C patient
K Szakszon, I Szegedi, Á Magyar, É Oláh, M Andrejkovics, P Balla, ...
european journal of paediatric neurology 18 (1), 75-78, 2014
Severe Shwachman-Diamond syndrome phenotype caused by compound heterozygous missense mutations in the SBDS gene
M Erdős, K Alapi, I Balogh, G Oroszlán, É Rákóczi, J Sümegi, L Maródi
Experimental hematology 34 (11), 1517-1521, 2006
Frequencies of two common mutations (c. 35delG and c. 167delT) of the connexin 26 gene in different populations of Hungary
A Bors, H Andrikovics, L Kalmár, N Erdei, S Galambos, A Losonczi, ...
International journal of molecular medicine 14 (6), 1105-1108, 2004
Activated protein C resistance in anterior ischaemic optic neuropathy
V Nagy, A Facsko, L Takacs, E Balazs, A Berta, I Balogh, I Edes, I Czuriga, ...
Acta Ophthalmologica Scandinavica 82 (2), 140-143, 2004
High prevalence of factor V Leiden mutation and 20210A prothrombin variant in Hungary
I Balogh, R Poka, G Pfliegler, M Dekany, Z Boda, L Muszbek
Thrombosis and haemostasis 81 (04), 660-661, 1999
Relation between biomarkers and clinical severity in patients with Smith–Lemli–Opitz syndrome
AV Oláh, GP Szabó, J Varga, L Balogh, G Csábi, V Csákváry, W Erwa, ...
European journal of pediatrics 172 (5), 623-630, 2013
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