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PubPharm (134)
81
Both positive and negative selection pressures contribute to the polymorphism pattern of the duplicated human CYP21A2 gene
enthalten in:
PloS one
| 2013
von
Szabó, J.
|
Szilágyi, .
|
Doleschall, Z.
| +6
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82
Comparative analysis of IL6 and IL6 receptor gene polymorphisms in mastocytosis
enthalten in:
British journal of haematology
| 2013
von
Rausz, E.
|
Szilágyi, A.
|
Nedoszytko, B.
| +12
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83
The use of ‘real-time’ complement analysis to differentiate atypical hemolytic uraemic syndrome from other forms of thrombotic microangiopathies
enthalten in:
Immunobiology
| 2012
von
Prohaszka, Z.
|
Szilágyi, .
|
Kiss, N.
| +2
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84
Consumption and dysregulation of complement classical and alternative pathways in patients with streptococcus pneumoniae-associated haemolytic uremic syndrome
enthalten in:
Immunobiology
| 2012
von
Szilagyi, A.
|
Kiss, N.
|
Varga, L.
| +1
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85
ACTH-induced cortisol release is related to the copy number of the C4B gene encoding the fourth component of complement in patients with non-functional adrenal incidentaloma
enthalten in:
Clinical endocrinology
| 2012
von
Bánlaki, Z.
|
Raizer, G.
|
Acs, B.
| +6
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86
ACTH‐induced cortisol release is related to the copy number of the C4B gene encoding the fourth component of complement in patients with non‐functional adrenal incidentaloma
enthalten in:
Clinical endocrinology
| 2012
von
Bánlaki, Z.
|
Raizer, G.
|
Ács, B.
| +6
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87
Analysis of the 8.1 ancestral MHC haplotype in severe, pneumonia-related sepsis
enthalten in:
Clinical immunology (Orlando, Fla.)
| 2011
von
Aladzsity, I.
|
Madách, K.
|
Szilágyi, A.
| +4
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88
Analysis of the 8.1 ancestral MHC haplotype in severe, pneumonia-related sepsis
enthalten in:
Clinical immunology
| 2011
von
Aladzsity, I.
|
Madách, K.
|
Szilágyi, .
| +4
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89
WIESLAB® Alternative Pathway assay as a specific test to support the diagnosis of atypical hemolytic-uremic syndrome: Results of a series of nine cases
enthalten in:
Molecular immunology
| 2010
von
Prohászka, Z.
|
Szilágyi, .
|
Füst, G.
| +1
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90
An old enigma revisited: Clinical course of hereditary angioedema is genetically determined
enthalten in:
Molecular immunology
| 2010
von
Füst, G.
|
Farkas, H.
|
Varga, L.
| +2
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CYP21A2 protein, human
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