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The functional promoter F12-46C/T variant predicts the asymptomatic phenotype of C1-INH-HAE.
Clin Exp Allergy. 2019 Nov;49(11):1520-1522. doi: 10.1111/cea.13470. Epub 2019 Jul 23.
Clin Exp Allergy. 2019.
PMID: 31334892
No abstract available.
Hereditary angioedema due to C1-inhibitor deficiency in Macedonia: clinical characteristics, novel SERPING1 mutations and genetic factors modifying the clinical phenotype.
Grivčeva-Panovska V, Košnik M, Korošec P, Andrejević S, Karadža-Lapić L, Rijavec M.
Grivčeva-Panovska V, et al.
Ann Med. 2018 May;50(3):269-276. doi: 10.1080/07853890.2018.1449959. Epub 2018 Mar 15.
Ann Med. 2018.
PMID: 29513108
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The CC2D2B is a novel genetic modifier of the clinical phenotype in patients with hereditary angioedema due to C1 inhibitor deficiency.
Rupar N, Šelb J, Košnik M, Zidarn M, Andrejević S, Čulav L, Grivčeva-Panovska V, Korošec P, Rijavec M.
Rupar N, et al. Among authors: grivceva panovska v.
Gene. 2024 Aug 15;919:148496. doi: 10.1016/j.gene.2024.148496. Epub 2024 Apr 27.
Gene. 2024.
PMID: 38679185
Free article.
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Henoch-Schönlein purpura in an adult patient: extragastric, cutaneous manifestation of helicobacter pylori infection.
Grivceva-Panovska V, Grivceva Stardelova K, Serafimoski V.
Grivceva-Panovska V, et al.
Prilozi. 2008 Jul;29(1):291-301.
Prilozi. 2008.
PMID: 18709017
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Frequency of delayed-type hypersensitivity to contact allergens in palmo-plantar psoriasis.
Caca-Biljanovska N, V'lckova-Laskoska M, Balabanova-Stefanova M, Grivceva-Panovska V.
Caca-Biljanovska N, et al. Among authors: grivceva panovska v.
Prilozi. 2005 Dec;26(2):131-41.
Prilozi. 2005.
PMID: 16400235
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