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» Authors » Hanna Gregorek

Hanna Gregorek

Explore the profile of Hanna Gregorek including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 25
Citations 442
Followers 0
Related Specialties
Allergy & Immunology
Hematology
General Medicine
Top 10 Co-Authors
Krystyna H Chrzanowska
Anna Wakulinska
Kazimierz Madalinski
Katarzyna Dzierzanowska-Fangrat
Malgorzata Syczewska
Barbara Pietrucha
Beata Wolska-Kusnierz
Malgorzata Pac
Barbara Piatosa
Edyta Heropolitanska-Pliszka
Published In
J Clin Immunol
Cent Eur J Immunol
Haematologica
Eur J Immunol
J Clin Periodontol
Affiliations
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Recent Articles
11.
Gaucher disease and dysgammaglobulinemia: a report of 61 patients, including 18 with GD type III
Jurecka A, Gregorek H, Kleinotiene G, Czartoryska B, Tylki-Szymanska A
Blood Cells Mol Dis . 2010 Aug; 46(1):85-7. PMID: 20729110
No abstract available.
12.
High prevalence of primary ovarian insufficiency in girls and young women with Nijmegen breakage syndrome: evidence from a longitudinal study
Chrzanowska K, Szarras-Czapnik M, Gajdulewicz M, Kalina M, Gajtko-Metera M, Walewska-Wolf M, et al.
J Clin Endocrinol Metab . 2010 May; 95(7):3133-40. PMID: 20444919
Context: Nijmegen breakage syndrome (NBS) is a severe chromosomal instability disorder characterized by microcephaly, growth retardation, immune deficiency, and predisposition for malignancy. It is caused by hypomorphic mutations in the...
13.
Loss of juxtaposition of RAG-induced immunoglobulin DNA ends is implicated in the precursor B-cell differentiation defect in NBS patients
van der Burg M, Pac M, Berkowska M, Goryluk-Kozakiewicz B, Wakulinska A, Dembowska-Baginska B, et al.
Blood . 2010 Apr; 115(23):4770-7. PMID: 20378756
The Nijmegen breakage syndrome (NBS) is a rare inherited condition, characterized by microcephaly, radiation hypersensitivity, chromosomal instability, an increased incidence of (mostly) lymphoid malignancies, and immunodeficiency. NBS is caused by...
14.
Nijmegen breakage syndrome: Long-term monitoring of viral and immunological biomarkers in peripheral blood before development of malignancy
Gregorek H, Chrzanowska K, Dzierzanowska-Fangrat K, Wakulinska A, Pietrucha B, Zapasnik A, et al.
Clin Immunol . 2010 Feb; 135(3):440-7. PMID: 20167538
Selected viruses and immune parameters were monitored in 57 patients with Nijmegen breakage syndrome as a proposed tool for early detection of changes preceding development of malignancy. The following parameters...
15.
Long-term monitoring of Epstein-Barr virus DNA load and humoral parameter abnormalities in pediatric liver transplant recipients before development of malignancy
Gregorek H, Jankowska I, Dzierzanowska-Fangrat K, Teisseyre J, Sawicka A, Kasztelewicz B, et al.
Pediatr Transplant . 2010 Feb; 14(5):629-35. PMID: 20158667
EBV loads and abnormalities of humoral responses were monitored in 51 pediatric liver transplant recipients as a proposed non-invasive laboratory tool for early detection of changes preceding severe clinical complications....
16.
Oral findings in patients with Nijmegen breakage syndrome: a preliminary study
Gregorek H, Olczak-Kowalczyk D, Dembowska-Baginska B, Pietrucha B, Wakulinska A, Gozdowski D, et al.
Oral Surg Oral Med Oral Pathol Oral Radiol Endod . 2009 Sep; 108(5):e39-45. PMID: 19782616
Objective: The objective of this study was to assess the oral cavity status of patients with Nijmegen breakage syndrome (NBS), an inherited genetic disorder that belongs to the group of...
17.
Functional C1-inhibitor diagnostics in hereditary angioedema: assay evaluation and recommendations
Wagenaar-Bos I, Drouet C, Aygoren-Pursun E, Bork K, Bucher C, Bygum A, et al.
J Immunol Methods . 2008 Jul; 338(1-2):14-20. PMID: 18655790
Hereditary angioedema (HAE) is an autosomal dominant disease characterized by recurrent episodes of potentially life-threatening angioedema. The most widespread underlying genetic deficiency is a heterozygous deficiency of the serine protease...
18.
Possible disease-modifying factors: the mannan-binding lectin pathway and infections in hereditary angioedema of children and adults
Cedzynski M, Madalinski K, Gregorek H, Swierzko A, Nowicka E, Obtulowicz K, et al.
Arch Immunol Ther Exp (Warsz) . 2008 Feb; 56(1):69-75. PMID: 18250972
Introduction: Hereditary angioedema (HAE) is caused by mutations in the C1inh gene, leading to dysfunction of the C1-esterase inhibitor (C1-INH). C1-INH interacts with MASP-1 and MASP-2 proteases, participating in the...
19.
[Persistence of hepatitis B virus in children after interferon-alpha therapy despite the seroconversion in HBsAg/anti-HBs system]
Gregorek H, Dzierzanowska-Fangrat K, Woynarowski M, Jozwiak P, Witkowska-Vogtt E, Wojda U, et al.
Przegl Epidemiol . 2006 Jan; 59(3):641-9. PMID: 16433306
Objective: The aim of our study was to assess: (1) whether seroconversion to IgG anti-HBs, induced by IFN-alpha therapy in children with chronic active hepatitis B, is maintained 4-10 years...
20.
The influence of surgical treatment of periodontal disease on selected lymphocyte subpopulations important for cellular and humoral immune responses
Gorska R, Laskus-Perendyk A, Gregorek H, Kowalski J
J Periodontol . 2005 Aug; 76(8):1304-10. PMID: 16101362
Background: Periodontal disease is a complex pathological process involving a wide spectrum of immunological reactions. The aim of the study was to evaluate the influence of surgical periodontal treatments on...