Sylwia Koltan
Overview
Explore the profile of Sylwia Koltan including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
45
Citations
277
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Geier C, Ellison M, Cruz R, Pawar S, Leiss-Piller A, Zmajkovicova K, et al.
J Clin Immunol
. 2022 Aug;
42(8):1748-1765.
PMID: 35947323
Warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome (WS) is a combined immunodeficiency caused by gain-of-function mutations in the C-X-C chemokine receptor type 4 (CXCR4) gene. We characterize a unique international...
12.
Samborska M, Baranska M, Wachowiak J, Skalska-Sadowska J, Thambyrajah S, Czogala M, et al.
Front Oncol
. 2022 Jul;
12:935373.
PMID: 35875115
Introduction: Myeloid sarcoma (MS) is an extramedullary malignant tumor composed of immature myeloid cells. It occurs in patients with acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), or chronic myeloid leukemia...
13.
Grzesk E, Dabrowska A, Urbanczyk A, Ewertowska M, Wysocki M, Koltan S
Postepy Dermatol Alergol
. 2021 Dec;
38(5):873-880.
PMID: 34849137
Introduction: Common variable immunodeficiency (CVID) is one of the primary humoral immunodeficiencies. Despite the inborn nature, the first symptoms may appear in both children and adults. It is characterized by...
14.
Oszer A, Babol-Pokora K, Koltan S, Pastorczak A, Mlynarski W
Mol Cytogenet
. 2021 Nov;
14(1):51.
PMID: 34781974
Background: Isolated Congenital Asplenia (ICA, OMIM #271400) is a rare, life-threatening abnormality causing immunodeficiency, which is characterized by the absence of a spleen. Diagnosis should be completed in early childhood...
15.
Koltan S, Koltan A, Soszynska K, Matiakowska K, Morgut-Klimkowska M, Grzesk E, et al.
Cent Eur J Immunol
. 2021 Nov;
46(2):210-216.
PMID: 34764789
Introduction: Acute lymphoblastic leukemia (ALL) is the most common malignancy diagnosed in children. The factors predisposing to ALL remain mostly unknown. Natural killer (NK) cells are a component of innate...
16.
Babol-Pokora K, Wolowiec M, Popko K, Jaworowska A, Bryceson Y, Tesi B, et al.
Arch Immunol Ther Exp (Warsz)
. 2021 Oct;
69(1):31.
PMID: 34677667
Hemophagocytic lymphohistiocytosis (HLH) is a clinical syndrome of life-threatening inflammation caused by an excessive, prolonged and ineffective immune response. An increasing number of HLH cases is recognized in Poland, but...
17.
Dimitrova D, Nademi Z, Maccari M, Ehl S, Uzel G, Tomoda T, et al.
J Allergy Clin Immunol
. 2021 May;
149(1):410-421.e7.
PMID: 34033842
Background: Activated phosphoinositide 3-kinase delta syndrome (APDS) is a combined immunodeficiency with a heterogeneous phenotype considered reversible by allogeneic hematopoietic cell transplantation (HCT). Objectives: This study sought to characterize HCT...
18.
Wolska-Kusnierz B, Pastorczak A, Fendler W, Wakulinska A, Dembowska-Baginska B, Heropolitanska-Pliszka E, et al.
Clin Cancer Res
. 2020 Oct;
27(2):575-584.
PMID: 33082212
Purpose: Nijmegen breakage syndrome (NBS) is a DNA repair disorder with a high predisposition to hematologic malignancies. Experimental Design: We describe the natural history of NBS, including cancer incidence, risk...
19.
Pac M, Bielecka T, Grzela K, Komarnicka J, Langfort R, Koltan S, et al.
Front Immunol
. 2020 Sep;
11:1950.
PMID: 32973798
Primary immunodeficiencies (PIDs) are rare disorders of the immune system encompassing inborn errors of immunity. Primary antibody deficiencies constitute the largest group of PID with common variable immunodeficiency (CVID) being...
20.
Sharapova S, Skomska-Pawliszak M, Rodina Y, Wolska-Kusnierz B, Dabrowska-Leonik N, Mikoluc B, et al.
Front Immunol
. 2020 Jul;
11:900.
PMID: 32655540
Variants in recombination-activating genes () are common genetic causes of autosomal recessive forms of combined immunodeficiencies (CID) ranging from severe combined immunodeficiency (SCID), Omenn syndrome (OS), leaky SCID, and CID...