Lisette van de Corput
Overview
Explore the profile of Lisette van de Corput including associated specialties, affiliations and a list of published articles.
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Articles
13
Citations
296
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0
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Recent Articles
1.
Pavlova S, Malcikova J, Radova L, Bonfiglio S, Cowland J, Brieghel C, et al.
Hemasphere
. 2025 Jan;
9(1):e70065.
PMID: 39840379
In chronic lymphocytic leukemia, the reliability of next-generation sequencing (NGS) to detect variants ≤10% allelic frequency (low-VAF) is debated. We tested the ability to detect 23 such variants in 41...
2.
van Eijs M, van der Wagen L, Mous R, Leguit R, van de Corput L, van Lindert A, et al.
Cancer Immunol Immunother
. 2022 Jun;
72(1):249-255.
PMID: 35691988
Immune checkpoint inhibition (ICI) can induce durable responses in patients with advanced malignancies. Three cases of hematological neoplasia following ICI for solid tumors have been reported to date. We present...
3.
Smits B, van Montfrans J, Merrill S, van de Corput L, van Gijn M, de Vries A, et al.
J Clin Immunol
. 2021 Mar;
41(6):1219-1228.
PMID: 33779897
Hemophagocytic lymphohistiocytosis (HLH) is a life-threatening immune dysregulation syndrome characterized by uncontrolled immune cell activation. Timely diagnosis is important, since early treatment can improve survival rates. However, completing all assessments...
4.
Le T, Sanders C, van de Corput L, van Erpecum K, Rockmann H
J Allergy Clin Immunol Pract
. 2015 Aug;
4(1):175-6.
PMID: 26298826
No abstract available.
5.
Mattheij M, Schatorje E, Gemen E, van de Corput L, Nooijen P, van der Burg M, et al.
Case Reports Immunol
. 2014 Nov;
2012:196417.
PMID: 25379303
We describe a girl, now 9 years of age, with chronic idiopathic thrombocytopenic purpura, persistent nonmalignant lymphadenopathy, splenomegaly, recurrent infections, and autoimmune hemolytic anemia. Her symptoms partly fit the definitions...
6.
Nijman I, van Montfrans J, Hoogstraat M, Boes M, van de Corput L, Renner E, et al.
J Allergy Clin Immunol
. 2013 Oct;
133(2):529-34.
PMID: 24139496
Background: Primary immunodeficiency (PID) disorders are a heterogeneous group of inherited disorders caused by a variety of monogenetic immune defects. Thus far, mutations in more than 170 different genes causing...
7.
Zhao X, Gazendam R, Drewniak A, Van Houdt M, Tool A, van Hamme J, et al.
Blood
. 2013 May;
122(1):109-11.
PMID: 23687090
Familial hemophagocytic lymphohistiocytosis (FHL) is caused by genetic defects in cytotoxic granule components or their fusion machinery, leading to impaired natural killer cell and/or T lymphocyte degranulation and/or cytotoxicity. This...
8.
van Montfrans J, Hoepelman A, Otto S, van Gijn M, van de Corput L, de Weger R, et al.
J Allergy Clin Immunol
. 2011 Dec;
129(3):787-793.e6.
PMID: 22197273
Background: CD27 is a lymphocyte costimulatory molecule that regulates T-cell, natural killer (NK) cell, B-cell, and plasma cell function, survival, and differentiation. On the basis of its function and expression...
9.
van de Ven A, Compeer E, Bloem A, van de Corput L, van Gijn M, van Montfrans J, et al.
J Allergy Clin Immunol
. 2011 Dec;
129(3):755-761.e7.
PMID: 22130422
Background: B cells of patients with common variable immunodeficiency (CVID) disorders display impairment in production of immunoglobulin class-switched antibodies, which is possibly contributed to by defects in early B-cell activation....
10.
Elstak E, Te Loo M, Tesselaar K, van Kerkhof P, Loeffen J, Grivas D, et al.
Pediatr Blood Cancer
. 2011 Jul;
58(4):598-605.
PMID: 21755595
Background: UNC13D, encoding the protein munc13-4, is essential in intracellular trafficking and exocytosis of lytic granules. Mutations in this gene are associated with familial hemophagocytic lymphohistiocytosis type 3 (FHL3), a...