F Arwert
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Explore the profile of F Arwert including associated specialties, affiliations and a list of published articles.
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Articles
89
Citations
1433
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Recent Articles
1.
Chen F, Medhurst A, de Winter J, Waisfisz Q, Rooimans M, Oostra A, et al.
Leukemia
. 2004 Sep;
18(11):1918-20.
PMID: 15356654
No abstract available.
2.
Hermsen M, Xie Y, Rooimans M, Meijer G, Baak J, Plukker J, et al.
Fam Cancer
. 2003 Oct;
1(1):39-43.
PMID: 14574014
Fanconi anemia (FA) is an autosomal recessive syndrome with a marked predisposition to malignancies, in particular acute myeloid leukemia and squamous cell carcinoma of the oral cavity. We examined oral...
3.
Geldof A, Versteegh LRT , van Mourik J, Rooimans M, Arwert F, Hermsen M, et al.
Thyroid
. 2001 Nov;
11(10):909-17.
PMID: 11716037
Starting from different regional samples taken from a heterogeneous follicular thyroid cancer recurrence in a male patient, a series of cell cultures was initiated. Three stable cancer cell lines were...
4.
5.
van den Berg J, Limburg M, Pals G, Arwert F, Westerveld A
Cerebrovasc Dis
. 2001 Feb;
11(2):92-4.
PMID: 11223659
We present a family with 2 female cousins with intracranial aneurysms and type III collagen deficiency. DNA analysis revealed no mutations in the COL3A1 gene, encoding type III collagen, and...
6.
Xie Y, de Winter J, Waisfisz Q, Nieuwint A, Scheper R, Arwert F, et al.
Br J Haematol
. 2001 Feb;
111(4):1057-64.
PMID: 11167740
Fanconi anaemia (FA) is an autosomal recessive disease strongly predisposing to bone marrow failure and acute myeloid leukaemia (AML). Four FA genes, corresponding to complementation groups A, C, F and...
7.
de Winter J, van der Weel L, de Groot J, Stone S, Waisfisz Q, Arwert F, et al.
Hum Mol Genet
. 2000 Nov;
9(18):2665-74.
PMID: 11063725
Fanconi anemia (FA) is a chromosomal instability syndrome associated with a strong predisposition to cancer, particularly acute myeloid leukemia and squamous cell carcinoma. At the cellular level, FA is characterized...
8.
de Winter J, Leveille F, van Berkel C, Rooimans M, van der Weel L, Steltenpool J, et al.
Am J Hum Genet
. 2000 Sep;
67(5):1306-8.
PMID: 11001585
Fanconi anemia (FA) is an autosomal recessive chromosomal instability syndrome with at least seven different complementation groups. Four FA genes (FANCA, FANCC, FANCF, and FANCG) have been identified, and two...
9.
Joenje H, Levitus M, Waisfisz Q, DAndrea A, Garcia-Higuera I, Pearson T, et al.
Am J Hum Genet
. 2000 Aug;
67(3):759-62.
PMID: 10936108
Fanconi anemia (FA) is an autosomal recessive disorder with diverse clinical symptoms and extensive genetic heterogeneity. Of eight FA genes that have been implicated on the basis of complementation studies,...
10.
Cheng N, van de Vrugt H, van der Valk M, Oostra A, Krimpenfort P, de Vries Y, et al.
Hum Mol Genet
. 2000 Aug;
9(12):1805-11.
PMID: 10915769
Fanconi anemia (FA) is a hereditary chromosomal instability syndrome with cancer predisposition. Bone marrow failure resulting in pancytopenia is the main cause of death of FA patients. Diagnosis of FA...