Zobrazeno 1 - 10 of 21 pro vyhledávání: '"R E, Kibbelaar"'
1
Expanding the clinical spectrum of self-limiting, rare Kikuchi disease - A case with overwhelming multi-organ involvement
Autor: H A, Hoogstins, R E, Kibbelaar, F L, Ubels, M H, Hemmelder, M, Hoogendoorn
Publikováno v: The Netherlands journal of medicine. 75(3)
Kikuchi disease is a rare disorder with an unknown pathogenesis and a typically self-limiting natural course in predominantly previously healthy young women. Here we present a 54-year-old woman suffering from an overwhelming presentation of Kikuchi d
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::9820c58bd512added2b362e54a534724
https://pubmed.ncbi.nlm.nih.gov/28469047
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2
Characterization of a New Human B Cell Line (Bonna-12) with Trisomy 9 and Trisomy 12 Chromosomal Abnormality
Autor: Joop H. Jansen, Hanneke C. Kluin-Nelemans, Hans W. Wessels, Geoffrey C. Beverstock, Gert-Jan H. M. Wientjens, Pieter Brederoo, R E Kibbelaar
Publikováno v: Leukemialymphoma. 5(5-6)
A new EBV positive human B-cell line, BONNA-12 was established from splenic cells of a patient with a hairy cell leukemia (HCL). BONNA-12 cells grew spontaneously and formed colonies in semisolid media. Although the BONNA-12 cell line was identical w
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dea131fa2959b19ecf6afef759f2f95e
https://pubmed.ncbi.nlm.nih.gov/27463354
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5
Severe cardiac defect in a patient with the OEIS complex
Autor: Sarina G. Kant, A Van Haeringen, M M Bartelings, R E Kibbelaar
Publikováno v: Clinical Dysmorphology. 6:371-374
The OEIS complex is an association of fetal malformations including omphalocele, exstrophy of the cloaca, imperforate anus and spinal defects. We present a fetus with the OEIS complex in combination with a cardiac defect. Until now very few cases wit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40afa83eb930d2f47f1b93cf1d6645f9
https://doi.org/10.1097/00019605-199710000-00012
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6
Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridization
Autor: Ph. M. Kluin, R E Kibbelaar, H. Van Kamp, H.L. Haak, J. W. Wessels, Willem E. Fibbe, E.J. Dreef, J.W.R. Mulder, Geoffrey C. Beverstock
Publikováno v: Blood. 82:904-913
Fluorescence in situ hybridization (FISH) is a powerful tool for detection of numerical and structural chromosomal aberrations. We have compared conventional banding techniques and FISH for the detection of monosomy 7 (-7) and trisomy 8 (+8) in 89 pa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f1b8a30d074171e54586d506779255b8
https://doi.org/10.1182/blood.v82.3.904.904
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7
Detection of monosomy 7 and trisomy 8 in myeloid neoplasia: a comparison of banding and fluorescence in situ hybridization
Autor: R E, Kibbelaar, J W, Mulder, E J, Dreef, H, van Kamp, W E, Fibbe, J W, Wessels, G C, Beverstock, H L, Haak, P M, Kluin
Publikováno v: Blood. 82:904-913
Fluorescence in situ hybridization (FISH) is a powerful tool for detection of numerical and structural chromosomal aberrations. We have compared conventional banding techniques and FISH for the detection of monosomy 7 (-7) and trisomy 8 (+8) in 89 pa
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::282dcda1bfa261ed41f23f07cff27e16
https://doi.org/10.1182/blood.v82.3.904.bloodjournal823904
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8
Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes
Autor: Johanna Kluin-Nelemans, Philippus Kluin, E.J. Dreef, Willem E. Fibbe, Geoffrey C. Beverstock, R E Kibbelaar, G de Groot-Swings, H. Van Kamp
Publikováno v: Blood. 79:1823-1828
Clonality of myeloid and lymphoid cell fractions obtained from peripheral blood (PB) or bone marrow (BM) of five patients with a myelodysplastic syndrome (MDS), was studied by combined immunophenotypic analysis and DNA in situ hybridization. This nov
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a91206b393e70f8bb8b16ba6f51e272a
https://doi.org/10.1182/blood.v79.7.1823.1823
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9
Nonradioactive in situ hybridisation of the translocation t(1;7) in myeloid malignancies
Autor: Anton K. Raap, H.L. Haak, R E Kibbelaar, Hans W. Wessels, Jan-Willem R. Mulder, Harmen van Kamp, E.J. Dreef, Philip M. Kluin, Geoffrey C. Beverstock
Publikováno v: Genes, Chromosomes and Cancer. 4:128-134
Bone marrow cells of four patients with t(1;7) and myelodysplasia or acute myeloid leukemia were analyzed using nonradioactive in situ hydridisation. As probes, centromeric alphoid DNA sequences of chromosomes 1 and 7, a satellite DNA probe for 1q12,
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1535b1763aab62bd7757184611099d08
https://doi.org/10.1002/gcc.2870040205
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10
Sustained engraftment of mice transplanted with IL-1-primed blood-derived stem cells
Autor: W E Fibbe, M S Hamilton, L L Laterveer, R E Kibbelaar, J H Falkenburg, J W Visser, R Willemze
Publikováno v: The Journal of Immunology. 148:417-421
IL-1 is considered the primary mediator of the acute phase response. One of the characteristic manifestations of this response is early neutrophilia that is probably caused by release of mature neutrophils from the bone marrow into the peripheral blo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::0311046de105f2cadc812067a88d4dbd
https://doi.org/10.4049/jimmunol.148.2.417
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