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Constitutional mismatch repair deficiency mimicking Lynch syndrome is associated with hypomorphic mismatch repair gene variants.
NPJ Precis Oncol. 2024 May 24;8(1):119. doi: 10.1038/s41698-024-00603-z.
NPJ Precis Oncol. 2024.
PMID: 38789506
Free PMC article.
Pediatric acute promyelocytic leukemia and Fanconi anemia: Case report and literature review.
Freycon C, Sepulchre E, Lavallée VP, Mitchell D, MacMillan ML, Vezina C, Goudie C.
Freycon C, et al. Among authors: sepulchre e.
Clin Genet. 2024 Apr 24. doi: 10.1111/cge.14537. Online ahead of print.
Clin Genet. 2024.
PMID: 38658784
Free article.
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Leukemic conversion involving RAS mutations of type 1 CALR-mutated primary myelofibrosis in a patient treated for HCV cirrhosis: a case report.
Gurban P, Mambet C, Botezatu A, Necula LG, Neagu AI, Matei L, Pitica IM, Nedeianu S, Chivu-Economescu M, Bleotu C, Ataman M, Mocanu G, Saguna C, Pavel AG, Stambouli D, Sepulchre E, Anton G, Diaconu CC, Constantinescu SN.
Gurban P, et al. Among authors: sepulchre e.
Front Oncol. 2023 Sep 29;13:1266996. doi: 10.3389/fonc.2023.1266996. eCollection 2023.
Front Oncol. 2023.
PMID: 37841434
Free PMC article.
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Red blood cell alloimmunisation in sickle cell disease patients in the Democratic Republic of the Congo.
Kambale-Kombi P, Djang'eing'a RM, Alworong'a Opara JP, Minon JM, Sepulchre E, Bours V, Floch A, Pirenne F, Tshilumba CK, Batina-Agasa S.
Kambale-Kombi P, et al. Among authors: sepulchre e.
Transfus Med. 2023 Apr;33(2):137-146. doi: 10.1111/tme.12939. Epub 2022 Nov 15.
Transfus Med. 2023.
PMID: 36377544
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Case Report Series: Aggressive HR Deficient Colorectal Cancers Related to BRCA1 Pathogenic Germline Variants.
Freire MV, Martin M, Thissen R, Van Marcke C, Segers K, Sépulchre E, Leroi N, Lété C, Fasquelle C, Radermacher J, Gokburun Y, Collignon J, Sacré A, Josse C, Palmeira L, Bours V.
Freire MV, et al. Among authors: sepulchre e.
Front Oncol. 2022 Feb 24;12:835581. doi: 10.3389/fonc.2022.835581. eCollection 2022.
Front Oncol. 2022.
PMID: 35280729
Free PMC article.
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Covid-19: contribution of clinical characteristics and laboratory features for early detection of patients with high risk of severe evolution.
Sepulchre E, Pittie G, Stojkovic V, Haesbroek G, Crama Y, Schyns M, Paridaens H, de Marchin J, Degesves S, Biemar C, Boccar S, Senterre JM, Minon JM.
Sepulchre E, et al.
Acta Clin Belg. 2022 Apr;77(2):261-267. doi: 10.1080/17843286.2020.1822078. Epub 2020 Sep 16.
Acta Clin Belg. 2022.
PMID: 32935644
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[Concerns about glycated haemoglobin and the limitations of its interpretations].
Sepulchre E, Lutteri L, Cavalier E, Guerci B, Radermecker RP.
Sepulchre E, et al.
Rev Med Liege. 2014 Sep;69(9):497-503.
Rev Med Liege. 2014.
PMID: 25796758
Free article.
Review.
French.
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