Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Laura Yissel Rengifo"'
Autor:
Laura Yissel Rengifo, Lucienne Michaux, Johan Maertens, Thomas Tousseyn, Liesbeth Lenaerts, Joris Robert Vermeesch, Peter Vandenberghe, Barbara Dewaele
Publikováno v:
Clinical Case Reports, Vol 8, Iss 10, Pp 1924-1927 (2020)
Abstract To the authors' best knowledge, this is the first report of acute myeloid leukemia (AML) detected by noninvasive prenatal testing. This was an aggressive case that otherwise would have been difficult to characterize due to disadvantages of "
Externí odkaz:
https://doaj.org/article/2a82322b56b84ef4b4571ecfa76e8385
Autor:
Laura Yissel Rengifo, Sanne Smits, Lieselot Buedts, Michel Delforge, Luc Dehaspe, Thomas Tousseyn, Nancy Boeckx, Stefan Lehnert, Lucienne Michaux, Joris Robert Vermeesch, Peter Vandenberghe, Barbara Dewaele
Publikováno v:
Cancer Treatment and Research Communications, Vol 28, Iss , Pp 100380- (2021)
Multiple myeloma (MM), is a heterogeneous disease in which chromosomal abnormalities are important for prognostic risk stratification. Cytogenetic profiling with FISH on plasma cells from bone marrow samples (BM-PCs) is the current gold standard, but
Externí odkaz:
https://doaj.org/article/85c27e840f814546b405842cb93ef777
Publikováno v:
Acta Biológica Colombiana, Vol 16, Iss 2 (2011)
El género Lagothrix se encuentra representado en Colombia por Lagothrix lagotricha lagotricha y Lagothrix lagotricha lugens y siendo un género llamativo para el tráfico y caza, se han realizado varios trabajos encaminados a conocer sobre su ecolog
Externí odkaz:
https://doaj.org/article/cac8165d944445f5819123db9f0cb92d
Autor:
Jenny Blanco, William Usaquén, Harvy Velasco, Laura Yissel Rengifo, Johanna Galvis, Andrea Casas-Vargas
Publikováno v:
Biomédica: revista del Instituto Nacional de Salud, Vol 39, Iss 4, Pp 622-630 (2019)
En la mayoría de los casos, la diferenciación sexual masculina ocurre con la participación del gen SRY. Sin embargo, se pueden presentar otros genotipos excepcionales, como en el caso que se presenta en este reporte.Se trata de un paciente adulto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bf6ffa21e05ef666d24522a5ea37334
https://doi.org/10.7705/biomedica.4687
https://doi.org/10.7705/biomedica.4687
Autor:
Sanne Smits, Stefan Lehnert, Lieselot Buedts, Peter Vandenberghe, Barbara Dewaele, Lucienne Michaux, Nancy Boeckx, Luc Dehaspe, Laura Yissel Rengifo, Joris Vermeesch, Thomas Tousseyn, Michel Delforge
Publikováno v:
Cancer Treatment and Research Communications, Vol 28, Iss, Pp 100380-(2021)
UNLABELLED: Multiple myeloma (MM), is a heterogeneous disease in which chromosomal abnormalities are important for prognostic risk stratification. Cytogenetic profiling with FISH on plasma cells from bone marrow samples (BM-PCs) is the current gold s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5803b3c89252d8afb7c2b22eec017fd
https://pubmed.ncbi.nlm.nih.gov/33962213
https://pubmed.ncbi.nlm.nih.gov/33962213
Autor:
Liesbeth Lenaerts, Thomas Tousseyn, Joris Vermeesch, Barbara Dewaele, Johan Maertens, Peter Vandenberghe, Lucienne Michaux, Laura Yissel Rengifo
Publikováno v:
Clinical Case Reports
Clinical Case Reports, Vol 8, Iss 10, Pp 1924-1927 (2020)
Clinical Case Reports, Vol 8, Iss 10, Pp 1924-1927 (2020)
To the authors' best knowledge, this is the first report of acute myeloid leukemia (AML) detected by noninvasive prenatal testing. This was an aggressive case that otherwise would have been difficult to characterize due to disadvantages of "gold‐st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdd6dd3692e017a760e0e9e08e78da9c
https://lirias.kuleuven.be/handle/123456789/657719
https://lirias.kuleuven.be/handle/123456789/657719
Autor:
Matthew S. Hestand, Ann Swillen, Elfi Vergaelen, Jeroen Breckpot, Adrian Odrzywolski, Lisanne Vervoort, Anne S. Bassett, Ania Fiksinski, Bernice E. Morrow, Laura Yissel Rengifo, Donna M. McDonald-McGinn, Vandana Shashi, Jacob A. S. Vorstman, Tracy Heung, Wolfram Demaerel, Joris Vermeesch, Janneke Zinkstok, Koen Devriendt, Eva W.C. Chow
Publikováno v:
Hum Mol Genet
The majority (99%) of individuals with 22q11.2 deletion syndrome (22q11.2DS) have a deletion that is caused by non-allelic homologous recombination between two of four low copy repeat clusters on chromosome 22q11.2 (LCR22s). However, in a small subse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39b9d251281485d3e8559478d6dd331c
https://pubmed.ncbi.nlm.nih.gov/31884517
https://pubmed.ncbi.nlm.nih.gov/31884517
Publikováno v:
American journal of primatology. 72(12)
There is a controversy regarding how many species the genus Lagothrix contains, since the Lagothrix lagothricha subspecies have been recently proposed to be actual species. Clarification of species status is of particular importance in the case of L.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22ce81d4ad1bb3918067c35ee95640a9
https://pubmed.ncbi.nlm.nih.gov/20815013
https://pubmed.ncbi.nlm.nih.gov/20815013