Zobrazeno 1 - 10
of 826
pro vyhledávání: '"C Vermylen"'
Autor:
C. Leonard, L. Conrard, M. Guthmann, H. Pollet, M. Carquin, C. Vermylen, P. Gailly, P. Van Der Smissen, M. P. Mingeot-Leclercq, D. Tyteca
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-17 (2017)
Abstract Although lipid domains have been evidenced in several living cell plasma membranes, their roles remain largely unclear. We here investigated whether they could contribute to function-associated cell (re)shaping. To address this question, we
Externí odkaz:
https://doaj.org/article/53b3e96f60d34bdbb6a7c77e0de021b1
Akademický článek
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Autor:
A.K. Lukusa, C. Vermylen
Publikováno v:
Haematologica, Vol 93, Iss 11 (2008)
Externí odkaz:
https://doaj.org/article/0bcc327bb4644bb9ba9caa2f805131ab
Publikováno v:
Vox Sanguinis. 66:122-129
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95d8ba4e075f3bb90360e583779797e7
https://doi.org/10.1159/000462490
https://doi.org/10.1159/000462490
Autor:
TEKCAN, Demet1 demet.kuscu@yahoo.com, CELIK, Ilknur KULHAS1, TARRANT, Teresa K.2, HERSFIELD, Michael S.2,3, ARTAC, Hasibe1
Publikováno v:
Asthma Allergy Immunology / Astim Allerji Immunoloji. Aug2024, Vol. 22 Issue 2, p213-216. 4p.
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 18(3)
Haemophilia A (HA) is caused by widespread mutations in the factor VIII gene. The high spontaneous mutation rate of this gene means that roughly 40% of HA mutations are private. This study aimed to describe the approaches used to confirm private dise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f9fc6884bc88c7bf9240e22aca0d6259
https://pubmed.ncbi.nlm.nih.gov/21883705
https://pubmed.ncbi.nlm.nih.gov/21883705
Autor:
Xavier Bossuyt, A. Uyttebroeck, Heidi Schaballie, Victoria Bordon, Isabelle Meyts, C Vermylen, Marleen Renard, Anniek Corveleyn, Lieve Sevenants, Filomeen Haerynck
Publikováno v:
Pediatric Rheumatology Online Journal, Vol 9, Iss Suppl 1, p P313 (2011)
Pediatric Rheumatology Online Journal
Europe PubMed Central
Pediatric Rheumatology Online Journal
Europe PubMed Central
Results In 10 patients an SBDS mutation was identified in both alleles, patient 11 was heterozygous. The mean age at diagnosis was 2.9 years. All patients had exocrine pancreatic insufficiency. Radiological evidence of skeletal dysplasia was present
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17e47a79ab45d0eb946146d839620d0d
https://doaj.org/article/7f2b236dbf9b434c847785acf788bdd5
https://doaj.org/article/7f2b236dbf9b434c847785acf788bdd5
Autor:
C Vermylen, A K Lukusa
Publikováno v:
Haematologica. 93(11)
We read with interest the paper by Berthaut et al.[1][1], who studied the influence of hydroxyurea on sperm parameters and fertility of human males. In that retrospective multicenter study, sperm parameters and fertility were evaluated in 44 adult pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c80e210f3c20ef0465dea4f18a6e03a5
https://pubmed.ncbi.nlm.nih.gov/18508803
https://pubmed.ncbi.nlm.nih.gov/18508803
Publikováno v:
Annales de chirurgie plastique et esthetique. 51(4-5)
Infantile hemangioma always involute in 5 to 7 years. However, 10% of proliferating hemangiomas will necessitate a therapeutic approach, often medical, in order to avoid life or organ threatening, fonctional or esthetic sequelae. "Which hemangioma ne
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::139c6d6318229762ec8486429772c2e4
https://pubmed.ncbi.nlm.nih.gov/16997446
https://pubmed.ncbi.nlm.nih.gov/16997446