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Akademický článek

Contribution of plasma membrane lipid domains to red blood cell (re)shaping

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

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Akademický článek

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Akademický článek

Use of hydroxyurea from childhood to adult age in sickle cell disease: semen analysis

Autor: A.K. Lukusa, C. Vermylen

Publikováno v: Haematologica, Vol 93, Iss 11 (2008)

Externí odkaz: https://doaj.org/article/0bcc327bb4644bb9ba9caa2f805131ab

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Problems in the Detection of Hemophilia Carriers Principles of a Factor VIII Assay on Capillary Blood

Autor: J. Vermylen, Verstraete M, C Vermylen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::40286776fd937af1d2baba88ed1d79bb
https://doi.org/10.1159/000384522

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Original Paper

Autor: S. Uyttendaele, H. Claeys, W. Mertens, H. Verhaert, C. Vermylen

Publikováno v: Vox Sanguinis. 66:122-129

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::95d8ba4e075f3bb90360e583779797e7
https://doi.org/10.1159/000462490

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Computational and molecular approaches for predicting unreported causal missense mutations in Belgian patients with haemophilia A

Autor: N, Lannoy, I, Abinet, A, Bosmans, C, Lambert, C, Vermylen, C, Hermans

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

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Shwachman-Diamond Syndrome: frequent misdiagnosis as Jeune Syndrome and other peculiarities

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

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

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Use of hydroxyurea from childhood to adult age in sickle cell disease: semen analysis

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

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[Medical treatment of juvenile hemangiomas]

Autor: L-M, Boon, A-C, Bataille, V, Bernier, C, Vermylen, G, Verellen

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

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[A particular hereditary anemia in a two-month-old infant: elliptocytosis]

Autor: F G, Debray, S, Ilunga, B, Brichard, C, Chantrain, J M, Scheiff, C, Vermylen

Publikováno v: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 12(2)

We report the case of a 2.5-month-old infant with severe anaemia discovered fortuitously during an acute febrile illness. The patient was admitted because of a septic arthritis of the knee. Initial biology showed a 3.5 g/dl haemoglobin concentration.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::321882a17310a7b198d2cf5f2d811f60
https://pubmed.ncbi.nlm.nih.gov/15694541

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