Researcher
Maissa Rayyan
- Disciplines:Laboratory medicine, Palliative care and end-of-life care, Regenerative medicine, Other basic sciences, Other health sciences, Nursing, Other paramedical sciences, Other translational sciences, Other medical and health sciences
Affiliations
- Faculty of Medicine (Faculty)
Member
From1 Oct 2020 → 30 Sep 2021 - Woman and Child (Division)
Member
From1 Apr 2013 → Today - Department of Development and Regeneration (Department)
Member
From1 Jan 2012 → 26 Apr 2022
Projects
1 - 2 of 2
- Oral drug absorption in specific patient populations: understanding the impact of gastrointestinal physiologyFrom1 Oct 2018 → 21 Jun 2023Funding: Own budget, for example: patrimony, inscription fees, gifts
- Characterizing the esophageal function of infants in the NICU.From1 Oct 2011 → 8 May 2020Funding: Own budget, for example: patrimony, inscription fees, gifts
Publications
21 - 30 of 68
- Improvised Hand Injury Treatment Using Traditional Veterinary Medicine in Ethiopia(2017)
Authors: Raf Aerts, Maissa Rayyan
Pages: 322 - 326 - Esophageal Atresia: Future Directions for Research on the Digestive Tract(2017)
Authors: Maissa Rayyan, Nathalie Rommel, Jan Tack, Jan Deprest, Karel Allegaert
Pages: 306 - 312 - Risk factors for spontaneous localized intestinal perforation in the preterm infant(2017)
Authors: Maissa Rayyan, Gunnar Naulaers, Karel Allegaert, Marc Miserez
Pages: 2617 - 2623 - The Potential Benefits of Applying Recent Advances in esophageal Motility Testing in Patients with esophageal Atresia(2017)
Authors: Nathalie Rommel, Maissa Rayyan, Taher Omari
Pages: 1 - 7 - Catch-up growth in the first two years of life in Extremely Low Birth Weight (ELBW) infants is associated with lower body fat in young adolescence(2017)
Authors: Anke Raaijmakers, Lotte Jacobs, Maissa Rayyan, Els Ortibus, Elena Levtchenko, Jan A Staessen, Karel Allegaert
- Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate(2016)
Authors: Jeroen Breckpot, Greet Hens, Maissa Rayyan, Eric Legius, Joris Vermeesch, Koenraad Devriendt
Pages: 51 - 8 - Chromosome 22q12.1 microdeletions: Confirmation of the MN1 gene as a candidate gene for cleft palate(2016)
Authors: Jeroen Breckpot, BM Anderlid, Y Alanay, M Blyth, A Brahimi, B Duban-Bedu, O Gozé, H Firth, MC Yakicier, G Hens, et al.
Pages: 51 - 58 - PP-10 CHARACTERIZATION OF ESOPHAGEAL MOTILITY IN INFANTS BORN WITH CONGENITAL DIAPHRAGMATIC HERNIA USING HIGH RESOLUTION MANOMETRY.(2015)
Authors: Maissa Rayyan, Karel Allegaert, Philippe Nafteux, Hans Van Veer, Jan Deprest, Nathalie Rommel
Pages: 524 - Pierre Robin sequence: Management of respiratory and feeding complications during the first year of life in a tertiary referral centre(2015)
Authors: Maissa Rayyan, Joseph Schoenaers, Anna Verdonck, Koenraad Devriendt, Vincent Vander Poorten, Greet Hens
Pages: 1206 - 12 - The correlation between the observed-to-expected total fetal lung volume and intra-thoracic organ herniation on magnetic resonance images in fetuses with isolated left-sided congenital diaphragmatic hernia(2015)
Authors: Mary Patrice Eastwood, Inga Sandaite, Philip DeKoninck, Filip Claus, Jute Richter, Maissa Rayyan, Jan Deprest
Pages: 162 - 167