Ghent University Academic Bibliography

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Your filters: cql: author="BONNET, D*" or (type exact bookEditor and editor="BONNET, D*")

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- Journal Article
- A1
- open access
Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

Danyel Lee, Jérémie Le Pen, Ahmad Yatim, Beihua Dong, Yann Aquino, Masato Ogishi, Rémi Pescarmona, Estelle Talouarn, Darawan Rinchai, Peng Zhang, et al.

(2023) SCIENCE. 379(6632).
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- Journal Article
- A1
- open access
SARS-CoV-2–related MIS-C : a key to the viral and genetic causes of Kawasaki disease?

Vanessa Sancho-Shimizu, Petter Brodin, Aurélie Cobat, Catherine M. Biggs, Julie Toubiana, Carrie L. Lucas, Sarah E. Henrickson, Alexandre Belot, Elie Haddad, Kathie Beland, et al.

(2021) JOURNAL OF EXPERIMENTAL MEDICINE. 218(6).
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- Miscellaneous
- open access
Arterial tortuosity syndrome : 40 new families and literature review (vol 20, pg 1236, 2017)

Aude Beyens (UGent) , Juliette Albuisson, Annekatrien Boel (UGent) , Mazen Al-Essa, Waheed Al-Manea, Damien Bonnet, Ozlem Bostan, Odile Boute, Tiffany Busa, Nathalie Canham, et al.

(2019) GENETICS IN MEDICINE. 21(8). p.1894-1895
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Recommendations from the Association for European Paediatric and Congenital Cardiology for training in pulmonary hypertension

Hannes Sallmon, Shahin Moledina, Dimpna C Albert, Maurice Beghetti, Rolf MF Berger, Damien Bonnet, Mila Bukova, Martin Koestenberger, Katharina Meinel, Zdenka Reinhardt, et al.

(2019) CARDIOLOGY IN THE YOUNG. 29(11). p.1323-1327
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Arterial tortuosity syndrome : 40 new families and literature review

Aude Beyens (UGent) , Juliette Albuisson, Annekatrien Boel (UGent) , Mazen Al-Essa, Waheed Al-Manea, Damien Bonnet, Ozlem Bostan, Odile Boute, Tiffany Busa, Nathalie Canham, et al.

(2018) GENETICS IN MEDICINE. 20(10). p.1236-1245
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- Conference Paper
- C3
Arterial tortuosity syndrome : 40 new families and literature review

Aude Beyens (UGent) , Juliette Albuisson, Annekatrien Boel (UGent) , Mazen Al-Essa, Damien Bonnet, O Bostan, Odile Boute, T Busa, N Canham, Ergun Cil, et al.

(2017) European Society of Human Genetics, 50th Annual meeting, Abstracts.
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CD64 distinguishes macrophages from dendritic cells in the gut and reveals the Th1-inducing role of mesenteric lymph node macrophages during colitis

Samira Tamoutounour, Sandrine Henri, Hugues Lelouard, Béatrice de Bovis, Colin de Haar, C Janneke van der Woude, Andrea M Woltman, Yasmin Reyal, Dominique Bonnet, Dorine Sichien (UGent) , et al.

(2012) EUROPEAN JOURNAL OF IMMUNOLOGY. 42(12). p.3150-3166
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Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 year

Chantal Stheneur, Laurence Faivre, Gwenaelle Collod-Beroud, Elodie Gautier, Christine Binquet, Claira-e Bonithon-Kopp, Mireille Claustres, Anne H Child, Eloisa Arbustini, Lesley C Ades, et al.

(2011) PEDIATRIC RESEARCH. 69(3). p.265-270
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- Journal Article
- A1
Key aspects of CdTe/CdS solar cells.

K DUROSE, D BOYLE, A ABKEN, CJ OTTLEY, Peter Nollet, Stefaan Degrave, Marc Burgelman (UGent) , R WENDT, J BEIER and D BONNET

(2002) PHYSICA STATUS SOLIDI B-BASIC RESEARCH. 229(2). p.1055-1064
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- Journal Article
- A1
The mutation spectrum in Holt-Oram syndrome.

SJ CROSS, YH CHING, QY LI, L ARMSTRONG-BUISSERET, S SPRANGER, S LYONNET, D BONNET, M PENTTINEN, P JONVEAUX, B LEHEUP, et al.

(2000) JOURNAL OF MEDICAL GENETICS. 37(10). p.785-787

Academic Bibliography

Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

SARS-CoV-2–related MIS-C : a key to the viral and genetic causes of Kawasaki disease?

Arterial tortuosity syndrome : 40 new families and literature review (vol 20, pg 1236, 2017)

Recommendations from the Association for European Paediatric and Congenital Cardiology for training in pulmonary hypertension

Arterial tortuosity syndrome : 40 new families and literature review

Arterial tortuosity syndrome : 40 new families and literature review

CD64 distinguishes macrophages from dendritic cells in the gut and reveals the Th1-inducing role of mesenteric lymph node macrophages during colitis

Prognosis factors in probands with an FBN1 mutation diagnosed before the age of 1 year

Key aspects of CdTe/CdS solar cells.

The mutation spectrum in Holt-Oram syndrome.

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