학술논문
'학술논문'
에서 검색결과 28건 | 목록
1~10
Academic Journal
Schuermans, N.; Bogaert, E.; Rosseel, T.; De Clercq, G.; Debackere, E.; Coucke, P.J.; Poppe, B.; Dermaut, B.; Dufour, S.; Impens, F.; El Chehadeh, S.; Depienne, C.; Hemelsoet, D.; Gautheron, J.; Vigouroux, C.; Auclair, M.; Jéru, I.; Vantyghem, M.-C.; Nouioua, S.; Cherif, F.R.; Tazir, M.; Okawa, F.; Mizushima, N.; Hilbert, P.; Van Doninck, N.; Taquet, M.-C.; Van Haverbeke, C.; Van Dorpe, J.; Urtizberea, J.A.; Chanson, J.-B.; Funalot, B.; Authier, F.-J.; Kaya, S.; Terryn, W.; Callens, S.; Depypere, B.; Vanlander, A.V.; Verloo, P.
In: Nature Genetics . (Nature Genetics, November 2023, 55(11):1929-1940)
Academic Journal
Schuermans, N.; Coucke, P.J.; Callewaert, B.; Bogaert, E.; Debackere, E.; Ghijsels, J.; LeBlanc, P.; Verdin, H.; Dermaut, B.; Poppe, B.; Hemelsoet, D.; Terryn, W.; Steyaert, S.; Callens, S.; Van Coster, R.; Verloo, P.; Vanlander, A.V.; Steyaert, W.; Naesens, L.; Haerynck, F.; De Bleecker, J.; Santens, P.; Boon, P.; Laureys, G.; Kerre, T.
In: Orphanet Journal of Rare Diseases . (Orphanet Journal of Rare Diseases, December 2022, 17(1))
Academic Journal
Tang, M.; Boel, A.; Castelluccio, N.; Cardona Barberán, A.; Christodoulaki, A.; Bekaert, B.; Popovic, M.; Vanden Meerschaut, F.; De Sutter, P.; Stoop, D.; Heindryckx, B.; Menten, B.; Symoens, S.; Coucke, P.J.; Vanlander, A.V.
In: Journal of Assisted Reproduction and Genetics . (Journal of Assisted Reproduction and Genetics, March 2022, 39(3):609-618)
Academic Journal
Rosier, K.; Monnens, Y.; Bhalla, K.; Aerts, L.; Régal, L.; Creemers, J.W.M.; McDevitt, M.T.; Floyd, B.J.; Bingman, C.A.; Rashan, E.H.; Pagliarini, D.J.; Smet, J.; Verschoore, M.; Vanlander, A.V.; Van Coster, R.; Marcaida, M.J.; Dal Peraro, M.; Lemmens, I.; Tavernier, J.; Cravatt, B.F.; Gounko, N.V.; Vints, K.
In: iScience . (iScience, 17 December 2021, 24(12))
Academic Journal
Jennions, E.; Törnhage, C.-J.; Darin, N.; Hedberg-Oldfors, C.; Oldfors, A.; Berglund, A.-K.; Kollberg, G.; Sterky, F.H.; Eklund, E.A.; Verloo, P.; Vanlander, A.V.; De Meirleir, L.; Seneca, S.
In: Journal of Inherited Metabolic Disease . (Journal of Inherited Metabolic Disease, 1 September 2019, 42(5):898-908)
Academic Journal
Vandecasteele, S.J.; Seneca, S.; Smet, J.; Reynders, M.; De Ceulaer, J.; Vanlander, A.V.; van Coster, R.
In Clinical Microbiology and Infection April 2018 24(4):431-431
Academic Journal
Hemelsoet, D.M.; Vanlander, A.V.; Smet, J.; Vantroys, E.; Van Coster, R.; Acou, M.; Goethals, I.; Sante, T.; Menten, B.; Seneca, S.
In: Neurology: Genetics . (Neurology: Genetics, 1 December 2018, 4(6))
Academic Journal
Vantroys, E.; Smet, J.; Vanlander, A.V.; Van Coster, R.; Vergult, S.; Menten, B.; De Bruyne, R.; Roels, F.; Stepman, H.; Roeyers, H.
In: Orphanet Journal of Rare Diseases . (Orphanet Journal of Rare Diseases, 21 May 2018, 13(1))
Academic Journal
Bogaert, D.J.; De Bruyne, M.; Haerynck, F.; Dullaers, M.; De Baets, F.; Bonroy, C.; De Baere, E.; Dehoorne, J.; Vanlander, A.V.; Kuehn, H.S.; Rosenzweig, S.D.; Calvo, K.R.; Cytlak, U.; Bigley, V.
In: Journal of Allergy and Clinical Immunology . (Journal of Allergy and Clinical Immunology, January 2018, 141(1):432-435.e7)
Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
Academic Journal
Alston, C.L.; Oláhová, M.; Yarham, J.W.; He, L.; Taylor, R.W.; Compton, A.G.; Thorburn, D.R.; Formosa, L.E.; Ryan, M.T.; Strecker, V.; Wittig, I.; Haack, T.B.; Prokisch, H.; Smet, J.; De Paepe, B.; Vanlander, A.V.; Van Coster, R.; Stouffs, K.; Seneca, S.; Diakumis, P.; Bahlo, M.; Ciara, E.; Pronicka, E.; Cassiman, D.; Van Hove, J.L.K.; Romain, N.; Haller, R.G.; Feichtinger, R.G.; Mayr, J.A.; Płoski, R.; Rokicki, D.
In: American Journal of Human Genetics . (American Journal of Human Genetics, 7 July 2016, 99(1):217-227)
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[AR] Vanlander, A.V.
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