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발행년	- (예 : 2010-2015)

Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling

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)

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C-terminal frameshift variant of TDP-43 with pronounced aggregation-propensity causes rimmed vacuole myopathy but not ALS/FTD

Academic Journal

Ervilha Pereira, P.; Schuermans, N.; LeBlanc, P.; Versluys, L.; Peetermans, M.; Debackere, E.; Vanakker, O.; Janssens, S.; Symoens, S.; Bogaert, E.; Dermaut, B.; Meylemans, A.; Verhoeven, K.; De Paepe, B.; De Bleecker, J.L.; Copley, K.E.; Rubien, J.D.; Shorter, J.; Altheimer, C.; Barmada, S.J.; Baets, J.; Lammens, M.

In: Acta Neuropathologica. (Acta Neuropathologica, June 2023, 145(6):793-814)

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Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)

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))

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Implementation of WES-based gene panel testing in patients with adult-onset neurological disorders at the University Hospital of Ghent: a retrospective observational analysis of 176 patients

Academic Journal

Schuermans, N.; Debackere, E.; Symoens, S.; Poppe, B.; Santens, P.; De Bleecker, J.; Hemelsoet, D.; Dermaut, B.

EUROPEAN JOURNAL OF HUMAN GENETICS; DEC 2020, 28 SUPPL 1, p404-p405, 2p. Supplement: 1

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Unexpected identification of a novel 11 bp deletion mutation in TARDBP causing a slowly progressive autosomal dominant myopathy

Academic Journal

Pereira, P. Ervilha; Schuermans, N.; Meylemans, A.; Roy, S.; Leblanc, P.; Aalders, J.; Debackere, E.; Vanakker, O.; Van Hengel, J.; Symoens, S.; De Bleecker, J.; Dermaut, B.; Bogaert, E.

EUROPEAN JOURNAL OF HUMAN GENETICS; DEC 2020, 28 SUPPL 1, p449-p450, 2p. Supplement: 1

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Between city and state. The local policy towards foreigners in Antwerp, 1830-1880

Academic Journal

Debackere, E.

In: Belgisch Tijdschrift voor Nieuwste Geschiedenis/ Revue Belge de Histoire Contemporaine. (Belgisch Tijdschrift voor Nieuwste Geschiedenis/ Revue Belge de Histoire Contemporaine, 2016, 46(3-4):258-259)

Web of Science JCR 저널정보 Scopus Find it@PNU

City history in Belgian and Dutch historical periodicals (2014)

Academic Journal

Puttevils, J.; Baguet, J.; Debackere, E.; Germonprez, D.; De Graef, P.; De Groot, J.; Horemans, B.; De Meulder, Y.; Muurling, S.; Schepers, M.; Vervaeke, A.

In: Stadsgeschiedenis. (Stadsgeschiedenis, 2016, 11(1):90-114)

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Belgian immigration policy in the nineteenth century: Circulars as communication channels between the central and local policy level (1830-1914)

Academic Journal

Coppens, A.; Debackere, E.

In: Belgisch Tijdschrift voor Nieuwste Geschiedenis/ Revue Belge de Histoire Contemporaine. (Belgisch Tijdschrift voor Nieuwste Geschiedenis/ Revue Belge de Histoire Contemporaine, 2015, 45(2-3):12-45)

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Understanding the mechanism of RNF216-mediated neurodegeneration: genetic, proteomic, neuropathological and cellular approach

Academic Journal

Roy, S.; Pereira, P. Ervilha; Schuermans, N.; Sieben, A.; Thery, F.; Mondragon Rezola, E.; Debackere, E.; LeBlanc, P.; Galas, M.; Santens, P.; Impens, F.; Bogaert, E.; Dermaut, B.

EUROPEAN JOURNAL OF HUMAN GENETICS; DEC 2020, 28 SUPPL 1, p387-p387, 1p. Supplement: 1

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