Antonia Felzen

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Speerpunten

Progressive familial inrahepatic cholestasis and related diseases

Opleiding / Academische kwalificatie

Bachelor of Science in Medicine, Rijksuniversiteit Groningen

1-sep.-2016 → 8-jul.-2019

Datum van toekenning: 8-jul.-2019

Bachelor Honours College , Honours College University of Groningen

1-sep.-2016 → 26-jun.-2019

Datum van toekenning: 26-jun.-2019

Master of Science in Medicine, Rijksuniversiteit Groningen

1-sep.-2019 → …

1 Conference contribution
1 Poster
1 Meeting Abstract
1 Article
Meer
- 1 Review article

The spectrum of Progressive Familial Intrahepatic Cholestasis diseases: Update on pathophysiology and emerging treatments
Felzen, A. & Verkade, H. J., nov.-2021, In: European journal of medical genetics. 64, 11, 8 blz., 104317.
Onderzoeksoutput › peer review

Open Access
Bestand

11 Citaten (Scopus)

139 Downloads (Pure)
Analysis of long-term treatment effects of odevixibat on clinical outcomes in children with progressive familial intrahepatic cholestasis in odevixibat clinical studies vs external controls from the NAPPED database
Hansen, B., Valcheva, V., Yu, Q., Wessel, D. V., Thompson, R., Gonzalès, E., Jankowska, I., Sokal, E., Grammatikopoulos, T., Kadaristiana, A., Jacquemin, E., Spraul, A., Lipiński, P., Czubkowski, P., Rock, N., Shagrani, M., Kumar, K., Alkuraya, F., Sateesh, M., Broering, D. C., & 32 anderenNicastro, E., Kelly, D., Nebbia, G., Arnell, H., Fischler, B., Serranti, D., Arıkan, C., Polat, E., Debray, D., Lacaille, F., Gonçalves, C., Llanillo, L. H., Bartolo, G. M., Mozer-Glassberg, Y., Azaz, A., Brecelj, J., Dezsőfi, A., Calvo, P. L., Grabhorn, E., Sturm, E., Woerd, W. L. V. D., Kamath, B. M., Wang, J-S., Liting, L., Durmaz, O., Önal, Z., Felzen, A., Nomden, M., Sonajalg, J., Stein, P., Ni, Q. & Verkade, H., jun.-2023, blz. S969-S970. 2 blz.
Onderzoeksoutput › Academic
Characterization of a novel bile salt export pump deficiency mouse model with the p.E297g mutation
Felzen, A., Hovingh, M., Havinga, R., Mulder, N., Koehorst, M., van de Sluis, B., de Boer, J. F., Kuipers, F. & Verkade, H., jun.-2023, ESPGHAN 55th Annual Meeting Abstracts. Wolters Kluwer, Vol. 76. blz. 671-672 2 blz.
Onderzoeksoutput › Academic › peer review

Open Access
Bestand

20 Downloads (Pure)
Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency
NAtural course and Prognosis of PFIC and Effect of biliary Diversion (NAPPED) Consortium, Felzen, A., van Wessel, D. B. E., Gonzales, E., Thompson, R. J., Jankowska, I., Shneider, B. L., Sokal, E., Grammatikopoulos, T., Kadaristiana, A., Jacquemin, E., Spraul, A., Lipiński, P., Czubkowski, P., Rock, N., Shagrani, M., Broering, D., Nicastro, E., Kelly, D., Nebbia, G., & 53 anderenArnell, H., Fischler, B., Hulscher, J. B. F., Serranti, D., Arikan, C., Polat, E., Debray, D., Lacaille, F., Goncalves, C., Hierro, L., Muñoz Bartolo, G., Mozer-Glassberg, Y., Azaz, A., Brecelj, J., Dezsőfi, A., Calvo, P. L., Grabhorn, E., Hartleif, S., van der Woerd, W. J., Kamath, B. M., Wang, J-S., Li, L., Durmaz, Ö., Kerkar, N., Jørgensen, M. H., Fischer, R., Jimenez-Rivera, C., Alam, S., Cananzi, M., Laverdure, N., Ferreira, C. T., Ordoñez Guerrero, F., Wang, H., Sency, V., Kim, K. M., Chen, H-L., de Carvalho, E., Fabre, A., Bernabeu, J. Q., Zellos, A., Alonso, E. M., Sokol, R. J., Suchy, F. J., Loomes, K. M., McKiernan, P. J., Rosenthal, P., Turmelle, Y., Horslen, S., Schwarz, K., Bezerra, J. A., Wang, K., Hansen, B. E. & Verkade, H., feb.-2023, In: JHEP reports : innovation in hepatology. 5, 2, 12 blz., 100626.
Onderzoeksoutput › Academic › peer review

Open Access
Bestand

34 Downloads (Pure)
THE PRESENCE OF A TRUNCATING MUTATION IN ABCB11 ABROGATES THE BENEFICIAL EFFECT OF A RESIDUAL FUNCTION MUTATION ON THE COURSE OF SEVERE BILE SALT EXPORT PUMP DEFICIENCY
Felzen, A., van Wessel, D., Thompson, R. J., Gonzales, E. M., Jankowska, I., Shneider, B. L., Sokal, E., Grammatikopoulos, T., Kadaristiana, A., Jacquemin, E., Spraul, A., Lipinski, P., Czubkowski, P., Rock, N., Shagrani, M., Broering, D., Algoufi, T., Mazhar, N., Nicastro, E., Kelly, D., & 53 anderenNebbia, G., Arnell, H., Fischler, B., Hulscher, J., Serranti, D., Arikan, C., Polat, E., Debray, D., Lacaille, F., Goncalves, C., Hierro, L., Bartolo, G. M., Mozer-Glassberg, Y., Azaz, A., Brecelj, J., Dezsofi, A., Calvo, P. L., Grabhorn, E., Hartleif, S., Van der Woerd, W., Kamath, B. M., Wang, J-S., Li, L., Durmaz, O., Kerkar, N., Jorgensen, M. H., Fischer, R. T., Jimenez-Rivera, C., Alam, S., Cananzi, M., Ruiz, M., Ferreira, C. T., Ferrero, F. O., Wang, H., Sency, V., Kim, K. M., Chen, H-L., Carvalho, E., Fabre, A., Bernabeu, J. Q., Alonso, E. M., Sokol, R. J., Suchy, F. J., Loomes, K. M., McKiernan, P. J., Rosenthal, P., Turmelle, Y., Horslen, S. P., Schwarz, K. B., Bezerra, J. A., Wang, K. S., Hansen, B. E. & Verkade, H. J., nov.-2020, In: Hepatology. 72, blz. 884A-886A 3 blz.
Onderzoeksoutput › Academic

Alex Mowat Prize
Felzen, Antonia (Recipient), 20-mei-2023
Prijs: Prize › Academic

Antonia Felzen

Persoonlijk profiel

Speerpunten

Opleiding / Academische kwalificatie

Samenwerkingen en hoofdonderzoeksgebieden uit de afgelopen vijf jaar

Duik in details

The spectrum of Progressive Familial Intrahepatic Cholestasis diseases: Update on pathophysiology and emerging treatments

Analysis of long-term treatment effects of odevixibat on clinical outcomes in children with progressive familial intrahepatic cholestasis in odevixibat clinical studies vs external controls from the NAPPED database

Characterization of a novel bile salt export pump deficiency mouse model with the p.E297g mutation

Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

THE PRESENCE OF A TRUNCATING MUTATION IN ABCB11 ABROGATES THE BENEFICIAL EFFECT OF A RESIDUAL FUNCTION MUTATION ON THE COURSE OF SEVERE BILE SALT EXPORT PUMP DEFICIENCY

Alex Mowat Prize

Antonia Felzen

Persoonlijk profiel

Speerpunten

Opleiding / Academische kwalificatie

Samenwerkingen en hoofdonderzoeksgebieden uit de afgelopen vijf jaar

Onderzoeksoutput

The spectrum of Progressive Familial Intrahepatic Cholestasis diseases: Update on pathophysiology and emerging treatments

Analysis of long-term treatment effects of odevixibat on clinical outcomes in children with progressive familial intrahepatic cholestasis in odevixibat clinical studies vs external controls from the NAPPED database

Characterization of a novel bile salt export pump deficiency mouse model with the p.E297g mutation

Genotype-phenotype relationships of truncating mutations, p.E297G and p.D482G in bile salt export pump deficiency

THE PRESENCE OF A TRUNCATING MUTATION IN ABCB11 ABROGATES THE BENEFICIAL EFFECT OF A RESIDUAL FUNCTION MUTATION ON THE COURSE OF SEVERE BILE SALT EXPORT PUMP DEFICIENCY

Prijzen

Alex Mowat Prize