Antonia Reimer (A Reimer-Taschenbrecker, A Reimer, Antonia Reimer-Taschenbrecker)

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 12

Top Topics

Intellectual Disability

Top Venues

Journal of the European Academy of Dermatology and Venereology : JEADV

The British journal of dermatology

Orphanet journal of rare diseases

This page only lists publications with an associated author ORCID identifier.

Publications

Antonia Reimer, M Hess, M Davidovic, A Hwang, S Hübner, M Hofsaess, S Gewert, Kilian Eyerich, Cristina Has
IL-6 levels dominate the serum cytokine signature of severe epidermolysis bullosa: A prospective cohort study. Journal of the European Academy of Dermatology and Venereology : JEADV (2024)
Mingfeng Li, Kenneth Lay, Andreas David Zimmer, Kristin Technau-Hafsi, Jasmine Wong, Antonia Reimer, Jan Rohr, Ebtesam Abdalla, Judith Fischer, Bruno Reversade, Cristina Has
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. The British journal of dermatology 188 (2) (2023)
Mingfeng Li, Kenneth Lay, Andreas David Zimmer, Kristin Technau-Hafsi, Jasmine Wong, Antonia Reimer, Jan Rohr, Ebtesam Abdalla, Judith Fischer, Bruno Reversade, Cristina Has
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. The British journal of dermatology 188 (2) (2023)
Mingfeng Li, Kenneth Lay, Andreas David Zimmer, Kristin Technau-Hafsi, Jasmine Wong, Antonia Reimer, Jan Rohr, Ebtesam Abdalla, Judith Fischer, Bruno Reversade, Cristina Has
A homozygous p.Leu813Pro gain-of-function NLRP1 variant causes phenotypes of different severity in two siblings. The British journal of dermatology 188 (2) (2023)
Cristina Has, Moritz Hess, Waltraud Anemüller, Ulrike Blume-Peytavi, Steffen Emmert, Regina Fölster-Holst, Jorge Frank, Kathrin Giehl, Claudia Günther, Johanna Hammersen, Kathrin Hillmann, Bettina Höflein, Peter H Hoeger, Alrun Hotz, Thuy Anh Mai, Vinzenz Oji, Holm Schneider, Kira Süßmuth, Iliana Tantcheva-Póor, Frederieke Thielking, Birgit Zirn, Judith Fischer, Antonia Reimer
Epidemiology of inherited epidermolysis bullosa in Germany. Journal of the European Academy of Dermatology and Venereology : JEADV (2022)
Antonia Reimer, M Hess, A Hotz, J Fischer, L Bruckner-Tuderman, Cristina Has
Plantar involvement correlates with obesity, pain and impaired mobility in epidermolysis bullosa simplex: a retrospective cohort study. Journal of the European Academy of Dermatology and Venereology : JEADV 35 (10) (2021)
Leonie Frommherz, A Krause, J Kopp, A Hotz, S Hübner, Antonia Reimer, F Casetti, B Zirn, J Fischer, Cristina Has
High rate of self-improving phenotypes in children with non-syndromic congenital ichthyosis: case series from south-western Germany. Journal of the European Academy of Dermatology and Venereology : JEADV 35 (11) (2021)
Agnes Schwieger-Briel, L Trefzer, H Schumann, Antonia Reimer, David Rafei-Shamsabadi, F Meiss, Cristina Has
Esophageal carcinoma in severe recessive dystrophic epidermolysis bullosa-an underestimated complication? Journal of the European Academy of Dermatology and Venereology : JEADV (2021)
Antonia Reimer, M Hess, A Schwieger-Briel, Dimitra Kiritsi, F Schauer, H Schumann, L Bruckner-Tuderman, Cristina Has
Natural history of growth and anaemia in children with epidermolysis bullosa: a retrospective cohort study. The British journal of dermatology 182 (6) (2019)
Antonia Reimer, S Lu, Y He, L Bruckner-Tuderman, K Technau-Hafsi, F Meiss, Cristina Has, D von Bubnoff
Combined anti-inflammatory and low-dose antiproliferative therapy for squamous cell carcinomas in recessive dystrophic epidermolysis bullosa. Journal of the European Academy of Dermatology and Venereology : JEADV 34 (1) (2019)
Antonia Reimer, Leena Bruckner-Tuderman, Hagen Ott
Mapping health care of rare diseases: the example of epidermolysis bullosa in Germany. Orphanet journal of rare diseases 13 (1) (2018)
Antonia Reimer, A Schwieger-Briel, Y He, J Leppert, F Schauer, Dimitra Kiritsi, H Schneider, H Ott, L Bruckner-Tuderman, Cristina Has
Natural history and clinical outcome of junctional epidermolysis bullosa generalized intermediate due to a LAMA3 mutation. The British journal of dermatology 178 (4) (2018)