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Dermatology Research and Practice
Volume 2009, Article ID 320403, 10 pages
http://dx.doi.org/10.1155/2009/320403
Review Article

Diagnostic Pitfalls in Newborns and Babies with Blisters and Erosions

Department of Dermatology, eb-house Austria, Paracelsus Private Medical University Salzburg, Muellner Hauptstraße 48, 5020 Salzburg, Austria

Received 6 July 2009; Accepted 27 October 2009

Academic Editor: Clay Cockerell

Copyright © 2009 Elke Nischler et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Citations to this Article [14 citations]

The following is the list of published articles that have cited the current article.

  • Gabriela Pohla-Gubo, Rodrigo Cepeda-Valdes, and Helmut Hintner, “Immunofluorescence Mapping for the Diagnosis of Epidermolysis Bullosa,” Dermatologic Clinics, vol. 28, no. 2, pp. 201–+, 2010. View at Publisher · View at Google Scholar
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  • Martin Laimer, Gabriela Pohla-Gubo, Lukas Kraus, Elke Nischler, V. Ahlgrimm-Siess, and Helmut Hintner, “Autoimmune Bullous Diseases in Austria,” Dermatologic Clinics, vol. 29, no. 4, pp. 691–+, 2011. View at Publisher · View at Google Scholar
  • Julio Cesar Salas-Alanis, Rodrigo Cepeda-Valdes, Jemima E. Mellerio, Angela M. Christiano, and Jouni Uitto, “Progress in epidermolysis bullosa: summary of a workshop in CILAD-2010,” International Journal Of Dermatology, vol. 51, no. 6, pp. 682–687, 2012. View at Publisher · View at Google Scholar
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  • Roberto Diaz, Jennifer M. Chan, and Amy L. Ladd, “Epidermolysis Bullosa,” Congenital Anomalies of the Upper Extremity, pp. 325–334, 2014. View at Publisher · View at Google Scholar
  • Catherine S. Yang, Daniela Kroshinksy, and Brian M. Cummings, “Neonatal Junctional Epidermolysis Bullosa: Treatment Conundrums and Ethical Decision Making,” American Journal of Clinical Dermatology, 2014. View at Publisher · View at Google Scholar
  • Peter Koelblinger, Roland Lang, Helmut Hintner, and Martin Laimer, “Bullous skin changes in a 5-month-old infant,” Journal der Deutschen Dermatologischen Gesellschaft, vol. 12, no. 7, pp. 632–636, 2014. View at Publisher · View at Google Scholar
  • Martin Laimer, Christine Prodinger, and Johann W. Bauer, “Hereditary epidermolysis bullosa,” Journal Der Deutschen Dermatologischen Gesellschaft, vol. 13, no. 11, pp. 1125–1134, 2015. View at Publisher · View at Google Scholar
  • Cathy Y. Zhao, and Dedee F. Murrell, “Blistering diseases in neonates,” Current Opinion in Pediatrics, vol. 28, no. 4, pp. 500–506, 2016. View at Publisher · View at Google Scholar
  • Hiroyuki Wakiguchi, Shunji Hasegawa, Shinji Maeba, Sasagu Kimura, Satoko Ito, Hiroshi Tateishi, Kazuhiro Ueda, and Shouichi Ohga, “A Sporadic Neonatal Case of Epidermolysis Bullosa Simplex Generalized Intermediate with KRT5 and KRT14 Gene Mutations.,” AJP reports, vol. 6, no. 1, 2016. View at Publisher · View at Google Scholar
  • Gang Wang, Huan-Huan Qu, and Cui-Ling Ma, “A case of infantile bullous pemphigoid,” Journal of Clinical Dermatology, vol. 46, no. 8, pp. 567–569, 2017. View at Publisher · View at Google Scholar
  • C. M. Prodinger, M. Laimer, J. Bauer, and H. Hintner, “Epidermolysis bullosa House Austria as a role model for the care of a rare disease,” Almanac of Clinical Medicine, vol. 41, no. 1, pp. 2–11, 2019. View at Publisher · View at Google Scholar