Literature DB >> 8006439

The National Epidermolysis Bullosa Registry.

J D Fine1, L B Johnson, C M Suchindran.   

Abstract

Since its inception in 1986, the NEBR has proved to be an excellent example of how a relatively small allocation of federal research funds for the development of a registry of cases of a single rare disease can have a major impact on the rapid expansion in the depth of knowledge of not only the disease itself but of a number of associated biologic principles, including keratinization and epithelial cell-extracellular matrix interactions. At present, the NEBR is generating extensive clinical, laboratory, and demographic data, both from cross-sectional and longitudinal perspectives, as well as establishing a centralized cell and tissue bank that will serve the scientific community at large as a valuable resource for future basic research on this oftentimes devastating genetic disease.

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Year:  1994        PMID: 8006439     DOI: 10.1111/1523-1747.ep12388622

Source DB:  PubMed          Journal:  J Invest Dermatol        ISSN: 0022-202X            Impact factor:   8.551


  6 in total

1.  Oral manifestations of epidermolysis bullosa dystrophica: a rare genetic disease.

Authors:  Anita Dundappa Parushetti; Jiwanasha Manish Agrawal; Lalita Girish Nanjannawar; Manish Suresh Agrawal
Journal:  BMJ Case Rep       Date:  2013-01-23

2.  Case report: Dystrophic Epidermolysis Bullosa: dental management and oral health promotion.

Authors:  A K Louloudiadis; K A Louloudiadis
Journal:  Eur Arch Paediatr Dent       Date:  2009-01

Review 3.  A review of scoring systems for ocular involvement in chronic cutaneous bullous diseases.

Authors:  Brendon W H Lee; Jeremy C K Tan; Melissa Radjenovic; Minas T Coroneo; Dedee F Murrell
Journal:  Orphanet J Rare Dis       Date:  2018-05-22       Impact factor: 4.123

4.  Safe Skin Management during Open Hepatectomy in a Patient with Recessive Dystrophic Congenital Epidermolysis Bullosa.

Authors:  Ikuo Watanobe; Hiroko Kida; Yuuki Sekine; Masaya Kawai; Shozo Miyano; Michio Machida; Toshiaki Kitabatake; Hiroyuki Sugo; Yoshifumi Lee; Kuniaki Kojima
Journal:  Case Rep Surg       Date:  2018-06-28

5.  Validity of first-time diagnoses of congenital epidermolysis bullosa in the Danish National Patient Registry and the Danish Pathology Registry.

Authors:  Mattias Hedegaard Kristensen; Sigrún Alba Jóhannesdóttir Schmidt; Line Kibsgaard; Mette Mogensen; Mette Sommerlund; Uffe Koppelhus
Journal:  Clin Epidemiol       Date:  2019-01-17       Impact factor: 4.790

6.  Prioritization of therapy uncertainties in Dystrophic Epidermolysis Bullosa: where should research direct to? an example of priority setting partnership in very rare disorders.

Authors:  Paula Davila-Seijo; Angela Hernández-Martín; Evanina Morcillo-Makow; Raúl de Lucas; Esther Domínguez; Natividad Romero; Eva Monrós; Marta Feito; Luis Carretero; Bea Aranegui; Ignacio García-Doval
Journal:  Orphanet J Rare Dis       Date:  2013-04-22       Impact factor: 4.123

  6 in total

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