H
Helmut Hintner
Researcher at Paracelsus Private Medical University of Salzburg
Publications - 104
Citations - 4736
Helmut Hintner is an academic researcher from Paracelsus Private Medical University of Salzburg. The author has contributed to research in topics: Epidermolysis bullosa & Exon. The author has an hindex of 34, co-authored 104 publications receiving 4487 citations.
Papers
More filters
Journal ArticleDOI
The classification of inherited epidermolysis bullosa (EB): Report of the Third International Consensus Meeting on Diagnosis and Classification of EB.
Jo-David Fine,Robin A.J. Eady,Eugene A. Bauer,Johann W. Bauer,Leena Bruckner-Tuderman,A.H.M. Heagerty,Helmut Hintner,Alain Hovnanian,Marcel F. Jonkman,Irene M. Leigh,John A. McGrath,Jemima E. Mellerio,Jemima E. Mellerio,Dedee F. Murrell,Hiroshi Shimizu,Jouni Uitto,Anders Vahlquist,David T. Woodley,Giovanna Zambruno +18 more
TL;DR: A revised classification system that takes into account the new advances, as well as encompassing other inherited diseases that should also be included within the EB spectrum, based on the presence of blistering and mechanical fragility is presented.
Journal ArticleDOI
Inherited epidermolysis bullosa: Updated recommendations on diagnosis and classification
Jo-David Fine,Leena Bruckner-Tuderman,Robin A.J. Eady,Eugene A. Bauer,Johann W. Bauer,Cristina Has,A.H.M. Heagerty,Helmut Hintner,Alain Hovnanian,Marcel F. Jonkman,Irene M. Leigh,M. Peter Marinkovich,M. Peter Marinkovich,Anna E. Martinez,John A. McGrath,Jemima E. Mellerio,Jemima E. Mellerio,Celia Moss,Dedee F. Murrell,Hiroshi Shimizu,Jouni Uitto,David T. Woodley,Giovanna Zambruno +22 more
TL;DR: In this article, the authors presented a new approach to classification of epidermolysis bullosa (EB) that takes into account sequentially the major EB type present (based on identification of the level of skin cleavage), phenotypic characteristics (distribution and severity of disease activity; specific extracutaneous features; other), mode of inheritance, targeted protein and its relative expression in skin, gene involved and type(s) of mutation present, and specific mutation(s), and their location(s).
Journal ArticleDOI
Revised classification system for inherited epidermolysis bullosa: Report of the second international consensus meeting on diagnosis and classification of epidermolysis bullosa
Jo-David Fine,Robin A.J. Eady,Eugene A. Bauer,Robert A. Briggaman,Leena Bruckner-Tuderman,Angela M. Christiano,Adrian Heagerty,Helmut Hintner,Marcel F. Jonkman,John A. McGrath,J McGuire,Alan N. Moshell,Hiroshi Shimizu,Gianluca Tadini,Jouni Uitto +14 more
Journal ArticleDOI
Generalized atrophic benign epidermolysis bullosa.
Helmut Hintner,Klaus Wolff +1 more
TL;DR: A new variant of hereditary epidermolysis bullosa (EB), generalized atrophic benign EB, is reported in this article, which is a junctional form of EB that, in contrast to EB letalis of Herlitz, has a good prognosis.
Journal ArticleDOI
Ribosomal proteins Rpl10 and Rps6 are potent regulators of yeast replicative life span.
Andreas G. Chiocchetti,Jia Zhou,Huashun Zhu,Thomas Karl,Olaf Haubenreisser,Mark Rinnerthaler,Gino Heeren,Kamil Oender,Johann W. Bauer,Helmut Hintner,Michael Breitenbach,Lore Breitenbach-Koller +11 more
TL;DR: Reduction of gene dosage of RP genes belonging to both the 60S and the 40S subunit affect lifespan, possibly altering the aging process by modulation of translation.