Leena Bruckner–Tuderman

Author

University of Münster

Also Known As

Leena Bruckner-Tuderman, Leena Bruckner–Tuderman

Publications

342

Citations

H-Index

Concepts

All Affiliations

University of Münster University of Zurich Jefferson College Thomas Jefferson University

About

Leena Bruckner–Tuderman is an author at University of Münster specializing in dermatopathology, dermatology, and medicine.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	218
2	Pathology	4	4	192
3	Education	1	1	56
4	Cell Biology	1	1	26
5	Molecular Genetics	1	1	81

Leena Bruckner–Tuderman

Publications

334

Citations

H-Index

Page 1

	Year	Citations
Novel ITGB4 Mutations in Lethal and Nonlethal Variants of Epidermolysis Bullosa with Pyloric Atresia: Missense versus Nonsense Leena Pulkkinen, Fatima Rouan, Leena Bruckner–Tuderman, The American Journal of Human Genetics	1998	116
Three Novel Homozygous Point Mutations and a New Polymorphism in the COL17A1 Gene: Relation to Biological and Clinical Phenotypes of Junctional Epidermolysis Bullosa Hauke Schumann, Nadja Hammami-Hauasli, Leena Pulkkinen, The American Journal of Human Genetics MedicineGeneticsCutaneous BiologyGenetic EpidemiologyPathology	1997	81
Animal Model for Dermolytic Mechanobullous Disease: Sheep with Recessive Dystrophic Epidermolysis Bullosa Lack Collagen VII Leena Bruckner–Tuderman, Franco Guscetti, F. Ehrensperger Journal of Investigative Dermatology Animal PhysiologyAnimal ScienceVeterinary PathologyAnimal ModelVeterinary Science	1991	56
Epidermolysis bullosa simplex with mottled pigmentation Leena Bruckner–Tuderman, A. Vogel, Silvia Rüegger, Journal of the American Academy of Dermatology Cutaneous BiologySurgical PathologyHistopathologyPathologyDermatology	1989	28
Esophageal stenosis in childhood: Dystrophic epidermolysis bullosa without skin blistering due to collagen VII mutations K. Zimmer, Hauke Schumann, Sabine Mecklenbeck, Gastroenterology Cutaneous BiologyEsophageal StenosisSkin BlisteringPathologyVii Mutations	2002	27
A Combination of a Common Splice Site Mutation and Frameshift Mutation in the COL7A1 Gene: Absence of Functional Collagen VII in Keratinocytes and Skin Nadja Hammami-Hauasli, D. Ulrike Kalinke, Hauke Schumann, Journal of Investigative Dermatology FibrosisCutaneous BiologyCol7a1 GeneFrameshift MutationDermatology	1997	26

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