Schumann H - Search Results

1

Molecular diagnostics facilitate distinction between lethal and non-lethal subtypes of junctional epidermolysis bullosa: a case report and review of the literature.

Bauer J, Schumann H, Sönnichsen K, Tomaske M, Bosk A, Bruckner-Tuderman L, Rassner G, Garbe C. Bauer J, et al. Among authors: schumann h. Eur J Pediatr. 2002 Dec;161(12):672-9. doi: 10.1007/s00431-001-0851-2. Epub 2001 Nov 15. Eur J Pediatr. 2002. PMID: 12447669 Review.

2

Esophageal stenosis in childhood: dystrophic epidermolysis bullosa without skin blistering due to collagen VII mutations.

Zimmer KP, Schumann H, Mecklenbeck S, Bruckner-Tuderman L. Zimmer KP, et al. Among authors: schumann h. Gastroenterology. 2002 Jan;122(1):220-5. doi: 10.1053/gast.2002.30428. Gastroenterology. 2002. PMID: 11781296

3

Network epidermolysis bullosa: molecular pathomechanisms and novel therapeutic approaches.

Volz A, Has C, Schumann H, Bruckner-Tuderman L. Volz A, et al. Among authors: schumann h. J Dtsch Dermatol Ges. 2007 Apr;5(4):274-9. doi: 10.1111/j.1610-0387.2006.06181.x. J Dtsch Dermatol Ges. 2007. PMID: 17376090 Review. English, German.

4

Molecular mechanisms of phenotypic variability in junctional epidermolysis bullosa.

Kiritsi D, Kern JS, Schumann H, Kohlhase J, Has C, Bruckner-Tuderman L. Kiritsi D, et al. Among authors: schumann h. J Med Genet. 2011 Jul;48(7):450-7. doi: 10.1136/jmg.2010.086751. Epub 2011 Feb 28. J Med Genet. 2011. PMID: 21357940 Free article.

5

A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy.

Fritsch A, Loeckermann S, Kern JS, Braun A, Bösl MR, Bley TA, Schumann H, von Elverfeldt D, Paul D, Erlacher M, Berens von Rautenfeld D, Hausser I, Fässler R, Bruckner-Tuderman L. Fritsch A, et al. Among authors: schumann h. J Clin Invest. 2008 May;118(5):1669-79. doi: 10.1172/JCI34292. J Clin Invest. 2008. PMID: 18382769 Free PMC article.

6

Collagenous transmembrane proteins: collagen XVII as a prototype.

Franzke CW, Tasanen K, Schumann H, Bruckner-Tuderman L. Franzke CW, et al. Among authors: schumann h. Matrix Biol. 2003 Jun;22(4):299-309. doi: 10.1016/s0945-053x(03)00051-9. Matrix Biol. 2003. PMID: 12935815 Review.

7

Contact dermatitis due to use of Octenisept in wound care.

Calow T, Oberle K, Bruckner-Tuderman L, Jakob T, Schumann H. Calow T, et al. Among authors: schumann h. J Dtsch Dermatol Ges. 2009 Sep;7(9):759-65. doi: 10.1111/j.1610-0387.2009.07035.x. J Dtsch Dermatol Ges. 2009. PMID: 19228295 Clinical Trial. English, German.

8

Acral peeling skin syndrome with TGM5 gene mutations may resemble epidermolysis bullosa simplex in young individuals.

Kiritsi D, Cosgarea I, Franzke CW, Schumann H, Oji V, Kohlhase J, Bruckner-Tuderman L, Has C. Kiritsi D, et al. Among authors: schumann h. J Invest Dermatol. 2010 Jun;130(6):1741-6. doi: 10.1038/jid.2010.23. Epub 2010 Feb 18. J Invest Dermatol. 2010. PMID: 20164844 Free article. No abstract available.

9

[Anaesthesia for children with epidermolysis bullosa].

Knab J, Schumann H, Kaltofen H, Steinmann D. Knab J, et al. Among authors: schumann h. Anasthesiol Intensivmed Notfallmed Schmerzther. 2010 Oct;45(10):618-24. doi: 10.1055/s-0030-1267526. Epub 2010 Oct 19. Anasthesiol Intensivmed Notfallmed Schmerzther. 2010. PMID: 20960366 Review. German.

10

Monoallelic Large Intragenic KRT5 Deletions Account for Genetically Unsolved Cases of Epidermolysis Bullosa Simplex.

Has C, Schumann H, Leppert J, He Y, Hartmann B, Hausser I, Kohlhase J. Has C, et al. Among authors: schumann h. J Invest Dermatol. 2017 Oct;137(10):2231-2234. doi: 10.1016/j.jid.2017.05.016. Epub 2017 May 30. J Invest Dermatol. 2017. PMID: 28576738 Free article. No abstract available.

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