Kohlhase J - Search Results

1

Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations.

Schumann H, Kiritsi D, Pigors M, Hausser I, Kohlhase J, Peters J, Ott H, Hyla-Klekot L, Gacka E, Sieron AL, Valari M, Bruckner-Tuderman L, Has C. Schumann H, et al. Among authors: kohlhase j. Br J Dermatol. 2013 Jul;169(1):115-24. doi: 10.1111/bjd.12317. Br J Dermatol. 2013. PMID: 23496044

2

Forty-two novel COL7A1 mutations and the role of a frequent single nucleotide polymorphism in the MMP1 promoter in modulation of disease severity in a large European dystrophic epidermolysis bullosa cohort.

Kern JS, Grüninger G, Imsak R, Müller ML, Schumann H, Kiritsi D, Emmert S, Borozdin W, Kohlhase J, Bruckner-Tuderman L, Has C. Kern JS, et al. Among authors: kohlhase j. Br J Dermatol. 2009 Nov;161(5):1089-97. doi: 10.1111/j.1365-2133.2009.09333.x. Epub 2009 Jun 5. Br J Dermatol. 2009. PMID: 19681861

3

Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype.

Arin MJ, Grimberg G, Schumann H, De Almeida H Jr, Chang YR, Tadini G, Kohlhase J, Krieg T, Bruckner-Tuderman L, Has C. Arin MJ, et al. Among authors: kohlhase j. Br J Dermatol. 2010 Jun;162(6):1365-9. doi: 10.1111/j.1365-2133.2010.09657.x. Epub 2010 Feb 25. Br J Dermatol. 2010. PMID: 20199538

4

Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VII.

Leverkus M, Ambach A, Hoefeld-Fegeler M, Kohlhase J, Schmidt E, Schumann H, Has C, Gollnick H. Leverkus M, et al. Among authors: kohlhase j. Br J Dermatol. 2011 May;164(5):1104-6. doi: 10.1111/j.1365-2133.2011.10230.x. Br J Dermatol. 2011. PMID: 21275939

5

Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutations.

Schumann H, Has C, Kohlhase J, Bruckner-Tuderman L. Schumann H, et al. Among authors: kohlhase j. Br J Dermatol. 2008 Aug;159(2):464-9. doi: 10.1111/j.1365-2133.2008.08695.x. Epub 2008 Jun 28. Br J Dermatol. 2008. PMID: 18565177

6

C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes.

Has C, Ludwig RJ, Herz C, Kern JS, Ussar S, Ochsendorf FR, Kaufmann R, Schumann H, Kohlhase J, Bruckner-Tuderman L. Has C, et al. Among authors: kohlhase j. Br J Dermatol. 2008 Nov;159(5):1192-6. doi: 10.1111/j.1365-2133.2008.08760.x. Epub 2008 Jul 22. Br J Dermatol. 2008. PMID: 18652585

7

Intronic ITGA3 Mutation Impacts Splicing Regulation and Causes Interstitial Lung Disease, Nephrotic Syndrome, and Epidermolysis Bullosa.

He Y, Balasubramanian M, Humphreys N, Waruiru C, Brauner M, Kohlhase J, O'Reilly R, Has C. He Y, et al. Among authors: kohlhase j. J Invest Dermatol. 2016 May;136(5):1056-1059. doi: 10.1016/j.jid.2015.11.031. Epub 2016 Feb 15. J Invest Dermatol. 2016. PMID: 26854491 Free article. Review. No abstract available.

8

Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteria.

Arnold AW, Itin PH, Pigors M, Kohlhase J, Bruckner-Tuderman L, Has C. Arnold AW, et al. Among authors: kohlhase j. Br J Dermatol. 2010 Oct;163(4):866-9. doi: 10.1111/j.1365-2133.2010.09929.x. Epub 2010 Sep 7. Br J Dermatol. 2010. PMID: 20618321

9

Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancer.

Has C, Burger B, Volz A, Kohlhase J, Bruckner-Tuderman L, Itin P. Has C, et al. Among authors: kohlhase j. Dermatology. 2010;221(4):309-12. doi: 10.1159/000320235. Epub 2010 Oct 11. Dermatology. 2010. PMID: 20938162

10

Alitretinoin in punctate palmoplantar keratoderma.

Yilmaz P, Medvecz M, Kohlhase J, Küsel J, Fischer J, Has C. Yilmaz P, et al. Among authors: kohlhase j. Br J Dermatol. 2019 Apr;180(4):931-932. doi: 10.1111/bjd.17336. Epub 2018 Dec 19. Br J Dermatol. 2019. PMID: 30339730 No abstract available.

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