Burger B - Search Results

1

Increased epidermal expression and absence of mutations in CARD14 in a series of patients with sporadic pityriasis rubra pilaris.

Eytan O, Qiaoli L, Nousbeck J, van Steensel MA, Burger B, Hohl D, Taïeb A, Prey S, Bachmann D, Avitan-Hersh E, Jin Chung H, Shemer A, Trau H, Bergman R, Fuchs-Telem D, Warshauer E, Israeli S, Itin PH, Sarig O, Uitto J, Sprecher E. Eytan O, et al. Among authors: burger b. Br J Dermatol. 2014 May;170(5):1196-8. doi: 10.1111/bjd.12799. Br J Dermatol. 2014. PMID: 24359224 No abstract available.

2

Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genes.

Nousbeck J, Sarig O, Magal L, Warshauer E, Burger B, Itin P, Sprecher E. Nousbeck J, et al. Among authors: burger b. Br J Dermatol. 2014 Dec;171(6):1521-4. doi: 10.1111/bjd.13176. Epub 2014 Oct 26. Br J Dermatol. 2014. PMID: 24909267

3

Immune-regulatory genes as possible modifiers of familial pityriasis rubra pilaris - lessons from a family with PRP and psoriasis.

Spoerri I, Herms S, Eytan O, Sarig O, Heinimann K, Sprecher E, Itin PH, Burger B. Spoerri I, et al. Among authors: burger b. J Eur Acad Dermatol Venereol. 2018 Oct;32(10):e389-e392. doi: 10.1111/jdv.15029. Epub 2018 Jul 24. J Eur Acad Dermatol Venereol. 2018. PMID: 29704870 No abstract available.

4

Description of the natural course and clinical manifestations of ichthyosis with confetti caused by a novel KRT10 mutation.

Burger B, Spoerri I, Schubert M, Has C, Itin PH. Burger B, et al. Br J Dermatol. 2012 Feb;166(2):434-9. doi: 10.1111/j.1365-2133.2011.10639.x. Epub 2011 Dec 5. Br J Dermatol. 2012. PMID: 21929535

5

The immigration delay disease: adermatoglyphia-inherited absence of epidermal ridges.

Burger B, Fuchs D, Sprecher E, Itin P. Burger B, et al. J Am Acad Dermatol. 2011 May;64(5):974-80. doi: 10.1016/j.jaad.2009.11.013. Epub 2010 Jul 8. J Am Acad Dermatol. 2011. PMID: 20619487

6

A mutation in a skin-specific isoform of SMARCAD1 causes autosomal-dominant adermatoglyphia.

Nousbeck J, Burger B, Fuchs-Telem D, Pavlovsky M, Fenig S, Sarig O, Itin P, Sprecher E. Nousbeck J, et al. Among authors: burger b. Am J Hum Genet. 2011 Aug 12;89(2):302-7. doi: 10.1016/j.ajhg.2011.07.004. Epub 2011 Aug 4. Am J Hum Genet. 2011. PMID: 21820097 Free PMC article.

7

Naegeli-Franceschetti-Jadassohn syndrome and dermatopathia pigmentosa reticularis: intrafamilial overlap of phenotypes in patients with the same KRT14 frameshift variant.

Burger B, Spoerri I, Imahorn E, Wariwoda H, Leeb T, Itin PH. Burger B, et al. Br J Dermatol. 2019 Oct;181(4):864-866. doi: 10.1111/bjd.17997. Epub 2019 Jul 15. Br J Dermatol. 2019. PMID: 30968399 No abstract available.

8

Epidermodysplasia verruciformis.

Burger B, Itin PH. Burger B, et al. Curr Probl Dermatol. 2014;45:123-31. doi: 10.1159/000356068. Epub 2014 Mar 17. Curr Probl Dermatol. 2014. PMID: 24643182 Review.

9

Mosaic manifestations of monogenic skin diseases.

Itin P, Burger B. Itin P, et al. Among authors: burger b. J Dtsch Dermatol Ges. 2009 Sep;7(9):744-48. doi: 10.1111/j.1610-0387.2009.07033.x. J Dtsch Dermatol Ges. 2009. PMID: 19302403 Review. English, German.

10

Discovery of heterozygous KRT10 alterations in MAUIE cases underlines the importance of regular skin cancer screening in ichthyosis with confetti.

Burger B, Ghosh A, Ng CKY, Piscuoglio S, Spoerri I, Itin PH, Greer K, Elbaum D. Burger B, et al. Br J Dermatol. 2020 Nov;183(5):954-955. doi: 10.1111/bjd.19218. Epub 2020 Jun 29. Br J Dermatol. 2020. PMID: 32407542 No abstract available.

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