Muss W - Search Results

1

A compound heterozygous one amino-acid insertion/nonsense mutation in the plectin gene causes epidermolysis bullosa simplex with plectin deficiency.

Bauer JW, Rouan F, Kofler B, Rezniczek GA, Kornacker I, Muss W, Hametner R, Klausegger A, Huber A, Pohla-Gubo G, Wiche G, Uitto J, Hintner H. Bauer JW, et al. Among authors: muss w. Am J Pathol. 2001 Feb;158(2):617-25. doi: 10.1016/S0002-9440(10)64003-5. Am J Pathol. 2001. PMID: 11159198 Free PMC article.

2

Characteristic immunohistochemical and ultrastructural findings indicate that Kindler's syndrome is an apoptotic skin disorder.

Lanschuetzer CM, Muss WH, Emberger M, Pohla-Gubo G, Klausegger A, Bauer JW, Hintner H. Lanschuetzer CM, et al. Among authors: muss wh. J Cutan Pathol. 2003 Oct;30(9):553-60. doi: 10.1034/j.1600-0560.2003.00119.x. J Cutan Pathol. 2003. PMID: 14507403

3

Ocular involvement in IgA-epidermolysis bullosa acquisita.

Bauer JW, Schaeppi H, Metze D, Muss W, Pohla-Gubo G, Hametner R, Ruckhofer J, Grabner G, Hintner H. Bauer JW, et al. Among authors: muss w. Br J Dermatol. 1999 Nov;141(5):887-92. doi: 10.1046/j.1365-2133.1999.03163.x. Br J Dermatol. 1999. PMID: 10583173

4

[Dental alterations in junctional epidermolysis bullosa--report of a patient with a mutation in the LAMB3-gene].

Sadler E, Laimer M, Diem A, Klausegger A, Pohla-Gubo G, Muss W, Hachleitner J, Stadlhuber R, Bauer JW, Hintner H. Sadler E, et al. Among authors: muss w. J Dtsch Dermatol Ges. 2005 May;3(5):359-63. doi: 10.1111/j.1610-0387.2005.05703.x. J Dtsch Dermatol Ges. 2005. PMID: 16372803 German.

5

Novel KIND1 gene mutation in Kindler syndrome with severe gastrointestinal tract involvement.

Sadler E, Klausegger A, Muss W, Deinsberger U, Pohla-Gubo G, Laimer M, Lanschuetzer C, Bauer JW, Hintner H. Sadler E, et al. Among authors: muss w. Arch Dermatol. 2006 Dec;142(12):1619-24. doi: 10.1001/archderm.142.12.1619. Arch Dermatol. 2006. PMID: 17178989

6

Functional correction of type VII collagen expression in dystrophic epidermolysis bullosa.

Murauer EM, Gache Y, Gratz IK, Klausegger A, Muss W, Gruber C, Meneguzzi G, Hintner H, Bauer JW. Murauer EM, et al. Among authors: muss w. J Invest Dermatol. 2011 Jan;131(1):74-83. doi: 10.1038/jid.2010.249. Epub 2010 Aug 19. J Invest Dermatol. 2011. PMID: 20720561 Free article.

7

Gene symbol: Kind1. Disease: kindler syndrome.

Lanschuetzer CM, Muss WH, Emberger M, Pohla-Gubo G, Klausegger A, Bauer JW, Hintner H. Lanschuetzer CM, et al. Among authors: muss wh. Hum Genet. 2004 Jul;115(2):175. Hum Genet. 2004. PMID: 15300990 No abstract available.

8

An ex vivo RNA trans-splicing strategy to correct human generalized severe epidermolysis bullosa simplex.

Peking P, Breitenbach JS, Ablinger M, Muss WH, Poetschke FJ, Kocher T, Koller U, Hainzl S, Kitzmueller S, Bauer JW, Reichelt J, Lettner T, Wally V. Peking P, et al. Among authors: muss wh. Br J Dermatol. 2019 Jan;180(1):141-148. doi: 10.1111/bjd.17075. Epub 2018 Oct 7. Br J Dermatol. 2019. PMID: 30099737 Free PMC article.

9

Skin grafting as a therapeutic approach in pretibially restricted junctional epidermolysis bullosa.

Laimer M, Bauer JW, Klausegger A, Koller J, Pohla-Gubo G, Muss W, Sadler E, Emberger M, Lanschuetzer CM, Hametner R, Wally V, Oender K, Hinter H. Laimer M, et al. Among authors: muss w. Br J Dermatol. 2006 Jan;154(1):185-7. doi: 10.1111/j.1365-2133.2005.06988.x. Br J Dermatol. 2006. PMID: 16403119 No abstract available.

10

Histopathology of human corneas after amniotic membrane and limbal stem cell transplantation for severe chemical burn.

Stoiber J, Muss WH, Pohla-Gubo G, Ruckhofer J, Grabner G. Stoiber J, et al. Cornea. 2002 Jul;21(5):482-9. doi: 10.1097/00003226-200207000-00009. Cornea. 2002. PMID: 12072723

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