Laimer M - Search Results

1

Adjuvante Anti-PD-1-Antikörpertherapie bei Stadium-III/IV-Melanom: Anwendungsdaten aus der klinischen Routine und gesundheitsökonomische Aspekte.

Koelblinger P, Hoellwerth M, Dernoscheg MT, Koch L, Richtig E, Wanner M, Nguyen VA, Ostermann H, Bauer JW, Laimer M. Koelblinger P, et al. Among authors: laimer m. J Dtsch Dermatol Ges. 2021 Aug;19(8):1186-1200. doi: 10.1111/ddg.14511_g. J Dtsch Dermatol Ges. 2021. PMID: 34390157 German.

2

Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay.

Buchroithner B, Klausegger A, Ebschner U, Anton-Lamprecht I, Pohla-Gubo G, Lanschuetzer CM, Laimer M, Hintner H, Bauer JW. Buchroithner B, et al. Among authors: laimer m. Lab Invest. 2004 Oct;84(10):1279-88. doi: 10.1038/labinvest.3700164. Lab Invest. 2004. PMID: 15311214 Free article.

3

Gene therapy of epidermolysis bullosa.

Bauer JW, Laimer M. Bauer JW, et al. Among authors: laimer m. Expert Opin Biol Ther. 2004 Sep;4(9):1435-43. doi: 10.1517/14712598.4.9.1435. Expert Opin Biol Ther. 2004. PMID: 15335311 Review.

4

Epidermolysis bullosa naevi reveal a distinctive dermoscopic pattern.

Lanschuetzer CM, Emberger M, Laimer M, Diem A, Bauer JW, Soyer HP, Hintner H. Lanschuetzer CM, et al. Among authors: laimer m. Br J Dermatol. 2005 Jul;153(1):97-102. doi: 10.1111/j.1365-2133.2005.06579.x. Br J Dermatol. 2005. PMID: 16029333

5

[Systemic ALlambda amyloidosis associated with vascular fragility].

Laimer M, Kaindl K, Emberger M, Hawranek T, Lanschützer CM, Bauer JW, Linke RP, Mlineritsch B, Hintner H. Laimer M, et al. J Dtsch Dermatol Ges. 2004 Nov;2(11):934-9. J Dtsch Dermatol Ges. 2004. PMID: 16281613 German.

6

[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: laimer m. 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.

7

Haploinsufficiency due to deletion within the 3'-UTR of C1-INH-gene associated with hereditary angioedema.

Laimer M, Klausegger A, Aberer W, Oender K, Steinhuber M, Lanschuetzer CM, Wally V, Hintner H, Bauer JW. Laimer M, et al. Genet Med. 2006 Apr;8(4):249-54. doi: 10.1097/01.gim.0000214302.90076.fa. Genet Med. 2006. PMID: 16617246 Free article.

8

Introducing a fast and simple PCR-RFLP analysis for the detection of mutant thiopurine S-methyltransferase alleles TPMT*3A and TPMT*3C.

Oender K, Lanschuetzer CM, Laimer M, Klausegger A, Paulweber B, Kofler B, Hintner H, Bauer JW. Oender K, et al. Among authors: laimer m. J Eur Acad Dermatol Venereol. 2006 Apr;20(4):396-400. doi: 10.1111/j.1468-3083.2006.01459.x. J Eur Acad Dermatol Venereol. 2006. PMID: 16643135

9

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: laimer m. Arch Dermatol. 2006 Dec;142(12):1619-24. doi: 10.1001/archderm.142.12.1619. Arch Dermatol. 2006. PMID: 17178989

10

Rapid, high-quality and epidermal-specific isolation of RNA from human skin.

Trost A, Bauer JW, Lanschützer C, Laimer M, Emberger M, Hintner H, Onder K. Trost A, et al. Among authors: laimer m. Exp Dermatol. 2007 Mar;16(3):185-90. doi: 10.1111/j.1600-0625.2006.00534.x. Exp Dermatol. 2007. PMID: 17286810

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