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22 results for Laimer,+Martin

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ArticlesPeer ReviewedFull Text
Small molecule drug development for rare genodermatoses – evaluation of the current status in epidermolysis bullosa
Author / Creator:Wally, Verena ; Reisenberger, Manuela ; Kitzmüller, Sophie ; Laimer, Martin
Publisher:London: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.1-292, Article 292
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Reflection on clinical and methodological issues in rare disease clinical trials
Author / Creator:Verbeeck, Johan ; Geroldinger, Martin ; Nyberg, Joakim ; Thiel, Konstantin E ; Hooker, Andrew C ; Bathke, Arne C ; Bauer, Johann W ; Molenberghs, Geert ; Laimer, Martin ; Zimmermann, Georg
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2025-06, Vol.20 (1), p.277-9
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Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials
Author / Creator:Geroldinger, Martin ; Verbeeck, Johan ; Hooker, Andrew C. ; Thiel, Konstantin E. ; Molenberghs, Geert ; Nyberg, Joakim ; Bauer, Johann ; Laimer, Martin ; Wally, Verena ; Bathke, Arne C. ; Zimmermann, Georg
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2023-12, Vol.18 (1), p.391-391, Article 391
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Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial
Author / Creator:Guttmann-Gruber, Christina ; Piñón Hofbauer, Josefina ; Tockner, Birgit ; Reichl, Victoria ; Klausegger, Alfred ; Hofbauer, Peter ; Wolkersdorfer, Martin ; Tham, Khek-Chian ; Lim, Seong Soo ; Common, John E. ; Diem, Anja ; Ude-Schoder, Katharina ; Hitzl, Wolfgang ; Lagler, Florian ; Reichelt, Julia ; Bauer, Johann W. ; Lang, Roland ; Laimer, Martin
Publisher:London: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2021-11, Vol.16 (1), p.1-473, Article 473
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Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa
Author / Creator:Prodinger, Christine ; Diem, Anja ; Ude-Schoder, Katherina ; Piñón-Hofbauer, Josefina ; Kitzmueller, Sophie ; Bauer, Johann W. ; Laimer, Martin
Publisher:England: BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2020-07, Vol.15 (1), p.182-182, Article 182
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Human dirofilariosis in Austria: the past, the present, the future
Author / Creator:Riebenbauer, Katharina ; Weber, Philipp B. ; Walochnik, Julia ; Karlhofer, Franz ; Winkler, Stefan ; Dorfer, Sonja ; Auer, Herbert ; Valencak, Julia ; Laimer, Martin ; Handisurya, Alessandra
Publisher:England: BioMed Central Ltd
Journal title:Parasites & vectors, 2021-04, Vol.14 (1), p.227-227, Article 227
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Recessive Dystrophic Epidermolysis bullosa due to Hemizygous 40 kb Deletion of COL7A1 and the Proximate PFKFB4 Gene Focusing on the Mutation c.425A>G Mimicking Homozygous Status
Author / Creator:Klausegger, Alfred ; Jeschko, Niklas ; Grammer, Markus ; Cemper-Kiesslich, Jan ; Neuhuber, Franz ; Diem, Anja ; Breitenbach-Koller, Hannelore ; Sander, Gabriele ; Kotzot, Dieter ; Bauer, Johann Wolfgang ; Laimer, Martin
Publisher:Switzerland: MDPI AG
Journal title:Diagnostics (Basel), 2022-10, Vol.12 (10), p.2460
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A Novel Homozygous 9385 bp Deletion in the FERMT1 (KIND1) Gene in a Malaysian Family with Kindler Epidermolysis bullosa and a Review of Large Deletions
Author / Creator:Klausegger, Alfred ; Leditzky, Fabian ; Krämer, Susanne ; Palisson, Francis ; Yubero, María Joao ; Véliz, Sebastián ; Koh, Mark Jean Aan ; Tan, Ene-Choo ; Laimer, Martin ; Bauer, Johann Wolfgang ; Fuentes, Ignacia
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2025-04, Vol.26 (9), p.4237
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COVID-19-Induced Reduction in Primary Melanoma Diagnoses: Experience from a Dermatopathology Referral Center
Author / Creator:Hoellwerth, Magdalena ; Kaiser, Andreas ; Emberger, Michael ; Brandlmaier, Matthias ; Laimer, Martin ; Egger, Alexander ; Bauer, Johann W. ; Koelblinger, Peter
Publisher:Basel: MDPI AG
Journal title:Journal of clinical medicine, 2021-09, Vol.10 (18), p.4059
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Clinical Perspectives of Gene-Targeted Therapies for Epidermolysis Bullosa
Author / Creator:Welponer, Tobias ; Prodinger, Christine ; Pinon-Hofbauer, Josefina ; Hintersteininger, Arno ; Breitenbach-Koller, Hannelore ; Bauer, Johann W. ; Laimer, Martin
Publisher:Cheshire: Springer Healthcare
Journal title:Dermatology and therapy, 2021-08, Vol.11 (4), p.1175-1197
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ArticlesPeer ReviewedFull Text
Low-dose calcipotriol can elicit wound closure, anti-microbial, and anti-neoplastic effects in epidermolysis bullosa keratinocytes
Author / Creator:Guttmann-Gruber, Christina ; Tockner, Birgit ; Scharler, Cornelia ; Hüttner, Clemens ; Common, John E. ; Tay, Angeline S. L. ; Denil, Simon L. I. J. ; Klausegger, Alfred ; Trost, Andrea ; Breitenbach, Jenny ; Schnitzhofer, Peter ; Hofbauer, Peter ; Wolkersdorfer, Martin ; Diem, Anja ; Laimer, Martin ; Strunk, Dirk ; Bauer, Johann W. ; Reichelt, Julia ; Lang, Roland ; Piñón Hofbauer, Josefina
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2018-09, Vol.8 (1), p.13430-14, Article 13430
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A novel humanized mouse model to study the function of human cutaneous memory T cells in vivo in human skin
Author / Creator:Klicznik, Maria M. ; Benedetti, Ariane ; Gail, Laura M. ; Varkhande, Suraj R. ; Holly, Raimund ; Laimer, Martin ; Stoecklinger, Angelika ; Sir, Andreas ; Reitsamer, Roland ; Neuper, Theresa ; Horejs-Hoeck, Jutta ; Rosenblum, Michael D. ; Campbell, Daniel J. ; Murauer, Eva M. ; Gratz, Iris K.
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2020-07, Vol.10 (1), p.11164-11164, Article 11164
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Recessive Dystrophic IEpidermolysis bullosa/I due to Hemizygous 40 kb Deletion of ICOL7A1/I and the Proximate IPFKFB4/I Gene Focusing on the Mutation c.425AG Mimicking Homozygous Status
Author / Creator:Klausegger, Alfred ; Jeschko, Niklas ; Grammer, Markus ; Cemper-Kiesslich, Jan ; Neuhuber, Franz ; Diem, Anja ; Breitenbach-Koller, Hannelore ; Sander, Gabriele ; Kotzot, Dieter ; Bauer, Johann Wolfgang ; Laimer, Ma
Publisher:MDPI AG
Journal title:Diagnostics (Basel), 2022-10, Vol.12 (10)
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Transcutaneous Gene Gun Delivery of hNC16A Induces BPAG2-Specific Tolerance
Author / Creator:Ettinger, Monika ; Peckl-Schmid, Doris ; Gruber, Christina ; Laimer, Martin ; Thalhamer, Josef ; Hintner, Helmut ; Gratz, Iris K. ; Bauer, Johann W.
Publisher:New York, NY: Elsevier Inc
Journal title:Journal of investigative dermatology, 2012-06, Vol.132 (6), p.1665-1671
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ArticlesPeer ReviewedFull Text
New diagnostics for melanoma detection: from artificial intelligence to RNA microarrays
Author / Creator:Ahlgrimm-Siess, Verena ; Laimer, Martin ; Arzberger, Edith ; Hofmann-Wellenhof, Rainer
Publisher:England: Future Medicine Ltd
Journal title:Future oncology (London, England), 2012-07, Vol.8 (7), p.819-827
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Skin clues of systemic diseases
Author / Creator:Laimer, Martin ; Hintner, Helmut
Publisher:London: Taylor & Francis
Journal title:Expert review of dermatology, 2011-12, Vol.6 (6), p.559-561
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8th European Conference on Rare Diseases Orphan Products
Author / Creator:Schlander, Michael ; Holm, Saren ; Nord, Erik ; Richardson, Jeff ; Garattini, Silvio ; Kolominsky-Rabas, Peter ; Marshall, Deborah ; Persson, Ulf ; Postma, Maarten ; Simoens, Steven ; de Sola Morales, Oriol ; Tolley, Keith ; Toumi, Mondher ; Telser, Harry ; Bonham, James R ; Hintner, Helmut ; Diem, Anja ; Laimer, Martin ; Hnbert, Rnjean ; Dasgupta, Nabarun ; Pierce, Carrie E ; Jordan, Melissa ; Bori, Barbara ; Fors, Mohanad ; Prazakova, Emilie ; Day, Simon ; Croce, Thomas J ; Fransson, Jonas ; Wood, Philip ; Lauridsen, Anne-Grethe ; Higgs, Joanne ; Aleksovska, Vesna Stojmirova ; Olsen, Christina ; Head, Ritchie ; Asero, Antonio ; Papa, Vincenzo ; van Kan, Christa ; Favennec, Loic ; Venturella, Silvana ; Salvador, Michela ; Krol, Alan ; Nielsen, Stephanie J ; Holm, Birthe B ; Lewi, Daniel ; DurA£o, Patricia ; Band, Heather ; West, Andrea ; Hammann, Marinda J. A ; Effing-Boele, Marije C ; Dekker, Hanka K ; Hunter, Amy ; Simpson, Amy ; Liu, Gumei ; Needleman, Katherine ; Lewis, Debra ; Rao, Gayatri ; Whitaker, Martin J ; Castro, Raquel
Publisher:BioMed Central Ltd
Journal title:Orphanet journal of rare diseases, 2016-11, Vol.11 (Suppl 1), p.1-9
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8th European Conference on Rare Diseases & Orphan Products (ECRD 2016): Edinburgh, UK. 26-28 May 2016
Author / Creator:Schlander, Michael ; Holm, Søren ; Nord, Erik ; Richardson, Jeff ; Garattini, Silvio ; Kolominsky-Rabas, Peter ; Marshall, Deborah ; Persson, Ulf ; Postma, Maarten ; Simoens, Steven ; de Solà Morales, Oriol ; Tolley, Keith ; Toumi, Mondher ; Telser, Harry ; Bonham, James R ; Hintner, Helmut ; Diem, Anja ; Laimer, Martin ; Hébert, Réjean ; Dasgupta, Nabarun ; Pierce, Carrie E. ; Jordan, Melissa ; Bori, Barbara ; Fors, Mohanad ; Prazakova, Emilie ; Day, Simon ; Croce, Thomas J. ; Fransson, Jonas ; Wood, Philip ; Lauridsen, Anne-Grethe ; Higgs, Joanne ; Aleksovska, Vesna Stojmirova ; Olsen, Christina ; Head, Ritchie ; Asero, Antonio ; Papa, Vincenzo ; van Kan, Christa ; Favennec, Loic ; Venturella, Silvana ; Salvador, Michela ; Krol, Alan ; Nielsen, Stephanie J. ; Holm, Birthe B. ; Lewi, Daniel ; Durão, Patricia ; Band, Heather ; West, Andrea ; Hammann, Marinda J. A. ; Effing-Boele, Marije C. ; Dekker, Hanka K. ; Hunter, Amy ; Simpson, Amy ; Liu, Gumei ; Needleman, Katherine ; Lewis, Debra ; Rao, Gayatri ; Whitaker, Martin J. ; Castro, Raquel
Publisher:London: BioMed Central
Journal title:Orphanet journal of rare diseases, 2016-11, Vol.11 (S1), p.1-9, Article 143
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Analysis of the LAMB3 gene in a junctional epidermolysis bullosa patient reveals exonic splicing and allele-specific nonsense-mediated mRNA decay
Author / Creator:Buchroithner, Birgit ; Klausegger, Alfred ; Ebschner, Ulrike ; Anton-Lamprecht, Ingrun ; Pohla-Gubo, Gabriele ; Lanschuetzer, Christoph M ; Laimer, Martin ; Hintner, Helmut ; Bauer, Johann W
Publisher:New York: Elsevier Inc
Journal title:Laboratory investigation, 2004-10, Vol.84 (10), p.1279-1288
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ArticlesPeer ReviewedFull Text
Haploinsufficiency due to deletion within the 3′-UTR of C1-INH-gene associated with hereditary angioedema
Author / Creator:Laimer, Martin ; Klausegger, Alfred ; Aberer, Werner ; Oender, Kamil ; Wally, Verena ; Hintner, Helmut ; Bauer, Johann W. ; Lanschuetzer, Christoph M. ; Steinhuber, Mathias
Publisher:United States
Journal title:Genetics in medicine, 2006-04, Vol.8 (4), p.249-254
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Showing 1 to 20 of 22 results

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Small molecule drug development for rare genodermatoses – evaluation of the current status in epidermolysis bullosa

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Reflection on clinical and methodological issues in rare disease clinical trials

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Statistical recommendations for count, binary, and ordinal data in rare disease cross-over trials

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Impact of low-dose calcipotriol ointment on wound healing, pruritus and pain in patients with dystrophic epidermolysis bullosa: A randomized, double-blind, placebo-controlled trial

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Profiling trial burden and patients’ attitudes to improve clinical research in epidermolysis bullosa

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Human dirofilariosis in Austria: the past, the present, the future

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Recessive Dystrophic Epidermolysis bullosa due to Hemizygous 40 kb Deletion of COL7A1 and the Proximate PFKFB4 Gene Focusing on the Mutation c.425A>G Mimicking Homozygous Status

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A Novel Homozygous 9385 bp Deletion in the FERMT1 (KIND1) Gene in a Malaysian Family with Kindler Epidermolysis bullosa and a Review of Large Deletions

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COVID-19-Induced Reduction in Primary Melanoma Diagnoses: Experience from a Dermatopathology Referral Center

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Clinical Perspectives of Gene-Targeted Therapies for Epidermolysis Bullosa

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Low-dose calcipotriol can elicit wound closure, anti-microbial, and anti-neoplastic effects in epidermolysis bullosa keratinocytes

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A novel humanized mouse model to study the function of human cutaneous memory T cells in vivo in human skin

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Recessive Dystrophic IEpidermolysis bullosa/I due to Hemizygous 40 kb Deletion of ICOL7A1/I and the Proximate IPFKFB4/I Gene Focusing on the Mutation c.425AG Mimicking Homozygous Status

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Transcutaneous Gene Gun Delivery of hNC16A Induces BPAG2-Specific Tolerance

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New diagnostics for melanoma detection: from artificial intelligence to RNA microarrays

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Skin clues of systemic diseases

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8th European Conference on Rare Diseases Orphan Products

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8th European Conference on Rare Diseases & Orphan Products (ECRD 2016): Edinburgh, UK. 26-28 May 2016

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

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

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