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Scientific Day on 10th March 2022 (from 9h AM to 2 PM)
Part1 on Bibliography for all thematic Groups
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time slotSubjecttiming1st publication2nd publi3rd publi
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minspeakerspeakerspeaker
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9hIntroduction5
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9h05 - 9h20Toxiten15Saskia OroSaskia OroBenoit Bensaid
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JAMA Dermatol . 2022 Feb 1;158(2):160-166.
Improvement of Mortality Prognostication in Patients with Epidermal Necrolysis : The Role of Novel Inflammatory Markers and Proposed Revision of SCORTEN (Re-SCORTEN). Hui Kai Koh et al

https://pubmed.ncbi.nlm.nih.gov/34935871/		JAAD Case Rep. 2022 Jan 7.
Erythema multiforme reactions after Pfizer/ BioNTech (BNT162b2) and Moderna
Q1 (mRNA-1273) COVID-19 vaccination: A case series. Karatas et al

https://pubmed.ncbi.nlm.nih.gov/35097177/		Sci Adv. 2021 Mar 19;7(12) : eabe 0013.
Massive clonal expansion of polycytotoxic skin and blood CD8+ T cells in patients with toxic epidermal necrolysis. Villani et al

https://pubmed.ncbi.nlm.nih.gov/33741590/
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9h20-9h35Allocate15Gregor JemecAngelo Marzano (Prof)Christos Zouboulis
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tbc(on "Current data on syndromic HS")

Dermatology. 2022 Jan 14;1-10.
Whole-Exome Sequencing in 10 Unrelated Patients with Syndromic Hidradenitis Suppurativa: A Preliminary Step for a Genotype-Phenotype Correlation. Marzano AV et al

https://pubmed.ncbi.nlm.nih.gov/35034021/
(on Atrophic Papulosis)

StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing
Malignant Atrophic Papulosis, Rice et al
Last Update: August 11, 2021

https://www.ncbi.nlm.nih.gov/books/NBK544329/
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9h35- 9h50DNA15Kevin KoschitzkiFanny Morice-PicardFanny Morice-Picard
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Photochem Photobiol. 2022 Jan 20. Research Article
Improved Spectral Purity of 222-nm Irradiation Eliminates Detectable Cyclobutylpyrimidine Dimers Formation in Skin Reconstructs even at High and Repetitive Disinfecting Doses. Ivanova et al

https://onlinelibrary.wiley.com/doi/epdf/10.1111/php.13594
Genet Med. 2021 Mar;23(3):479-487.
Dopachrome tautomerase variants in patients with oculocutaneous albinism.
Pennamen et al

https://pubmed.ncbi.nlm.nih.gov/33100333/		Genet Med. 2020 Oct;22(10):1613-1622
BLOC1S5 pathogenic variants cause a new type of Hermansky-Pudlak syndrome.
Pennamen et al

https://pubmed.ncbi.nlm.nih.gov/32565547/

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9h50 - 10h05EB15Cristina HasRoland ZaunerMarjon Pasmooij
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J Invest Dermatol . 2022 Feb 8;S0022-202X(22)00090-2.
Predominance of Staphylococcus correlates with wound burden and disease activity in dystrophic epidermolysis bullosa: a prospective case-control study. Reimer-Taschenbrecker et al

https://pubmed.ncbi.nlm.nih.gov/35149000/

Int J Mol Sci. 2022 Jan 17;23(2):1007.
Transcriptome-Guided Drug Repurposing for Aggressive SCCs. Zauner R et al

https://pubmed.ncbi.nlm.nih.gov/35055192/		J Invest Dermatol. 2021 Nov 26;S0022-202X(21)02584-7.
Natural Occurrence of Autoantibodies against Basement Membrane Proteins in Epidermolysis Bullosa. Gostyński et al

https://pubmed.ncbi.nlm.nih.gov/34843678/
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10h05 - 10h20ED15Nicolai Peschel (flexible for time slot)Holm Schneider Smail Hadj-Rabia
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Am J Med Genet A. 2021 Aug;185(8):2417-2433.
TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study. Bowles et al

https://pubmed.ncbi.nlm.nih.gov/34042254/		Orphanet J Rare Dis. 2021 Sep 3;16(1):373.
Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia. Hennig et al

https://pubmed.ncbi.nlm.nih.gov/34479575/		J Med Genet. 2021 Jun;58(6):415-421.
Telangiectasia-ectodermal dysplasia-brachydactyly-cardiac anomaly syndrome is caused by de novo mutations in protein kinase D1. Alter et al

https://pubmed.ncbi.nlm.nih.gov/32817298/
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10h20 - 10h35IPPK15Edwin Cuperus - Suzanne PasmansJuliette MazereeuwKathrin Giehl
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J Eur Acad Dermatol Venereol. 2022 Mar 3.
Proposal for a 6-step-approach for differential diagnosis of neonatal erythroderma. E Cuperus et al

https://pubmed.ncbi.nlm.nih.gov/35238435/		JAMA Dermatol . 2022 Feb 16;e215917. .
Development and Initial Validation of a Novel System to Assess Ichthyosis Severity. Sun et al

https://pubmed.ncbi.nlm.nih.gov/35171201/		J Allergy Clin Immunol. 2022 Feb 23;S0091-6749(22)00228-7.
Understanding immune profiles in ichthyosis may lead to novel therapeutic targets. Masashi Akiyama
https://pubmed.ncbi.nlm.nih.gov/35218769//
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10h35 - 10h50pause 15 min
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10h50 - 11h05AIBD15Matthias GoebelerMatthias GoebelerMatthias Goebeler
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N Engl J Med. 2021 Jun 17;384(24):2295-2305.
Rituximab versus Mycophenolate Mofetil in Patients with Pemphigus Vulgaris. Werth et al

https://pubmed.ncbi.nlm.nih.gov/34097368/		Br J Dermatol. 2021 Oct 5.
Treatment of pemphigus vulgaris and foliaceus with efgartigimod, a neonatal Fc receptor inhibitor: a phase II multicentre, open-label feasibility trial. Goebeler et al

https://pubmed.ncbi.nlm.nih.gov/34608631/
J Clin Invest. 2020;130(12):6317-6324.
Antigen-specific B cell depletion for precision therapy of mucosal pemphigus vulgaris. Jinmin Lee et al

https://www.jci.org/articles/view/138416/pdf
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11h05- 11h20MOSAIC15Eulalia Baselga TorresClaire van Eijsden - Suzanne PasmansOlivia Boccara
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Europ Journal of dermato, 2021 Dec,1;31(6): 785-790.
Saquelae following infantile haemangiomas treated with popanodol Baselga et al

https://pubmed.ncbi.nlm.nih.gov/35107070/		Br J Dermatol . 2021 Aug;185(2):371-379.
Development of an international core domain set for medium, large and giant congenital melanocytic naevi as a first step towards a core outcome set for clinical practice and research. Oei et al
https://pubmed.ncbi.nlm.nih.gov/33237568/

J Eur Acad Dermatol Venereol. 2020 Feb;34(2):267-273.
Protocol for the development of core set of domains of the core outcome set for patients with congenital melanocytic naevi (OCOMEN project). Oei et al
https://pubmed.ncbi.nlm.nih.gov/31419337/

Br J Dermatol . 2021 Nov;185(5):970-977.
Domains and outcomes of the core outcome set of congenital melanocytic naevi for clinical practice and research (the OCOMEN project): part 2. Fledderus et al
https://pubmed.ncbi.nlm.nih.gov/33959942/		J Am Acad Dermatol 2021 Dec 24;S0190-9622(21)02996-0.
Central nervous system screening in capillary malformation-arteriovenous malformation syndrome: An observational study. Boccara et al

https://pubmed.ncbi.nlm.nih.gov/34954287/
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11h20 - 11h35MCTD15Bert CallewaertJessica Warnink-KavelaarsJessica Warnink-Kavelaars
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Am J Hum Genet. 2021 Jun 3;108(6):1095-1114.
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome. Pottie et al
(illustration of the potential of the use of zebrafish for skin disorders)

https://pubmed.ncbi.nlm.nih.gov/33991472/		Genes 2021, 12(6), 831;
Heritable Connective Tissue Disorders in Childhood: Increased Fatigue, Pain, Disability and Decreased General Health. Warnink-Kavelaars et al

https://www.mdpi.com/2073-4425/12/6/831		Heritable Connective Tissue Disorders in Childhood: Decreased Health Related Quality of Life and Mental Health. Warnink-Kavelaars et al

Link tbc
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