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Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity

Journal of the European Academy of Dermatology and Venereology, 2022-01, Vol.36 (1), p.133-143

2022

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EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa

British journal of dermatology (1951), 2020-03, Vol.182 (3), p.794-797

2020

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Signatures mutationnelles des carcinomes épidermoïdes cutanés survenant chez les patients atteints d’épidermolyse bulleuse dystrophique récessive

Annales de dermatologie et de vénéréologie, 2020-12, Vol.147 (12), p.A142-A143

2020

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Marked intrafamilial phenotypic heterogeneity in dystrophic epidermolysis bullosa caused by inheritance of a mild dominant glycine substitution and a novel deep intronic recessive COL7A1 mutation

British journal of dermatology (1951), 2016-05, Vol.174 (5), p.1122-1125

2016

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Prurigo chronique des membres: penser à l’épidermolyse bulleuse dystrophique prurigineuse

Annales de dermatologie et de vénéréologie, 2019-12, Vol.146 (12), p.A115-A116

2019

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Immune reactivity to type VII collagen: implications for gene therapy of recessive dystrophic epidermolysis bullosa

Gene therapy, 2010-07, Vol.17 (7), p.930-937

2010

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Confirmation of RAX gene involvement in human anophthalmia

Clinical genetics, 2008-10, Vol.74 (4), p.392-395

2008

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Risque de carcinome épidermoïde cutané au cours de l’épidermolyse bulleuse héréditaire : faut-il surveiller aussi les formes simples de type Dowling-Meara ?

Annales de dermatologie et de vénéréologie, 2015-12, Vol.142 (12), p.S520-S521

2015

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844 Improvement of in vivo survival of mesenchymal stromal cells in immunodeficient mice

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S145-S145

2023

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807 Revertant mosaicism in the first case of recessive epidermolysis bullosa simplex caused by KRT5 mutations

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S137-S137

2018

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896 Exon skipping using palmitoyl conjugated tricyclo-DNA antisense oligonucleotides for recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2023-05, Vol.143 (5), p.S153-S153

2023

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290 Strategies to improve in vivo survival of Mesenchymal Stromal Cells after injection in immunodeficient mice

Journal of investigative dermatology, 2022-12, Vol.142 (12), p.S230-S230

2022

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490 Splice modulation as a therapeutic strategy applied to deep intronic mutations in COL7A1 causing recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S83

2022

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Spi-1/PU.1 transgenic mice develop multistep erythroleukemias

Molecular and Cellular Biology, 1996-05, Vol.16 (5), p.2453-2463

1996

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102 Citrullinated histone H3, a marker for neutrophil extracellular traps, is associated with poorer prognosis in recessive dystrophic epidermolysis bullosa patients with cutaneous squamous cell carcinoma

Journal of investigative dermatology, 2022-08, Vol.142 (8), p.S17

2022

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The mouse synemin gene encodes three intermediate filament proteins generated by alternative exon usage and different open reading frames

Experimental cell research, 2004-08, Vol.298 (2), p.431-444

2004

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The Mpl Receptor Is Expressed in the Megakaryocytic Lineage From Late Progenitors to Platelets

Blood, 1995-01, Vol.85 (2), p.391-401

1995

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183 Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity

Journal of investigative dermatology, 2021-10, Vol.141 (10), p.S179-S179

2021

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L’Elisa-collagène 7 (C7) sur la protéine entière (Elisa-C7 total) est plus sensible que celui sur les domaines NC1 et NC2 (Elisa-C7-NC1/NC2) pour le diagnostic d’épidermolyse bulleuse acquise (EBA)

Annales de dermatologie et de vénéréologie, 2013-12, Vol.140 (12), p.S383-S383

2013

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Diagnosis of Epidermolysis Bullosa Acquisita: Multicentre Comparison of Different Assays for Serum Anti-type VII Collagen Reactivity

Acta dermato-venereologica, 2021-03, Vol.101 (3), p.adv00420-adv00420

2021

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Lens cell targetting for gene therapy of prevention of posterior capsule opacification

Gene therapy, 2006-10, Vol.13 (19), p.1422-1429

2006

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237 Diagnostic challenge of compound heterozygosity for dominant and recessive COL7A1 mutations in dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2017-10, Vol.137 (10), p.S233-S233

2017

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425 Optimization of gentamicin therapy for recessive dystrophic epidermolysis bullosa patients harboring nonsense mutations

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S72-S72

2018

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809 Intradermal injection of bone marrow-MSC corrects recessive dystrophic epidermolysis bullosa in a xenograft model

Journal of investigative dermatology, 2018-05, Vol.138 (5), p.S137-S137

2018

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170 Bone marrow-derived MSCs show therapeutic potential for recessive dystrophic epidermolysis bullosa

Journal of investigative dermatology, 2016-09, Vol.136 (9), p.S190-S190

2016

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Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity

EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosa

Signatures mutationnelles des carcinomes épidermoïdes cutanés survenant chez les patients atteints d’épidermolyse bulleuse dystrophique récessive

Marked intrafamilial phenotypic heterogeneity in dystrophic epidermolysis bullosa caused by inheritance of a mild dominant glycine substitution and a novel deep intronic recessive COL7A1 mutation

Prurigo chronique des membres: penser à l’épidermolyse bulleuse dystrophique prurigineuse

Immune reactivity to type VII collagen: implications for gene therapy of recessive dystrophic epidermolysis bullosa

Confirmation of RAX gene involvement in human anophthalmia

Risque de carcinome épidermoïde cutané au cours de l’épidermolyse bulleuse héréditaire : faut-il surveiller aussi les formes simples de type Dowling-Meara ?

844 Improvement of in vivo survival of mesenchymal stromal cells in immunodeficient mice

807 Revertant mosaicism in the first case of recessive epidermolysis bullosa simplex caused by KRT5 mutations

896 Exon skipping using palmitoyl conjugated tricyclo-DNA antisense oligonucleotides for recessive dystrophic epidermolysis bullosa

290 Strategies to improve in vivo survival of Mesenchymal Stromal Cells after injection in immunodeficient mice

490 Splice modulation as a therapeutic strategy applied to deep intronic mutations in COL7A1 causing recessive dystrophic epidermolysis bullosa

Spi-1/PU.1 transgenic mice develop multistep erythroleukemias

102 Citrullinated histone H3, a marker for neutrophil extracellular traps, is associated with poorer prognosis in recessive dystrophic epidermolysis bullosa patients with cutaneous squamous cell carcinoma

The mouse synemin gene encodes three intermediate filament proteins generated by alternative exon usage and different open reading frames

The Mpl Receptor Is Expressed in the Megakaryocytic Lineage From Late Progenitors to Platelets

183 Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunity

L’Elisa-collagène 7 (C7) sur la protéine entière (Elisa-C7 total) est plus sensible que celui sur les domaines NC1 et NC2 (Elisa-C7-NC1/NC2) pour le diagnostic d’épidermolyse bulleuse acquise (EBA)

Diagnosis of Epidermolysis Bullosa Acquisita: Multicentre Comparison of Different Assays for Serum Anti-type VII Collagen Reactivity

Lens cell targetting for gene therapy of prevention of posterior capsule opacification

237 Diagnostic challenge of compound heterozygosity for dominant and recessive COL7A1 mutations in dystrophic epidermolysis bullosa

425 Optimization of gentamicin therapy for recessive dystrophic epidermolysis bullosa patients harboring nonsense mutations

809 Intradermal injection of bone marrow-MSC corrects recessive dystrophic epidermolysis bullosa in a xenograft model

170 Bone marrow-derived MSCs show therapeutic potential for recessive dystrophic epidermolysis bullosa

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