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E Bourrat

Showing results (61-70 of 91) with videos related to

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The British Journal of Dermatology|October 25, 2019
Severe early-onset manifestations of pseudoxanthoma elasticum resulting from the cumulative effects of several deleterious mutations in ENPP1, ABCC6 and HBB: transient improvement in ectopic calcification with sodium thiosulfateL Omarjee, Y Nitschke, S Verschuere, et al.
The British Journal of Dermatology|December 24, 2018
Naevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal naevus) and mosaic FGFR3 and FGFR2 mutationsD Bessis, A Petit, M Battistella, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 25, 2014
[Superficial skin infections and bacterial dermohypodermitis]M Lorrot, E Bourrat, C Doit, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 20, 2021
Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunityD Darbord, G Hickman, N Pironon, et al.
The British Journal of Dermatology|July 7, 2011
Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosisC Bodemer, E Bourrat, J Mazereeuw-Hautier, et al.
The British Journal of Dermatology|March 25, 2011
Palmoplantar keratodermas in black patients (Fitzpatrick skin phototype V-VI) of African descent: a multicentre comparative and descriptive seriesE Bourrat, P-P Cabotin, M Baccard, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
The British Journal of Dermatology|September 27, 2019
EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosaS Gaucher, S M Lwin, M Titeux, et al.
The British Journal of Dermatology|September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosisA Hotz, C Fagerberg, A Vahlquist, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 15, 2019
French expert opinion for the management of juvenile dermatomyositisB Bader-Meunier, C Gitiaux, A Belot, et al.
Pageof 10

Showing results (61-70 of 91) with videos related to

Sort By:
Pageof 10
The British Journal of Dermatology|October 25, 2019
Severe early-onset manifestations of pseudoxanthoma elasticum resulting from the cumulative effects of several deleterious mutations in ENPP1, ABCC6 and HBB: transient improvement in ectopic calcification with sodium thiosulfateL Omarjee, Y Nitschke, S Verschuere, et al.
The British Journal of Dermatology|December 24, 2018
Naevoid acanthosis nigricans or RAVEN (rounded and velvety epidermal naevus) and mosaic FGFR3 and FGFR2 mutationsD Bessis, A Petit, M Battistella, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 25, 2014
[Superficial skin infections and bacterial dermohypodermitis]M Lorrot, E Bourrat, C Doit, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 20, 2021
Dystrophic epidermolysis bullosa pruriginosa: a new case series of a rare phenotype unveils skewed Th2 immunityD Darbord, G Hickman, N Pironon, et al.
The British Journal of Dermatology|July 7, 2011
Short- and medium-term efficacy of specific hydrotherapy in inherited ichthyosisC Bodemer, E Bourrat, J Mazereeuw-Hautier, et al.
The British Journal of Dermatology|March 25, 2011
Palmoplantar keratodermas in black patients (Fitzpatrick skin phototype V-VI) of African descent: a multicentre comparative and descriptive seriesE Bourrat, P-P Cabotin, M Baccard, et al.
The British Journal of Dermatology|January 3, 2013
Unexpected extradermatological findings in 31 patients with xeroderma pigmentosum type CS Hadj-Rabia, D Oriot, N Soufir, et al.
The British Journal of Dermatology|September 27, 2019
EBGene trial: patient preselection outcomes for the European GENEGRAFT ex vivo phase I/II gene therapy trial for recessive dystrophic epidermolysis bullosaS Gaucher, S M Lwin, M Titeux, et al.
The British Journal of Dermatology|September 15, 2017
Identification of mutations in SDR9C7 in six families with autosomal recessive congenital ichthyosisA Hotz, C Fagerberg, A Vahlquist, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 15, 2019
French expert opinion for the management of juvenile dermatomyositisB Bader-Meunier, C Gitiaux, A Belot, et al.
Pageof 10